Phylogeny of Aphantochilinae and Strophiinae sensu Simon (Araneae; Thomisidae)
This study tests the monophyly of ant‐mimicking Thomisidae (Aphantochilinae and Strophiinae sensu Simon), redefines the composition of these taxa, proposes tribes and discusses aspects of their myrmecomorphy and biogeography. The analysis is based on a matrix composed of 113 morphological characters...
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| Published in: | Zoologica scripta Vol. 43; no. 1; pp. 65 - 78 |
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| Format: | Journal Article |
| Language: | English |
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01-01-2014
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| Abstract | This study tests the monophyly of ant‐mimicking Thomisidae (Aphantochilinae and Strophiinae sensu Simon), redefines the composition of these taxa, proposes tribes and discusses aspects of their myrmecomorphy and biogeography. The analysis is based on a matrix composed of 113 morphological characters and 37 terminal taxa (11 Aphantochilinae, 16 Strophiinae and 10 belonging to the out‐group). The 12 most parsimonious trees with 232 steps, obtained with equally weighted characters, support the monophyly of Aphantochilinae sensu Simon. Strophiinae emerges as a paraphyletic group divided into two clades: a basal clade that groups Strophius and Strigoplus (Strophiini new status) and another clade that includes Ceraarachne, Simorcus and Ulocymus (Ceraarachnini new status) as the sister group of Aphantochilus + Bucranium (Aphantochilini new status). Diagnoses are presented for the tribes and genera in this analysis. The synonymy between Bucranium and Aphantochilus is rejected. Majellula and Acracanthostoma are considered junior synonyms of Bucranium, and Synstrophius of Ceraarachne. The monophyly of Synstrophius is not recovered, S. blanci is transferred to Ceraarachne and S. muricatus is transferred to Ulocymus. Ant‐preying behaviour appears to be basal and has been documented for Strophiini and Aphantochilini species. Myrmecomorphy, which was documented for Aphantochilus, is presumably derived. The biogeographical analysis of Aphantochilinae and Strophiinae suggests an ancient relation between Neotropical, Afrotropical and Oriental species, with probable origin after the breakup of Gondwana, that is, in early Paleogene. |
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| AbstractList | This study tests the monophyly of ant‐mimicking Thomisidae (Aphantochilinae and Strophiinae
sensu
Simon), redefines the composition of these taxa, proposes tribes and discusses aspects of their myrmecomorphy and biogeography. The analysis is based on a matrix composed of 113 morphological characters and 37 terminal taxa (11 Aphantochilinae, 16 Strophiinae and 10 belonging to the out‐group). The 12 most parsimonious trees with 232 steps, obtained with equally weighted characters, support the monophyly of Aphantochilinae
sensu
Simon. Strophiinae emerges as a paraphyletic group divided into two clades: a basal clade that groups
Strophius
and
Strigoplus
(Strophiini new status) and another clade that includes
Ceraarachne
,
Simorcus
and
Ulocymus
(Ceraarachnini new status) as the sister group of
Aphantochilus
+
Bucranium
(Aphantochilini new status). Diagnoses are presented for the tribes and genera in this analysis. The synonymy between
Bucranium
and
Aphantochilus
is rejected
. Majellula
and
Acracanthostoma
are considered junior synonyms of
Bucranium
, and
Synstrophius
of
Ceraarachne
. The monophyly of
Synstrophius
is not recovered,
S. blanci
is transferred to
Ceraarachne
and
S. muricatus
is transferred to
Ulocymus
. Ant‐preying behaviour appears to be basal and has been documented for Strophiini and Aphantochilini species. Myrmecomorphy, which was documented for
Aphantochilus
, is presumably derived. The biogeographical analysis of Aphantochilinae and Strophiinae suggests an ancient relation between Neotropical, Afrotropical and Oriental species, with probable origin after the breakup of Gondwana, that is, in early Paleogene. This study tests the monophyly of ant-mimicking Thomisidae (Aphantochilinae and Strophiinae sensu Simon), redefines the composition of these taxa, proposes tribes and discusses aspects of their myrmecomorphy and biogeography. The analysis is based on a matrix composed of 113 morphological characters and 37 terminal taxa (11 Aphantochilinae, 16 Strophiinae and 10 belonging to the out-group). The 12 most parsimonious trees with 232 steps, obtained with equally weighted characters, support the monophyly of Aphantochilinae sensu Simon. Strophiinae emerges as a paraphyletic group divided into two clades: a basal clade that groups Strophius and Strigoplus (Strophiini new status) and another clade that includes Ceraarachne, Simorcus and Ulocymus (Ceraarachnini new status) as the sister group of Aphantochilus + Bucranium (Aphantochilini new status). Diagnoses are presented for the tribes and genera in this analysis. The synonymy between Bucranium and Aphantochilus is rejected. Majellula and Acracanthostoma are considered junior synonyms of Bucranium, and Synstrophius of Ceraarachne. The monophyly of Synstrophius is not recovered, S. blanci is transferred to Ceraarachne and S. muricatus is transferred to Ulocymus. Ant-preying behaviour appears to be basal and has been documented for Strophiini and Aphantochilini species. Myrmecomorphy, which was documented for Aphantochilus, is presumably derived. The biogeographical analysis of Aphantochilinae and Strophiinae suggests an ancient relation between Neotropical, Afrotropical and Oriental species, with probable origin after the breakup of Gondwana, that is, in early Paleogene. This study tests the monophyly of ant‐mimicking Thomisidae (Aphantochilinae and Strophiinae sensu Simon), redefines the composition of these taxa, proposes tribes and discusses aspects of their myrmecomorphy and biogeography. The analysis is based on a matrix composed of 113 morphological characters and 37 terminal taxa (11 Aphantochilinae, 16 Strophiinae and 10 belonging to the out‐group). The 12 most parsimonious trees with 232 steps, obtained with equally weighted characters, support the monophyly of Aphantochilinae sensu Simon. Strophiinae emerges as a paraphyletic group divided into two clades: a basal clade that groups Strophius and Strigoplus (Strophiini new status) and another clade that includes Ceraarachne, Simorcus and Ulocymus (Ceraarachnini new status) as the sister group of Aphantochilus + Bucranium (Aphantochilini new status). Diagnoses are presented for the tribes and genera in this analysis. The synonymy between Bucranium and Aphantochilus is rejected. Majellula and Acracanthostoma are considered junior synonyms of Bucranium, and Synstrophius of Ceraarachne. The monophyly of Synstrophius is not recovered, S. blanci is transferred to Ceraarachne and S. muricatus is transferred to Ulocymus. Ant‐preying behaviour appears to be basal and has been documented for Strophiini and Aphantochilini species. Myrmecomorphy, which was documented for Aphantochilus, is presumably derived. The biogeographical analysis of Aphantochilinae and Strophiinae suggests an ancient relation between Neotropical, Afrotropical and Oriental species, with probable origin after the breakup of Gondwana, that is, in early Paleogene. |
| Author | Campos, Luiz A. Teixeira, Renato A. Lise, Arno A. |
| Author_xml | – sequence: 1 givenname: Renato A. surname: Teixeira fullname: Teixeira, Renato A. email: renatoaug.tx@gmail.com organization: Departamento de Zoologia, Universidade Federal do Rio Grande do Sul, Prédio 43435, 91501-970, Porto Alegre, Brazil – sequence: 2 givenname: Luiz A. surname: Campos fullname: Campos, Luiz A. organization: Departamento de Zoologia, Universidade Federal do Rio Grande do Sul, Prédio 43435, 91501-970, Porto Alegre, Brazil – sequence: 3 givenname: Arno A. surname: Lise fullname: Lise, Arno A. organization: Laboratório de Aracnologia, Museu de Ciências e Tecnologia, Pontifícia Universidade Católica do Rio Grande do Sul, 90619-900, Porto Alegre, Brazil |
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| ContentType | Journal Article |
| Copyright | 2013 The Norwegian Academy of Science and Letters |
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| Notes | ArticleID:ZSC12036 Appendix S1. List of terminals: exemplar taxa and their voucher specimens (with locality and deposition data).Appendix S2. List of characters.Appendix S3. Figures 3-19: Figs. 3-6 are clades showing the non-ambiguous transformations and Figs. 7-19 showing selected character states listed in Appendix S2.Appendix S4. Data matrix showing characters states for each terminal taxon, the number of steps and the consistency and retention index (in percentage) are showed below.Appendix S5. Matrix in .txt format.Appendix S6. Similarity between consensus trees with different K index (Mirande, ). Similarity measure by SPR distance.Appendix S7. Strict consensus depicting ingroup relationships under equal weighting, .xml format.Appendix S8. Geographic coordinates in .xyd format. CNPq - No. 141425/2010-5 istex:140E2C26EE63A5DFB12FD4D4778565B16E56B8C6 ark:/67375/WNG-J50PMR2P-K ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
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| Snippet | This study tests the monophyly of ant‐mimicking Thomisidae (Aphantochilinae and Strophiinae sensu Simon), redefines the composition of these taxa, proposes... This study tests the monophyly of ant‐mimicking Thomisidae (Aphantochilinae and Strophiinae sensu Simon), redefines the composition of these taxa, proposes... This study tests the monophyly of ant-mimicking Thomisidae (Aphantochilinae and Strophiinae sensu Simon), redefines the composition of these taxa, proposes... |
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| SubjectTerms | Araneae Thomisidae |
| Title | Phylogeny of Aphantochilinae and Strophiinae sensu Simon (Araneae; Thomisidae) |
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