Does salinity enhance Cd toxicity to soil alkaline phosphatase?

The aim of this study was to provide data to assess the additive effects of soil salinity on the toxicity of Cd to soil alkaline phosphatase (EC 3.1.3.1). Two soils (Langroud acid soil and Shervedan calcareous soil) were artificially salinized with NaCl. The natural and salinized soils were treated with CdSO₄ solutions to give a Cd concentration in the range 3–5000 mg kg^?1. Soil alkaline phosphatase activity was measured after 3 days of incubation. Salinity enhanced the extractable Cd concentration in both Langroud and Shervedan soils. The percentage of soil alkaline phosphatase activity inhibited by Cd was significantly increased from 27.8 to 45 in the Langroud acid soil as salinity increased from natural levels to 28 dS m^?1. An increase in the inhibition percentage was not observed in the Shervedan soil. Lower values for the ecological dose causing 50% inhibition (ED₅₀) under saline conditions in the Shervedan soil supported the hypothesis that Cd may be more toxic to soil alkaline phosphatase when the soil is more saline. We conclude that Cd toxicity to soil alkaline phosphatase is salinity dependent and that higher Cd concentrations under saline conditions are probably responsible for the enhanced Cd toxicity to soil alkaline phosphatase.     

The genome of the African trypanosome Trypanosoma brucei

African trypanosomes cause human sleeping sickness and livestock trypanosomiasis in sub-Saharan Africa. We present the sequence and analysis of the 11 megabase-sized chromosomes of Trypanosoma brucei. The 26-megabase genome contains 9068 predicted genes, including approximately 900 pseudogenes and approximately 1700 T. brucei-specific genes. Large subtelomeric arrays contain an archive of 806 variant surface glycoprotein (VSG) genes used by the parasite to evade the mammalian immune system. Most VSG genes are pseudogenes, which may be used to generate expressed mosaic genes by ectopic recombination. Comparisons of the cytoskeleton and endocytic trafficking systems with those of humans and other eukaryotic organisms reveal major differences. A comparison of metabolic pathways encoded by the genomes of T. brucei, T. cruzi, and Leishmania major reveals the least overall metabolic capability in T. brucei and the greatest in L. major. Horizontal transfer of genes of bacterial origin has contributed to some of the metabolic differences in these parasites, and a number of novel potential drug targets have been identified.     

Comparison of Caudal Epidural Anesthesia with Lidocaine-distilled Water and Lidocaine-MgSO4 Mixture in Horses

This study was performed to compare the onset and duration of analgesia produced by either a lidocaine−MgSO₄ or lidocaine−distilled water combination administration in the caudal epidural space of horse. Seven healthy adult horses, aged 11.7 ± 1.4 years (mean ± SD), body weight (kg) 567 ± 32.5 (mean ± SD), were selected for this study. Caudal epidural anesthesia was produced in all horses by administering 2% lidocaine (0.22 mg/kg) diluted in 1 mL distilled water and repeated with 2% lidocaine (0.22 mg/kg) diluted in 1 mL 10% MgSO₄ 2 weeks later. Time to onset (minutes), duration (minutes), and cranial spread of epidural analgesia were recorded. Heart rate (HR), respiratory rate (RR), and body temperature (°C) were recorded. Measurements were taken at 0 (as a baseline value before epidural administrations) and at 5, 10, 15, 30, 60, and 75 minutes after the epidural administrations of each treatment. Statistical analyses included paired Student t test and analysis of variance (computer program SPSS, Analytical Software, version 15.00). Statistical significance was set at P < .05. Onset of analgesia was significantly different (P < .001) between lidocaine-distilled water (2.38 ± 0.47 minutes) and lidocaine−MgSO₄ (4.62 ± 0.54 minutes). Duration of analgesia after lidocaine−MgSO₄ (186.0 ± 7.0 minutes) was longer than lidocaine-distilled water (54.5 ± 7.3 minutes). No significant differences were recorded for HR, RR, and body temperature in comparison with baseline values for each group. Using the lidocaine−MgSO₄ combination for obstetric and surgical procedures could commence relatively soon after epidural injection and could be completed without readministration of anesthetic agent.     

Immunolocalization of Na+, K+-ATPase-rich cells in the gill and urinary system of Persian sturgeon, Acipenser persicus, fry

Localization of Na⁺, K⁺-ATPase-rich cells in the gill and urinary system of Acipenser persicus fry was performed through immunofluorescence light microscopy using a mouse monoclonal antibody IgGα₅ raised against the α-subunit of chicken Na⁺, K⁺-ATPase. Different types of epithelia were clearly identified in the gill epithelium: epithelia of branchial arch, interbranchial septum, filament and lamellar epithelium. The Na⁺, K⁺-ATPase-rich cells were found in the epithelia of branchial arch, interbranchial septum, filament, interlamellar region and also in the lamellae. Histologically, the urinary system is divided into head kidney, trunk kidney and short caudal kidney. The head kidney is composed of the pronephric tubules and the haemopoietic tissues, while the trunk kidney is composed of a large number of glomeruli and convoluted nephrons. Each nephron consisted of a large glomerulus and tubules (neck, proximal, distal and collecting tubules) which connected to ureters. Posteriorly, ureters extended and joined together to form a small urinary bladder. In the urinary system, no specific fluorescence staining was observed in the glomerulus, neck segment and proximal tubules. The distal tubule cells and collecting tubule cells showed a strong immunostaining of Na⁺, K⁺-ATPase. Epithelia of ureters and urinary bladder also showed several isolated immunofluorescent cells. Immunofluorescent cells were rich in Na⁺, K⁺-ATPase enzyme which is very important for osmoregulation.     

Determination of grapefruit (Citrus paradisi) peel extract bio‐active substances and its application in Caspian white fish (Rutilus frisii kutum) diet: Growth,haemato‐biochemical parameters and intestinal morphology

In this study, total phenolic and flavonoid contents of grapefruit peel extract (GPE) were equal to 117.3 ± 0.3 µg of gallic acid/mg and 39.30 ± 0.1 µg of quercetin/mg respectively. Caspian white fish (n = 180, 4 ± 0.9 g body weight) was fed with supplemented diets, including 0, 6.25, 12.5 and 25 mg of GPE/kg for 60 days at 25 ± 1°C. The growth performance was markedly improved in fish fed with 25 mg/kg of GPE compared to others (p < 0.05). Moreover, fish fed with 25 mg/kg of GPE showed a significant increase in red blood cell (2.65·10⁶ cell/mm³), white blood cell (17.75·10³ cell/mm³), packed cell volume (48%) and haemoglobin concentrations (8.75 g/dl) compared to the control (p < 0.05). However, the highest alanine aminotransferase (140 U/L), alanine transaminase (14.5 U/L), and alkaline phosphatase (18.5 U/L) were observed in control group. Morphological analysis of intestine revealed the highest amount of villus width (8.4 µM), height (32.86 µM) and surface area (342.7 µM²) in fish fed with 25 mg/kg of GPE (p < 0.05). In conclusion, supplementing feed with GPE at 25 g/kg can improve growth performance and haemato‐biochemical parameters of Caspian white fish fry.     

Interactions between Heterodera filipjevi and Fusarium culmorum,and between H. filipjevi and Bipolaris sorokiniana in winter wheat

Journal of Plant Diseases and Protection - Pot experiments with winter wheat were conducted for two successive years to study the relationship between the cereal cyst nematode, Heterodera...     

Canopy cover or remotely sensed vegetation index,explanatory variables of above-ground biomass in an arid rangeland,Iran

Estimation of above-ground biomass is vital for understanding ecological processes. Since direct measurement of above-ground biomass is destructive, time consuming and labor intensive, canopy cover can be considered as a predictor if a significant correlation between the two variables exists. In this study, relationship between canopy cover and above-ground biomass was investigated by a general linear regression model. To do so, canopy cover and above-ground biomass were measured at 5 sub-life forms(defined as life forms grouped in the same height classes) using 380 quadrats, which is systematic-randomly laid out along a 10-km transect, during four sampling periods(May, June, August, and September) in an arid rangeland of Marjan, Iran. To reveal whether obtained canopy cover and above-ground biomass of different sampling periods can be lumped together or not, we applied a general linear model(GLM). In this model, above-ground biomass was considered as a dependent or response variable, canopy cover as an independent covariate or predictor factor and sub-life forms as well as sampling periods as fixed factors. Moreover, we compared the estimated above-ground biomass derived from remotely sensed images of Landsat-8 using NDVI(normalized difference vegetation index), after finding the best regression line between predictor(measured canopy cover in the field) and response variable(above-ground biomass) to test the robustness of the induced model. Results show that above-ground biomass(response variable) of all vegetative forms and periods can be accurately predicted by canopy cover(predictor), although sub-life forms and sampling periods significantly affect the results. The best regression fit was found for short forbs in September and shrubs in May, June and August with R~2 values of 0.96, 0.93 and 0.91, respectively, whilst the least significant was found for short grasses in June, tall grasses in August and tall forbs in June with R~2 values of 0.71, 0.73 and 0.75, respectively. Even though the estimated above-ground biomass by NDVI is also convincing(R~2=0.57), the canopy cover is a more reliable predictor of above-ground biomass due to the higher R~2 values(from 0.75 to 0.96). We conclude that canopy cover can be regarded as a reliable predictor of above-ground biomass if sub-life forms and sampling periods(during growing season) are taken into account. Since,(1) plant canopy cover is not distinguishable by remotely sensed images at the sub-life form level, especially in sparse vegetation of arid and semi-arid regions, and(2) remotely sensed-based prediction of above-ground biomass shows a less significant relationship(R~2=0.57) than that of canopy cover(R~2 ranging from 0.75 to 0.96), which suggests estimating of plant biomass by canopy cover instead of cut and weighting method is highly recommended. Furthermore, this fast, nondestructive and robust method that does not endanger rare species, gives a trustworthy prediction of above-ground biomass in arid rangelands.     

Investigating the effects of temperature on seed germination of cutleaf geranium (Geranium dissectum L.) and determination of its cardinal temperatures

Phytoparasitica - Cutleaf geranium is a weed infesting crop fields in various parts of the world. The present study was conducted to determine the cardinal temperatures of germination for its seeds...     

Improvement of biochar capability in Cr immobilization via modification with chitosan and hematite and inoculation with Pseudomonas putida

ABSTRACT

Modification of biochar using chitosan and hematite made the biochar product more effective for hexavalent chromium (Cr (VI)) reduction in contaminated soils. Release experiment was conducted to examine Cr (VI) reduction in different treatments (control, unmodified biochar and two modified biochars with chitosan or hematite). The results indicated that the application of all treatments significantly decreased the release rate of Cr in comparison to the control treatment. Chitosan-modified biochar application increased Cr (VI) reduction from 28.53% (biochar) to 46.23%. In the case of hematite-modified biochar, it increased Cr (VI) reduction from 28.55% (biochar) to 38.95%. Two kinetic equations including pseudo-first-order and pseudo-second-order models employed to describe the time-dependent Cr release data. Between the kinetic equations estimated, the pseudo-second order best fitted to experimental data. In the presence of Pseudomonas putida, cumulative Cr release rate decreased by 2.38 mg kg^?1 (50.29%) in hematite–biochar and 1.768 mg kg^?1 (39.73%) in unmodified biochar as compared with control (4.43 mg kg^?1). According to results reported herein, modification of biochar with chitosan or hematite is promising since made biochar more effective in removing Cr from Cr-polluted calcareous soils.