Rust-proofing wheat for a changing climate

This paper offers projections of potential effects of climate change on rusts of wheat and how we should factor in a changing climate when planning for the future management of these diseases. Even though the rusts of wheat have been extensively studied internationally, there is a paucity of information on the likely effects of a changing climate on the rusts and their influence on wheat production. Due to the lack of published empirical research we relied on the few published studies of other plant diseases, our own unpublished work and relevant information from the vast literature on rusts of wheat to prepare this overview. Three broad areas of potential risks from a changing climate were described: increased loss from wheat rusts, new rust pathotypes evolving faster and the reduced effectiveness of rust resistances. Increased biomass of wheat crops grown in the presence of elevated CO₂ concentrations and higher temperatures will increase the leaf area available for attack by the pathogen leading to increased inoculum production. If changed weather conditions were to accelerate the life cycle of a pathogen, the increased inoculum can lead to severe rust epidemics in many environments. Likewise should the effects of climate change result in more conducive conditions for rust development there will also be a corresponding increase in the rate of evolution of new pathotypes which could increase the rate of appearance of new virulences. The effectiveness of some rust resistance genes is influenced by temperature and crop development stage. Climate change may directly or indirectly influence the effectiveness of some resistance genes but this can not be ascertained due to a complete lack of knowledge. Since disease resistance breeding is a long term strategy it is important to determine if any of the important genes may become less effective due to climate change. Studies must be made to acquire new information on the rust disease triangle to increase the adaptive capacity of wheat under climate change. Leadership within the Borlaug Global Rust Initiative (BGRI) is needed to broker research on rust evolution and the durability of resistance under climate change.     

Optimization of curing process for polymer-matrix composites based on orthogonal experimental method

In this paper, the orthogonal experimental method was carried out to optimize the curing process of aeronautical composite X850/T800 in autoclave process. Four important curing parameters including curing pressure, heating rate, curing temperature and heat preservation time were taken into account, and sixteen samples were fabricated to study the effects of the four parameters mentioned above on the curing quality by interlaminar properties test and microstructure analysis. The interlaminar properties and the interfacial bonding quality of these samples were studied by the short-beam three points bending test and scanning electron microscopy, respectively. Results revealed that the optimal curing process of X850/T800 composite laminate should be as follows: curing pressure of 0.6 MPa, heating rate of 1.5 °C/min, curing temperature of 160 °C, and heat preservation time of 120 min.     

A novel method to analyze the moisture liberation of textile fabrics

In this paper, a purpose-built apparatus was used to analyze the moisture liberation of textile fabrics. Fabrics were wetted and placed in an air-conditioned room to test the variation of weight and surface temperature during the process of moisture liberation. Effects of textile materials and fabric structures on the velocities of moisture liberation of fabrics were analyzed; the temperature variation and its relationship with moisture regains of fabrics in the moisture liberation were also studied. Moisture liberation velocities of polyester and silk fabrics are much higher than that of wool and cotton fabrics. For the same textile materials, knitted fabrics absorbed more water and thus took longer time to liberate the water. The surface temperature of fabrics showed three stages during moisture liberation. With the decrease of moisture regain, fabric temperature decreased gradually and jumped quickly to ambient temperature. In this way we could evaluate the moisture desorption of fabrics and develop quick-drying fabrics with imporved moisture and thermal properties.     

Temperature-dependent differences in biological traits between two strains of <Emphasis Type="Italic">Trichogramma cacoeciae</Emphasis> (Hymenoptera: Trichogrammatidae)

Parasitoids’ efficiency in controlling pests depends not only on their ability to parasitize their hosts but also on how much they are adapted to climatic conditions (notably temperature) of the area where they are planned to be released. In addition, the optimal conditions for production of parasitoids used for inundative releases like Trichogramma spp. may also vary largely as a function of strains. Using the parasitoid Trichogramma cacoeciae Marchal as biological model, we studied how temperature affects important parasitoid efficiency-related biological traits under laboratory conditions. Emergence, mortality rates and fecundity of two strains of T. cacoeciae, one originating from France (Alsace) and the other one from Tunisia (Degache), were compared at constant temperatures of 15, 20, 25 and 30°C. The parasitoids of the French strain showed highest fecundity at 25°C with wasps that had been reared at 20 or 25°C. The Tunisian strain showed the highest fecundity at 25°C, but only when wasps were previously reared at 25 or 30°C. For both strains, the highest mortality occurred among wasps that had laid eggs at 30°C. Emergence rates were relatively high at all temperatures, although the French strain did better at 15–25°C and the Tunisian one at 20–30°C. Because of the differences in biological traits of these two T. cacoeciae strains in relation to the temperature, a judicious choice must be made among the various strains when using this species in biological control programs.     

High water content silk protein-based hydrogels with tunable elasticity fabricated via a Ru(II) mediated photochemical cross-linking method

Silk is very promising in the field of biomaterials as a natural biomacromolecule. Silk protein can be made into various forms of materials, including hydrogels. However, silk protein-based hydrogels have not attracted much attention due to its weak mechanical properties. Here, we report high water content silk protein-based hydrogels with tunable elasticity which were fabricated through Ru(II) mediated photochemically cross-linking tyrosine residues in regenerated silk protein. The regenerated silk protein was characterized by Fourier transform infrared spectroscopy (FTIR). The gelation kinetics of the silk protein was studied by rheology measurements. The compressive mechanical properties of the silk protein-based hydrogels was investigated using compressive tests and dynamic mechanical analysis (DMA). Compressive modulus of the hydrogels reached 349±64 MPa at 15 % strain. The fabricated silk protein-based hydrogels were also characterized by Scanning electron microscopy (SEM), revealing an interconnected porous network structure, typical of hydrogels, with an average pore size of approximately 130 μm. Finally, biocompatibility of the silk protein-based hydrogels was demonstrated through cell culture studies using a human fibroblast cell line, HFL1. The reported silk protein-based hydrogels represent a promising candidate for biomaterial applications.     

Artificial polyploidy in medicinal plants: Advancement in the last two decades and impending prospects

Medicinal plants are in huge demand since the consumption is widespread and ever-increasing globally. The conventional breeding programs are generally environmental dependent; prone to different biotic and abiotic stresses as well as the secondary metabolite content is too low to harvest. In this context, developing polyploid individuals artificially would be a remarkable approach to increase vigor and attain this objective. Polyploids often exhibit some morphological features that are different or greater in forms than their diploid progenies. Polyploidization can be induced by quite a few antimitotic agents. The most frequently used antimitotic chemicals are colchicine, trifluralin, and oryzalin. The whole method of induced chromosome doubling consists of a series of steps, including an induction phase, regrowth phase, and a confirmation technique to evaluate the rate of achievement. The induction phase depends on different factors, such as explant types, antimitotic agents, its different concentrations, and exposure durations. To evaluate the accomplishment of polyploidization, morphological or anatomical observations are recorded as a rapid method. However, chromosome count and flow cytometry are the most eminent method for absolute confirmation. Despite significant prospects of polyploidization, there has been very little research on medicinal plants. The current review gives an overview of the different parameters of in vitro chromosome doubling, the history of the technique, and progress made over the last two decades.     

Rapid detection of <Emphasis Type="Italic">Peste des Petits Ruminants</Emphasis> (PPR) virus antigen in Sudan by agar gel precipitation (AGPT) and haemagglutination (HA) Tests

AGPT and HA tests were employed for rapid diagnosis of PPRV infection in sheep and goats in Sudan. Forty lymph nodes and spleen samples from suspected cases of PPR in both sheep and goats were examined by AGPT and HA tests for detection of PPRV antigen. Viral antigen was detected from (77.5%) of the samples tested by AGPT and (92.5%) tested by HA test. The results of both tests revealed that HA test was more sensitive than AGPT for detection of PPRV antigen (Kappa statistics 0.4366). Another advantage of the HA test over AGPT was that it can differentiate PPRV from RPV. Thus the HA test represents a quick, easy, simple, cheap and reliable confirmatory test for the diagnosis of PPR and differential diagnosis of PPRV and RPV. The HA test was carried out using chicken, goat and pig RBCs. Chicken RBCs were found to be the most sensitive for detection of PPRV antigen, followed by goat then pig RBCs. The HA time when using chicken RBCs was 20–25 minutes, using goat RBCs was 25–30 minutes and using pig RBCs was 40–45 minutes. The distribution of PPR infection in four different regions of Sudan was investigated.     

Guava (<Emphasis Type="Italic">Psidium guajava L</Emphasis>. cv. Red Suprema) Crude Extract Protect Human Dermal Fibroblasts against Cytotoxic Damage Mediated by Oxidative Stress

We analyzed guava fruits (Psidium guajava L. cv. Red Suprema) from Cuba to determine their chemical composition, total antioxidant capacity, as well as their protective effect against oxidative damage using an in vitro model of human dermal fibroblasts. The guava fruit is a natural source of bioactive compounds, such as polyphenols, vitamin C, folates and beta carotenes with proven health benefits. Human dermal fibroblasts were pre-incubated with different concentrations of guava crude extract and then subjected to oxidative stress using the AAPH stressor. The number of apoptotic and dead cells, as well as the markers of oxidative damage such as lipid and protein oxidation significantly decreased when cells were pre-incubated with guava crude extract and then exposed to the stressor. The activity of antioxidant enzymes also improved when cells were pre-incubated with guava crude extract in comparison to cells subjected to stress without prior pre-incubation with the guava extract. The results obtained in this study highlight the health benefits of guava regarding oxidative stress, proving it to be an important source of bioactive compounds associated with important biological properties.