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The spider tree of life: phylogeny of Araneae based on target‐gene analyses from an extensive taxon sampling

We present a phylogenetic analysis of spiders using a dataset of 932 spider species, representing 115 families (only the family Synaphridae is unrepresented), 700 known genera, and additional representatives of 26 unidentified or undescribed genera. Eleven genera of the orders Amblypygi, Palpigradi,...

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Published in:Cladistics 2017-12, Vol.33 (6), p.574-616
Main Authors: Wheeler, Ward C., Coddington, Jonathan A., Crowley, Louise M., Dimitrov, Dimitar, Goloboff, Pablo A., Griswold, Charles E., Hormiga, Gustavo, Prendini, Lorenzo, Ramírez, Martín J., Sierwald, Petra, Almeida‐Silva, Lina, Alvarez‐Padilla, Fernando, Arnedo, Miquel A., Benavides Silva, Ligia R., Benjamin, Suresh P., Bond, Jason E., Grismado, Cristian J., Hasan, Emile, Hedin, Marshal, Izquierdo, Matías A., Labarque, Facundo M., Ledford, Joel, Lopardo, Lara, Maddison, Wayne P., Miller, Jeremy A., Piacentini, Luis N., Platnick, Norman I., Polotow, Daniele, Silva‐Dávila, Diana, Scharff, Nikolaj, Szűts, Tamás, Ubick, Darrell, Vink, Cor J., Wood, Hannah M., Zhang, Junxia
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Language:English
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Summary:We present a phylogenetic analysis of spiders using a dataset of 932 spider species, representing 115 families (only the family Synaphridae is unrepresented), 700 known genera, and additional representatives of 26 unidentified or undescribed genera. Eleven genera of the orders Amblypygi, Palpigradi, Schizomida and Uropygi are included as outgroups. The dataset includes six markers from the mitochondrial (12S, 16S, COI) and nuclear (histone H3, 18S, 28S) genomes, and was analysed by multiple methods, including constrained analyses using a highly supported backbone tree from transcriptomic data. We recover most of the higher‐level structure of the spider tree with good support, including Mesothelae, Opisthothelae, Mygalomorphae and Araneomorphae. Several of our analyses recover Hypochilidae and Filistatidae as sister groups, as suggested by previous transcriptomic analyses. The Synspermiata are robustly supported, and the families Trogloraptoridae and Caponiidae are found as sister to the Dysderoidea. Our results support the Lost Tracheae clade, including Pholcidae, Tetrablemmidae, Diguetidae, Plectreuridae and the family Pacullidae (restored status) separate from Tetrablemmidae. The Scytodoidea include Ochyroceratidae along with Sicariidae, Scytodidae, Drymusidae and Periegopidae; our results are inconclusive about the separation of these last two families. We did not recover monophyletic Austrochiloidea and Leptonetidae, but our data suggest that both groups are more closely related to the Cylindrical Gland Spigot clade rather than to Synspermiata. Palpimanoidea is not recovered by our analyses, but also not strongly contradicted. We find support for Entelegynae and Oecobioidea (Oecobiidae plus Hersiliidae), and ambiguous placement of cribellate orb‐weavers, compatible with their non‐monophyly. Nicodamoidea (Nicodamidae plus Megadictynidae) and Araneoidea composition and relationships are consistent with recent analyses. We did not obtain resolution for the titanoecoids (Titanoecidae and Phyxelididae), but the Retrolateral Tibial Apophysis clade is well supported. Penestomidae, and probably Homalonychidae, are part of Zodarioidea, although the latter family was set apart by recent transcriptomic analyses. Our data support a large group that we call the marronoid clade (including the families Amaurobiidae, Desidae, Dictynidae, Hahniidae, Stiphidiidae, Agelenidae and Toxopidae). The circumscription of most marronoid families is redefined here. Amaurobiidae i
ISSN:0748-3007
1096-0031
DOI:10.1111/cla.12182