Analytical insight into degradation processes of aminopolyphosphonates as potential factors that induce cyanobacterial blooms

Environmental Science and Pollution Research - Aminopolyphosphonates (AAPs) are commonly used industrial complexones of metal ions, which upon the action of biotic and abiotic factors undergo a...     

Coupling of the Water Cycle with Patterns of Urban Growth in the Baltimore Metropolitan Region,United States

Regional municipal water plans typically do not recognize complex coupling patterns or that increased withdrawals in one location can result in changes in water availability in others. We investigated the interaction between urban growth and water availability in the Baltimore metropolitan region where urban growth has occurred beyond the reaches of municipal water systems into areas that rely on wells in low‐productivity Piedmont aquifers. We used the urban growth model SLEUTH and the hydrologic model ParFlow.CLM to evaluate this interaction with urban growth scenarios in 2007 and 2030. We found decreasing groundwater availability outside of the municipal water service area. Within the municipal service area we found zones of increasing storage resulting from increased urban growth, where reduced vegetation cover dominated the effect of urbanization on the hydrologic cycle. We also found areas of decreasing storage, where expanding impervious surfaces played a larger role. Although the magnitude of urban growth and change in water availability for the simulation period were generally small, there was considerable spatial heterogeneity of changes in subsurface storage. This suggests that there are locally concentrated areas of groundwater sensitivity to urban growth where water shortages could occur or where drying up of headwater streams would be more likely. The simulation approach presented here could be used to identify early warning indicators of future risk.     

Anaerobic incorporation of the radiolabeled explosive TNT and metabolites into the organic soil matrix of contaminated soil after different treatment procedures

Four bioreactor designs were performed to evaluate the level of incorporation of 14C-labeled 2,4,6-trinitrotoluene (TNT) and metabolites into the organic soil matrix of different anaerobically treated contaminated soils. The contaminated soils were amended with molasses slivers (80:20% per weight) as auxiliary substrate to enhance microbial activity. After 5 weeks (bioreactors 1 and 2), 8 weeks (bioreactor 3) and 12 weeks (bioreactor 4) of anaerobic incubation, we determined 41%, 58%, 72%, and 54%, respectively, of the initially applied radioactivity immobilized in various soil fractions. After alkaline hydrolyses of the solvent-extracted soils, low quantities of radiolabel were found in the humic and fulvic acid fractions, whereas the bulk of 14C activity was found to be strongly bound to the humin fraction (solid soil residues). The amounts of solvent extractable radioactivity were 53%, 40%, 16%, and 29% for bioreactors 1, 2, 3, and 4, respectively. The level of TNT transformation at the end of the experiments was within 90-94%. Regarding the results presented in this study, we can assume that there is the possibility of high incorporation levels of TNT metabolites into the soil organic matrix mediated by microbial cometabolism under strictly anoxic conditions.     

Umweltrelevanz von Diphenylamin — Ein Stoff der 3. EU-Altstoffprioritätenliste

Diphenylamine (DPA), the simplest secondary aromatic amine, is a compound from the third European Union (EU) list of priority pollutants. It was assigned to Germany to assess and control its environmental risks. DPA is most commonly used as a stabilizer agent in nitrocellulose-containing explosives and propellants, in the perfumery, and as an antioxidant in the rubber and elastomer industry. DPA is also widely used to prevent the post-harvest deterioration of apple and pear crops. It is a parent compound of many derivatives which are used for the production of dyes, pharmaceuticals, photography chemicals and further small-scale applications. At the beginning of the eighties, the estimated world production of DPA was ?40,000 tons per year (in Germany ?4,000 tons per year). The compound is still produced world-wide by the chemical industries. Recently published reports showed that DPA was found in soil and groundwater (within the ppb to ppm range). Some ecotoxicological reports demonstrated the potential hazard of various diphenylamines to the aquatic environment and to bacteria and animals as well. Studies on the biodegradability of DPA and its derivatives are very sparse. Therefore, further investigations are required to determine the complete dimensions of the potential environmental hazard and to introduce possible (bio)remediation techniques for sites that are contaminated with this compound or its derivatives. This review summarizes the environmental relevance of DPA as has been published in the literature thus far. It may possibly support the German authorities in their assessment of the risks of this priority pollutant.     

Diphenylamine and derivatives in the environment: a review

Diphenylamine (DPA) is a compound from the third European Union (EU) list of priority pollutants. It was assigned by the EU to Germany to assess and control its environmental risks. DPA and derivatives are most commonly used as stabilizers in nitrocellulose-containing explosives and propellants, in the perfumery, and as antioxidants in the rubber and elastomer industry. DPA is also widely used to prevent post-harvest deterioration of apple and pear crops. DPA is a parent compound of many derivatives, which are used for the production of dyes, pharmaceuticals, photography chemicals and further small-scale applications. Diphenylamines are still produced worldwide by the chemical industries. First reports showed that DPA was found in soil and groundwater. Some ecotoxicological studies demonstrated the potential hazard of various diphenylamines to the aquatic environment and to bacteria and animals. Studies on the biodegradability of DPA and its derivatives are very sparse. Therefore, further investigation is required to determine the complete dimension of the potential environmental hazard and to introduce possible (bio)remediation techniques for sites that are contaminated with this class of compounds. This is the first detailed review on DPA and some derivatives summarizing their environmental relevance as it is published in the literature so far and this review will recommend conducting further research in the future.     

Impact of Changing Climate and Land Cover on Flood Magnitudes in the Delaware River Basin,USA

Changing climate and land cover are expected to impact flood hydrology in the Delaware River Basin over the 21st Century. HEC‐HMS models (U.S. Army Corps of Engineers Hydrologic Engineering Center‐Hydrologic Modeling System) were developed for five case study watersheds selected to represent a range of scale, soil types, climate, and land cover. Model results indicate that climate change alone could affect peak flood discharges by ?6% to +58% a wide range that reflects regional variation in projected rainfall and snowmelt and local watershed conditions. Land cover changes could increase peak flood discharges up to 10% in four of the five watersheds. In those watersheds, the combination of climate and land cover change increase modeled peak flood discharges by up to 66% and runoff volumes by up to 44%. Precipitation projections are a key source of uncertainty, but there is a high likelihood of greater precipitation falling on a more urbanized landscape that produces larger floods. The influence of climate and land cover changes on flood hydrology for the modeled watersheds varies according to future time period, climate scenario, watershed land cover and soil conditions, and flood frequency. The impacts of climate change alone are typically greater than land cover change but there is substantial geographic variation, with urbanization the greater influence on some small, developing watersheds.     

Umweltrelevanz von Diphenylamin — Ein Stoff der 3. EU-Altstoffpriorit?tenliste

Zusammenfassung  Diphenylamin (DPA), das einfachste, rein aromatische sekund?re Amin, ist ein Stoff der dritten Altstoffpriorit?tenliste priorit?tenliste der Europ?ischen Union (EU). Es wurde der Bundesrepublik Deutschland zugewiesen, die von diesem Stoff ausgehenden Umweltrisiken zu erfassen und zu bewerten. DPA wird als Stabilisator in Nitrocellulose-haltigen Explosivstoffen und Treibladungspulvern eingeserzt, au?erdem als Stabilisator in der Parfümerie und als Antioxidationsmittel in der Gummi- und Elastomer-Industrie. DPA wird auch vielfach genutzt, um ?pfel und Birnen nach der Ernte vor vorzeitigem Altern bzw. Verfall zu bewahren. Ferner ist es Ausgangsverbindung zahlreicher Derivate, welche u.a. in der Produktion von Farben, Pharmazeutika und Fotografiechemikalien Anwendung finden. Anfang der 80er Jahre wurden weltweit sch?tzungsweise ca. 40.000 t DPA pro Jahr produziert (in Deutschland ca. 10% davon). Die Chemikalie wird noch heute weltweit von der chemischen Industrie hergestellt. Neuere Publikationen zeigen, da? DPA bereits im Boden und im Grundwasser (in ppb- bis ppm-Konzentrationen) nachgewiesen werden konnte. Einige ?kotoxikologische Ver?ffentlichungen demonstrierten die Gef?hrlichkeit verschiedener DPA-Derivate gegenüber der aquatischen Umwelt und auch gegenüber Bakterien und Tieren. Studien bezüglich der biologischen Abbaubarkeit von DPA und Derivaten sind sehr sp?rlich vorhanden. Aus diesem Grund sind weiterführende Forschungsarbeiten notwendig, um das volle Ausma\ der Umweltgef?hrdung für mit DPA und DPA-Derivaten kontaminierte Bereiche zu bestimmen, und um entsprechende (biologische) Sanierungsverfahren einzuleiten. Dieser übersichtsbeitrag fa\t die zug?ngliche Literatur zusammen, welche die Umweltrelevanz von DPA aufzeigt. Er kann m?glicherweise die deutschen Beh?rden bzw. Gutachter bei der Bewertung von Risiken dieses Altstoffes der EU-Priorit?tenliste unterstützen.      

Identification of oxidized TNT metabolites in soil samples of a former ammunition plant

Water extracts of soil samples of the former ammunition plant “Tanne” near Clausthal-Zellerfeld, Lower Saxony, Germany, were investigated for highly polar oxidized 2,4,6-trinitrotoluene (TNT) metabolites. 0.4 to 9.0 mg/kg dry soil 2,4,6-trinitrobenzoic acid (TNBA) and 5.8 to 544 mg/kg dry soil 2-amino-4,6-dinitrobenzoic acid (2-ADNBA) were found. In addition to the oxidized metabolites, TNT, 4- and 2-aminodinitrotoluene (4- and 2-ADNT), and 2,4-dinitrotoluene (2,4-DNT) were extractable with water. Most interestingly, in one sample, 2-ADNBA represented the main contaminant. The origin of the oxidized nitroaromatics is unknown at this time. They might be generated chemically or photochemically. Furthermore, a biological synthesis seems possible.