Mitigating the catastrophic impacts of torrential rivers in semi-arid environments: a case of the Gash River in eastern Sudan

The climatic, geomorphic, hydrologic and aquifer characteristics of the torrential Gash River across mountainous areas, in far eastern Sudan, were analyzed in order to mitigate its recurring catastrophic impacts. Hydrologic and climatic data and interpretation of Gash River satellite images were from relevant research works carried out in Gash Basin from 1985 to 2008. The results indicated that the total catchment area of Gash River is about 21,000 km2, and the basin area is 31,000 km2. The total length of Gash River is 450 km and the average slope is 200 cm/km. The width of the catchment varies from 30 m to 90 m and that of the basin is from 100 m to 800 m, and the course of the river is varied. During the period of 1980?2008, the mean annual rainfall was 250 mm and the mean annual discharge was 6.8 ×10~8 m~3, and the flooding is approximately one time per 5 years. Torrential floods measured at Kassala town since 1907 showed that an absolute maximum discharge was 876 m3/s and a mean maximum discharge was 365 m3/s. These characteristics differ widely between catchment and basin areas. The author proposes that, by analyzing the climatic, geomorphic, hydrologic and aquifer characteristics of the Gash River and considering the role of community, a concise database could be provided to formulate the aquifer, geomorphic, hydrologic and climatic (AQUIGEOHYCLIM) regional approach to mitigate Gash River recurring catastrophic impacts.     

A new pyrrole alkaloid from seeds of Castanea sativa

A new pyrrole alkaloid, methyl-(5-formyl-1H-pyrrole-2-yl)-4-hydroxybutyrate (1), was isolated from sweet chestnut seeds and its structure elucidated on the basis of data from NMR spectroscopy and by comparison with synthetic analogues.     

Chemical composition,insecticidal and biochemical effects of essential oils of different plant species from Northern Egypt on the rice weevil,Sitophilus oryzae L.

The extensive use of synthetic insecticides and fumigants for control stored-product insects has led to the development of resistance. Essential oils from aromatic plants may provide proper alternatives to currently used insect control agents. Essential oils from 20 Egyptian plants were obtained by hydrodistillation. The chemical composition of the oils was identified by gas chromatograph/mass spectrometer. Fumigant and contact toxicities of the essential oils were evaluated against Sitophilus oryzae. The inhibitory effects of the essential oils on acetylcholinesterase and adenosine triphosphatases activities were examined. The oils were composed of monoterpene hydrocarbons (i.e., limonene, sabinene, β-pinene and γ-terpinene) and oxygenated monoterpenes (i.e., terpinen-4-ol, β–thujone, 4-terpineol, α-citral and 1,8-cineole) with the exception of the oil of Schinus terebinthifolius which was contained sesquiterpenes, and the oil of Vitex agnus-castus which contained similar amounts of monoterpenes and sesquiterpenes. In the fumigation assay, the oils of Origanum vulgare (LC₅₀ = 1.64 mg/L air), Citrus lemon (LC₅₀ = 9.89 mg/L air), Callistemon viminals (LC₅₀ = 16.17 mg/L air), Cupressus sempervirens (LC₅₀ = 17.16 mg/L air), and Citrus sinensis (LC₅₀ = 19.65 mg/L air) showed high toxicity to S. oryzae. In the contact assay, the oils of Artemisia judaica, C. viminals, and O. vulgare caused the highest toxicity to S. oryzae with LC₅₀ values of 0.08, 0.09, and 0.11 mg/cm², respectively. The oil of A. judaica (I₅₀ = 16.1 mg/L) invoked the highest inhibitory effect on AChE activity, while the oils of C. viminals and O. vulgare were the most potent inhibitors to ATPases activity with I₅₀ values of 4.69 and 6.07 mg/L, respectively. The results indicate that the essential oils of A. Judaica, O. vulgare, C. limon, C. viminals, and C. sempervirens could be applicable to the management of populations of S. oryzae.     

Reaction of EDTA,DTPA, and EDDHA Complexes of Zinc,Copper, and Manganese with a Calcareous Soil

Solutions of Zn, Cu and Mn chelates of EDTA, DTPA and EDDHA were reacted separately with a calcareous soil for periods up to 28 days. DTPA was an effective chelate for Zn and Cu; more than 77 and 55% of the added Zn and Cu, respectively, remained soluble after 28 days of reaction with the soil. The stability of Zn-EDTA and Cu-EDTA was relatively less than those of the respective DTPA chelates, whereas Zn-EDDHA and Cu-EDDHA were highly unstable in the soil. The loss of soluble Mn from Mn-EDTA, Mn-DTPA and Mn-EDDHA additions to soil was very rapid and completed in about one week. It was found that adsorption of Zn-EDDHA, Cu-EDDHA and Mn-EDDHA molecules by the soil was the main process removing Zn, Cu and Mn from solution. Whereas, replacement of the metal in the metal-chelate molecule by Ca ion from the soil was a more serious factor affecting the stability of DTPA and EDTA chelates of Zn, Cu, and Mn.     

Incidence of antibiotic resistant bacteria in drinking water in Cairo

The presence of antibiotic resistant bacteria was found among standard plate count (SPC) populations of chlorinated drinking water from two districts in Cairo. SPC values obtained were low, ranging between 20 and 3 800 mL^?1. Most strains appeared to be ampicillin resistant (89.7%). Those were followed by sulfaguanidine (78.1%) and streptomycin (56.9%). The majority of the tested strains were resistant to two or more antibiotics (multiple antibiotic resistant, MAR) which represent 62.4 to 98 % of the total isolates of the mean obtained in a month. Identification of 363 MAR strains revealed that gram-positive rods were dominant in chlorinated drinking water. Gram-negative fermentative-rods, gram-positive cocci and gramnegative nonfermentative rods represent the second, third and fourth group of the identified MAR phenotypes. The impact of the antibiotic resistant bacteria in drinking water as a health hazard is discussed.     

Leachability of Lead from Lead Tailings

Laboratory column studies were used to predict the effect on the leachability of lead when using fly ash or a fly ash/sludge mixture as a cover for a lead tailings site. A high pH fly ash cover produced a leachate with a pH 12. This was sufficiently high to allow for the formation of lead hydroxide complexes which are slightly soluble. Therefore, the leachate had an average lead concentration of about 5 mg L^-1, while the pH in the leachate from the column with only tailings was 7.8 and a lead concentration below the detection limit (≤0.1 mg L^-1). The fly ash cover changed the availability of the remaining lead, making it less available. Rainfall rate did not affect the fly ash cover, but did have an effect on the fly ash/sludge cover.     

Effect of Cadmium on Lipid Peroxidation and on Some Antioxidants in the Liver,Kidneys and Testes of Rats Given Diet Containing Cadmium-polluted Radish Bulbs

The aim of this study was to examine the effects of cadmium (Cd), incorporated in radish bulbs, on malondialdehyde and glutathione levels and on superoxide dismutase activity in the liver, kidneys and testes of male rats. The control animals were given diet containing ordinary radish bulbs for 4, 8 and 12 weeks, while contaminated animals were given diet containing Cd-polluted radish bulbs (1.1 mg Cd/g of diet) for the same periods as in the controls. At each time point, rats were euthanized and the liver, kidneys and testes were removed. The results indicated that the body weight gain of contaminated rats was identical to that of the control rats. Cd concentrations in the liver, kidneys and testes increased significantly and gradually from the 4th to 12th week of treatment. Malondialdehyde concentrations decreased significantly in the liver and increased significantly in the kidneys and testes after 12 weeks of treatment, while glutathione levels increased significantly in the liver, and decreased significantly in the kidneys and testes at the same time. No changes were observed in SOD activity in the liver, while in the kidneys and testes, this activity was increased after 12 weeks of treatment as compared with the control rats.     

Elemental characterization of commercial mate tea leaves (Ilex paraguariensis A. St.-Hil.) before and after hot water infusion using ion beam techniques

Ilex paraguariensis A. St.-Hil. is used to prepare a traditional tealike beverage widely appreciated in Argentina, Paraguay, Uruguay, and southern Brazil. In these countries, the tea is popularly known as mate or chimarr?o. The aim of this work is to characterize the elemental composition of commercial Ilex paraguariensis and determine the portion of each element present in the leaves that is eluted in the water during the infusion process and consequently ingested by the drinker. Using the particle-induced X-ray emission technique, we verified the presence of Mg, Al, Si, P, S, Cl, K, Ca, Ti, Mn, Fe, Cu, Zn, and Rb at different concentrations, which accounts for about 3.4% of the total mass. The results show a loss of about 90% of K and Cl, 50% of Mg and P, and 20% of Mn, Fe, Cu, Zn, and Rb by the leaves after the infusion. The volume of water used in the infusion affects only the concentration of elements such as Cl, P, K, and Mg until the first 600 mL of water, where a steep decrease in the concentration of these elements was observed in brewed leaves. Furthermore, higher water temperatures (typical temperatures used in infusions, between 80 and 100 degrees C) favor the extraction of K and Cl into the infusion, while the concentration of other elements remains practically constant as a function of temperature.     

Effect of oxazolidine E on collagen fibril formation and stabilization of the collagen matrix

Oxazolidine E, an aldehydic cross-linking agent, is used to impart hydrothermal stability to collagen. The purpose of this study was to investigate the exact nature of oxazolidine E induced cross-links with collagen by using synthetic peptides having sequence homology with collagen type I. Tandem mass spectrometry revealed the formation of methylol and Schiff-base adducts upon reaction of oxazolidine E with the peptides. This was confirmed by allowing the reaction to proceed under reducing conditions using cyanoborohydride. Mass spectrometry (MS)-MS analysis clearly showed interaction of tryptophan and lysine residues with oxazolidine E and demonstrated that arginine could be cross-linked with glycine in the presence of oxazolidine E through the formation of a methylene bridge. Collagen fibrils regenerated from monomers in the presence and absence of oxazolidine E were studied using atomic force microscopy to investigate morphological alterations. Regenerated fibrils showing the typical 65 nm D-banding pattern were obtained from those formed both in the presence and absence of oxazolidine E, and there was no evidence of a change in the D-periodicity of these fibrils. This indicated that oxazolidine E does not hinder collagen molecules from correctly aligning to form the quarter-stagger structure.     

Development of Highly Selective and Efficient Prototype Sensor for Potential Application in Environmental Mercury Pollution Monitoring

Mercury (Hg) is an environmental pollutant which is detrimental to the health of living beings due to the toxicity in its all oxidation states. To control mercury pollution development of low cost, efficient and highly sensitive prototype mercury sensor remains a challenge. In the present work, we have proposed a low-cost prototype device based on silver nanoparticle-impregnated poly(vinyle alcohol) (PVA-Ag-NPs) nanocomposite thin film for mercury detection. The thin film, fabricated through a facile protocol, is shown to be a fast, efficient, and selective sensor for Hg²⁺ in aqueous medium with a detection limit of 10 ppb. We have utilized the aggregation and amalgamation of Ag-NPs with Hg²⁺ to develop the low-cost, highly efficient and feasible prototype mercury sensor. In the presence of Hg²⁺, the yellowish thin film turned into colourless due to the loss of intense surface plasmon resonance (SPR) absorption band of the silver nanoparticles (Ag-NPs) through aggregation and amalgamation with mercury. The developed sensor has high selectivity for Hg²⁺ ions over a wide range of other competing heavy metal ions, generally present in water of natural sources. The sensor response is found to be linear over the Hg²⁺ ion concentration regime from 10 ppb to 5 ppm. The developed sensor has shown to determine a trace Hg²⁺ ions in real water samples. Finally, using the proposed technique, we have developed a simple and inexpensive prototype device for monitoring in field environmental mercury pollution.

Open image in new window

Graphical Abstract ?