Understanding the evolution of complex traits is among the major challenges in biology. One such trait is the cuticular hydrocarbon (CHC) layer in insects. It protects against desiccation and provides communication signals, especially in social insects. CHC composition is highly diverse within and across species. To understand the adaptive value of this chemical diversity, we must understand how it affects biological functionality. So far, CHCs have received ample research attention, but their physical properties were little studied. We argue that these properties determine their biological functionality, and are vital to understanding how CHC composition affects their adaptive value. We investigated melting behaviour and viscosity of CHCs from 11 ant species using differential scanning calorimetry and a novel microrheological technique. CHCs began melting below −45°C, and often were entirely liquid only above 30°C. Thus, they formed a solid-liquid mixture under ambient conditions, which contrasts to previous assumptions of entirely solid layers in many species. This may be adaptive as only biphasic CHC layers ensure uniform coating of the insect body, which is necessary for waterproofing. CHC viscosity was mostly between 0.1 and 0.2 Pa s −1 , thus similar to motor oils. Surprisingly, chemically different CHC profiles had similar viscosities, suggesting that a certain viscosity level is adaptive and ensures that communication signals can be perceived. With this study, we draw attention to the importance of studying the physics of CHC layers. Only by understanding how chemical and physical mechanisms enable CHC functionality can we understand the causes and consequences of CHC diversification.

A new sulfonation strategy enables the preparation of durable aromatic polymers with octasulfonated biphenyl units. This leads to polyelectrolytes with extremely high degrees of sulfonation, reaching high proton conductivities at low water contents.

One of the challenges in tailoring the dynamics of active, self-propelling agents lies in arresting and releasing these agents at will. Here, we present an experimental system of active droplets with thermally controllable and reversible states of motion, from unsteady over meandering to persistent to arrested motion. These states depend on the Péclet number of the chemical reaction driving the motion, which we can tune by using a temperature sensitive mixture of surfactants as a fuel medium. We quantify the droplet dynamics by analysing flow and chemical fields for the individual states, comparing them to canonical models for autophoretic particles. In the context of these models, we are able to observe in situ the fundamental first transition between the isotropic, immotile base state and self-propelled motility.