Archives of Environmental Contamination and Toxicology (Arch Environ Contam Toxicol)

Publisher: Springer Verlag

Journal description

Archives of Environmental Contamination and Toxicology is a repository of significant, full-length articles describing original experimental or theoretical research work pertaining to the scientific aspects of contaminants in the environment. It provides a place for the publication of detailed, definitive, complete, credible reports concerning advances and discoveries in the fields of air, water, and soil contamination and pollution, human health aspects, and in disciplines concerned with the introduction, presence, and effects of deleterious substances in the total environment. Acceptable manuscripts for the Archives are the ones that deal with some aspects of environmental contaminants, including those that lie in the domains of analytical chemistry, biochemistry, pharmacology, toxicology, agricultural, air, water, and soil chemistry.

Current impact factor: 1.96

Impact Factor Rankings

2015 Impact Factor Available summer 2015
2013 / 2014 Impact Factor 1.96
2012 Impact Factor 2.012
2011 Impact Factor 1.927
2010 Impact Factor 1.93
2009 Impact Factor 1.743
2008 Impact Factor 1.864
2007 Impact Factor 1.62
2006 Impact Factor 1.419
2005 Impact Factor 1.408
2004 Impact Factor 1.612
2003 Impact Factor 1.857
2002 Impact Factor 1.516
2001 Impact Factor 1.301
2000 Impact Factor 1.437
1999 Impact Factor 1.173
1998 Impact Factor 1.065
1997 Impact Factor 1.102
1996 Impact Factor 1.396
1995 Impact Factor 1.307
1994 Impact Factor 1.182
1993 Impact Factor 1.252
1992 Impact Factor 1.221

Impact factor over time

Impact factor
Year

Additional details

5-year impact 2.15
Cited half-life 9.90
Immediacy index 0.35
Eigenfactor 0.01
Article influence 0.57
Website Archives of Environmental Contamination and Toxicology website
Other titles Archives of environmental contamination and toxicology (Online), Environmental contamination and toxicology
ISSN 1432-0703
OCLC 41210730
Material type Document, Periodical, Internet resource
Document type Internet Resource, Computer File, Journal / Magazine / Newspaper

Publisher details

Springer Verlag

  • Pre-print
    • Author can archive a pre-print version
  • Post-print
    • Author can archive a post-print version
  • Conditions
    • Author's pre-print on pre-print servers such as arXiv.org
    • Author's post-print on author's personal website immediately
    • Author's post-print on any open access repository after 12 months after publication
    • Publisher's version/PDF cannot be used
    • Published source must be acknowledged
    • Must link to publisher version
    • Set phrase to accompany link to published version (see policy)
    • Articles in some journals can be made Open Access on payment of additional charge
  • Classification
    ​ green

Publications in this journal

  • [Show abstract] [Hide abstract]
    ABSTRACT: A rapid and sensitive method using liquid chromatography coupled with mass spectrometry triple quadrupole direct aqueous injection for analysis of atrazine and ametrine herbicides in surface waters was developed. According to the validation method, water samples from six different locations in the Piracicaba River were collected monthly from February 2011 to January 2012 and injected into a liquid chromatographer/dual mass spectrometer without the need for sample extraction. The method was validated and shown to be precise and accurate; limits of detection and quantification were 0.07 and 0.10 µg L(-1) for atrazine and 0.09 and 0.14 µg L(-1) for ametrine. During the sampling period, concentrations of atrazine ranged from 0.11 to 1.92 µg L(-1) and ametrine from 0.25 to 1.44 µg L(-1). After analysis of the herbicides, Danio rerio were exposed a range of concentrations found in the river water to check the induction of micronuclei and nuclear abnormalities (NAs) in erythrocytes. Concentrations of atrazine and ametrine >1.0 and 1.5 µg L(-1), respectively, induced MN formation in D. rerio. Ametrine was shown to be more genotoxic to D. rerio because a greater incidence of NAs was observed compared with atrazine. Therefore, environmentally relevant concentrations of atrazine and ametrine found in the Piracicaba River are dangerous to the aquatic biota.
    Archives of Environmental Contamination and Toxicology 06/2015; DOI:10.1007/s00244-015-0171-6
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    ABSTRACT: This study was designed to investigate the molecular (transcriptional expression), biochemical (oxidative stress and neurotoxicity), and histopathological effects of metal contamination in the gill of clams (Ruditapes decussatus) sampled from the Tunis lagoon. The concentrations of five heavy metals (Cd, Pb, Hg, Cu, and Zn) in surface sediments and their accumulation in soft tissues of R. decussatus were evaluated in three sites (Z1, Z2, and Z3). A metal contamination state of Tunis lagoon sediments was noted with spatial variations with relatively high levels at Z2. Biomarker analyses showed an increase in glutathione S-transferase and catalase activities and lipid peroxidation levels and a decrease in acetylcholinesterase activity in the studied sites. Molecular investigation showed a significant overexpression of: cytochrome c oxidase subunit I, ribosomal RNA 16S, Cu/Zn superoxide dismutase, heat shock protein 70, and metallothioneins in the three sampling sites. Moreover, our data were correlated to severe and diverse histopathological alterations in the clam gills. The principal component analysis showed that the Z2 region is more affected by metal contamination than Z1 and Z3 regions. Current field results suggest the use of several combined biomarkers at different cell levels instead of individual ones in monitoring programs.
    Archives of Environmental Contamination and Toxicology 06/2015; DOI:10.1007/s00244-015-0185-0
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    ABSTRACT: The concentrations of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs), as well as the levels of a number of heavy metals, have been periodically measured in samples of soil and vegetation collected around a municipal solid waste incinerator (MSWI) in Tarragona (Catalonia, Spain) for approximately 20 years. Since 2007, the levels of the above-mentioned pollutants have also been determined in air samples by means of either active or passive samplers. In the present study, data regarding the environmental impact of the MSWI, in terms of PCDD/Fs and heavy metals, are updated. The temporal trends of these pollutants were evaluated by comparison with data from previous surveys. In the current survey (2013-2014), mean concentrations of PCDD/Fs in soil, vegetation, and air were 0.63 ng I-TEQ/g, 0.07 ng I-TEQ/g, and 10.1 fg WHO-TEQ/m(3), respectively. Decreases of 47 and 35 % of PCDD/Fs in soil and vegetation, respectively, were observed in relation to the background study (1999). Regarding air samples, a slight temporal decrease of the PCDD/F levels was also found with the remaining concentrations staying nearly constant through time. With respect to metals, notable fluctuations in the concentrations were noted, being dependent on each specific environmental monitor. Overall, the current exposure to PCDD/Fs and metals does not mean any additional health risks for the population living near the facility. In conclusion, the results of the present study show that the environmental impact of the Tarragona MSWI is not significant, in terms of PCDD/Fs and heavy metals, after >20 years of continuous operation.
    Archives of Environmental Contamination and Toxicology 06/2015; DOI:10.1007/s00244-015-0168-1
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    ABSTRACT: The contamination of aquatic ecosystems with copper (Cu) poses a serious threat to aquatic organisms. Although the histopathological changes caused by Cu in fish gills are well documented, knowledge about the impact of this metal in gill specific cell types, such as neuroendocrine cells (NECs) and eosinophilic granule cells (EGCs), is still limited. In the present work, Nile tilapia (Oreochromis niloticus) were exposed for 21 days to nominal concentrations of Cu (40 and 400 µg L(-1)). Stereological methods were used to estimate the volumetric density of both NECs and EGCs in fish gill filament after 3, 7, 14, and 21 days of exposure. The results showed that Cu significantly increased the relative volume of NECs, whereas the relative volume of EGCs decreased. NECs were more affected by Cu in the first 7 days of exposure, during which a greater increase in their relative volume was observed. The Cu exposure induced a progressive decrease in the relative volume of EGCs, which reached statistical significance after 14 days of exposure. An exception was observed in subepithelial EGCs with a slight increase in their relative volume after 3 days of exposure. Our findings confirm that Cu can modulate both neuroendocrine and immune systems and becomes immunotoxic after a prolonged exposure.
    Archives of Environmental Contamination and Toxicology 06/2015; DOI:10.1007/s00244-015-0170-7
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    ABSTRACT: In the present study, gas chromatographic analysis of pesticide residues in bovine milk (n = 312) from Punjab, India, showed chlorpyrifos, DDT, and γ-HCH as the predominant contaminants. In addition, the presence of β-endosulfan, endosulfan suphate, cypermethrin, cyhalothrin, fenvalerate, deltamethrin, malathion, profenofos, and ethion was reported in milk samples. In this study, it was observed that 12 milk samples exceeded the maximum residue limits (MRLs) for γ-HCH (lindane), 18 for DDT and chlorpyrifos, and 1 sample each for endosulfan, cypermethrin, and profenophos. In India, DDT is still permitted for a malaria control program, which may be the plausible reason for its occurrence in milk samples. The spatial variation for presence of pesticide residues in milk indicated greater levels in cotton-growing areas of Punjab. At current levels of pesticide residues in bovine milk, the human health risk assessment in terms of noncancer and cancer hazard was calculated based on both lower-bound [LB (mean residue levels)] and upper-bound [UP (95th percentile level)] limits. It was noticed that cancer and noncancer risk were within United States Environmental Protection Agency prescribed limits for both adults and children at the LB, but children were being exposed to greater risk for DDT and HCH at the 95th-percentile UB level.
    Archives of Environmental Contamination and Toxicology 05/2015; DOI:10.1007/s00244-015-0163-6
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    ABSTRACT: Sediment and water samples collected from 8 sites of the Yangtze River in Nanjing section were characterized with 31 congeners of polychlorodibenzothiophenes (PCDTs). Concentrations and percentage compositions of these PCDTs in water and sediments were analyzed by gas chromatography-mass spectrometry. Results showed that ∑PCDT concentrations in sediments were higher (0.86-1.75 μg/kg) than those in water (0.56-1.30 μg/L). A linear relationship existed between ∑PCDT concentrations and total organic carbon content in sediments, whereas there was a poor linearity between ∑PCDTs concentrations and dissolved organic carbon content in water phase. Moreover, percentage compositions showed that penta-chlorinated DTs were the predominant congeners both in sediments and water. Differences existed in the percentage compositions between water and sediments. Highly chlorinated DTs accounted for a larger proportion in sediments than those in water. In conclusion, the present study showed the prevalent contamination by PCDTs in sediments and water from the Nanjing section of the Yangtze River.
    Archives of Environmental Contamination and Toxicology 05/2015; DOI:10.1007/s00244-015-0159-2
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    ABSTRACT: Microplastics are ubiquitous within the marine environment. The last 10 years have seen research directed at understanding the fate and effect of microplastics within the marine environment; however, no studies have yet addressed how concentrations of these particles could affect sedimentary processes such as nutrient cycling. Herein we first determine the concentration and spatial distribution of microplastics within Baynes Sound, a key shellfish-growing area within coastal British Columbia (BC). We also determined sediment grain size and % organic matter (OM) such that we could relate spatial patterns in sediment microplastic concentrations to sedimentary processes that determine zones of accretion and erosion. Using field-determined concentrations of microplastics, we applied laboratory microcosms studies, which manipulated sediment concentrations of microplastics, OM, and bivalves to determine the influence of sediment microplastics on ammonium cycling within intertidal sediments. Concentrations of microplastics determined within the intertidal sediment varied spatially and were similar to those found in other coastal regions of high urban use. Concentrations were independent of grain size and OM suggesting that physical processes other than those that govern natural sediment components determine the fate of microplastics within sediments. Under laboratory conditions, concentrations of ammonium were significantly greater in the overlying water of treatments with microplastics, clams, and OM compared with treatments without microplastics. These preliminary studies suggest that high concentrations of microplastics have the potential to alter key sedimentary processes such as ammonium flux. This could have serious implications, for example, contributing to eutrophication events in regions of the coast that are highly urbanized.
    Archives of Environmental Contamination and Toxicology 04/2015; DOI:10.1007/s00244-015-0156-5
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    ABSTRACT: The presence and distribution characteristics of microplastics become a big issue due to the adverse effects on marine organisms caused by not only microplastics but any incorporated and/or adsorbed pollutants. Distribution of microplastics (50- to 5000-μm size) was determined for three sandy beaches on an isolated island in a high-tidal costal region to elucidate spatial distributions in relation to beach locations. The abundances of microplastics (n = 21) measured were 56-285,673 (46,334 ± 71,291) particles/m(2) corresponding to the highest level globally. Out of observed polymer types, expanded polystyrene was overwhelmingly dominant. Although lying toward the estuary of the largest river in the country, the north-side beach contained a 100-fold lower abundance than two south-side beaches that faced southerly wind and currents that were prevalent throughout the study season. In addition, distinct differences between the beaches on either side were also present in terms of size distribution and spatial homogeneity of microplastics on the same beach. Winds and currents are therefore considered to be the driving forces in the distribution of microplastics.
    Archives of Environmental Contamination and Toxicology 04/2015; DOI:10.1007/s00244-015-0155-6