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Herbicide runoff and the effects of a narrow vegetative filter strip (VFS) were studied on an arable field in the low-lying plains of the Veneto Region (north-east Italy). Cultivated plots were compared with and without a 6m wide VFS composed of trees, shrubs and grass. Natural and simulated runoff were monitored during 2000 and 2001. Herbicides applied on the field were: metolachlor (2184-2254 g ha(-1)), terbuthylazine (1000-1127 g ha(-1)) and isoproturon (1000 g ha(-1)). The VFS reduced both runoff depth (10.2-91.2%) and herbicide losses (85.7-97.9%) in the monitored rainfall events. Total herbicide loss with runoff was low (0.69-3.98 g ha(-1) without VFS, less than 0.27 g ha(-1) with VFS), but concentrations were sometimes very high, especially of terbuthylazine and isoproturon during the first events after treatment. In these events there was a high probability of exceeding the ecotoxicological endpoint for algae, but the VFS helped to reduce the potential risk. Two VFS effectiveness mechanisms were identified: (i) dilution, and (ii) a "sponge-like" effect, which temporarily trapped chemicals inside the VFS before releasing them.  相似文献   
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Habitat loss and degradation are main global threats to biodiversity, and land-use changes in agriculture-dominated landscapes are crucial for an important portion of biodiversity, especially in Europe. We evaluated the effects of land-use changes (1954–2012) on a threatened species, the ortolan bunting, in an agricultural area crucial for its conservation in Italy. We built a distribution model for ortolan bunting in current landscapes and then re-projected it to past scenarios (1954 and 1999–2000). We evaluated the most important land-use changes occurred and estimated their effects on habitat suitability. Bunting occurrence was mostly affected by the extent of grassland (positively; used as foraging/breeding ground), shrubland (quadratic effect; perches/shelter), forest and urbanized land (negatively), and by solar radiation (positively) and slope (quadratic), consistent with other studies carried out especially in southern Europe. The potential distribution of the species was much larger in the past: the estimated decline in suitable habitat is 44–72 % (since 1999–2000/1954), coherent with historical data suggesting strong decline and contraction. Changes in suitability (1954–2012) were mostly associated with changes in the cover of forest, vineyards and abandoned areas (negatively), and shrubland (positively). Land-use/land-cover changes are the main drivers of species occurrence and of habitat decline. The heterogeneous landscape of hilly/low-mountain sites in this area, characterized by a mix of habitats offering complementary resources to ortolan buntings and other species of conservation concern, is currently threatened by abandonment and intensification, but its maintenance may be promoted by a correct definition of Rural Development Programme measures.  相似文献   
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Environmental Science and Pollution Research - Toxic trace elements from both, natural and anthropogenic origin, pose a threat to aquatic environments and marine wildlife due to their long-range...  相似文献   
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Objectives

To evaluate the clinical significance of nuchal translucency (NT) between the 95th–99th percentile in terms of typical and atypical chromosomal abnormalities (ACAs), associated fetal congenital defects and postnatal outcome.

Methods

A retrospective cohort study of fetuses with NT between the 95th–99th percentile. Data regarding the rate of associated fetal defects, genetic abnormalities and postnatal outcome were collected.

Results

A total of 306 cases of fetuses with an NT between the 95th–99th percentiles were included. The overall rate of genetic abnormalities was 12.1% (37/306). Chromosomal abnormalities were found in 10.1% (31/306) of cases and 2% were ACA (6/306). Within this group, two were pathogenic Copy Number Variants (CNVs) and four were single gene disorders. The overall rate of fetal congenital defects was 13.7% (42/306). All ACAs were found in fetuses with congenital defects. Postnatally, a new diagnosis of a single gene disorder was made in 0.85% of cases (2/236).

Conclusions

The presence of an NT between the 95th–99th percentiles carries a 10-fold increased risk of fetal defects, representing an indication for referral for a detailed fetal anatomy evaluation. The risk of ACA is mainly related to the presence of fetal defects, irrespective of the combined test risk.  相似文献   
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