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Phylogeny of the orb-weaving spider family Araneidae (Araneae: Araneoidea)

  • Nikolaj Scharff
  • , Jonathan A. Coddington
  • , Todd A. Blackledge
  • , Ingi Agnarsson
  • , Volker W. Framenau
  • , Tamás Szűts
  • , Cheryl Y. Hayashi
  • , Dimitar Dimitrov

Research output: Contribution to journalArticlepeer-review

Abstract

We present a new phylogeny of the spider family Araneidae based on five genes (28S, 18S, COI, H3 and 16S) for 158 taxa, identified and mainly sequenced by us. This includes 25 outgroups and 133 araneid ingroups representing the subfamilies Zygiellinae Simon, 1929, Nephilinae Simon, 1894, and the typical araneids, here informally named the “ARA Clade”. The araneid genera analysed here include roughly 90% of all currently named araneid species. The ARA Clade is the primary focus of this analysis. In taxonomic terms, outgroups comprise 22 genera and 11 families, and the ingroup comprises three Zygiellinae and four Nephilinae genera, and 85 ARA Clade genera (ten new). Within the ARA Clade, we recognize ten informal groups that contain at least three genera each and are supported under Bayesian posterior probabilities (≥ 0.95): “Caerostrines” (Caerostris, Gnolus and Testudinaria), “Micrathenines” (Acacesia, Micrathena, Ocrepeira, Scoloderus and Verrucosa), “Eriophorines” (Acanthepeira, Alpaida, Eriophora, Parawixia and Wagneriana), “Backobourkiines” (Acroaspis, Backobourkia, Carepalxis, Novakiella, Parawixia, Plebs, Singa and three new genera), “Argiopines” (Arachnura, Acusilas, Argiope, Cyrtophora, Gea, Lariniaria and Mecynogea), “Cyrtarachnines” (Aranoethra, Cyrtarachne, Paraplectana, Pasilobus and Poecilopachys), “Mastophorines” (Celaenia, Exechocentrus and Mastophora,), “Nuctenines” (Larinia, Larinioides and Nuctenea), “Zealaraneines” (Colaranea, Cryptaranea, Paralarinia, Zealaranea and two new genera) and “Gasteracanthines” (Augusta, Acrosomoides, Austracantha, Gasteracantha, Isoxya, Macracantha, Madacantha, Parmatergus and Thelacantha). Few of these groups are currently corroborated by morphology, behaviour, natural history or biogeography. We also include the large genus Araneus, along with Aculepeira, Agalenatea, Anepsion, Araniella, Cercidia, Chorizopes, Cyclosa, Dolophones, Eriovixia, Eustala, Gibbaranea, Hingstepeira, Hypognatha, Kaira, Larinia, Mangora, Metazygia, Metepeira, Neoscona, Paraplectanoides, Perilla, Poltys, Pycnacantha, Spilasma and Telaprocera, but the placement of these genera was generally ambiguous, except for Paraplectanoides, which is strongly supported as sister to traditional Nephilinae. Araneus, Argiope, Eriophora and Larinia are polyphyletic, Araneus implying nine new taxa of genus rank, and Eriophora and Larinia two each. In Araneus and Eriophora, polyphyly was usually due to north temperate generic concepts being used as dumping grounds for species from southern hemisphere regions, e.g. South-East Asia, Australia or New Zealand. Although Araneidae is one of the better studied spider families, too little natural history and/or morphological data are available across these terminals to draw any strong evolutionary conclusions. However, the classical orb web is reconstructed as plesiomorphic for Araneidae, with a single loss in “cyrtarachnines”–“mastophorines”. Web decorations (collectively known as stabilimenta) evolved perhaps five times. Sexual dimorphism generally results from female body size increase with few exceptions; dimorphic taxa are not monophyletic and revert to monomorphism in a few cases.

Original languageEnglish
Pages (from-to)1-21
Number of pages21
JournalCladistics
Volume36
Issue number1
DOIs
Publication statusPublished - 1 Feb 2020

Bibliographical note

Funding Information: JC and NS acknowledge NSF EAR-0228699 (Assembling the Tree of Life: phylogeny of Spiders). TAB and NS acknowledge NSF DEB-0516038 (Collaborative Research: Araneid Phylogeny and Evolution of Spider Silk Phenotypes). DD and NS received support by the Danish National Research Foundation grant DNRF96 to the Center for Macroecology Evolution and Climate. NS acknowledges the Danish Natural Science Research Council Award 21020502. NS and TS acknowledge Marie Curie Intra European Fellowship Award 025850. NS and VWF received support by the Australian Biological Resources Study (ABRS grant no. 205-24). Access to the Abel computing facilities at the University of Oslo was granted through the Norwegian Metacenter for Computational Science (NOTUR; project NN9601K) to DD. We thank Joel Duff for access to his molecular laboratory. We thank Alpana Chaudhuri, Mariam Lekveishvili and Kimberly Lorentz for assistance with sequencing of many specimens. In addition to specimens collected by ourselves, we thank David Britton, Matthew Bruce, David Court, Paula Cushing, Mike Gray, Charles Griswold, Aaron Harmer, Mark Harvey, Ken Haynes, Marshal Hedin, Marie Herberstein, Miki Kusahara, Laura Leibensperger, Astri and John Leroy, Brent Opell, Phil Sirvid, Helen Smith, Mark Stowe, Akio Tanikawa, Cor Vink and Ken Yeargan for providing specimens. We thank Miquel Arnedo, Charles Griswold and Martín Ramírez for their constructive criticism of a previous version of the manuscript. We thank associate editor Lorenzo Prendini for assistance with the manuscript. Publisher Copyright: © The Willi Hennig Society 2019

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