Intensity of tropical cyclones during pre- and post-monsoon seasons in relation to accumulated tropical cyclone heat potential over Bay of Bengal

The aim of the present study is to understand the impact of oceanic heat potential in relation to the intensity of tropical cyclones (TC) in the Bay of Bengal during the pre-monsoon (April–May) and post-monsoon (October–November) cyclones for the period 2006–2010. To accomplish this, the two-layer gravity model (TLGM) is employed to estimate daily tropical cyclone heat potential (TCHP) utilizing satellite altimeter data, satellite sea surface temperature (SST), and a high-resolution comprehensive ocean atlas developed for Indian Ocean, subsequently validated with in situ ARGO profiles. Accumulated TCHP (ATCHP) is estimated from genesis to the maximum intensity of cyclone in terms of minimum central pressure along their track of all the cyclones for the study period using TLGM generated TCHP and six-hourly National Centre for Environmental Prediction Climate Forecast System Reanalysis data. Similarly, accumulated sea surface heat content (ASSHC) is estimated using satellite SST. In this study, the relationship between ATCHP and ASSHC with the central pressure (CP) which is a function of TC intensity is developed. Results reveal a distinct relationship between ATCHP and CP during both the seasons. Interestingly, it is seen that requirement of higher ATCHP during pre-monsoon cyclones is required to attain higher intensity compared to post-monsoon cyclones. It is mainly attributed to the presence of thick barrier layer (BL) resulting in higher enthalpy fluxes during post-monsoon period, where as such BL is non-existent during pre-monsoon period.     

An Optimised 1,10‐Phenanthroline Method for the Determination of Ferrous and Ferric Oxides in Silicate Rocks,Soils and Minerals

A precise, accurate and rapid method for the sequential determination of FeO and Fe₂O₃ in rocks, soils and some non‐refractory minerals by 1,10‐phenanthroline spectrophotometry is described. Fe(II) and Fe(III) were leached from the sample (?200 mesh) using a mixture of NH₄HF₂ and H₂SO₄ at 40–80 °C for 10 min on a hot plate. Both Fe(II) and Fe(III) could be conveniently estimated sequentially from the same reaction mixture at the μg g^?1 to percentage level. The method is better than the existing wet chemical methods, including the commonly used Pratt's titrimetric redox method, for Fe(II) and Fe(III) determinations in rock and soil samples in terms of precision, accuracy and rapidity. The throughput of the method was very high; at least forty to fifty samples could be estimated easily in a day. The results obtained compare favourably with those obtained by Pratt's method, as well as for certified/recommended values of a set of eleven certified reference materials having FeO and Fe₂O₃ contents in the range 0.21–14.63% and 0.58–8.48%, respectively. The optimised 1,10 phenanthroline method was found to be accurate to within 0.21% m/m FeO and 0.30% m/m Fe₂O₃ compared with the literature values of the certified reference materials studied.     

Occurrence, physiological responses and toxicity of nickel in plants

The focus of the review is on the specific aspects of nickel’s effects on growth, morphology, photosynthesis, mineral nutrition and enzyme activity of plants. The mobility of nickel in the environment and the consequent contamination in soil and water is of great concern. Also, the detrimental effects of excessive nickel on plant growth have been well known for many years. Toxic effects of nickel on plants include alterations in the germination process as well as in the growth of roots, stems and leaves. Total dry matter production and yield was significantly affected by nickel and also causes deleterious effects on plant physiological processes, such as photosynthesis, water relations and mineral nutrition. Nickel strongly influences metabolic reactions in plants and has the ability to generate reactive oxygen species which may cause oxidative stress. More recent evidence indicates that nickel is required in small amounts for normal plant growth and development. Hence, with the increasing level of nickel pollution in the environment, it is essential to understand the functional roles and toxic effects of nickel in plants.     

Temporal variation in the arsenic and metal accumulation in the maritime pine tree grown on contaminated soils

The uptake of arsenic and other metals (iron, manganese, copper, zinc, lead, nickel and tungsten) by Pinus pinaster Aiton (the maritime pine tree) growing in soils and tailings around an abandoned mine (northern Portugal) was investigated. Aerial parts of Pinus pinaster trees were sampled from three substrate areas: a background area, in mine contaminated soils and in tailings. Vegetation material was separated into needles and stems and subdivided into tissues of different maturities (1-, 2-, 3- and 4-years-old). The sampling of the substrate in each area was also undertaken. In general, vegetation concentrations were strongly related to substrate concentrations. The results show that the contents of several elements depend as much on the plant organ as on the age of the tissue. For the researched elements, this species shows a great variability in behavior depending on the age of the organ. The data indicate that the older needles constitute the best samples for use in a conjunct biogeochemical analysis of these elements.     

An integrated approach to investigate saline water intrusion and to identify the salinity sources in the Central Godavari delta, Andhra Pradesh, India

The Central Godavari delta is located along the Bay of Bengal Coast, Andhra Pradesh, India, and is drained by Pikaleru, Kunavaram and Vasalatippa drains. There is no groundwater pumping for agriculture as wells as for domestic purpose due to the brackish nature of the groundwater at shallow depths. The groundwater table depths vary from 0.8 to 3.4 m and in the Ravva Onshore wells, 4.5 to 13.3 m. Electrical Resistivity Tomography (ERT) surveys were carried out at several locations in the delta to delineate the aquifer geometry and to identify saline water aquifer zones. Groundwater samples collected and analyzed for major ions for assessing the saline water intrusion and to identify the salinity origin in the delta region. The results derived from ERT indicated low resistivity values in the area, which can be attributed to the existence of thick marine clays from ground surface to 12–15 m below ground level near the coast and high resistivity values are due to the presence of coarse sand with freshwater away from the coast. The resistivity values similar to saline water <0.01 Ω m is attributed to the mixing of the saline water along surface water drains. In the Ravva Onshore Terminal low resistivity values indicated up coning of saline water and mixing of saline water from Pikaleru drain. The SO ₄ ^?2 /Cl^?and Na⁺²/Cl^?ratios did not indicate saline water intrusion and the salinity is due to marine palaeosalinity, dilution of marine clays and dissolution of evaporites.     

Change in entropy of non-spinning black holes w.r.t. the radius of event horizon in XRBs

The present research paper discusses the derivation for the change in entropy of Non- spinning black holes with respect to the change in the radius of event horizon applying the first law of black hole mechanics ( $\delta M = \frac{\kappa}{8\pi} \delta A + \varOmega\delta J - \upsilon\delta Q$ ) with the relation for the change in entropy δS=8πMδM. When the work is further extended with proper operation, the entropy of black hole is obtained almost the same as the Bekenstein-Hawking entropy of black hole. This is the entirely new method to obtain the change in entropy of Non-spinning black holes w.r.t. the radius of event horizon and Hawking entropy of black hole. We have also calculated their values for different types of test non-spinning black holes having masses 5–20M _⊙ found in X-ray binaries (Narayan, gr-qc/0506078v1, 2005).     

Removal of Selenium by Adsorption onto Granular Activated Carbon (GAC) and Powdered Activated Carbon (PAC)

The present work involves the study of Se(IV) adsorption onto granular activated carbon (GAC) and powdered activated carbon (PAC). The adsorbents are coated with ferric chloride solution for the effective removal of selenium. The physico-chemical characterization of the adsorbents is carried out using standard methods, e. g., proximate analysis, scanning electron microscopy (SEM), fourier transform infrared spectroscopy (FTIR), thermo-gravimetric (TGA) and differential thermal analysis (DTA), etc. The FTIR spectra of the GAC and PAC indicate the presence of various types of functional groups, e. g., free and hydrogen bonded OH groups, silanol groups (Si-OH), alkenes, and CO group stretching from aldehydes and ketones on the surface of adsorbents. Batch experiments are carried out to determine the effect of various factors such as adsorbent dose (w), initial pH, contact time (t), and temperature (T) on the adsorption process. The optimum GAC and PAC dosage is found to be 10 g/L and 8 g/L, respectively, for Se(IV) removal with C₀ = 100 mg/L. The percent removal of Se(IV) increases with increasing adsorbent concentration, while removal per unit weight of adsorbent increases with decreasing adsorbent concentration. Se(IV) adsorption onto both the GAC and PAC adsorbents is high at low pH values, and decreases with increased initial pH. The results obtained are analyzed by various kinetic models. The parameters of pseudo-first order, pseudo-second order kinetics, and Weber-Morris intra particle kinetics are determined. It is seen that the sorption kinetics of Se(IV) onto GAC and PAC can be best represented by the pseudo-second order kinetic model.     

Adsorption of Selenium Using Bagasse Fly Ash

The present work involves the study of Se(IV) adsorption onto bagasse fly ash. The adsorbents were coated with a ferric chloride solution for the effective removal of selenium. The physico‐chemical characterization of the adsorbent was carried out using standard methods, e. g., proximate analysis, scanning electron microscopy, Fourier transform infrared spectroscopy, thermo‐gravimetric analysis and differential thermal analysis. Batch experiments were carried out to determine the effect of various parameters such as adsorbent dose, initial pH, contact time, and temperature on the adsorption process. Results obtained from these studies were analyzed using various kinetic models and isotherms. Se(IV) adsorption onto adsorbent was high at low pH values, and decreased with an increase in initial pH. A temperature study showed that the uptake of Se(IV) was greatest at 293 K, within the temperature range studied. The parameters of pseudo first order, pseudo second order, and Weber‐Morris intra‐particle kinetic models were determined. Equilibrium isotherms were analyzed using Langmuir, Freundlich, and Temkin isotherms. Error analyses were also carried out using hybrid fractional error function and Marquardt's percent standard deviation.     

Characteristics of Flaring Sites in Solar Active Regions

The properties of the flaring sites in the active region NOAA 6555 and 6659 are presented in this paper. Although, several locations of these active regions displayed high magnetic shear, the X-class flares occurred only at one of them. Our investigations show that these locations are characterized by the `crossing' of magnetic and velocity field neutral lines. Based on a new parameter to define the stressed magnetic fields, we show that some of these flaring locations possessed highly stressed magnetic field which disappeared after the flare. This revised version was published online in July 2006 with corrections to the Cover Date.     

Temperature and pH Dependence of Some Metals Leaching from Fly Ash of Municipal Solid Waste

Abstract. Municipal solid waste combustion leads to concentration of various metals in the solid residue (fly ash) remaining after combustion. These metals pose serious environmental hazard and require proper handling and monitoring in order to control their harmful effects. Leachability of some metals from fly ash was examined in fly ash and Milli-Q water mixture (liquid-to-solid ratio, 100) under various temperature and pH conditions in the laboratory. The leaching experiments conducted for 24 hours showed that pH was generally more important than temperature in controlling the amount of metals leached out of the fly ash. However, at a given pH, rise in temperature led to different degree of (usually one to two fold) enhanced or reduced leaching of metals. Owing to amphoteric nature of oxides of Al, Cr, Pb and Zn, these metals often yielded typical pattern of increase and decrease in their concentrations with change in pH. The extent of leaching of Cr and Pb in our experiments suggests that decrease of pH to acidic range in the case of Pb and to neutral to acidic range for Cr over a long period of storage of fly ash at solid waste dumping site may facilitate leaching of these metals from fly ash, leading to contamination of groundwater to the level that exceeds beyond the level permitted by the environmental laws.