Response of antioxidant enzymes in Nicotiana tabacum clones during phytoextraction of heavy metals

Background, aim, and scope  Tobacco, Nicotiana tabacum, is a widely used model plant for growth on heavy-metal-contaminated sites. Its high biomass and deep rooting system make it interesting for phytoextraction. In the present study, we investigated the antioxidative activities and glutathione-dependent enzymes of different tobacco clones optimized for better Cd and Zn accumulation in order to characterize their performance in the field. Main features  The improved heavy metal resistance also makes the investigated tobacco clones interesting for understanding the plant defense enzyme system in general. Freshly harvested plant material (N. tabacum leaves) was used to investigate the antioxidative cascade in plants grown on heavy metal contaminated sites with and without amendments of different ammonium nitrate and ammonium sulfate fertilizers. Materials and methods  Plants were grown on heavily polluted soils in north-east Switzerland. Leaves were harvested at the field site and directly deep frozen in liquid N₂. Studies were concentrated on the antioxidative enzymes of the Halliwell–Asada cycle, and spectrophotometric measurements of catalase (CAT, EC 1.11.1.6), ascorbate peroxidase (APX, EC 1.11.1.11), superoxide dismutase (SOD, EC 1.15.1.1), glutathione peroxidase (GPX, EC 1.11.1.9), glutathione reductase (GR, EC 1.6.4.2), glutathione S-transferase (GST, EC 2.5.1.18) were performed. Results and discussion  We tried to explain the relationship between fertilizer amendments and the activity of the enzymatic defense systems. When tobacco (N. tabacum) plants originating from different mutants were grown under field conditions with varying fertilizer application, the uptake of cadmium and zinc from soil increased with increasing biomass. Depending on Cd and Zn uptake, several antioxidant enzymes showed significantly different activities. Whereas SOD and CAT were usually elevated, several other enzymes, and isoforms of GST were strongly inhibited. Conclusions  Heavy metal uptake represents severe stress to plants, and specific antioxidative enzymes are induced at the cost of more general reactions of the Halliwell–Asada cycle. In well-supplied plants, the glutathione level remains more or less unchanged. The lack of certain glutathione S-transferases upon exposure to heavy metals might be problematic in cases when organic pollutants coincide with heavy metal pollution. When planning phytoremediation of sites, mixed pollution scenarios have to be foreseen and plants should be selected according to both, their stress resistance and hyperaccumulative capacity.     

Development and validation of a new fluorescence-based bioassay for aquatic macrophyte species

Bioassays with unicellular algae are frequently used as ecotoxicological test systems to evaluate the toxicity of contaminated environmental samples or chemicals. In contrast, aquatic macrophyte test systems are still rarely used as they are laborious to handle because species exhibit distinct ecological requirements. The aim of this study was to establish a fast and reproducible measuring system for aquatic macrophyte species to overcome those limitations for use. Thus, a newly developed pulse-amplitude modulated chlorophyll fluorometer (Imaging-PAM) was applied as an effect detection in short-term bioassays with aquatic macrophyte species. This multiwell-plate-based measuring device enables the incubation and measurement of up to 24 samples in parallel. The Imaging-PAM was used (i) to establish and validate the sensitivity of the test systems to three Photosystem II (PSII) inhibitors (atrazine, prometryn, isoproturon), (ii) to compare the test systems with established biotests for macrophytes and (iii) to define necessary time scales in aquatic macrophyte testing. The results showed that fluorescence-based measurements with the Imaging-PAM allow rapid and parallel analysis of large amounts of aquatic macrophyte samples and of toxicants effects of the PSII inhibitors tested on aquatic macrophytes. Measurements revealed a good correlation between obtained median effective concentrations (EC50s) for the new and the established biotest systems. Hence, the Imaging-PAM measuring device is a promising tool to allow fast chemical effect screening for high amounts of samples with little time and material and thus offers scope for high-throughput biotesting using aquatic macrophyte species.     

Assessing the transformation of chlorinated ethenes in aquifers with limited potential for natural attenuation: added values of compound-specific carbon isotope analysis and groundwater dating

The evaluation of biotransformation of chlorinated ethenes (CEs) in contaminated aquifers is challenging when variable redox conditions and groundwater flow regime are limiting factors. By using compound-specific stable carbon isotope analysis (C-CSIA) and ³H-³He based groundwater dating, we assessed three CE-contaminated field sites that differed in groundwater flow velocities, redox conditions, and level of contamination. CE isotopic signatures and carbon isotopic mass balances were applied to quantify CE transformation, whereas groundwater dating allowed determining degradation timescales and assessing hydrodynamic regimes. The combination of these techniques enabled at all field sites to indicate zones within the aquifers where CE dechlorination preferably occurred, sometimes even to metabolites of no toxic concern. However, the natural transformation processes were insufficient to mitigate the entire CE contamination at the studied sites. Such situations of limited transformation are worldwide far more common than sites where optimal natural (mainly redox) conditions are enabling complete CEs degradation. Despite such constraints for natural transformation, this study showed that even under non-favorable biogeochemical CEs degradation, the combination of CSIA and groundwater dating provide valuable information to the understanding of the fate of the CEs, thus, being an important contribution in the definition of efficient remediation measures at any given biogeochemical conditions.     

Toxizitätsänderungen in Photoreaktionen von Azaarenen

The azaarenes and the structurally analogous PAH accompany each other and occur ubiquitously in nature. Photochemical conversions like direct photolysis or the photoreaction with nitrate are important natural degradation reactions of azaarenes. Furthermore, photoreactions with chlorine and bromine radicals can be expected in nature. The reactions generate a large number of oxidized, nitrated and halogenated products with unknown toxicity. In this paper, a first screening of changes is reported in acute toxicity during the course of the photochemical reactions. As test system luminescent bacteria are used. For quinoline, isoquinoline and phthalazine the investigations show different changes of the toxicity of the reaction mixtures in dependence on the respective reaction type. The toxicity of the reaction mixtures of quinazoline and quinoxaline increases in all reactions investigated. Furthermore the reactions of bromine radicals with azaarenes also show an increase of the toxicity in all cases. Compared with the azaarenes in all reactions products with significantly higher toxicity are formed.     

Aktive Stoffe als Handlungsoption gegen die Verschleppung von Organismen durch Seeschiffe?

Background and Scope

The marine shipping lanes have become the most important path for the invasion of foreign aquatic organisms. The increasing global trade results in an increase in the number of marine vessels. Without any protective measures, with every ship carrying foreign organisms the risk of biological invasions will rise.

Results

The International Martime Organization (IMO) of the United Nations developed a convention to reduce the transfer of organisms with ballast water. After the entry-into-force of this convention the fleet of the world has to be equipped with effective ballast water management technology before 2016. This article discusses potential options for action. To comply with the limit values of the ballast water convention, the current state of the art demands the use of active substances. Any decision on the approval of active substances used for ballast water treatment and the environmental impact assessment lies with the IMO. Proposed to day are UV-radiation, active chlorine, active oxygen, the creation of biocides through electrolysis and a change in gases contained in the ballast water. The technologies and the potential risks are presented.

Conclusions

Despite the introduction of an approval procedure by IMO any reliable assessment of the real risks involved in the use of biocides is impossible, as the risk assessment approaches have still to be developed. On the regulatory level, the main focus in data requirements for the risk assessment is on a comprehensive testing of the toxic potential of the biocides proposed. Strategies for the identification and evaluation of the chemical resulting from the treatment of limnic, marine and brackish water are not fully developed. An integrating assessment of risks involved in the introduction of foreign organisms versus the toxic effects of the substances used or created during treatment is still missing.     

The International Lead and Zinc Study Group and the metals market

The International Lead and Zinc Study Group was founded by the United Nations in 1959. There are 32 member countries which together cover over 90% of world production and consumption of total lead and zinc. The Study Group, inter alia provides opportunities for consultation on lead and zinc, provides information regarding supply and demand, collects and disseminates statistics, studies different aspects of the world situation in lead and zinc and considers possible solutions to any special problems. This paper presents excerpts of the activities of the International Lead and Zinc Study Group in each of the above areas.     

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.