Sediment analysis to support the recent glacial origin of DDT pollution in Lake Iseo (Northern Italy)

In the present study, a depth-related distribution of Persistent Organic Pollutants (POPs) in sediments of Lake Iseo, one of the major southern Alpine Italian lakes, is reported in order to further test the hypothesis of melting Alpine glaciers as a secondary source of contamination. In a previous paper, a “glacier contamination hypothesis” was suggested to explain the unexpected contamination of the biota of Lake Iseo, mainly fed by the Alpine melting ice.The sediment core analyses covered around the last 50 years. The organic matter profile evaluated as a Loss-On-Ignition percentage indicated transition of the basin from an oligotrophic to a mesotrophic status at around the early 1970s, but there was no evidence of the shift to eutrophy in the 1980s. Among DDTs, pp’DDE was the predominant metabolite, accounting on average for 79.4% of the total DDT concentrations and ranging from 6.4 to 447.5 ng g⁻¹ d.w. PCBs ranged from 5.0 to 163.7 ng g⁻¹ d.w. The maximum PCB concentrations were found in sediment layers corresponding to the 1970s when the highest production and use of these compounds occurred in Italy. In contrast, concentrations of DDTs showed a sharp increase from the early 1990s, long after their agricultural use was banned in Italy. This delayed pollution provides support for the hypothesis that the recent retreat of glaciers represents a secondary pollution source for old pesticides that were stored in the ice at the time of their use in agriculture.     

Environmental ozone exposure and oxidative DNA damage in adult residents of Florence, Italy

In 71 adults residing in Florence, Italy, enrolled in a prospective study, we investigated the correlation between individual levels of oxidative DNA damage detected by the Comet assay in circulating lymphocytes, and a specific ozone exposure score calculated in 10 different time-windows (0-5 to 0-90 days) before blood drawing, based on daily measurements provided by the local environmental monitoring system.Overall, statistically significant positive correlations between average ozone concentrations and DNA damage emerged in almost all time-windows considered; correlations were more evident among males, non-smokers, and traffic-exposed workers. Multivariate regression analyses taking into account selected individual characteristics, showed an independent effect on DNA damage of average ozone concentrations in the last 60-90 days before blood drawing. Local residents showed a divergent pattern with correlations restricted to shorter time-windows.Our results suggest that ozone concentrations at ground levels modulate oxidative DNA damage in circulating lymphocytes of residents of polluted areas.     

Laser induced fluorescence instrument for NO2 measurements: Observations at a central Italy background site

A laser induced fluorescence (LIF) instrument has been developed to measure tropospheric NO₂ with low detection limit. The instrument design, development and first measurements are reported. There are also details of the temporal gate system built for the fluorescence acquisition. The instrument is able to make fast measurements (up to 4 Hz) and shows a limit of detection of 10 pptv/60 s. Continuous observations (2 weeks in summer 2007) in a small town in central Italy were used to test the performance of the instrument and to study the photochemistry of ozone in a background site. LIF and a commercial chemiluminescence (CL) instrument simultaneous observations of NO₂ show a good linearity (LIF = 1.02 CL + 0.6 (ppb), R² = 0.98) but there is a bias of the commercial instrument of about 0.60 ppbv on average. The overestimation of the CL system is probably due to conversion of NO_y species into NO by the molybdenum converter used in the CL instrument to detect NO₂. Analysis of 1 s data is used to test the instrument response and the coupling between nitrogen oxides and ozone.     

Synergies and trade‐offs in achieving global biodiversity targets

After their failure to achieve a significant reduction in the global rate of biodiversity loss by 2010, world governments adopted 20 new ambitious Aichi biodiversity targets to be met by 2020. Efforts to achieve one particular target can contribute to achieving others, but different targets may sometimes require conflicting solutions. Consequently, lack of strategic thinking might result, once again, in a failure to achieve global commitments to biodiversity conservation. We illustrate this dilemma by focusing on Aichi Target 11. This target requires an expansion of terrestrial protected area coverage, which could also contribute to reducing the loss of natural habitats (Target 5), reducing human‐induced species decline and extinction (Target 12), and maintaining global carbon stocks (Target 15). We considered the potential impact of expanding protected areas to mitigate global deforestation and the consequences for the distribution of suitable habitat for >10,000 species of forest vertebrates (amphibians, birds, and mammals). We first identified places where deforestation might have the highest impact on remaining forests and then identified places where deforestation might have the highest impact on forest vertebrates (considering aggregate suitable habitat for species). Expanding protected areas toward locations with the highest deforestation rates (Target 5) or the highest potential loss of aggregate species’ suitable habitat (Target 12) resulted in partially different protected area network configurations (overlapping with each other by about 73%). Moreover, the latter approach contributed to safeguarding about 30% more global carbon stocks than the former. Further investigation of synergies and trade‐offs between targets would shed light on these and other complex interactions, such as the interaction between reducing overexploitation of natural resources (Targets 6, 7), controlling invasive alien species (Target 9), and preventing extinctions of native species (Target 12). Synergies between targets must be identified and secured soon and trade‐offs must be minimized before the options for co‐benefits are reduced by human pressures.     

Chemical Recovery of Useful Chemicals from Polyester (PET) Waste for Resource Conservation: A Survey of State of the Art

In this paper we present the main technologies developed over the last decades on chemical recycle of PET from a practical and economical point of view. We show details of plants used to carry out solvolitic reactions emphasising steps of purification, which are sometimes not considered when discussing chemical, recycle but which, in fact, are the key feasibility factors. The recycling or modification of PET to obtain monomers and other useful chemicals as intermediates and additives is carefully considered.     

Integrated waste management in a zone of northern Italy: compost production and use, and analytical control of compost, soil, and crop

Agricultural soils of two Italian maize farms were treated for five years with an industrially produced high-quality compost. Cattle manure and the usual mineral fertilizer were used for comparison purposes. The effects of the organic and mineral fertilizer treatments were studied by analyzing the compost and manure, cultured soils, and harvested material. The grain yield was also determined. Organic fertilization improved soil pH, CEC, content of organic matter and NPK. Soil respiration and N mineralization were found to be higher than in the purely mineral-treated soil. Plant K take-up was improved, whereas grain yield was not affected. It was confirmed that organic fertilization, particularly compost use, maintained and increased soil fertility. The study demonstrated the feasibility of using in loco analytical facilities to follow the entire recycling process-from waste to compost production-and the use of the final product in the field.     

Isotopic composition, growth rates and biological behaviour of Chamelea gallina and Callista chione from the Bay of Trieste (Italy)

Shells of the bivalve molluscs Chamelea gallina L. and Callista chione L. from the Bay of Trieste (northern Adriatic) were analysed for their oxygen and carbon isotopic composition. The main purpose of this study was to obtain detailed information on the biological behaviour and, particularly, on the growth rates and the settlement time of these two species. Isotopic measurements were carried out on "spot" samples collected from the umbo to the ventral margin of each shell. The results obtained from nine specimens of C. gallina (plus some 20 specimens studied only for the isotopic composition of their initial umbo and for the last section of their ventral edge) and from two specimens of C. chione allow the following conclusions: (1) the calcium carbonate of C. gallina shells is not deposited under isotopic equilibrium conditions with the environmental variables (temperature and oxygen isotopic composition of seawater); (2) this species usually initiates precipitation of carbonate during the springtime, although some late summer-early autumn generation also occurs; (3) the rate of calcium carbonate deposition decreases with increasing age, and the overall accretion rate is a rather slow one; (4) there is a negative correlation between the carbon isotopic composition and the size of each shell; (5) the mean growth rate of the shells can be easily evaluated according to the oxygen isotopic composition of the spot measurements; (6) the specimens of C. chione do not precipitate the calcium carbonate of their shells in isotopic equilibrium with environmental conditions; (7) their accretion rate is rather fast during the first years of their life and progressively and considerably reduced after about 5 years; (8) the carbon isotopic composition of these shells does not show the marked evolution towards more negative values shown by C. gallina, suggesting that neither respiratory CO₂ nor carbon species derived from the oxidation of organic matter are systematically used for the precipitation of shell carbonate; and (9) a marked preference for the warmer half of the year is shown by the oldest specimen of C. chione (12 years).     

Organic compounds and trace metals of anthropogenic origin in sediments from Montego Bay,Jamaica: assessment of sources and distribution pathways

Surface sediments throughout Montego Bay, Jamaica were collected in 1995 and analyzed for their trace metal and trace organic contaminant content. A variety of trace metals, petroleum hydrocarbons, polycyclic aromatic hydrocarbons, coprostanol as well as chlorinated hydrocarbons such as pesticides and polychlorinated biphenyls were detected and provide evidence for several anthropogenic inputs to the bay. Two main sources of these chemicals are the Montego River and the North Gully, the latter being more significant. Particle-associated pollutants were found to be distributed along the Montego River plume, as well as being transported by the prevailing water currents to the South-Western sections of the bay, probably through re-suspension of enriched fine sediments from the North Gully outfall area.