Laboratory and field evaluation of the pathogenicity of entomopathogenic nematodes to the red palm weevil, Rhynchophorus ferrugineus (Oliv.) (Col.: Curculionidae)

Ten Egyptian and imported entomopathogenic nematodes were evaluated for their pathogenicity to R. ferrugineus in both the laboratory and the field. In the laboratory, most nematodes were pathogenic to the pest larvae, pupae and adults. Larvae and adults were more susceptible to nematode infection (mostly 100% mortality) than pupae enclosed in their cocoons. In the field however, the highest insect larval mortality was 66.67% and most of nematodes failed in controlling the pest. Such failure could be due to hot weather, the tunnelling behaviour of the pest larvae and the too much sap in the infested sites in the trunks of palm trees.     

Perineal Nets of Proteoglycans and Glycoproteins in Albino Rat Hippocampus

Perineuronal nets (PNs) of condensed extracellular matrix (ECM) have been shown to characterize the microenvironment of individual neurons and the chemoarchitecture of some brain regions. In the present study, PNs in the hippocampus were visualized with a cationic iron colloid method for sulphated proteoglycan content and a plant lectin from Vicia villosa agglutinin (VVA) for N-acetylgalactosamine containing glycoconjugates. The ECM molecules were organized in reticular coats (PNs) around non-pyramidal cells in the Ammons horn (Corneu Ammons, CA) and subicular region, in addition to pyramidal neurons located in CA2 and CA3 regions. CA2 stratum pyramidale exhibited the most intense staining of its PNs and a diffuse intervening neutrophil labelling, while CA3 region showed a graded fashion of staining intensity. The subiculum displayed intensely stained perineuronal coats. Notably, the hippocampal perineuronal nets revealed overlapped staining characteristics with both staining methods. However, cell coats of the subicular neurons showed various degrees of labelling characteristics with both markers. It is suggested that the PNs in the hippocampus are correlated with the fast spiking inhibitory GABAergic neurons and their target pyramidal cells, and this is important to keep the excitatory elements under control and therefore control the information processes within the hippocampus.     

Effects of different high constant and alternating temperatures on the development and prey consumption of <Emphasis Type="Italic">Dicyphus tamaninii</Emphasis> Wagner (Heteroptera,Miridae) with <Emphasis Type="Italic">Aphis gossypii</Emphasis> Glover (Homoptera,Aphididae) as prey

The present work aimed to study the effects of high constant and alternating temperatures on the development and prey consumption by Dicyphus tamaninii Wagner (Het., Miridae) with Aphis gossypii Glover (Hom., Aphididae) as prey.Results showed that the predator was able to successfully develop and reach the adult stage, on average, after 20.1 () and 20.6 () days at a temperature of 30 ± 1 °C with A. gossypii as prey. On the other hand, it was not able to develop at 35 ± 1 °C, here all N₁ instars used at the beginning of the experiments had died even before moulting to N₂ instar. At alternating temperatures of 25/15 ± 1 °C, the predator reached the adult stage 23.7 () and 23.5 () days after egg hatching, whereas when the temperatures were increased to 35/22 ± 1 °C, it took a significantly shorter period: 20.6 () and 20.9 () days. In general, the highest mortality occurred during the first two nymphal instars. The total percentage mortality during development from N₁ to adult stage was 30 % and 100 % at the constant temperatures 30 ± 1 °C and 35 ± 1 °C, respectively. At the alternating temperatures of 25/15 ± 1 °C, it was lowest with 16.5 %, while at 35/22 ± 1 °C, it was 20 %.The results of the experiments on prey consumption showed that an individual D. tamaninii consumed during its development to adult stage at 30 ± 1 °C an average of 442.2 (), 433.6 () aphids. At the constant temperature of 35 ± 1 °C, the average daily prey consumption started with 4 aphids and decreased continuously till it approached nil on the 9th day, where all predatory nymphs died. At the alternating temperatures of 25/15 ± 1 °C, the total prey consumption during development was, on average, 359.3 () and 297.0 () aphids, while at 35/22 ± 1 °C it was 348.5 () and 334.0 () aphids. The effect of the four temperatures on the prey consumption by D. tamaninii during the first 10 days after emergence was also studied. At a constant temperature of 30 ± 1 °C, a total of 446.4 () and 372.0 () aphids were consumed, compared to 40.6 () and 39.0 () at 35 ± 1 °C. At alternating temperatures of 25/15 ± 1 °C, the predatory adult consumed, on average, a total of 267.0 () and 207.0 () aphids. Increasing the temperature to 35/22 ± 1 °C resulted in a higher prey consumption by the adult predator, reaching 351.5 () and 267.7 () aphids over the same period.In conclusion, results indicated that D. tamaninii is a promising predator of the melon aphid at a temperature spectrum ranging from 15 ± 1 °C up to 35 ± 1 °C.     

Two new flavonoids from Retama raetam

Two new flavones were isolated from the aerial parts of Retama raetam subsp. raetam. Their structures were established as luteolin 4'-O-neohesperidoside (1) and 5,4'-dihydroxy-(3",4"-dihydro-3", 4"-dihydroxy)-2",2"-dimethylpyrano-(5",6":7,8)-flavone (2) by means of spectroscopic methods. Also present was ephedroidin (4',5, 7-trihydroxy-8-(2-hydroxy-3-butenyl)-flavone).     

Effect of feeding Aspergillus awamori and canola seed on the growth performance and muscle fatty acid profile in broiler chicken

The aim of this study was to examine effects of dietary supplementation with Aspergillus awamori and feeding canola seed on the growth and fatty acid profile in broilers. Twenty‐eight chicks (15 days old) were assigned to the following groups: (1) control, fed a basal diet; (2) awamori, fed the basal diet supplemented with 0.05% A. awamori; (3) canola, fed a diet containing 5% canola seed; and (4) canola + awamori, fed the canola diet supplemented with A. awamori (seven birds/group). Body weight gain was increased by A. awamori but not influenced by canola seed. Breast muscle weight was increased in either awamori or canola groups. Although plasma triglyceride and cholesterol were decreased by feeding A. awamori or canola seed, fat content in the breast muscle were increased, accompanied by decrease in saturated fatty acids and increase in unsaturated fatty acids. Moreover, decreased thiobarbituric acid reactive substance and increased α‐tocopherol content in the breast muscle was observed in all experimental groups. In conclusion, these results suggested that feeding canola seed and A. awamori might improve growth performance, and modified muscle fatty acid profile and α‐tocopherol content, suggesting that they may improve meat quality.     

The origin of mangosteen: A review

Genetic Resources and Crop Evolution - Mangosteen (Garcinia mangostana var. mangostana) is an obligate apomictic species which does not require a fertilization process to produce seeds. The absence...     

Minimizing instrumentation requirement for estimating crop water stress index and transpiration of maize

Research was conducted in northern Colorado in 2011 to estimate the crop water stress index (CWSI) and actual transpiration (T _a) of maize under a range of irrigation regimes. The main goal was to obtain these parameters with minimum instrumentation and measurements. The results confirmed that empirical baselines required for CWSI calculation are transferable within regions with similar climatic conditions, eliminating the need to develop them for each irrigation scheme. This means that maize CWSI can be determined using only two instruments: an infrared thermometer and an air temperature/relative humidity sensor. Reference evapotranspiration data obtained from a modified atmometer were similar to those estimated at a standard weather station, suggesting that maize T _a can be calculated based on CWSI and by adding one additional instrument: a modified atmometer. Estimated CWSI during four hourly periods centered on solar noon was largest during the 2 h after solar noon. Hence, this time window is recommended for once-a-day data acquisition if the goal is to capture maximum stress level. Maize T _a based on CWSI during the first hourly period (10:00–11:00) was closest to T _a estimates from a widely used crop coefficient model. Thus, this time window is recommended if the goal is to monitor maize water use. Average CWSI over the 2 h after solar noon and during the study period (early August to late September, 2011) was 0.19, 0.57, and 0.20 for plots under full, low-frequency deficit, and high-frequency deficit irrigation regimes, respectively. During the same period (50 days), total maize T _a based on the 10:00–11:00 CWSI was 218, 141, and 208 mm for the same treatments, respectively. These values were within 3 % of the results of the crop coefficient approach.     

Antibody-coated gold nanoparticles immunoassay for direct detection of Aeromonas salmonicida in fish tissues

Aeromonas salmonicida is the causative agent of furunculosis, a disease that affects both salmonid and non‐salmonid fish. Detection of A. salmonicida can be labour intensive and time consuming because of the difficulties in distinguishing the bacterium from other species given the wide variety of existing biochemical profiles and the slow growth characteristics which allow other organisms to overgrow the A. salmonicida. Herein, we report the development of a specific immunoassay using gold‐conjugated polyclonal antibodies for the rapid detection of A. salmonicida in fish tissues. Monodispersible 13‐nm gold nanoparticles were coated with polyclonal antibodies specific to A. salmonicida. Reddish purple agglutination of gold particles indicated the presence of A. salmonicida in samples. Positive reactions were detected visually with the naked eye. No agglutination was observed when A. salmonicida antibody‐coated gold nanoparticles were tested with other common bacterial fish pathogens, thereby verifying the specificity of the assay. The assay could detect A. salmonicida in fish tissues down to 1 × 10⁴ CFU mL^?1, and results were obtained within 45 min. The antibody‐coated gold nanoparticles were stable for at least 2 months at 4°C. The immunoassay using antibody‐coated gold nanoparticles represents a promising tool for the rapid and specific detection of A. salmonicida in fish tissues.