Robust DNA Methylation in the Clonal Raider Ant Brain.

Social insects are promising model systems for epigenetics due to their immense morphological and behavioral plasticity. Reports that DNA methylation differs between the queen and worker castes in social insects [1-4] have implied a role for DNA methylation in regulating division of labor. To better understand the function of DNA methylation in social insects, we performed whole-genome bisulfite sequencing on brains of the clonal raider ant Cerapachys biroi, whose colonies alternate between reproductive (queen-like) and brood care (worker-like) phases [5]. Many cytosines were methylated in all replicates (on average 29.5% of the methylated cytosines in a given replicate), indicating that a large proportion of the C. biroi brain methylome is robust. Robust DNA methylation occurred preferentially in exonic CpGs of highly and stably expressed genes involved in core functions. Our analyses did not detect any differences in DNA methylation between the queen-like and worker-like phases, suggesting that DNA methylation is not associated with changes in reproduction and behavior in C. biroi. Finally, many cytosines were methylated in one sample only, due to either biological or experimental variation. By applying the statistical methods used in previous studies [1-4, 6] to our data, we show that such sample-specific DNA methylation may underlie the previous findings of queen- and worker-specific methylation. We argue that there is currently no evidence that genome-wide variation in DNA methylation is associated with the queen and worker castes in social insects, and we call for a more careful interpretation of the available data

Ant genomics sheds light on the molecular regulation of social organization.

Ants are powerful model systems for the study of cooperation and sociality. In this review, we discuss how recent advances in ant genomics have contributed to our understanding of the evolution and organization of insect societies at the molecular level

The Sheffield study Report on the filming of bus boarding

7.50SIGLELD:3487.019(CIT-CTS--22) / BLDSC - British Library Document Supply CentreGBUnited Kingdo

The Sheffield study Costs and maintenance of the split step and kneeling mechanism

SIGLELD:3487.019(CIT-CTS--21) / BLDSC - British Library Document Supply CentreGBUnited Kingdo

The Sheffield study Bus boarding survey

SIGLELD:3487.019(CIT-CTS--20) / BLDSC - British Library Document Supply CentreGBUnited Kingdo

Competitive Weighted Matching

Consider a bipartite graph with a set of left-vertices and a set of right-vertices. All the edges adjacent to the same left-vertex have the same weight. We present an algorithm that, given the set of right-vertices and the number of left-vertices, processes a uniformly random permutation of the left-vertices, one left-vertex at a time. In processing a particular left-vertex, the algorithm either permanently matches the left-vertex to a thus-far unmatched right-vertex, or decides never to match the left-vertex. The weight of the matching returned by our algorithm is within a constant factor of that of a maximum weight matching, generalizing the recent results of Babaioff et al

Social regulation of insulin signaling and the evolution of eusociality in ants.

Queens and workers of eusocial Hymenoptera are considered homologous to the reproductive and brood care phases of an ancestral subsocial life cycle. However, the molecular mechanisms underlying the evolution of reproductive division of labor remain obscure. Using a brain transcriptomics screen, we identified a single gene, <i>insulin-like peptide 2</i> ( <i>ilp2</i> ), which is always up-regulated in ant reproductives, likely because they are better nourished than their nonreproductive nestmates. In clonal raider ants ( <i>Ooceraea biroi</i> ), larval signals inhibit adult reproduction by suppressing <i>ilp2</i> , thus producing a colony reproductive cycle reminiscent of ancestral subsociality. However, increasing ILP2 peptide levels overrides larval suppression, thereby breaking the colony cycle and inducing a stable division of labor. These findings suggest a simple model for the origin of ant eusociality via nutritionally determined reproductive asymmetries potentially amplified by larval signals