Releases of phosphate fertilizer industry in the surrounding environment: Investigation on heavy metals and polonium-210 in soil

Distribution of Cu,Zn,Pb,Cr,Ni,Mn concentrations and the activity of polonium-210 in the surrounding area of a phosphate fertilizer industry located on the eastern coast of the Mediterranean Sea has been determined.Nineteen sampling sites were distributed around the industrial zone on a surface area of about 100,000 m2.Atomic absorption spectroscopy and Alpha spectroscopy were used to quantify the heavy elements and polonium-210,respectively.Investigation on a particle scale was conducted by TEM and SEM coupled to EDX and X-ray cartography to determine the nature of heavy elements carriers and their distribution.Heavy elements were mainly concentrated inside the particle size fraction 50 μm.Their levels decreased with distance increasing from the industry.According to the reference soil,enrichment factors were about 10,15,32 and 100 times for Zn,Pb,Cu,and Cr,respectively inside the particle size fraction 50 μm on the closest sites to the industry.The main contaminant sources were transport and storage of row materials and the free release of phosphogypsum waste.Heavy elements were entrapped inside agglomerates of sulfates,phosphates and iron oxihydroxides in a di used shape.Polonium-210 with an enrichment factor of about 56,showed the same behavior of the spatial distribution of the trace elements.     

Litter decomposition and nitrogen release in a sloping Mediterranean subtropical agroecosystem on the coast of Granada (SE, Spain): Effects of floristic and topographic alteration on the slope

On the coast of Granada (SE, Spain), an economically important area for subtropical fruit cultivation, the crops are grown on orchard terraces. Also, high amounts of fertilizers, often excessive, are used in this type of intensive agriculture. However, each year significant fractions of nutrients taken up by the trees return to the soil by fallen leaves. Using a litter-bag technique, we assessed the decomposition rates and N-release in various types of litter. Our main purpose was to compare two different agroecosystem scenarios: (1) an unaltered slope consisting mainly of a mixture of herbaceous plants (Papaver rhoeas, Convolvulus sp., Malva sylvestris, Reseda phyteuma, Anacyclus sp., Sinapis arvensis, Medicago sp.) among spontaneous perennial woody shrubs (Genista umbellata, Olea europaea, Lavandula officinalis, Phlomis purpurea, Retama sphaerocarpa), and (2) an altered slope cultivated with subtropical trees on terraces: loquat (Eriobotrya japonica), mango (Mangifera indica), avocado (Persea americana), and cherimoya (Annona cherimola), with groundcover plantings of aromatic, medicinal, and melliferous plants (AMMPs) on the taluses of the terraces, which are usually used for erosion control: Lavandula dentata, Thymus mastichina, Satureja obovata, Rosmarinus officinalis, Anthyllis cytisoides. In the leaves from the subtropical crops, we found the highest decomposition rates in cherimoya and the lowest in mango (1.30 and 0.64 years⁻¹, respectively). Leaves from mango and loquat registered initial peaks of N immobilization and later N-release, which was highest in cherimoya and avocado leaves (71.2 and 56.8% of the initial remaining N). In the spontaneous woody shrubs, O. europaea and G. umbellata were the slowest in decomposing (1.18 and 1.01 years⁻¹, respectively) contrary to L. officinalis, which decomposed fastest (2.22 years⁻¹). Only L. officinalis and P. purpurea registered a net N-release at the end of the study. The AMMPs showed different decomposition patterns: L. dentata registered the highest decomposition rates and Rosmarinus the lowest (1.9 and 1.1 years⁻¹, respectively). T. mastichina, L. dentata, and S. obovata had the highest N-release, whereas R. officinalis and A. cytisoides showed N immobilization (183 and 122% of the initial N). Knowledge of the dynamics of nutrient release and litter decomposition will be useful for predicting nutrient availability and nutrient cycles in these types of agroecosystems where subtropical orchards are grown on terraces.     

Yield and Water Productivity of Winter Wheat under Various Irrigation Capacities

The Agricultural Production Systems sIMulator model validated in a prior study for winter wheat was used to simulate yield, aboveground crop biomass (BM), transpiration (T), and evapotranspiration under four irrigation capacities (ICs) (0, 1.7, 2.5, and 5 mm/day) with two nitrogen (N) application rates (N1, 94 kg N/ha; N2, 160 kg N/ha) to (1) understand the performance of winter wheat under different ICs and (2) develop crop water production function under various ICs and N rates. Evaluation was based on yield, aboveground crop BM, transpiration productivity (TP), crop water productivity (WP), and irrigation WP (IWP). Simulation results showed winter wheat yield increased with increase in N application rate and IC. However, the rate of yield increase gradually reduced with additional irrigation beyond 2.5 mm/day. A 5 mm/day IC required a total of 190 mm irrigation and produced a 5%–16% yield advantage over 2.5 mm/day. This indicates it is possible to reduce groundwater use for wheat by 50% incurring only 5%–16% yield loss relative to 5 mm/day. The TP and IWP for grain were slightly higher under IC of 1.7 mm/day (15.2–16.1 kg/ha/mm and 0.98–1.6 kg/m³) when compared to 5 mm/day (14.7–15.5 kg/ha/mm and 0.6–1.06 kg/m³), respectively. Since TP and IWPs are relatively higher under lower ICs, winter wheat could be a suitable crop under lower ICs in the region. Relationship between yield–T and yield–ET was linear with a slope of 15–16 and 9.5–10 kg/ha/mm, respectively. Editor's note : This paper is part of the featured series on Optimizing Ogallala Aquifer Water Use to Sustain Food Systems. See the February 2019 issue for the introduction and background to the series.     

ERD of Residual TCE DNAPL Achieving Nondetect from a Single Injection of Food‐Grade Waste

Residual dense nonaqueous phase liquid (DNAPL) composed of trichloroethene (TCE) was identified in a deeper interval of an overburden groundwater system at a manufacturing facility located in northern New England. Site hydrostratigraphy is characterized by two laterally continuous and transmissive zones consisting of fully‐saturated fine sand with silt and clay. The primary DNAPL source was identified as a former dry well with secondary contributions from a proximal aboveground TCE storage tank. A single additive‐injection mobilization in 2001 utilizing a food‐grade injectate formulated with waste dairy product and inactive yeast enhanced residual TCE DNAPL destruction in situ by stimulating biotic reductive dechlorination. The baseline TCE concentration was detected up to 97,400 μg/L in the deeper interval of the overburden groundwater system, and enhanced reductive dechlorination (ERD) achieved >99 percent reduction in TCE concentrations in groundwater over nine years with no evidence of sustained rebound. TCE concentrations have remained nondetect below 2.0 μg/L for the last five consecutive sampling rounds between 2013 and 2015. ERD utilizing a food‐grade injectate is a green remediation technology that has destroyed residual DNAPL at the site and achieved similar results at other residual DNAPL sites during both pilot‐ and full‐scale applications. ©2016 Wiley Periodicals, Inc.     

Biodegradation and Ecotoxicity of Polyethylene Films Containing Pro-Oxidant Additive

The worldwide accumulation of non-degradable plastic materials, such as plastic bags, is one of the most important environmental concerns nowadays. The use of degradable materials is an option to mitigate the environmental impact generated by the consumption of plastics. One of the technologies used for the manufacture and use of degradable plastics is the use of pro-degradant additives that are incorporated in conventional plastics to promote their degradation under certain conditions. The aim of this study is to evaluate the process of oxidation, biodegradation and potential ecotoxicity of polyethylene films containing an oxo-degradable additive, according to the standard ASTM D-6954. This method establishes a procedure in which the samples are subjected to consecutive steps of accelerated oxidation, biodegradation by composting and ecotoxicity assessment. Furthermore, the effect of the presence of printing ink in the polyethylene samples with oxo-degradable additive was evaluated, and the results were compared with those obtained for samples of conventional polyethylene and polylactic acid. After 180 days of laboratory controlled composting, the samples reached the following percentages of biodegradation: polylactic acid, 41 %; printed oxo-degradable polyethylene, 32.24 %; oxo-degradable polyethylene, 25.84 %; printed polyethylene, 18.23 % and polyethylene, 13.48 %. The cellulose sample used as a control was mineralized in 58.45 %. Ecotoxicity assessment showed that the products of biodegradation of the samples tested, did not generate a negative effect on germination or development of the vegetal species studied. Under proper waste management conditions, these plastics can be used as an option to decrease the environmental impact of plastic films.     

PLA Chemical Recycling Process Optimization: PLA Solubilization in Organic Solvents

The recycling of used, post-industrial and post-consumer PLA is crucial to reduce both the consumption of renewable resources for the monomer synthesis and the environmental impact related to its production and disposal. Several processes are actually available: among these, there is a particular interest on the chemical recycling of PLA with production of its monomer. The aim of this work is to analyse the PLA dissolution behaviour in different organic solvents (acetone and Ethyl lactate) at different water concentrations in order to optimize the chemical depolymerisation process of PLA. New experimental data are presented and a kinetic model is provided for a first analysis. Preliminary results suggest that acetone based solvents (i.e., acetone water mixtures at various concentrations) are more effective to solubilize the PLA rather than the Ethyl-lactate based solvent. Anyway, an increase of water concentration in the solvent phase, determines both a reduction of the solvent power and a reduction of mass transport coefficient for the two solvents tested.     

Implications of climate change on mitigation potential estimates for forest sector in India

Climate change is projected to impact forest ecosystems, including biodiversity and Net Primary Productivity (NPP). National level carbon forest sector mitigation potential estimates are available for India; however impacts of projected climate change are not included in the mitigation potential estimates. Change in NPP (in gC/m²/yr) is taken to represent the impacts of climate change. Long term impacts of climate change (2085) on the NPP of Indian forests are available; however no such regional estimates are available for short and medium terms. The present study based on GCM climatology scenarios projects the short, medium and long term impacts of climate change on forest ecosystems especially on NPP using BIOME4 vegetation model. We estimate that under A2 scenario by the year 2030 the NPP changes by (−5) to 40% across different agro-ecological zones (AEZ). By 2050 it increases by 15% to 59% and by 2070 it increases by 34 to 84%. However, under B2 scenario it increases only by 3 to 25%, 3.5 to 34% and (−2.5) to 38% respectively, in the same time periods. The cumulative mitigation potential is estimated to increase by up to 21% (by nearly 1 GtC) under A2 scenario between the years 2008 and 2108, whereas, under B2 the mitigation potential increases only by 14% (646 MtC). However, cumulative mitigation potential estimates obtained from IBIS—a dynamic global vegetation model suggest much smaller gains, where mitigation potential increases by only 6% and 5% during the period 2008 to 2108.     

Equilibrium partitioning of PCB congeners in the water column: Field measurements from the Hudson River

The environmental behavior of hydrophobic organic compounds in water is driven by partitioning between dissolved and sorbed phases. Partitioning behavior of a compound is often based on empirical relationships to other properties of the chemical, such as water solubility and octanol-water partition coefficients, but actual partitioning in the environment may differ significantly from such predictions. We conducted intensive studies of the distribution of PCBs in the fresh water portion of the Hudson River, using sensitive capillary-column gas chromatography methods to calibrate and resolve quantitations for 90 PCB congeners in 48 samples at 10 locations. A linear equilibrium model of PCB congener partitioning, when corrected for temperature and suspended-matter organic carbon content, provides a good representation of phase distribution. When particulate-phase concentrations are predicted from dissolved concentrations with a two-phase model, the predictions are unbiased for the majority of samples and the average percent difference between observed and predicted particulate concentrations is ±43 percent. Estimated in situ partition coefficients show systematic differences from partition coefficients predicted from octanol-water partitioning. Partitioning to colloids appears to be a significant component of total concentration for mono- and dichlorobiphenyls, but not for more highly chlorinated congeners.The colloidal fraction may still cause significant overestimation of the bioavailable fraction for more hydrophobic congeners when a two-component model is used.     

Organochlorine Contaminants in Herring Gull Eggs from the Great Lakes, 1974-1995: Change Point Regression Analysis and Short-Term Regression

The temporal trends (1974-1995) of 11 organochlorine contaminants in herring gull eggs from 13 colonies throughout the Great Lakes were statistically analyzed using two regression methods on logarithmically transformed data. Change point analysis was used to determine if there had been significant year to year fluctuations in contaminant levels and/or changes in long-term trends. Short-term regressions were conducted on 6 major compounds for two time periods (early 1990s and early 1980s) to compare the rates of decline. Overall, change point analyses indicated that for most of the comparisons (75%) there had been significant year to year fluctuations in contaminant levels. They also indicated that for most of the comparisons (67%) the rate of decline after the change point was as fast as or faster than before the change point, this pattern was most common for dieldrin and heptachlor epoxide at certain locations. In 19% of the comparisons the rates of decline had slowed or stabilized, this was most common for PCB and pentachlorobenzene. In 14% of the comparisons there were no significant temporal trends, this was most common for photomirex and mirex. Results for short-term regression showed that out of 78 comparisons for each time period, 5 (6%) were declining significantly in the early 1990s and 11 (14%) were declining significantly in the early 1980s. Both types of regression indicated that, for most of the herring gull egg contaminant database, recent logarithmic rates of decline were similar to those seen previously in the sampling period. For PCB 1254:1260, a group of compounds of particular toxicological importance, change point analyses indicated that the logarithmic rates of decline in herring gull eggs from western Lake Ontario were slower from 1987-1995 than they were from 1974-1986. At both Lake Superior colonies and the Niagara River colony PCB 1254:1260 concentrations ceased to decline in the mid-1980s. At the colony in Green Bay, Lake Michigan, PCB 1254:1260 levels have shown no significant temporal trend since 1976. At the remaining 8 colonies, PCB 1254:1260 levels continue a logarithmic decline in recent years at the same rate as or faster than previously.