Phylogeography of the widespread Caribbean spiny orb weaver Gasteracantha cancriformis

PeerJ. 2020 Apr 30:8:e8976. doi: 10.7717/peerj.8976. eCollection 2020.

Abstract

Background: Modern molecular analyses are often inconsistent with pre-cladistic taxonomic hypotheses, frequently indicating higher richness than morphological taxonomy estimates. Among Caribbean spiders, widespread species are relatively few compared to the prevalence of single island endemics. The taxonomic hypothesis Gasteracantha cancriformis circumscribes a species with profuse variation in size, color and body form. Distributed throughout the Neotropics, G. cancriformis is the only morphological species of Gasteracantha in the New World in this globally distributed genus.

Methods: We inferred phylogenetic relationships across Neotropical populations of Gasteracantha using three target genes. Within the Caribbean, we estimated genetic diversity, population structure, and gene flow among island populations.

Results: Our findings revealed a single widespread species of Gasteracantha throughout the Caribbean, G. cancriformis, while suggesting two recently divergent mainland populations that may represent separate species, diverging linages, or geographically isolated demes. The concatenated and COI (Cytochrome c oxidase subunit 1) phylogeny supported a Caribbean clade nested within the New World. Genetic variability was high between island populations for our COI dataset; however, gene flow was also high, especially between large, adjacent islands. We found structured genetic and morphological variation within G. cancriformis island populations; however, this variation does not reflect genealogical relationships. Rather, isolation by distance and local morphological adaptation may explain the observed variation.

Keywords: Color polymorphism; Gene flow; Genetic diversity; Haplotype network; Intraspecific relationships; Morphology; Phylogeny; Species delimitation.

Associated data

  • Dryad/10.5061/dryad.sf7m0cg2s

Grants and funding

This work was supported by the National Science Foundation (DEB-1314749 and DEB-1050253) to Ingi Agnarsson and Greta Binford. Additional funds came from the Smithsonian Laboratories of Analytical Biology, a 2013 SI Barcode Network to Jonathan Coddington and Ingi Agnarsson, from Slovenian Research Agency (ARRS) grants to Matjaz Kuntner. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.