Pyrethroid residue dynamics in insects depends on the circadian clock

Many factors may affect pesticide effectiveness against pests. One of the factors that should be considered is circadian rhythmicity. In this study, we evaluated daily variations in pyrethroid susceptibility in the house cricket, Acheta domesticus L. Crickets were exposed to a standard dose of ß-cyfluthrin at different times of a day, and pesticide residue levels were evaluated using gas chromatography. Results demonstrate that the time of pyrethroid disappearance is correlated with the circadian clock, with the highest decomposition rate at night. Furthermore, crickets also showed the highest resistance to the insecticide at night, expressed as a high survival rate. Moreover, ß-cyfluthrin induced significant changes in thermal preferences of intoxicated crickets. This is the first report showing that pyrethroid residue levels in the crickets' body depend on its circadian clock.     

Mathematical modeling to predict residential solid waste generation

One of the challenges faced by waste management authorities is determining the amount of waste generated by households in order to establish waste management systems, as well as trying to charge rates compatible with the principle applied worldwide, and design a fair payment system for households according to the amount of residential solid waste (RSW) they generate. The goal of this research work was to establish mathematical models that correlate the generation of RSW per capita to the following variables: education, income per household, and number of residents. This work was based on data from a study on generation, quantification and composition of residential waste in a Mexican city in three stages. In order to define prediction models, five variables were identified and included in the model. For each waste sampling stage a different mathematical model was developed, in order to find the model that showed the best linear relation to predict residential solid waste generation. Later on, models to explore the combination of included variables and select those which showed a higher R(2) were established. The tests applied were normality, multicolinearity and heteroskedasticity. Another model, formulated with four variables, was generated and the Durban-Watson test was applied to it. Finally, a general mathematical model is proposed to predict residential waste generation, which accounts for 51% of the total.     

Reactivity of the plant growth regulator paclobutrazol (cultar) with two tropical soils of the northeast semiarid region of Brazil

The reactivity of paclobutrazol (PBZ, a plant growth retardant) with a Yellow Ultisol and a Vertisol from the semiarid northeast region of Brazil was evaluated through batch sorption experiments and modeling. Although not instantaneous, the sorption kinetic of PBZ (pure and formulated) was fast (a few hours) in both soils. The sorption kinetics were well described by a second-order (dS(t)/dt=k(2)(S(e2)-S(t))(2)) but not by a first-order model. The sorption isotherms were found to be linear and the calculated K(D) values were 8.8 +/- 0.11 and 7.4 +/- 0.2 L kg(-1) for pure PBZ in the Ultisol and the Vertisol, respectively. The corresponding K(OC) values were 1275 +/- 34 (logK(OC) = 3.11) and 1156 +/- 49 (logK(OC) = 3.06) L kg(-1), respectively. Considering the very different texture of the two soils and the similar K(OC) values determined, these results showed that in both soils, the sorption of PBZ is dominantly controlled by organic matter, although some interactions of PBZ with iron oxides (goethite) were observed in the Ultisol. Based on these sorption parameters a low leachability potential of PBZ in soils is anticipated, as they correspond to a groundwater ubiquity score (GUS) ranging from 2.0 to 2.7, i.e., moderately to not mobile, in contradiction with the actual groundwater situation in Brazil. This work stresses the need to evaluate and predict the risk associated with aquifer contamination by this widely used plant growth regulator.     

Phosphorus fractionation in volcanic lake sediments (Azores - Portugal)

The phosphorus distribution in volcanic sediments of three lakes that are under different anthropogenic pressures in S?o Miguel island (Azores - Portugal) was evaluated using a sequential extraction scheme. The P-fractionation scheme employs sequential extractions of sediment with NH4Cl, bicarbonate-dithionite (BD), NaOH (at room temperature), HCl and NaOH (at 85 degrees C) to obtain five P-fractions. The P-fractionation shows that in lakes with higher trophic status (Lake Furnas and Lake Sete Cidades), the NaOH extracted P is the dominant fraction, that contribute with more than 50% to total sedimentary phosphorus. The rank order of P-fractionation for these two lakes was NaOH>NaOH (85 degrees C)>HCl>BD>NH4Cl for Furnas lake and NaOH>HCl>NaOH (85 degrees C)>NH4Cl>BD for Sete Cidades lake. On the other hand, the trend of P contribution in the oligotrophic lake Fogo shows that the most inert P pools have the higher concentrations, with more than 50% of the P contribution from the last extraction step with NaOH at 85 degrees C. For this lake, the rank order of P-fractionation was NH4Cl>BD>NaOH>HCl>NaOH (85 degrees C). The Phosphorus Maximum Solubilization Potential (P-MSP) was also calculated and the results show that for the more bio-available P-fractions (first and second extraction step), the P-MSP values for Furnas and Sete Cidades lakes are sensibly higher than the results obtained in Fogo lake, an indication of the non-point diffuse load discharged in the first ones.     

Life cycle inventory for an organic swine waste treatment system

Journal of Material Cycles and Waste Management - The aim of this study was to analyze the efficiency of a system of treatment of organic swine waste as a management tool in the transformation of...     

Energy Use and CO2 Production in Tropical Agriculture and Means and Strategies for Reduction or Mitigation

Carbon dioxide emissions due to fossil fuel consumption are well recognized as a major contributor to climate change. In the debate on dealing with this threat, expectations are high that agriculture based economies of the developing world can help alleviate this problem. But, the contribution of agricultural operations to these emissions is fairly small. It is the clearing of native ecosystems for agricultural use in the tropics that is the largest non-fossil fuel source of CO₂ input to the atmosphere. Our calculation show that the use of fossil energy and the concomitant emission of CO₂ in the agricultural operational sector - i.e. the use of farm machinery, irrigation, fertilization and chemical pesticides - amounts to merely 3.9% of the commercial energy use in that part of the world. Of this, 70% is associated with the production and use of chemical fertilizers. In the absence of fertilizer use, the developing world would have converted even more land for cultivation, most of which is completely unsuitable for cultivation. Current expectations are that reforestation in these countries can sequester large quantities of carbon in order to mitigate excessive emissions elsewhere. But, any program that aims to set aside land for the purpose of sequestering carbon must do so without threatening food security in the region. The sole option to liberate the necessary land for carbon sequestration would be the intensification of agricultural production on some of the better lands by increased fertilizer inputs. As our calculations show, the sequestration of carbon far outweighs the emissions that are associated with the production of the extra fertilizer needed. Increasing the fertilizer use in the developing world (without China) by 20%, we calculated an overall net benefit in the carbon budget of between 80 and 206 Mt yr^?1 dependent on the carbon sequestration rate assumed for the regrowing forest. In those regions, where current fertilizer use is low, the relative benefits are the highest as responding yield increases are highest and thus more land can be set aside without harming food security. In Sub-Saharan Africa a 20% fertilizer increase, which amounts to 0.14 Mt of extra fertilizer, can tie up somewhere between 8 and 19 Mt of CO₂ per year (average: 96 t CO₂ per 1 t fertilizer). In the Near East and North Africa with a 20%-increased fertilizer use of 0.4 Mt yr^-1 between 10 and 24 Mt of CO₂ could be sequestered on the land set aside (40 t CO₂ per 1 t fertilizer). In South Asia this is 22–61 Mt CO₂ yr?1 with an annual additional input of 2.15 Mt fertilizer (19 t CO₂ per 1 t fertilizer). In fact, carbon credits may be the only way for some of the farmers in these regions to afford the costly inputs. Additionally, in regions with already relatively high fertilizer inputs such as in South Asia, an efficient use of the extra fertilizer must be warranted. Nevertheless, the net CO₂ benefit through implementation of this measure in the developing world is insignificant compared to the worldwide CO₂ output by human activity. Thus, reforestation is only one mitigating measure and not the solution to unconstrained fossil fuel CO₂ emissions. Carbon emissions should, therefore, first of all be reduced by the avoidance of deforestation in the developing world and moreover by higher energy efficiency and the use of alternative energy sources.     

The influence of lipids on the energetics of uptake of polycyclic aromatic hydrocarbons by natural organic matter

Although most of the organic carbon in soils and sediments may be composed of humic substances, their interaction with other compounds, especially their sorption interactions, may be significantly affected by the presence of small amounts of the other components of natural organic matter (NOM). In this investigation, the influence of the lipid fraction of NOM on the sorption thermodynamics of fluorene, phenanthrene, and pyrene to several geosorbent samples was examined before and after extraction of lipids. Batch experiments were performed at the same concentration for all polycyclic aromatic hydrocarbons (PAHs) (0.025 x their solubility in water) at different temperatures (10, 20, 30, and 40 degrees C), and the thermodynamic parameters were calculated. Removal of the lipids increases the sorption capacity of the samples as well as the exothermicity of the process. The free energy change was negative for all the samples and no significant differences were noticed on lipid removal. The entropy changes were small and positive for the whole geosorbent samples, but even smaller or more negative when the lipids were removed. This indicates that the interaction of PAHs with soils and sediments in the absence of extractable lipids is stronger and the mechanisms involved may be different, changing from a partitioning-like mechanism to specific adsorption. Because of the competition between lipids and PAHs for the same sorption sites, the lipids can be viewed as an "implicit sorbate."     

Development and calibration of a portable radon sampling system for groundwater Rn activity concentration measurements

The assembling of a system for field sampling and activity concentration measurement of radon dissolved in groundwater is described. Special attention is given in presenting the calibration procedure to obtain the radon activity concentration in groundwater from the raw counting rate registered in a portable scintillation detector and in establishing the precision of the activity concentration measurements. A field procedure was established and the system tested during one year of monthly observations of ²²²Rn activity concentration in groundwater drawn from two wells drilled on metamorphic rocks exposed at Eastern São Paulo State, Brazil. The observed mean ²²²Rn activity concentrations are 374 Bq/dm³ in one well and about 1275 Bq/dm³ in the other one. In both wells the ²²²Rn activity concentrations showed a seasonal variation similar to variations previously reported in the literature for the same region.