28 research outputs found
Mouse retinal specializations reflect knowledge of natural environment statistics
Pressures for survival drive sensory circuit adaption to a species’ habitat, making it essential to statistically characterise natural scenes. Mice, a prominent visual system model, are dichromatic with enhanced sensitivity to green and UV. Their visual environment, however, is rarely considered. Here, we built a UV-green camera to record footage from mouse habitats. We found chromatic contrast to greatly diverge in the upper but not the lower visual field, an environmental difference that may underlie the species’ superior colour discrimination in the upper visual field. Moreover, training an autoencoder on upper but not lower visual field scenes was sufficient for the emergence of colour-opponent filters. Furthermore, the upper visual field was biased towards dark UV contrasts, paralleled by more light-offset-sensitive cells in the ventral retina. Finally, footage recorded at twilight suggests that UV promotes aerial predator detection. Our findings support that natural scene statistics shaped early visual processing in evolution
Compensation to positive as well as negative lenses can occur in chicks reared in bright UV lighting
Hybrid Poly(urethane–urea)/Silica Nanocapsules with pH-Sensitive Gateways
We have produced hybrid poly(urethane–urea)/silica
nanocapsules
with controlled molecular-scale regimes of silica that break upon
introduction into basic media. The miniemulsion technique used is
simple and scalable but yields complex molecular-scale morphologies
that create molecular gates for the release of hydrophilic components.
The hybrid nanocapsules displayed no microphase separation, indicating
the formation of microscopically mixed regions of silica and poly(urethane–urea).
Using atomic force microscopic techniques, we characterize the mechanical
properties of individual capsules and identify the tailorability of
the capsule modulus by changing the ratio of isocyanate to silica
in the precursor mixture. The compositions of the hybrids were confirmed
by infrared spectroscopy and thermogravimetric analysis. The change
in size of a nanocapsule with pH and time was monitored by fluorescence
correlation spectroscopy to evaluate their potential as nanocontainers
and show a pH-responsive release
Fluorescence Correlation Spectroscopy in Dilute Polymer Solutions: Effects of Molar Mass Dispersity and the type of fluorescent Labeling
© 2015 American Chemical Society. Fluorescence correlation spectroscopy (FCS) has become an important tool in polymer science. Among various other applications the method is often applied to measure the hydrodynamic radius and the degree of fluorescent labeling of polymers in dilute solutions. Here we show that such measurements can be strongly affected by the molar mass dispersity of the studied polymers and the way of labeling. As model systems we used polystyrene and poly(methyl methacrylate) synthesized by atom transfer radical polymerization or free-radical polymerization. Thus, the polymers were either end-labeled bearing one fluorophore per chain or side-labeled with a number of fluorophores per chain proportional to the degree of polymerization.The experimentally measured autocorrelation curves were fitted with a newly derived theoretical model that uses the Schulz-Zimm distribution function to describe the dispersity in the degree of polymerization. For end-labeled polymers having a molecular weight distribution close to Schulz-Zimm, the fits yield values of the number-average degree of polymerization and the polydispersity index similar to those obtained by reference gel permeation chromatography. However, for the side-labeled polymers such fitting becomes unstable, especially for highly polydisperse systems. Brownian dynamic simulations showed that the effect is due to a mutual dependence between the fit parameters, namely, the polydispersity index and the number-average molecular weight. As a consequence, an increase of the polydispersity index can be easily misinterpreted as an increase of the molecular weight when the FCS autocorrelation curves are fitted with a standard single component model, as commonly done in the community.status: publishe