Phillip Barden, David A. Grimaldi  Current Biology 

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Adaptive Radiation in Socially Advanced Stem-Group Ants from the Cretaceous  Phillip Barden, David A. Grimaldi  Current Biology  Volume 26, Issue 4, Pages 515-521 (February 2016) DOI: 10.1016/j.cub.2015.12.060 Copyright © 2016 Elsevier Ltd Terms and Conditions

Figure 1 Social Assemblages of Cretaceous Worker Ants (A–F) Top: photomicrograph of entire piece of JZC Bu1814, with detailed views of its six workers of Gerontoformica spiralis. The 0° to 180° axis was used to measure orientations of the ants. Bottom: JZC Bu116 sections A and B, containing 12 worker ants (labeled A–L). Bottom left: photomicrographs of entire piece with two sections fitting together as in the original resin flow. Bottom right: CT scans, with 10 of the 11 Gerontoformica spiralis workers in orange and one Haidomyrmex zigrasi Barden and Grimaldi in blue (one G. spiralis worker, labeled B, was not recovered by X-ray imaging); red arrows indicate orientation of body axis. The large insect is a roach. See also Figure S1. Current Biology 2016 26, 515-521DOI: (10.1016/j.cub.2015.12.060) Copyright © 2016 Elsevier Ltd Terms and Conditions

Figure 2 Workers of Two Species of Gerontoformica in Burmese Amber, G. tendir and G. spiralis, Captured while Fighting Specimen JZC Bu1646. (A) Photomicrograph of entire specimens. (B) Photomicrographic detail of interaction. (C) Illustration of anterior portion of specimens, clarifying positions of appendages. Current Biology 2016 26, 515-521DOI: (10.1016/j.cub.2015.12.060) Copyright © 2016 Elsevier Ltd Terms and Conditions

Figure 3 Preferred Timescaled Consensus Cladogram of Cretaceous and Exemplar Extant Ants Based on a parsimony-based analysis of 42 morphological characters using implied weighting (K = 6.875) and a crown-group topology constrained by previous molecular hypotheses [9]. Timescale included to demonstrate range of Cretaceous fauna: nodes and branch lengths do not correspond to actual diversification times or morphological change, although the earliest divergences are constrained not to exceed the age of the earliest aculeates (Bethylonymidae) in the very Late Jurassic [42]. Node values represent bootstrap support measures. See Supplemental Information for details of analytical procedures. Current Biology 2016 26, 515-521DOI: (10.1016/j.cub.2015.12.060) Copyright © 2016 Elsevier Ltd Terms and Conditions

Figure 4 PCA Plot of Exemplar Living and Cretaceous Ant Workers and Assemblage of Mouthpart Diversity in Cretaceous Stem-Group Ants Top: generated by PCA analysis (PC1 96% and PC2 3% of variance) of four body proportions of 107 living species in 96 genera and 19 Cretaceous species in five genera. For data and analyses see Supplemental Information. Gray and black lines circumscribe living and Cretaceous morphospace, respectively. Body shapes and sizes of six living and extinct exemplar species are presented to same scale, with the exception of the minute ants Carebara and Zigrasimecia (which are greatly enlarged). Bottom: a summary of diversity and homology among Cretaceous stem-group ant mouthparts. Note that not all structures are preserved in known specimens of Sphecomyrma freyi, S. mesaki, and Myanmyrma gracilis, and, therefore, some components are missing. See also Figures S2 and S3. Current Biology 2016 26, 515-521DOI: (10.1016/j.cub.2015.12.060) Copyright © 2016 Elsevier Ltd Terms and Conditions