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1.
Three different growth forms of lichens belonging to six species; Phaeophyscia hispidula, Parmotrema praesorediosum (foliose); Caloplaca subsoluta, Diploschistes candidissmus (crustose) and Peltula euploca, Phylliscum indicum (squamulose) were studied comparatively for the biomonitoring of Al, Cd, Cr, Cu, Fe, Ni and Zn in Mandav city in central India. Based on the anthropogenic activities three sites were selected for lichen collection. To identify the sources of heavy metal pollution, their concentration was analyzed in thallus as well as in their respective substrates. The thallus of studied lichens showed higher concentration of metals such as Cd, Cr, Ni and Zn, while most of the metals were absent or present in negligible amount in substrates (Fe, Al, Cu), which proves that the accumulated metals were air borne. The foliose lichens (P. hispidula and P. praesorediosum) found highly significant in metal accumulation at each sites followed by crustose and squamulose forms. Lichen samples collected from site 2, adjacent to road side accumulated maximum quantities of Zn, Ni, Cd and Cr whereas the city centre (Site 1) had maximum concentrations of Fe, Cu and Al. The site 3 situated away from the city had lowest amount of all the metals. The analysis of variance and LSD indicated that the metal concentrations among lichen species as well as between substratum is significant at p < 0.05% and P < 0.01% level respectively.  相似文献   

2.
A simple system was constructed for the separation and collection of atmospheric particles and gases. The five-stage sampling train consists of a particle filter followed by four 7LiOH-impregnated filters to collect acidic gases. The treated filters quantitatively collect acidic gas-phase species of B, S, Cl, Br, I, As, Se, Sb and Hg. Simultaneous sampling with activated charcoal-impregnated and 7LiOH-treated filters revealed that B, S, and As species were found only as acidic gases, while the others had both acidic and nonacidic contributions. Concentrations of up to 48 elements on the particle filters and nine elements on the treated filters were determined using instrumental neutron activation analysis and neutron capture prompt -ray activation analysis. Minimum sampling volume estimates, average filter blank concentrations, and average atmospheric concentrations at College Park, MD and Wallops Island, VA are presented.  相似文献   

3.
A detailed set of reactions treating the gas and aqueous phase chemistry of the most important iodine species in the marine boundary layer (MBL) has been added to a box model which describes Br and Cl chemistry in the MBL. While Br and Cl originate from seasalt, the I compounds are largely derived photochemically from several biogenic alkyl iodides, in particular CH2I2, CH2ClI, C2H5I, C3H7I, or CH3I which are released from the sea. Their photodissociation produces some inorganic iodine gases which can rapidly react in the gas and aqueous phase with other halogen compounds. Scavenging of the iodine species HI, HOI, INO2, and IONO2 by aerosol particles is not a permanent sink as assumed in previous modeling studies. Aqueous-phase chemical reactions can produce the compounds IBr, ICl, and I2, which will be released back into the gas phase due to their low solubility. Our study, although highly theoretical, suggests that almost all particulate iodine is in the chemical form of IO-3. Other aqueous-phase species are only temporary reservoirs and can be re-activated to yield gas phase iodine. Assuming release rates of the organic iodine compounds which yield atmospheric concentrations similar to some measurements, we calculate significant concentrations of reactive halogen gases. The addition of iodine chemistry to our reaction scheme has the effect of accelerating photochemical Br and Cl release from the seasalt. This causes an enhancement in ozone destruction rates in the MBL over that arising from the well established reactions O(1D) + H2O 2OH, HO2 + O3 OH + 2O2, and OH + O3 HO2 + O2. The given reaction scheme accounts for the formation of particulate iodine which is preferably accumulated in the smaller sulfate aerosol particles.  相似文献   

4.
To assess the impact of ultraviolet B (UV-B) radiation under laboratory conditions on lichens from different biomonitoring sites, thalli of the lichen Ramalina lacera were transplanted from a clean air site to nine different polluted sites in Israel. Our objective was to determine the probability of synergistic/antagonistic effects on physiological parameters by considering two stressors: chemical contamination and UV-B. Exposure to both airborne pollutants in the field and subsequent UV-B radiation in the laboratory which led to a severe disintegration of cell membranes, followed by electrolyte leakage, indicate the probability of a synergistic effect. The impairment of the potential quantum yield of electron transfer through photosystem II (PSII) of photosynthesis indicated by a significant decrease of the ratio Fv/Fm, further demonstrated the synergistic effect of both chemical contamination and UV-B radiation. Besides enlarged amounts of stress-ethylene in lichens at contaminated sites, the reduced levels of ethylene production upon UV-B radiation in the present study suggest the likelihood of an antagonistic effect of xenobiotic elements and UV-B radiation as a result of an impaired ethylene-producing system.  相似文献   

5.
A field study was carried out in the spring and summer of 2003 (2 months each), to assess the efficiency of alternative exposure modes of biological monitors – lichen biomass and tree-bark biomass – together with prospective, non-biological monitors – cellulose acetate and Chelex-100 resin – versus conventional transplants of the same species. After exposure to the marine atmosphere of Sines (SW Portugal), saline elements (Cl, Na, K, Mg) contents were determined in all samples by instrumental neutron activation analysis (INAA). Manganese was used as the crustal reference for data normalisation. As a whole, the results pointed to a consistent elemental accumulation regardless of the season (spring, summer), and to some fair reproducibility of data. There were good correlations between Cl and Na in terms of both raw and normalised data, for either the biomonitors or the cellulose acetate. Elemental ratios generally agreed with the average relative composition of bulk seawater. The degree of association between Cl and Na appeared rather unaffected by the normalisation procedure, which suggests that (i) both elements most likely had an almost exclusive marine origin; and (ii) accounting for crustal inputs via Mn did not bias the results. Other sources than the sea-spray might contribute to the Mg levels, though, as only Mn-normalised data showed intrinsic (correlation) and extrinsic (ratio) consistency. The performance of the Chelex-100 resin was rather disappointing when compared to the other monitors.  相似文献   

6.
Arsenic and its chemical species were determined in transplanted lichens (Parmelia caperata) and tree bark (Platanus hybrida), in order to get a better understanding of their atmospheric cycling and the suitability of these materials for biomonitoring purposes. Various strategies were used (discontinuous and cumulative exposure of transplants) to biomonitor two locations in Portugal, viz. the northern Lisbon area and Sines, both highly industrialised areas.Analytical techniques comprised instrumental nuclear activation analysis (INAA), inductively coupled plasma-mass spectrometry (ICP-MS) and high performance liquid chromatography-hydride generation atomic fluorescence spectrometry (HPLC-HGAFS) for determination of total arsenic in solid materials, total arsenic in extracts of solid materials and arsenic species in extracts of solid materials, respectively.Only a fraction (up to 50%) of the extracted arsenic species could be identified and quantified in the transplanted lichens, being mainly inorganic arsenic and some methylated arsenic species. Since in a previous study these methylated arsenic species were not found in aerosols collected in the same area, it is probable that the lichen transplants studied (Parmelia caperata) do not behave as genuine passive biomonitors but are able to actively methylate inorganic arsenic to methylated arsenic species. Furthermore, this lichen-induced methylation occurs with some delay, possibly as a reaction to the transplantation of the lichen itself, and therefore transplanted lichens are only suitable for long-term biomonitoring studies. For tree bark only total arsenic concentration data could be generated since speciation analysis failed due to too low an initial total arsenic concentrations.  相似文献   

7.
Many lichens are very sensitive to air pollution due to their symbiotic nature. However, they are generally less sensitive to toxic effects of trace elements; therefore they can be used as accumulator organisms for estimating concentrations of these elements in the environment. Heavy metal accumulation in lichens is a commonly used bioindication method for assessing heavy metal ambient levels. An active biomonitoring method was used for the determination of short-term accumulation of zinc, lead, arsenic and cadmium by epiphytic lichens transplanted at different localities in Slovenia polluted by heavy metals. The atomic absorption spectrophotometry method was used for the determination of heavy metal content in lichen thalli. The content of heavy metals in lichens collected in the background area with clean air (Rogla, Pohorje Mountains) was used as the reference value. Lichens were transplanted from Rogla using the branch transplantation technique for a period of 6 months in the surroundings of Slovenian thermal power plants (Velenje, otanj, Zavodnje, Veliki Vrh, Vnajnarje, and Dobovec) and close to the lead and zinc ore smelter at erjav. The monthly accumulation of heavy metals was comparable within years at selected locations. Heavy metal pollution was the highest at erjav despite of remediation of lead and zinc ore smelter. The monthly accumulation of all four heavy metals was statistically significantly higher in lichens exposed at erjav than at other localities.  相似文献   

8.
The occurrence of CH2Br2, CH2BrCl, CH2I2, CH2ClI, CHBr3, CHBr2Cl, CHBrCl2 and CH2Br-CH2Br in marine air and seawater from various sampling sites in the region of the Atlantic Ocean have been measured and evaluated. A correlation exists between high concentrations of these compounds in air and in water and the occurrence of algae at the coastlines of various islands (The Azores, Bermuda, Tenerife) and in a region of high bioactivity in the Atlantic Ocean near the West African coast.Real-world air-water concentration ratios derived from measurements in the open ocean identify the water mass near the African coast with its high primary production as a source for the above compounds. This region has to be discussed also as a possible secondary source in which CHBr2Cl, CHBrCl2 and CH2ClI can be formed via halogen-exchange. Whether CHBrCl2 and CH2ClI under-go transformation to CHCl3 and CH2Cl2, respectively, is open to further investigations.Direct photolysis and degradation by OH-radicals lead to a gradient in the marine troposphere with reduced concentrations for the organobromides above the tropospheric boundary layer.Partly presented at: 2nd International Symposium on Biosphere-Atmosphere Exchange, Mainz, F.R.Germany, 16–21 March, 1986. Part VII: Chemosphere 15 (1986) 429–436.  相似文献   

9.
The diversity of epiphytic lichens and mercury concentrations in lichen samples were measured to monitor the release of airborne pollutants from the industrial exploitation of geothermal resources in the Mt. Amiata area (Italy). The lichen biodiversity showed a general condition of moderate environmental alteration around the geothermal power plants, contrasting with the low environmental alteration of the remaining sites investigated. According to the accumulated Hg in lichen thalli, it was possible to estimate mean Hg and H2S concentrations in the air, which resulted in very good agreement with values measured instrumentally. Based on these data and the correlation between lichen diversity values and Hg concentrations in lichens, it was possible to calculate the threshold of 8 μg/m3 H2S as responsible for the worsening from low to moderate environmental alteration according to the biodiversity of epiphytic lichens, and to infer that around geothermal power plants, although not toxic to humans, H2S concentrations are such to alter the nasal quality of the air. Based on the growth rate of X. parietina, it was possible to convert Hg concentrations into estimates of average Hg deposition rates, which showed fluxes of the order of 65–100 mg/ha/y, indicating a dispersions factor of about 104 for the Hg emitted from the geothermal power plants.  相似文献   

10.
The Atlantic Forest, a hotspot in the world with a great diversity of plants and animals, is located in the most industrialized area of Brazil, a potential source of chemical elements for the atmosphere. From its original area about 10% has been preserved mainly through the implementation of conservation units, among which the Parque Estadual Carlos Botelho (PECB) is one of the most representative. Here, leaves of the predominant species in the PECB were analyzed by instrumental neutron activation analysis (INAA) for the establishment of natural backgrounds of As, Ba, Br, Ca, Cd, Ce, Co, Cs, Fe, Hg, K, Na, Rb, Sc, Se, Sr and Zn. Biomonitoring of the Atlantic Forest was realized through the tree community study taking in account the interspecies and the intraspecies variability of chemical concentrations. Results pointed out the low status of pollution based on the concentrations of chemical elements of environmental concerning. However, Br concentrations were higher in the understory species, which could be related to the possible effects of atmospheric pollution or sea influence. In addition, some Hyeronima alchorneoides trees showed to be hyperaccumulators of Co.  相似文献   

11.
The sorption studies of Hg2+, CH3Hg+ and elemental mercury (Hg0) were carried out on lichen (Parmelia sulcata) and moss (Funaria hygrometrica) samples under laboratory conditions. Desorption studies with HCl indicate that inorganic mercury (Hg+2) and methyl mercury could be completely desorbed with 1 M HCl and 0.5 M HCl, respectively. Samples loaded with elemental mercury, however, needed 4–5 M HCl concentration for complete desorption of the adsorbed elemental mercury. When similar desorption studies were carried out with field samples collected around a thermometer factory with elevated levels of mercury (8 mg/kg), it was found that only about 10–15% of total mercury was desorbed with 1M HCl, while 4–5 M acid was required for complete desorption. We have tried to correlate this information to understand the transformations of mercury species that may occur either in the atmosphere or on the biomonitors. The results indicated that the elemental mercury, the principal form of mercury contamination around the thermometer factory, is converted into a strongly held form by some chemical binding agents on the surface of lichen/moss, or elemental mercury could diffuse into the cells of the lichen/moss, which then needs the stronger acid to release it. Sorption capacity studies suggest that the lichens and mosses can also be used as sorbent material for the decontamination of inorganic and methyl mercury from aqueous solutions.  相似文献   

12.
Measurements of Hg (total gas-phase, precipitation-phase andparticulate-phase), aerosol mass, particulate 210Pb and7Be and precipitation 210Pb were made at an atmosphericcollection station located in a near remote area of northcentral Wisconsin,U.S.A. (46°10N, 89°50W) during the summers of 1993, 1994and 1995. Total Hg and 210Pb were observed to correlate strongly(slope = 0.06 ± 0.03 ng mBq-1; r 2 =0.72) in rainwater. Mercury to 210Pb ratios in particulate matter(0.03 ± 0.02 ng mBq-1; r 2 = 0.06) wereconsistent with the ratio in rain. Enrichment of the Hg/mass ratio (approx.5–50×) relative to soil and primary pollutant aerosols indicatedthat gas-to-particle conversion had taken place during transport. Comparisonof these results with models for the incorporation of Hg into precipitationindicates that atmospheric particles deliver more Hg to precipitation than canbe explained by the presence of soot. A lack of correlation between totalgas-phase Hg (TGM) and a 7Be/210Pb function suggests novertical concentration gradient within the troposphere, and allows an estimateof TGM residence time of 1.5 ± 0.6 yr be made based on surface airsamples.  相似文献   

13.
In the year 2000, the elemental composition of mosses collected from 528 French sites has been studied as part of the 2000 European Moss Survey. Five moss species were collected: Scleropodium purum (56%), Pleurozium schreberi (18%), Hypnum cupressiforme (18%), Thuidium tamariscinum (4.5%.) and Hylocomium splendens (3.5%). Mosses were kept whole for analysis, including green and brownish parts. Summary statistics on element concentrations (Al, Ba, Ca, Cd, Co, Cr, Cu, Fe, Hg, K, Li, Mg, Mn, Na, Ni, P, Pb, Rb, Sr, V and Zn), and comparisons made with data from the other 27 participating European countries are shown here. The sources of these elements are identified using calculations of enrichment factors (EF) and principal component analysis (PCA). Finally, the spatial distribution in France of 10 elements is also shown, using maps underscoring areas showing highest concentration levels for each metal.  相似文献   

14.
In situ AGAGE GC-MS measurements of methyl bromide (CH3Br) and methyl chloride (CH3Cl) at Mace Head, Ireland and Cape Grim, Tasmania (1998–2001) reveal a complex pattern of sources. At Mace Head both gases have well-defined seasonal cycles with similar average annual decreases of 3.0% yr−1 (CH3Br) and 2.6% yr−1 (CH3Cl), and mean northern hemisphere baseline mole fractions of 10.37 ± 0.05 ppt and 535.7 ± 2.2 ppt, respectively. We have used a Lagrangian dispersion model and local meteorological data to segregate the Mace Head observations into different source regions, and interpret the results in terms of the known sources and sinks of these two key halocarbons. At Cape Grim CH3Br and CH3Cl also show annual decreases in their baseline mixing ratios of 2.5% yr−1 and 1.5% yr−1, respectively. Mean baseline mole fractions were 7.94 ± 0.03 ppt (CH3Br) and 541.3 ± 1.1 ppt (CH3Cl). Although CH3Cl has astrong seasonal cycle there is no well-defined seasonal cycle in the Cape Grim CH3Br record. The fact that both gases are steadily decreasing in the atmosphere at both locations implies that a change has occurred which is affecting a common, major source of both gases (possibly biomass burning) and/or their major sink process (destruction by hydroxyl radical).  相似文献   

15.
The present work evaluates the stress effects in two epiphytic lichen species with different thallus morphology, the foliose Parmelia caperata and the fruticose Evernia prunastri, as resulting from transplanting from an unpolluted to an air-polluted area. Lichen samples were collected in Portugal in a clean area, during the spring 2003, and transplanted (1) to the same zone nearby and (2) to a polluted area as affected by an industrial complex. Transplant samples were taken periodically during four months in both places. At the same time lichen samples from the clean-air site native (in-situ) populations were also collected. For each sample were measured the chlorophyll content, the chlorophyll degradation and the cell membrane damage, the latter represented by leacheate conductivity. During the experiment the meteorological conditions were registered. The results indicate the absence of stress effects of transplanting as such, and suggest that leachate conductivity may be the more sensitive indicator of general lichen vitality.  相似文献   

16.
Six locations across mainland Portugal were selected for exposing Parmelia sulcata, for a one-year period (8 months for one site), with simultaneous measurement of total (dry + wet) deposition (one-month periods). The exposed lichens and the total (dry + wet) deposition were analysed for cobalt contents by INAA (instrumental neutron activation analysis) and ICP-MS (inductively coupled plasma mass spectroscopy), respectively. The designated wet deposition was evaluated through the collected water volume; the designated dry deposition was assessed after the (dried) residual mass of the wet deposition. An excellent agreement between Co contents in exposed lichens and the cumulative (1) Co contents in the dry deposition, (2) dry deposition, and (3) wet deposition has been found for the locations with alternate drought and precipitation months, high dry deposition, and high Co contents in the latter. Continuous rainfall was found to hinder the Co accumulation in the lichen due to its release from the lichen and/or lower Co contents in the dry deposition. At three locations, P. sulcata Co contents, after subtraction of the background (before exposure), equalled or exceeded the Co contents in the cumulative dry deposition at the end of the exposure time. The optimal exposure period for this species likely depends on the exposure conditions.  相似文献   

17.
The evaluation of air quality is an important topic. It is well known that lichens have a set of characteristics that make them well suited for biomonitoring purposes. Sampling lichen diversity is not as expensive as chemical analysis, allowing a dense sampling grid and reducing the costs. Lichen diversity can be used to identify more disturbed areas, resulting from pollution, land use or ecological variables. In recent years, in order to enable extended use of lichens and to reduce ambiguities, i.e., variations due to unwanted environmental variables, efforts have been made to develop a feasible protocol for lichen sampling for biomonitoring purposes. This work aims at providing the information needed a priori for an air quality assessment study, in the form of a map showing areas where lichen diversity and abundance is lower. This study was done by sampling foliose and fruticulose lichen diversity and frequency, in a region in southwest Portugal (Sines) with large industrial facilities. A long-term study has been underway in the same area since the 1970s using lichens as bioindicators to evaluate air quality. In this work, we used a standard protocol to determine a lichen diversity value (LDV), to be used as an indicator of environmental quality. In order to reduce uncertainty concerning the type of disturbance affecting lichens, sampling sites were restricted using well-defined criteria. Whenever possible, sampling site variables were quantified. This method allowed us to reduce the many sources of variability affecting lichen diversity.  相似文献   

18.
A one-dimensional photochemical model was used to explore the role of chlorine atoms in oxidizing methane and other nonmethane hydrocarbons (NMHCs) in the marine troposphere and lower stratosphere. Where appropriate, the model predictions were compared with available measurements. Cl atoms are predicted to be present in the marine troposphere at concentrations of approximately 103 cm-3, mostly as a consequence of the reaction of OH with HCl released from sea spray. Despite this low abundance, our results indicate that 20 to 40% of NMHC oxidation in the troposphere (0–10 km) and 40 to 90% of NMHC oxidation in the lower stratosphere (10–20 km) is caused by Cl atoms. At 15 km, NMHC-Cl reactions account for nearly 80% of the PAN produced.The model was also used to test the longstanding hypothesis that NOCl is an intermediate to HCl formation from sea salt aerosols. It was found that the NOCl concentration required (10 ppt) would be incompatible with field observations of reactive nitrogen and ozone abundance. Chlorine nitrate (ClONO2) and methyl nitrate (CH3ONO2) were shown to be minor components of the total NO y abundance. Heterogeneous reactions that might enhance photolysis of halocarbons or convert ClONO2 to HOCl or Cl2 were determined to be relatively unimportant sources of Cl atoms. Specific and reliable measurements of HCl and other reactive chlorine species are needed to better assess their role in tropospheric chemistry.  相似文献   

19.
Kinetics and products of the gas-phase reactions of dimethylsulphide (DMS), dimethylsulphoxide (DMSO) and dimethylsulphone (DMSO2) with Br atoms and BrO radicals in air have beeninvestigated using on-line Fourier Transform Infrared Spectroscopy (FT-IR) as analytical technique at 740 ± 5 Torr total pressure and at 296 ± 3 K in a480 L reaction chamber. Using a relative rate method for determining the rate constants; the following values (expressed in cm3molecule–1 s–1) were found: kDMS+Br = (4.9 ±1.0) ×10–14, kDMSO + Br < 6 × 10–14,kDMSO 2 + Br 1 × 10–15,kDMSO + BrO = (1.0 ± 0.3) × 10–14 andkDMSO 2 + BrO 3 × 10–15 (allvalues are given with one on the experimental data). DMSO, SO2, COS, CH3SBr andCH3SO2Br were identified as the main sulphur containing products of the oxidation of DMS by Br atoms. From the reaction between DMSO and Br atoms, DMSO2and CH3SO2Br were the only sulphur containing products thatwere identified. DMSO, DMSO2 and SO2 were identified as themain sulphur containing products of the reaction between DMS and BrO.DMSO2 was found to be the only product of the reaction between DMSO and BrO. For the reactions of DMSO2 with Br and BrO no products were identified because the reactions were too slow.The implications of these results for atmospheric chemistry are discussed.  相似文献   

20.
To assess the impact of UV-B radiation combined with NaHSO3 in solution under laboratory conditions, we compared the amounts of stress-ethylene produced by two lichen species of the same genus. Ramalina lacera, an epiphytic Mediterranean lichen, was found to be rather sensitive to UV-B combined with NaHSO3, relative to the epilithic desert lichen R. maciformis. The impact of high temperatures with FeCl2 in solution, measured by amounts of stress ethylene accentuated the adaptability of R. maciformis to desert conditions, whereas R. lacera appeared to be rather sensitive to extreme temperatures especially in the case of chemical contamination. The adaptability of R. maciformis to UV-B appears to be related to the photoprotective capabilities of lichen substances.  相似文献   

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