Analyses account 8 missing species | |||||||||||||||||||
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−0 | −0 | K0 | −1 | −1 | K1 | t_shift | log-LH | Akaike weight | −0 | −0 | K0 | −1 | −1 | K1 | t_shift | log-LH | Akaike weight | ||
Calisto diversification | |||||||||||||||||||
CR0 | constant λ and μ (birth-death) | 0.07 | 0 | - | - | - | - | - | −124.437 | 0.00 | 0.08 | 0 | - | - | - | - | - | −123.853 | 0.00 |
CR1 | − declining as div-dep. No μ (DDL) | 0.175 | - | 40.119 | - | - | - | - | −118.715 | 0.03 | - | - | - | - | - | - | - | - | - |
CR2 | div-dep with μ (DDL + E) depend in λ | 0.163 | 0 | 43.055 | - | - | - | - | −118.926 | 0.01 | 0.163 | 0 | 54.745 | - | - | - | - | −118.774 | 0.02 |
SR0 | Yule-2-rate | 0.122 | - | 36.641 | 0.3 | - | K0 | 13.567 | −116.243 | 0.12 | 0.122 | - | 45.321 | 0.298 | - | K1 | 13.567 | −116.487 | 0.16 |
*SR1 | shift in K | 0.306 | 0 | 13.132 | λ 0 | μ 0 | 36.62 | 13.567 | −113.877 | 0.48 | 0.295 | 0 | 14.456 | λ 0 | μ 0 | 45.466 | 13.567 | −114.384 | 0.47 |
SR2 | shift in K and μ | 0.306 | 0 | 13.13 | −0 | 0 | 36.617 | 13.567 | −113.878 | 0.18 | 0.3 | 0.006 | 14.342 | −0 | 0 | 45.355 | 13.567 | −114.369 | 0.18 |
SR3 | shift in K and λ | 0.322 | 0 | 13.025 | 0.298 | −0 | 36.713 | 13.567 | −113.863 | 0.18 | 0.289 | 0 | 14.507 | 0.298 | −0 | 45.414 | 13.567 | −114.382 | 0.17 |
KI1 | shift in K in subclade | 0.133 | 0 | 27.172 | −0 | −0 | Inf. | 13.567 | −118.634 | 0.00 | 0.139 | 0 | 37.103 | −0 | −0 | Inf. | 13.567 | −121.355 | 0.00 |
KI2 | shift in K and μ in subclade | 0.133 | 0 | 27.159 | −0 | 0 | Inf. | 13.567 | −118.651 | 0.00 | 0.139 | 0 | 36.965 | −0 | 0 | Inf. | 13.567 | −121.371 | 0.00 |
KI3 | shift in K and λ in subclade | 0.164 | 0 | 25.591 | 0.115 | −0 | Inf. | 13.567 | −118.319 | 0.00 | 0.17 | 0 | 34.419 | 0.114 | −0 | Inf. | 13.567 | −120.853 | 0.00 |
KI4 | shift in K, λ and μ in subclade | 0.162 | 0 | 25.779 | 0.111 | 0 | Inf. | 13.567 | −118.302 | 0.00 | 0.17 | 0 | 34.434 | 0.114 | 0 | Inf. | 13.567 | −120.852 | 0.00 |
Hispaniolan lineages diversification | |||||||||||||||||||
CR0 | constant λ and μ (birth-death) | 0.056 | 0 | - | - | - | - | - | −85.5 | 0.00 | 0.066 | 0 | - | - | - | - | - | −84.936 | 0.00 |
CR1 | − declining as div-dep. No μ (DDL) | 0.186 | - | 24.646 | - | - | - | - | −78.905 | 0.19 | - | - | - | - | - | - | - | - | - |
CR2 | div-dep with μ (DDL + E) depend in λ | 0.165 | 0 | 26.665 | - | - | - | - | −80.231 | 0.02 | 0.166 | 0 | 36.387 | - | - | - | - | −79.968 | 0.04 |
SR0 | Yule-2-rate | 0.141 | - | 24 | 0.335 | - | K0 | 12.843 | −77.021 | 0.17 | 0.141 | - | 32 | 0.347 | - | K1 | 12.843 | −77.219 | 0.20 |
*SR1 | shift in K | 0.33 | 0.001 | 11.991 | λ 0 | μ 0 | 23.918 | 14.352 | −75.372 | 0.32 | 0.339 | 0.001 | 15.518 | λ 0 | μ 0 | 31.942 | 12.843 | −75.477 | 0.42 |
SR2 | shift in K and μ | 0.318 | 0.001 | 11.964 | −0 | 0 | 24 | 14.352 | −75.219 | 0.14 | 0.327 | 0 | 15.593 | −0 | 0 | 32.023 | 12.844 | −75.427 | 0.16 |
SR3 | shift in K and λ | 0.333 | 0 | 12.98 | 0.245 | −0 | 24.135 | 12.843 | −75.09 | 0.16 | 0.295 | 0.001 | 15.743 | 0.355 | −0 | 31.948 | 12.843 | −75.372 | 0.17 |
Cuban lineage diversification | |||||||||||||||||||
CR0 | constant λ and μ (birth-death) | 0.09 | 0 | - | - | - | - | - | −40.903 | 0.01 | - | - | - | - | - | - | - | - | - |
CR1 | − declining as div-dep. No μ (DDL) | 0.27 | - | 14.568 | - | - | - | - | −38.31 | 0.14 | - | - | - | - | - | - | - | - | - |
CR2 | div-dep with μ (DDL + E) depend in λ | 0.219 | 0 | 17.498 | - | - | - | - | −39.235 | 0.02 | - | - | - | - | - | - | - | - | - |
*SR0 | Yule-2-rate | 0.099 | - | 14 | 0.493 | - | K 0 | 10.475 | −35.409 | 0.35 | - | - | - | - | - | - | - | - | - |
SR1 | shift in K | 0.502 | 0.012 | 2.323 | −0 | −0 | 13.644 | 11.894 | −35.377 | 0.13 | - | - | - | - | - | - | - | - | - |
*SR2 | shift in K and λ | 0.426 | 0.024 | 1.864 | λ 0 | 0 | 13.982 | 13.567 | −33.981 | 0.20 | - | - | - | - | - | - | - | - | - |
SR3 | shift in K and λ | 0.162 | 0.009 | 1.884 | 0.466 | −0 | 13.718 | 13.573 | −34.287 | 0.15 | - | - | - | - | - | - | - | - | - |