AeDES: a next-generation monitoring and forecasting system for environmental suitability of Aedes-borne disease transmission.

Aedes-borne diseases, such as dengue and chikungunya, are responsible for more than 50 million infections worldwide every year, with an overall increase of 30-fold in the last 50 years, mainly due to city population growth, more frequent travels and ecological changes. In the United States of America, the vast majority of Aedes-borne infections are imported from endemic regions by travelers, who can become new sources of mosquito infection upon their return home if the exposed population is susceptible to the disease, and if suitable environmental conditions for the mosquitoes and the virus are present. Since the susceptibility of the human population can be determined via periodic monitoring campaigns, the environmental suitability for the presence of mosquitoes and viruses becomes one of the most important pieces of information for decision makers in the health sector. We present a next-generation monitoring and forecasting system for [Formula: see text]-borne diseases' environmental suitability (AeDES) of transmission in the conterminous United States and transboundary regions, using calibrated ento-epidemiological models, climate models and temperature observations. After analyzing the seasonal predictive skill of AeDES, we briefly consider the recent Zika epidemic, and the compound effects of the current Central American dengue outbreak happening during the SARS-CoV-2 pandemic, to illustrate how a combination of tailored deterministic and probabilistic forecasts can inform key prevention and control strategies .

Advances in photoelectrocatalysis with nanotopographical photoelectrodes.

The design of photoelectrodes for high efficiency solar fuel energy conversion devices is based on the search for adequate surface conditioning to achieve efficient light harvesting, stability, minimized surface recombination losses and high electron-transfer rates at the electrolyte interface. An overview on established and novel approaches is given. A recent viable solution is provided by electroplating of nanoscale catalytic metals on passivated semiconductor surfaces, thereby forming reactive centers and avoiding contact between the semiconductor surface and the electrolyte. At these nano-dimensioned Schottky-type junctions, light-induced excess minority carriers are scavenged and transferred to the electrolyte. Various possible device configurations are outlined and envisaged systems for hydrogen or oxygen evolution and carbon dioxide reduction are presented. The role of ultrathin passivating films is emphasized and methods to fabricate open as well as compact conformal films are described.

Complex surface dynamics during anodic dissolution of Ni.

The evolution of the surface roughness during the anodic dissolution of polycrystalline Ni was investigated by means of ex situ AFM in acid phosphate solutions. To characterize the time and spatial scaling behavior of surface roughness, the interface width and the power spectral density of the surface at different dissolution stages were analyzed in terms of dynamic scaling theories. The time dependence of global surface roughness, W(L,t), shows an unstable behavior characterized by a continuous increase without saturation following the relation W approximately t(beta), where beta > 0.5. The unstable behavior results from the development of wide grooves that originates a surface consisting of mounds. Two scaling regimes at scales shorter and larger than the mound dimensions (l(c)) were observed. For l < l(c), we found alpha approximately 1 consistent with mounds exhibiting smooth (faceted) walls, whereas an anomalous scaling behavior with a proper local roughness exponents (alpha(loc) < 1) dominates at l > l(c). The introduction of nitrite in the solution, a common additive used in phosphating baths, leads to some changes in the scaling behavior as a consequence of different generated chemical surface conditions during dissolution. The different dissolution rates of the exposed crystal orientations and surface diffusion of adatoms were identified as the physical processes that govern the interface dynamic for this system.

Influence of the adsorption of N species on the anodic dissolution of Ni.

The dissolution and passivation of Ni in nitrite-containing acid solutions are investigated by Auger spectroscopy, atomic force microscopy, and conventional electrochemical techniques. The dissolution/ passivation of the Ni surface is consistent with a competition between adsorbed OH- and nitrogen-containing species with a potential-dependent surface coverage. Nitrogen-containing species hinder the passivation of the Ni surface, shifting the formation of the complex nickel hydroxide/oxide film to more positive potential values. The dynamics of the dissolving interface, followed by atomic force microscopy, reflect first the competition of adsorbed species, leading to the development of protrusions and cavities, and finally the formation of the passive film that promotes surface smoothening by a preferential dissolution of the protrusion tips under ohmic control.