Complex response in size-related traits of bulb mites (Rhizoglyphus robini) under elevated thermal conditions - an experimental evolution approach.

Temperature is a key environmental factor affecting almost all aspects of life history in ectotherms. Theory predicts that they grow faster, reach smaller sizes and produce smaller offspring when temperature increases. In addition, temperature changes, through their effects on metabolism, may also influence the expression of alternative reproductive phenotypes (ARPs) in ectotherms. Although many studies have investigated the phenotypic plasticity of life history traits in relation to temperature change, little is known about how those traits and phenotypic plasticity may evolve together. In our study we subjected bulb mites (non-model, soil organisms that normally experience rather stable thermal conditions) to experimental evolution in two temperature treatments: control (24°C) and elevated (28°C). After 18 generations, we measured adult body size, egg size and development time of both treatments at control as well as at elevated temperatures (test temperatures). Thus, we were able to detect genetic changes (the effects of selection temperature) and environmental effects (the effects of test temperature). We also observed the ARP expression throughout the experimental evolution. Our results revealed quite complex patterns of life history in traits response to temperature. Mites developed faster and reached smaller sizes at increased temperature, but evolutionary responses to increased temperature were not always parallel to the observed phenotypic plasticity. Additionally, despite smaller body sizes, females laid larger eggs at higher temperature. This effect was more pronounced in animals evolving at elevated temperature. Evolution at increased temperature also affected ARP expression, with the proportion of armored fighters decreasing from generation to generation. We propose that this could be the consequence of temperature sensitivity of the cost-to-benefits ratio of expressing ARPs.

Removing cadmium ions from water via nanoparticle-enhanced ultrafiltration.

Here we evaluate removal of cadmium ions from water by nanoparticle-enhanced ultrafiltration using polymer and zeolite nanoparticles. This evaluation considered nanoparticle physical-chemical properties, metal-binding kinetics, capacity and reversibility, and ultrafiltration separation for a Linde type A zeolite nanocrystals, poly(acrylic acid), alginic acid, and carboxyl-functionalized PAMAM dendrimers in simple, laboratory prepared ionic solutions. The three synthetic materials exhibited fast binding kinetics and strong affinity for cadmium, with good regeneration capabilities. Only the zeolite nanoparticles were completely rejected by the ultrafiltration membranes tested. Overall, colloidal zeolites performed similar to conventional metal binding polymers, but were more easily recovered using relatively loose filtration membranes (i.e., lower energy consumption). Further, the superhydrophilic colloidal zeolites caused relatively little flux decline even in the presence of divalent cations which caused dense, highly impermeable polymer gels to form over the membranes. These results suggest zeolite nanoparticles may compete with polymeric materials in low-pressure hybrid filtration processes designed to remove toxic metals from water.

Influence of zeolite crystal size on zeolite-polyamide thin film nanocomposite membranes.

Zeolite-polyamide thin film nanocomposite membranes were coated onto polysulfone ultrafiltration membranes by interfacial polymerization of amine and acid chloride monomers in the presence of Linde type A zeolite nanocrystals. A matrix of three different interfacial polymerization chemistries and three different-sized zeolite crystals produced nanocomposite thin films with widely varying structure, morphology, charge, hydrophilicity, and separation performance (evaluated as reverse osmosis membranes). Pure polyamide film properties were tuned by changing polymerization chemistry, but addition of zeolite nanoparticles produced even greater changes in separation performance, surface chemistry, and film morphology. For fixed polymer chemistry, addition of zeolite nanoparticles formed more permeable, negatively charged, and thicker polyamide films. Smaller zeolites produced greater permeability enhancements, but larger zeolites produced more favorable surface properties; hence, nanoparticle size may be considered an additional "degree of freedom" in designing thin film nanocomposite reverse osmosis membranes. The data presented offer additional support for the hypothesis that zeolite crystals alter polyamide thin film structure when they are present during the interfacial polymerization reaction.