Biochemical composition of sedimentary organic matter in the coral reefs of Lakshadweep Archipelago,Indian Ocean

Surface sediments were collected from the shore and lagoons of Kavaratti, Kadamat Agatti and Pitti islands of Lakshadweep Archipelago during May 2015 and analysed for biochemical composition and quality of organic matter. The biochemical composition of sedimentary organic matter from the entire study area was characterised by the dominance of carbohydrates (CHO) followed by proteins (PRT) and finally lipids (LPD). PRT:CHO ratios were less than 1 and indicated the presence of aged organic matter in the islands. The poor nutritional quality of sediments to support benthic fauna was evident from the values of LPD:CHO ratios. The refractory nature of sediments and less availability of food to benthic source was supported by BPC:TOC ratios. Based on estimated ratios and biopolymeric carbon values, the trophic status of the study area was categorised as oligotrophic.     

Photochemical decomposition of tetrachlorovinphos

The photochemical degradation of tetrachlorovinphos in solvents and as a solid has been investigated. Photoproducts have been isolated and characterized by spectroscopic methods and comparison with authentic samples. The rate of phototransformation of this compound has also been studied.     

Physiological effects of arsenate on transplant thalli of the lichen Pyxine cocoes (Sw.) Nyl

Introduction

The changes in photosynthetic pigments, chlorophyll fluorescence, protein content, and antioxidant enzymes were investigated in a foliose lichen Pyxine cocoes, which was subjected to increasing concentrations of arsenate.

Methods

The arsenate concentrations of 10, 25, 50, 75, 100, and 200???M were sprayed every alternate day on the lichen thallus. The thalli were then harvested on 10, 20, 30, and 45?days.

Results

The quantity of photosynthetic pigments exhibited a decreasing trend till 20?days but increased from 30?days onwards. Concomitantly, chlorophyll fluorescence also showed a decreasing trend with increasing arsenic treatment duration as well as concentration. The higher concentration of arsenate was found to be deleterious to the photosynthesis of lichen as the chlorophyll fluorescence and the amount of pigments decreased significantly. The protein content of lichen increased uninterruptedly as the concentration of arsenate as well as duration of treatment increased. The activities of superoxide dismutase and ascorbate peroxide increased initially at lower concentration of arsenate but declined at higher concentrations and longer duration of treatment.

Conclusions

The catalase activity was found to be most susceptible to arsenate stress as its activity started declining from very beginning of the experiment. P. cocoes also proved to be an excellent accumulator of arsenate whose concentration increased in the thallus corresponding to its increase in the treatment and duration. Thus, it can be utilized for active biomonitoring of arsenic pollution.     

Behaviour and Quantification Studies of Terbacil and Lenacil in Environmental Samples Using Cyclic and Adsorptive Stripping Voltammetry at Hanging Mercury Drop Electrode

The cyclic voltammograms of terbacil and lenacil at the hanging mercury drop electrode showed a single well defined four electron irreversible peak in universal buffer of pH 4.0 for both compounds. The peak potentials were shifted to more negative values on the increase of pH of the medium, implying the involvement of protons in the electrode reaction and that the proton transfer reaction precedes the proper electrode process. The four electron single peak may be attributed to the simultaneous reduction of carbonyl groups present in 2 and 4 in pyrimidine ring of terbacil and lenacil to the corresponding hydroxy derivative. Based on the interfacial adsorptive character of the terbacil and lenacil onto the mercury electrode surface, a simple sensitive and low cost differential pulse adsorptive stripping voltammetric procedure was optimized for the analysis of terbacil and lenacil. The optimal operational conditions of the proposed procedure were accumulation potential E _acc = −0.4 V, accumulation time t _acc = 80 s, scan rate = 40 mV s⁻¹, pulse amplitude = 25 mV using a universal buffer pH 4.0 as a supporting electrolyte. The linear concentration range was found to be 1.5 × 10⁻⁵ to 1.2 × 10⁻⁹ mol/l and 1.5 × 10⁻⁵ to 2.5 × 10⁻⁸ mol/l with the lower detection limit of 1.22 × 10⁻⁹ and 2.0 × 10⁻⁸ mol/l. The correlation coefficient and relative standard deviation values are found to be 0.942, 0.996, 1.64% and 1.23%, respectively, for 10 replicants. The procedure was successfully applied for determination of terbacil and lenacil in formulations, mixed formulations, environmental samples such as fruit samples and spiked water samples.     

Trace metal fractionation in the Pichavaram mangrove–estuarine sediments in southeast India after the tsunami of 2004

The geochemistry of coastal sediments of southern India was altered after the tsunami in 2004. A five-step sequential extraction procedure was applied to assess the effects of tsunami on mobility and redistribution of selected elements (Cd, Cr, Cu, Fe, Mn, Ni, Pb, and Zn). Ten surface sediments and three cores were analyzed for different metal fractions (exchangeable, carbonate, reduced, oxidized, and residual). Total metal concentrations increased in mangrove sediments after the tsunami, but their spatial distribution did not show significant variation (except Mn). The sediments were mixed by the tsunami, and there was lack of variation in metal concentrations in different fractions with depth (except Pb and Mn). High concentrations of Pb and Zn occurred in the oxide fractions, whereas Cu, Cr, Cd, and Ni were high in the organic and sulfide-rich fractions. Metals in the residual fraction (lattice bound) had the highest concentration suggesting their non-availability and limited biological uptake in the system. Most of the metals (except Mn) do not constitute a risk based on the different geochemical indices.     

Statistical Modeling of Health Effects on Climate-Sensitive Variables and Assessment of Environmental Burden of Diseases Attributable to Climate Change in Nepal

An ecological time-series study is conducted to quantify health-effect coefficients associated with climate-sensitive variables namely temperature, rainfall, relative humidity, and wind speed and estimate environmental burden of diseases attributed to temperature as the main climatic variable together with climate change in Nepal. The study is based upon daily data of climate-sensitive variables and hospitalizations collected for 5 years between 2009 and 2014. Generalized linear model is used to estimate health-effect coefficients accounting distributed lag effects. Results show 3.08%, 10.14%, and 3.27% rise in water-borne, vector-borne, and renal disease hospitalizations, respectively, and 3.67% rise in water- and vector-borne disease deaths per 1 °C rise in average temperature. Similarly, 2.45% and 1.44% rise in heart disease hospitalization and all-cause mortality, respectively per 1 °C rise in absolute difference of average temperature with its overall average (20 °C). The computed attributable fractions are 0.3759, 0.6696, 0.2909, and 0.1024 for water-borne, vector-borne, renal, and heart disease hospitalizations, respectively, and 0.0607 and 0.4335 for all-cause mortality and disease-specific mortality of water- and vector-borne diseases, respectively. The percent change in attributable burdens due to climate change are found to be 4.32%, 4.64%, 7.20%, and ?2.29% for water-borne, vector-borne, renal, and heart disease hospitalizations, respectively, and ?1.39% and 6.55% for all-cause deaths and water-borne and vector-borne disease deaths, respectively. In conclusion, climate-sensitive variables have significant effects on many major health burdens in Nepal. In the context of changing climatic scenarios around the world including that of Nepal, such changes are bound to affect the health burden of Nepalese people.     

Synthesis of 2-furyl-4-arylidene-5(4H)-oxazolones as new potent antibacterial agents against phyto-pathogenic and nitrifying bacteria

Crop losses due to bacterial pathogens are a major global concern. Most of the available pesticides for these pathogens suffer from various drawbacks such as complicated synthesis, high cost, high toxicity, pesticide resistance and environmental hazards. To overcome these drawbacks, the present study was undertaken to find a potent bactericide. Therefore, a series of compounds comprising bioactive furyl and oxazolone rings was synthesized under microwave irradiation and screened for in vitro antibacterial activity. The reactions were completed in fewer than 2 minutes with minimal use of solvents and resulted in high yields. These compounds were screened for antibacterial activity against plant pathogens, Xanthomonas oryzae, Ralstonia solanacearum and nitrifying bacteria, Nitrosomonas species under laboratory conditions. Five compounds were active as antibacterial agents against Xanthomonas oryzae and Ralstonia solanacearum. However, all compounds were effective against the Nitrosomonas species and the best one was 2-furyl-4-(3-methoxy-4-hydroxybenzylidene)-5(4H)-oxazolone. The study revealed the fast and environmentally friendly synthesis of bioactive title compounds, which also hold promise to be used as prototypes for the discovery of potent analogues.     

Partial characterization,UV-induction and photoprotective function of sunscreen pigment,scytonemin from Rivularia sp. HKAR-4

Scytonemin, located in the extracellular polysaccharide sheath of some cyanobacterial species is considered an efficient natural photoprotectant against lethal doses of ultraviolet (UV) radiations. In the present study, scytonemin from the cyanobacterium Rivularia sp. HKAR-4 was partially characterized and investigated for its induction by UV radiation as well as its role in photoprotection. High-performance liquid chromatography (HPLC) with photodiode-array detection studies revealed the presence of an UV-absorbing compound with absorption maximum at 386 nm. Based on its absorption spectrum and ion trap liquid chromatography/mass spectrometry (LC/MS) analysis, the compound was confirmed as scytonemin. In comparison to photosynthetically active radiation, a significant induction in the synthesis of scytonemin was found under UV-stress. Scytonemin also exhibited efficient photoprotective ability by detoxifying the in vivo reactive oxygen species (ROS) generated by UV radiation and by reducing the formation of thymine dimers. To the best of our knowledge this is the first report on the UV-screening effects of scytonemin on in vivo ROS generation and thymine dimer formation in any cyanobacterial strain. Based on these findings, we conclude that scytonemin may play a vital role in the survival and sustainability of cyanobacterial life in adverse environmental conditions such as under high solar irradiances.     

Brown marine algae turbinaria conoides as biosorbent for Malachite green removal: Equilibrium and kinetic modeling

In this study, the biosorption of Malachite green (MG) onto Turbinaria conoides, brown marine algae, was studied with respect to initial pH, temperature, initial dye concentration, and sorbent dosage. The optimum initial pH and temperature values for MG removal were found to be 8.0 and 30°C, respectively. Sorbent dosage was found to strongly influence the removal of MG. Equilibrium studies were carried out to test the validity of the Langmuir (q _max = 66.6 mg/g and b = 0.526 mL mol/L) and the Freundlich (n = 1.826 and K = 3.751 mg/g) isotherms. The kinetic studies indicated the validity of the pseudo first-order and second-order equation.     

Spatial variation of phosphorus fractionation in the coral reef sediments of Lakshadweep Archipelago,Indian Ocean

Surface sediments were collected from the shore and lagoons of Kavaratti, Kadamat and Agatti islands of Lakshadweep Archipelago during May 2015 and analysed for the spatial distribution of the micronutrient element, phosphorus. Phosphorus was separated by sequential extraction procedure into five fractions – exchangeable (Ex-P), iron bound, (Fe-P), calcium bound (Ca-P), organic and residual fractions (OP) and total phosphorus (TP). The average relative contribution of each P species to TP was: OP?>?Ca –P?>?Ex – P?>?Fe – P. The high concentration of organic and residual phosphorus (87–96%) compared to inorganic phosphorus is particularly evident at stations characterised by higher total phosphorus concentrations. Among the three forms of IP in the sediments, Ca-P was dominant at all stations. The OC/OP ratio ranged from 3 to 163 in the sediments, suggesting that the organic matter in sediments had been subjected to degradation. Hence, the major contribution towards organic and residual phosphorus form is from the residual fraction comprising biologically resistant or non-available phosphorus form composed of refractory materials. The concentration of phosphorus reported in the present study is higher than that of the earlier studies in Lakshadweep, indicating a terrestrial and anthropogenic in?uence on the sediment.