@ARTICLE{TreeBASE2Ref23506,
author = {P?vel Matos-Marav? and Rayner N??ez ?guila and Carlos Pe?a and Jacqueline Y. Miller and Andrei Sourakov and Niklas Wahlberg},
title = {Causes of endemic radiation in the Caribbean: evidence from the historical biogeography and diversification of the butterfly genus Calisto (Nymphalidae: Satyrinae: Satyrini)},
year = {2014},
keywords = {Caribbean, ecological limits, historical biogeography, intra-island diversification, island-island vicariance, Lepidoptera, molecular phylogeny},
doi = {10.1186/s12862-014-0199-7},
url = {http://www.biomedcentral.com/1471-2148/14/199},
pmid = {25220489},
journal = {BMC Evolutionary Biology},
volume = {14},
number = {},
pages = {199},
abstract = {Background
Calisto is the largest butterfly genus in the West Indies but its systematics, historical biogeography and the causes of its diversification have not been rigorously evaluated previously. Several studies attempting to explain Calisto diversity gave different weights to vicariance, dispersal and adaptive radiation. We utilized molecular phylogenetic approaches and secondary calibrations points to estimate lineage ages. We used the dispersal-extinction-cladogenesis model and the Caribbean paleogeographical information to reconstruct ancestral geographical distributions. We also evaluated different models of diversification to estimate the dynamics of lineage radiation within Calisto. By understanding the evolution of Calisto butterflies, we attempt to identify the main processes acting on insular insect diversity, the causes of its origin and maintenance.
Results
The crown age of the genus was estimated to the early Oligocene (31 ? 5 Ma), and one shift in diversification rate following a diversity-dependent process was the best explanation for its extant diversity assemblage. A major increase in diversification rate was recovered at 14 Ma, right after the geological arrangements that favoured the availability of empty niches. Inferred ancestral distributional ranges suggested that the origin of extant Calisto is in agreement with a vicariant model and the origin of the Cuban lineage was likely the result of the Cuba-Hispaniola split vicariance. Long-distance dispersal is supported for the colonization of Jamaica and the Bahamas.
Conclusions
The ancestral geographical distribution of Calisto is in line with the paleogeographical model of Caribbean colonization which favours island-island vicariance. Because the sister lineage of Calisto remains ambiguous, its arrival to the West Indies remains to be elucidated, although, given its age and historical biogeography, the hypothesized land bridge GAARlandia might have been a plausible introduction route from continental America. Intra-island radiation caused by ecological innovation and abiotic creation of niche spaces was found to be the main force shaping Calisto diversity and island endemism in Hispaniola and Cuba.
}
}
Taxa for matrix 23604 of Study 16186

Citation title:
"Causes of endemic radiation in the Caribbean: evidence from the historical biogeography and diversification of the butterfly genus Calisto (Nymphalidae: Satyrinae: Satyrini)".

Study name:
"Causes of endemic radiation in the Caribbean: evidence from the historical biogeography and diversification of the butterfly genus Calisto (Nymphalidae: Satyrinae: Satyrini)".

This study is part of submission 16186
(Status: Published).
Taxa
Return to matrix row view
| ID |
Taxon Label |
NCBI taxid |
uBIO namebankID |
| 1574960 |
Brintesia circe CP B01 |
111891
|
2961948
|
| 1574986 |
Calisto arcas CP19 01 |
|
7633738
|
| 1574975 |
Calisto arcas CP20 04 |
|
7633738
|
| 1574984 |
Calisto arcas NW149 16 |
|
7633738
|
| 1574995 |
Calisto archebates RN02 14 |
|
6837010
|
| 1574980 |
Calisto batesi RN03 02 |
|
6195002
|
| 1574946 |
Calisto bradleyi PM07 24 |
|
7633780
|
| 1574973 |
Calisto bradleyi PM07 25 |
|
7633780
|
| 1574925 |
Calisto bradleyi PM07 26 |
|
7633780
|
| 1574996 |
Calisto brochei PM07 03 |
|
|
| 1574948 |
Calisto brochei PM20 04 |
|
|
| 1575003 |
Calisto brochei PM20 05 |
|
|
| 1574935 |
Calisto bruneri PM07 15 |
|
|
| 1574983 |
Calisto bruneri PM07 16 |
|
|
| 1574997 |
Calisto bruneri PM07 17 |
|
|
| 1575005 |
Calisto bruneri PM07 21 |
|
|
| 1574924 |
Calisto chrysaoros RN04 01 |
|
7633745
|
| 1574988 |
Calisto clenchi RN06 01 |
|
6786082
|
| 1574974 |
Calisto clydoniata RN02 16 |
|
6786083
|
| 1575000 |
Calisto confusa DR016 |
|
3386680
|
| 1574930 |
Calisto confusa DR032 |
|
3386680
|
| 1574982 |
Calisto crypta CP19 05 |
|
6701422
|
| 1574981 |
Calisto crypta CP20 01 |
|
6701422
|
| 1574945 |
Calisto crypta CP20 02 |
|
6701422
|
| 1574959 |
Calisto crypta CP20 03 |
|
6701422
|
| 1574969 |
Calisto crypta NW149 17 |
|
6701422
|
| 1574922 |
Calisto debarriera DR019 |
|
7633747
|
| 1574920 |
Calisto eleleus CP19 06 |
|
7633749
|
| 1574951 |
Calisto eleleus RN03 01 |
|
7633749
|
| 1574991 |
Calisto franciscoi CP19 14 |
|
6701423
|
| 1574992 |
Calisto galii DR017 |
|
6837011
|
| 1574947 |
Calisto galii RN02 17 |
|
6837011
|
| 1574965 |
Calisto grannus CP19 08 |
|
6255543
|
| 1574989 |
Calisto grannus NW149 15 |
|
6255543
|
| 1574990 |
Calisto grannus RN06 02 |
|
6255543
|
| 1574938 |
Calisto grannus RN06 03 |
|
6255543
|
| 1574976 |
Calisto herophile PM07 07 |
|
3386681
|
| 1574970 |
Calisto herophile PM07 12 |
|
3386681
|
| 1575007 |
Calisto herophile PM07 22 |
|
3386681
|
| 1574941 |
Calisto herophile PM15 06 |
|
3386681
|
| 1575001 |
Calisto herophile PM20 06 |
|
3386681
|
| 1574936 |
Calisto herophile RN02 25 |
|
3386681
|
| 1574926 |
Calisto herophile RN02 26 |
|
3386681
|
| 1575006 |
Calisto hysius CP20 11 |
|
6058493
|
| 1574923 |
Calisto hysius RN04 02 |
|
6058493
|
| 1574929 |
Calisto israeli PM07 01 |
|
|
| 1575002 |
Calisto israeli PM07 02 |
|
|
| 1575004 |
Calisto loxias RN02 18 |
|
7633760
|
| 1574957 |
Calisto lyceius DR075 |
|
7633762
|
| 1574999 |
Calisto lyceius DR081 |
|
7633762
|
| 1574964 |
Calisto muripetens PM07 08 |
|
7633784
|
| 1574917 |
Calisto muripetens RN01 04 |
|
7633784
|
| 1574919 |
Calisto muripetens RN01 05 |
|
7633784
|
| 1574928 |
Calisto nubila CP19 10 |
|
3386682
|
| 1574968 |
Calisto nubila PR 1 3 |
|
3386682
|
| 1574956 |
Calisto obscura DR005 |
681776
|
3386683
|
| 1574921 |
Calisto obscura DR080 |
681776
|
3386683
|
| 1574932 |
Calisto obscura NW149 12 |
681776
|
3386683
|
| 1574931 |
Calisto obscura NW150 1 |
681776
|
3386683
|
| 1574942 |
Calisto obscura NW150 2 |
681776
|
3386683
|
| 1574994 |
Calisto obscura RN06 04 |
681776
|
3386683
|
| 1574985 |
Calisto occulta PM07 04 |
|
|
| 1574916 |
Calisto occulta PM07 10 |
|
|
| 1574962 |
Calisto occulta PM07 18 |
|
|
| 1574993 |
Calisto occulta PM07 19 |
|
|
| 1574940 |
Calisto occulta PM07 23 |
|
|
| 1574950 |
Calisto pulchella DR003 |
669534
|
6734208
|
| 1574987 |
Calisto pulchella DR015 |
669534
|
6734208
|
| 1574927 |
Calisto raburni CAL Sat102 |
|
6701427
|
| 1574998 |
Calisto schwartzi DR059 |
|
6701428
|
| 1574954 |
Calisto schwartzi DR063 |
|
6701428
|
| 1574934 |
Calisto sibylla RN02 22 |
|
7633786
|
| 1574967 |
Calisto sibylla RN02 23 |
|
7633786
|
| 1574939 |
Calisto smintheus PM07 05 |
|
7633778
|
| 1574966 |
Calisto smintheus PM07 09 |
|
7633778
|
| 1574955 |
Calisto smintheus PM07 13 |
|
7633778
|
| 1574933 |
Calisto smintheus PM07 14 |
|
7633778
|
| 1574953 |
Calisto sommeri CP19 11 |
|
6195008
|
| 1574944 |
Calisto sp PM07 06 |
|
|
| 1574978 |
Calisto tasajera CP20 07 |
|
6305142
|
| 1574949 |
Calisto tasajera CP20 08 |
|
6305142
|
| 1574961 |
Calisto zangis RN02 12 |
|
3386684
|
| 1574943 |
Cyllopsis pertepida NW165 3 |
366046
|
2605364
|
| 1574972 |
Erebia oeme EW24 7 |
242259
|
2973611
|
| 1574977 |
Eretris CP04 62 |
|
|
| 1574952 |
Euptychia spn2 CP01 33 |
|
|
| 1574937 |
Manerebia cyclopina CP03 63 |
366106
|
2963135
|
| 1574958 |
Maniola jurtina EW4 5 |
191418
|
2969036
|
| 1574979 |
Melanargia galathea EW24 17 |
111923
|
2966507
|
| 1574918 |
Pararge aegeria EW1 1 |
116150
|
2957239
|
| 1574971 |
Pronophila thelebe CP03 70 |
366166
|
2980142
|
| 1574963 |
Steremnia umbracina CP07 89 |
366184
|
7646183
|
| 1575008 |
Taygetis virgilia NW108 3 |
270093
|
2981719
|