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791.
Use of Descriptors of Ecosystem Functioning for Monitoring a National Park Network: A Remote Sensing Approach 总被引:1,自引:0,他引:1
Baseline assessments and monitoring of protected areas are essential for making management decisions, evaluating the effectiveness
of management practices, and tracking the effects of global changes. For these purposes, the analysis of functional attributes
of ecosystems (i.e., different aspects of the exchange of matter and energy) has advantages over the traditional use of structural
attributes, like a quicker response to disturbances and the fact that they are easily monitored through remote sensing. In
this study, we described the spatiotemporal patterns of different aspects of the ecosystem functioning of the Spanish national
parks and their response to environmental changes between 1982 and 2006. To do so, we used the NOAA/AVHRR-GIMMS dataset of
the Normalized Difference Vegetation Index (NDVI), a linear estimator of the fraction of photosynthetic active radiation intercepted
by vegetation, which is the main control of carbon gains. Nearly all parks have significantly changed during the last 25 years:
The radiation interception has increased, the contrast between the growing and nongrowing seasons has diminished, and the
dates of maximum and minimum interception have advanced. Some parks concentrated more changes than others and the degree of
change varied depending on their different environmental conditions, management, and conservation histories. Our approach
identified reference conditions and temporal changes for different aspects of ecosystem functioning, which can be used for
management purposes of protected areas in response to global changes. 相似文献
792.
Cecilia Håkansson 《Journal of Environmental Planning and Management》2009,52(3):345-363
This paper presents a cost-benefit analysis (CBA) of a trade-off between salmon and hydropower production in the Ume/Vindel River, northern Sweden. A distinctive element of this analysis is that estimated changes in resource conditions are based on detailed river-specific data. A salmon population model was used to develop the scenario and a novel willingness to pay (WTP) question, which caters for uncertainty in a different manner, provided an interval estimate. Non-use values are the major contributors to the benefit (96–517 millions of Swedish kronor (MSEK)) of increasing the stock of wild salmon. Sensitivity analysis suggests that the opportunity costs in terms of lost electricity are typically higher than the estimated benefits. 相似文献
793.
Biosorption of nickel(II) from aqueous solution by Aspergillus niger: Response surface methodology and isotherm study 总被引:1,自引:0,他引:1
In the present study, the effects of biosorbent Aspergillus niger dosage, initial solution pH and initial Ni(II) concentration on the uptake of Ni(II) by NaOH pretreated biomass of A. niger from aqueous solution were investigated. Batch experiments were carried out in order to model and optimize the biosorption process. The influence of three parameters on the uptake of Ni(II) was described using a response surface methodology (RSM) as well as Langmuir and Freundlich isotherm models. Optimum Ni(II) uptake of 4.82 mg Ni(II) g−1 biomass (70.30%) was achieved at pH 6.25, biomass dosage of 2.98 g L−1 and initial Ni(II) concentration of 30.00 mg L−1 Ni(II). Langmuir and Freundlich were able to describe the biosorption isotherm fairly well. However, prediction of Ni(II) biosorption using Langmuir and Freundlich isotherms was relatively poor in comparison with RSM approaches. The biosorption mechanism was also investigated by using Fourier transfer infrared (FT-IR) analysis of untreated, NaOH pretreated, and Ni(II) loaded A. niger biomass. 相似文献
794.
This study investigated the possible effects of a commonly used foliar herbicide 2,4-dichlorophenoxyacetic acid (2,4-D) formulation on medulla spinalis of lebistes. Fish were exposed to 2,4-D (15, 30, 45 mg L−1), behavioral changes were monitored. Fish were fixed, histopathological examination was carried out on sections taken from the upper parts of the fish body. Histopathology showed increase in neuronal loss, swelling indicating formation of intracellular edema, vacuolization noticed as the formation of vacuoles within or adjacent to cells, deformation in the Nissl granules, pyknosis and gliosis in medulla spinalis. Behavioral changes were decreased general activity, grouping, shortness in breath, sudden rotations and jumping, loss of equilibrium and colour. In conclusion, this commercial formulation of 2,4-D is considerably neurotoxic to lebistes. Fish constitute the last link in the chain of the feeding cycle in aquatic eco-system, number of studies investigating acute and chronic neurotoxicity of various herbicides in fish should be increased. 相似文献
795.
Degradation of pentachlorobiphenyl by a sequential treatment using Pd coated iron and an aerobic bacterium (H1) 总被引:1,自引:0,他引:1
The reductive dechlorination and biodegradation of 2,2′4,5,5′-pentachlorobiphenyl (PCB#101) was investigated in a laboratory-scale. Palladium coated iron (Pd/Fe) was used as a catalytic reductant for the chemical degradation of 2,2′4,5,5′-pentachlorobiphenyl, and an aerobic bacteria was used for biodegradation following the chemical reaction in this study. Dechlorination was affected by several factors such as Pd loading, initial soil pH and the amount of Pd/Fe used. The results showed that higher Pd loading, higher dosage of Pd/Fe and slightly acid condition were beneficial to the catalytic dechlorination of 2,2′,4,5,5′-pentachlorobiphenyl. In laboratory batch experiments, 2,2′4,5,5′-pentachlorobiphenyl was reduced in the presence of Pd/Fe bimetal, which was not further degraded by aerobic bacteria. 2,2′,4-trichlorobiphenyl (PCB#17), a reduction product from 2,2′4,5,5′-pentachlorobiphenyl, was readily biodegraded in the presence of a aerobic bacterial strain. It is suggested that an integrated Pd/Fe catalytic reduction-aerobic biodegradation process may be a feasible option for treating PCB-contaminated soil. 相似文献
796.
Huan Zhong 《Environmental pollution (Barking, Essex : 1987)》2009,157(3):981-986
This study compared the relative importance of three types of sorption (organic matter-particle, mercury-organic matter and mercury-particle) in controlling the overall mercury partitioning and bioavailability in sediments. We found that all three types of sorption were important for both inorganic mercury (Hg) and methylated mercury (MeHg). Mercury-particle sorption was more important than mercury-fulvic acid (FA) sorption in increasing the mercury concentrations with increasing aging. Bioavailability (quantified by gut juice extraction from sipunculans) was mainly controlled by mercury-particle sorption, while FA-particle and mercury-FA sorption were not as important, especially for MeHg. Bacterial activity also increased the partitioning of Hg or MeHg in the sediments and was further facilitated by the presence of organic matter. The bioavailability of Hg or MeHg from sediments was only slightly influenced by bacterial activity. This study highlights the importance of sorption from various sources (especially mercury-particle sorption) as well as bacteria in controlling the partitioning and bioavailability of Hg or MeHg in sediments. 相似文献
797.
Tobias Frische Michael Faust Wiebke Meyer Thomas Backhaus 《Environmental science and pollution research international》2009,16(5):593-603
Background, aim and scope
Estrogenic and non-estrogenic chemicals typically co-occur in the environment. Interference by non-estrogenic chemicals may confound the assessment of the actual estrogenic activity of complex environmental samples. The aim of the present study was to investigate whether, in which way and how seriously the estrogenic activity of single estrogens and the observed and predicted joint action of estrogenic mixtures is influenced by toxic masking and synergistic modulation caused by non-estrogenic chemical confounders.Materials and methods
The yeast estrogen screen (YES) was adapted so that toxicity and estrogenicity could be quantified simultaneously in one experimental run. Mercury, two organic solvents (dimethyl sulfoxide (DMSO) and 2,4-dinitroaniline), a surfactant (LAS-12) and the antibiotic cycloheximide were selected as toxic but non-estrogenic test chemicals. The confounding impact of selected concentrations of these toxicants on the estrogenic activity of the hormone 17ß-estradiol was determined by co-incubation experiments. In a second step, the impact of toxic masking and synergistic modulation on the predictability of the joint action of 17ß-estradiol, estrone and estriol mixtures by concentration addition was analysed.Results
Each of the non-estrogenic chemicals reduced the apparent estrogenicity of both single estrogens and their mixtures if applied at high, toxic concentrations. Besides this common pattern, a highly substance- and concentration-dependent impact of the non-estrogenic toxicants was observable. The activity of 17ß-estradiol was still reduced in the presence of only low or non-toxic concentrations of 2,4-dinitroaniline and cycloheximide, which was not the case for mercury and DMSO. A clear synergistic modulation, i.e. an enhanced estrogenic activity, was induced by the presence of slightly toxic concentrations of LAS-12. The joint estrogenic activity of the mixture of estrogens was affected by toxic masking and synergistic modulation in direct proportion to the single estrogens, which allowed for an adequate adaptation of concentration addition and thus unaffected predictability of the joint estrogenicity in the presence of non-estrogenic confounders.Discussion
The modified YES proved to be a reliable system for the simultaneous quantification of yeast toxicity and estrogen receptor activation. Experimental results substantiate the available evidence for toxic masking as a relevant phenomenon in estrogenicity assessment of complex environmental samples. Synergistic modulation of estrogenic activity by non-estrogenic confounders might be of lower importance. The concept of concentration addition is discussed as a valuable tool for estrogenicity assessment of complex mixtures, with deviations of the measured joint estrogenicity from predictions indicating the need for refined analyses.Conclusions
Two major challenges are to be considered simultaneously for a reliable analysis of the estrogenic activity of complex mixtures: the identification of known and suspected estrogenic compounds in the sample as well as the substance- and effect-level-dependent confounding impact of non-estrogenic toxicants.Recommendations and perspectives
The application of screening assays such as the YES to complex mixtures should be accompanied by measures that safeguard against false negative results which may be caused by non-estrogenic but toxic confounders. Simultaneous assessments of estrogenicity and toxicity are generally advisable. 相似文献798.
Robert Kase Peter D. Hansen Birgit Fischer Werner Manz Peter Heininger Georg Reifferscheid 《Environmental science and pollution research international》2009,16(1):54-64
Background, aim, and scope The enzyme-linked receptor assay (ELRA) detects estrogenic and anti-estrogenic effects at the molecular level of receptor
binding and is a useful tool for the integrative assessment of ecotoxicological potentials caused by hormonally active agents
(HAA) and endocrine disrupting compounds (EDC). The main advantage of the ELRA is its high sample throughput and its robustness
against cytotoxicity and microbial contamination. After a methodological adaptation to salinity of the ELRA, according to
the first part of this study, which increased its salinity tolerance and sensitivity for 17-β-estradiol, the optimised ELRA
was used to investigate 13 native sediments characterised by different levels of salinity and chemical contamination. The
applicability of the ELRA for routine analysis in environmental assessment was evaluated. Salinity is often a critical factor
for bioassays in ecotoxicological sediment assessment. Therefore, salinity of the samples was additionally adjusted to different
levels to characterise its influence on elution and binding processes of receptor-binding substances.
Materials and methods The ELRA was carried out with the human estrogen receptor α (ER) in a 96-well microplate format using the experimental setup
known from the competitive immunoassay based on ligand–protein interaction. It is an important improvement that a physiologically
relevant receptor was used as a linking protein instead of an antibody. The microplates were coated with a 17-β-estradiol-BSA
conjugate, and dilution series of estradiol and of native sediment samples were added and incubated with the ER. After a washing
step, a biotinylated mouse anti-ER antibody was added to each well. Receptor binding to estradiol, agonistic and antagonistic
receptor binding, were determined by a streptavidin-POD-biotin complex with subsequent measurement of the peroxidase activity
at the wavelength of 450 nm using a commercial ELISA multiplate reader. The sediment elutriates and pore water samples of
sediments were tested in a dilution series to evaluate at which dilution step the receptor-binding potential ends. In the
elution process (see Section 2.1 to 2.2), a method was developed to adjust the salinity to the levels of the reference testings, which offers an appropriate option
to adjust the salinity in both directions. Statistical evaluation was made with a combination of the Mann–Whitney U test and the pT-method.
Results This part of the study characterised the environmental factor ‘salinity’ for prospective applications of the ELRA. Using reference
substances such as 17-β-estradiol, the ELRA showed sigmoid concentration-effect relations over a broad range from 0.05 μg/l
to 100 μg/l under physiological conditions. After methodological optimisation, both sensitivity and tolerance of the assay
against salinity could be significantly raised, and the ELRA became applicable under salinity conditions up to concentrations
of 20.5‰. The mean relative inter-test error (n = 3) was around 11% with reference substances and below 5% for single sediments elutriates in three replicates each. For
sediment testings, the pore water and different salinity-adjusted elutriates of 13 sediments were used. A clear differentiation
of the receptor-binding potential could be reached by application of the pT-method. Thereby, pT-values from one to six could
be assigned to the sediments, and the deviation caused by the different salinity conditions was one pT-value. The mean standard
deviation in the salinity adaptation procedure of the elutriates was below 5%.
Discussion Although the ELRA has already been used for assessments of wastewater, sludge and soil, its applicability for samples to different
salinity levels has not been investigated so far. Even if the ELRA is not as sensitive as the E-screen or the YES-assay, with
regard to reference substances like 17-β-estradiol, it is a very useful tool for pre-screening, because it is able to integrate
both estrogenic as well as anti-estrogenic receptor-binding effects. According to the results of sediment testing, and given
the integrative power to detect different directions of effects, the ELRA shows sufficient sensitivity and salinity tolerance
to discriminate receptor-binding potentials in environmental samples.
Conclusions The optimised ELRA assay is a fast, cost-effective, reliable and highly reproducible tool that can be used for high-throughput
screening in a microplate format in detecting both estrogenic and anti-estrogenic effects. Additionally, the ELRA is robust
against microbial contaminations, and is not susceptible towards cytotoxic interferences like the common cell-culture methods.
The general applicability and sufficient sensitivity of the ELRA was shown in freshwater environments. Marine and brackish
samples can be measured up to salinity levels of 20.5‰.
Recommendations and perspectives In view of the proven sensitivity, functionality and the fastness of the ELRA, it is recommendable to standardise the test
method. At the moment, no adequate in vitro test procedure exists which is standardised to DIN or ISO levels. The E-screen
and the yeast estrogen/androgen screens (YES/YAS) sometimes underlie strong cytotoxic effects, as reported in the first part
of this study. Further development of an ELRA assay using human androgen receptors appears to be very promising to gain information
about androgenic and anti-androgenic effects, too. This would offer a possibility to use the ELRA as a fast and reliable pre-screening
tool for the detection of endocrine potentials, thus minimising time and cost-expensive animal experiments. 相似文献
799.
Jan Bernd Barhorst Roland Kubiak 《Environmental science and pollution research international》2009,16(5):582-589
Background, aim and scope The use of sodium hypochlorite (HYP) in viticulture results in effluents which are contaminated with halogenated substances.
These disinfection by-products (DBPs) can be quantified as group parameter ‘adsorbable organic halogens’ (AOX) and have not
been determined in effluents of viticulture yet. The substances that are detected as AOX are unknown. The AOX can be composed
of harmless substances, but even toxic contaminants. Thus, it is impossible to assess ecological impacts. The aim of this
study is to determine the quantification of AOX and DBPs after the use of HYP. This will be helpful to reduce environmental
pollution by AOX.
Materials and methods The potential of HYP to generate AOX was determined in laboratory-scale experiments. Different model solutions were treated
with HYP according to disinfection processes in viticulture and conditions of AOX formation in effluents were simulated. AOX
were quantified using the flask-shaking method and identified DBPs were investigated by gas chromatography–mass spectrometry.
Results Treatment with HYP resulted in the formation of AOX. The percentage conversion of HYP to AOX was up to 11%. Most important
identified DBPs in viticulture are chloroform, dichloroacetic acid and trichloroacetaldehyde. In addition, the formation of
carbon tetrachloride (CT), 1,1,1-trichloropropanone, 2,4-dichlorobenzoic acid and 2-chloro-/2,4-dichlorophenylacetic acid
was investigated. It was demonstrated that reaction temperature, concentration of HYP and type of organic matter have important
influence on the formation of chlorinated DBPs.
Discussion The percentage conversion of HYP to AOX was similar to other published studies. Although a correlation of single compounds
and AOX is difficult, chloroform was the predominant AOX. Generation of the volatile chloroform should be avoided due to possible
adverse effects. The generation of dichloroacetic acid is of minor importance on account of biodegradation. Trichloroacetaldehyde
and 1,1,1-trichloropropanone are weak mutagens and their formation should be avoided.
Conclusions The generation of AOX and chlorinated DBPs can be minimised by reducing the concentrations of the organic materials in the
effluents. The removal of organic matter before disinfection results in a decreased formation of AOX. HYP is an effective
disinfectant; therefore, it should be used at low temperatures and concentrations to reduce the amount of AOX. If possible,
disinfection should be accomplished by the use of no chlorine-containing agents. By this means, negative influences of HYP
on the quality of wine can also be avoided.
Recommendations and perspectives Our results indicate that HYP has a high potential to form AOX in effluents of viticulture. The predominant by-products are
chloroform, dichloroacetic acid and trichloroacetaldehyde. In further research, wastewaters from a winery and the in- and
outflows of two sewage treatment plants were sampled during vintage and analysed. These results will be discussed in a following
paper. 相似文献
800.
Siedlecka EM Stepnowski P 《Environmental science and pollution research international》2009,16(4):453-458
Background, aim, and scope Ionic liquids are regarded as essentially “green” chemicals because of their insignificant vapor pressure and, hence, are
a good alternative to the emissions of toxic conventional volatile solvents. Not only because of their attractive industrial
applications, but also due to their very high stability, ionic liquids could soon become persistent contaminants of technological
wastewaters and, moreover, break through into natural waters following classical treatment systems. The removal of harmful
organic pollutants has forced the development of new methodologies known as advanced oxidation processes (AOPs). Among them,
the Fenton and Fenton-like reactions are usually modified by the use of a higher hydrogen peroxide concentration and through
different catalysts. The aim of this study was to assess the effect of hydrogen peroxide concentration on degradation rates
in a Fenton-like system of alkylimidazolium ionic liquids with alkyl chains of varying length and 3-methyl-N-butylpyridinium chloride.
Materials and methods The ionic liquids were oxidized in dilute aqueous solution in the presence of two different concentrations of hydrogen peroxide.
All reactions were performed in the dark to prevent photoreduction of Fe(III). The concentrations of ionic liquids during
the process were monitored with high-performance liquid chromatography. Preliminary degradation pathways were studied with
the aid of 1H NMR.
Results Degradation of ionic liquids in this system was quite effective. Increasing the H2O2 concentration from 100 to 400 mM improved ionic liquid degradation from 57–84% to 87–100% after 60 min reaction time. Resistance
to degradation was weaker, the shorter the alkyl chain.
Discussion The compound omimCl was more resistant to oxidation then other compounds, which suggests that the oxidation rates of imidazolium
ionic liquids by OH· are structure-dependent and are correlated with the n-alkyl chain length substituted at the N-1-position. The level of degradation was dependent on the type of head group. Replacing
the imidazolium head group with pyridinium increased resistance to degradation. Nonetheless, lengthening the alkyl chain from
four to eight carbons lowered the rate of ionic liquid degradation to a greater extent than changing the head group from imidazolium
to pyridinium. 1H-NMR spectra show, in the first stage of degradation, that it is likely that radical attack is nonspecific,
with any one of the carbon atoms in the ring and the n-alkyl chain being susceptible to attack.
Conclusions The proposed method has proven to be an efficient and reliable method for the degradation of imidazolium ionic liquids by
a Fenton-like reagent deteriorated with lengthening n-alkyl substituents and by replacing the imidazolium head group with pyridinium. The enhanced resistance of 1-butyl-3-methylpyridinium
chloride when the resistance of imidazolium ionic liquids decreases with increasing H2O2 concentration is probably indicative of a change in the degradation mechanism in a vigorous Fenton-like system. H-NMR spectra
showed, in the first stage of degradation, that radical attack is nonspecific, with any one of the carbon atoms in the ring
and the n-alkyl chain being susceptible to attack.
Recommendations and perspectives Since ionic liquids are now one of the most promising alternative chemicals of the future, the degradation and waste management
studies should be integrated into a general development research of these chemicals. In the case of imidazolium and pyridinium
ionic liquids that are known to be resistant to bio- or thermal degradation, studies in the field of AOPs should assist the
future structural design as well as tailor the technological process of these chemicals 相似文献