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Biology subjects

Stephenson, A. B.

Publications and source records attributed to Stephenson, A. B..

2 recordsLinked to original sources

On metallic luster and iridescence in animal coloration

Some structural colors in nature are frequently described as metallic. For example, hummingbird plumage, jewel beetles and Morpho butterflies have this attribute. While much attention has been paid to describing the often-shifting hues of these structural colors, there has been little interest in explaining why they appear metallic. In this paper, we argue that the metallic luster (the metallic appearance or sheen) of some structural colors arises in part from a combination of two factors: a colored specular reflection and a very low diffuse reflection. Reflections with these characteristics are found in metals and are distinct from other material reflections in nature. We propose that metallic luster can be classified based on these two reflectance properties (colored specular reflection and low diffuse reflection). We also suggest that some of the ambiguity surrounding the term "iridescent structural color" can be traced to the frequent confounding of metallic luster with a common definition of iridescence: a shift of peak spectral wavelength (often referred to as hue) with viewing angle. We show using optical models and cross-polarization imaging of bird plumage that two types of structural colors that are often classified as "iridescent" and "non-iridescent" both display iridescence--but only one type has metallic luster. By considering metallic luster and iridescence separately, we simultaneously clarify terminology in structural colors and open up many new lines of inquiry regarding the perception of metallic luster in animals.

evolutionary biology↗

Liposome-assisted in-situ cargo delivery to artificial cells and cellular subcompartments

We report on liposome-mediated targeted delivery of membrane-impermeable constituents into surface-adhered giant lipid compartments, employed as artificial cells. Soluble cargo compounds are delivered by means of an open-space microfluidic device, which perfuses selected lipid compartments with loaded small unilamellar vesicles (SUVs) composed of cationic lipids. The SUV membranes fuse with the surface-adhered containers, merging their contents. We monitored the fusion process via Forster resonance energy transfer (FRET) by labeling both the membranes of the SUVs and the target compartments with a fluorophore pair. We established that, upon fusion, water-soluble dyes, fluorescently labeled genetic polymers, sugars and proteins carried by the SUVs can be successfully internalized at high yield. Finally, by transferring carbonic anhydrase (CA) to the giant lipid compartments, enzymatic hydrolysis of the prefluorescent carboxyfluorescein diacetate (CFDA) is demonstrated by the emission intensity increase emanating from the product carboxyfluorescein (CF). Spontaneous subcompartmentalization occurred during liposomal delivery of the enzyme, leading to CF formation in an organelle-like subcompartment. The reported targeted delivery technique enables chemical reactions and cell-free gene expression in synthetic cell models with unprecedented ease and precision, and opens pathways to protocell architectures with distinct functional subcompartments in the context of origins of life research.

biophysics↗