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101.
E. V. Milanova 《Environmental monitoring and assessment》1995,37(1-3):239-244
Scale-dependent present-day landscape mapping and assessment were used to study the relationship among physical environment, land use, and degree of landscape modification in the Aral Sea region and the Karakum Desert, areas prone to desertification in the Commonwealth of Independent States (CIS). Applying geographic information system (GIS) techniques at global (1:15,000,000), regional (1:1,000,000), and local (1:300,000) scales, researchers found that large-scale landscape assessment and mapping allow them to recognize landscape changes under desertification processes and assess the type and intensity of these processes. Remote sensing has been widely used to evaluate data reliability, to fill information gaps, and to reveal the dynamics of land use types resulting from landscape changes. 相似文献
102.
Methods derived from time-series analysis are proposed for processing monitoring data. The necessity for the use of these methods is demonstrated. In a case study time-series analysis was applied to assess the impact of the closure of the Grevelingen estuary (S. W. Netherlands) in 1971 on a local wintering population of Oystercatchers (Haematopus ostralegus) in the adjacent Oosterschelde estuary.Communication No. 328 of the Delta Institute for Hydrobiological Research. 相似文献
103.
104.
G. L. Sia C. N. Ong S. E. Chia H. Y. Ong W. H. Phoon K. T. Tan 《Environmental monitoring and assessment》1991,19(1-3):401-411
This study was conducted to evaluate the usefulness of various biological parameters for monitoring of workers exposed to methyl ethyl ketone (MEK). Fifty male workers from a large magnetic videotape factory participated in this study. Personal air samples were collected using 3M organic vapor monitors and analysed for MEK by gas chromatography with flame ionisation detector (FID). 10 mL of urine; blood (1 mL) and exhaled air were also collected at the end of an 8-hour workshift. The headspace GC method was applied for measurement of urinary and blood MEK. MEK in expired air was analysed directly by using a GC/FID.The correlation coefficients (r) between environmental MEK and all other biological parameters measured show significant positive relationships. The r for environmental MEK and urine MEK was 0.84; for blood 0.73 and for breath 0.64. The correlation coefficients between blood and urine was 0.72; blood and breath was 0.88 and urine and breath 0.60. These findings suggest that measurements of unmetabolised MEK in blood, exhaled air and urine can be used for biological monitoring of MEK exposure. Nevertheless, laboratory methodological assessment is in favour of measuring urinary MEK as it is non-invasive and does not have to be analysed immediately after collection. 相似文献
105.
A water quality assessment was conducted on three Appalachian streams polluted by coal mining at the Big South Fork National River and Recreation Area, Tennessee and Kentucky. Results showed that sulfate was an excellent parameter for detecting the effects of coal mining and that sulfate analyses used in conjunction with conductivity readings provided the best detection index. Acidity and pH readings were relatively insensitive indicators, reflecting the mining pollution only after sulfate concentrations already indicated severe pollution levels.Hydrologist, Big South Fork NRRA, during the study; presently at Cape Lookout National SeashoreHydrologist, NPS, during the study; presently with USDA-Forest Service, Washington, DC. 相似文献
106.
Off-line solid-phase extraction (SPE) combined with liquid chromatography-electrospray tandem mass spectrometry (LC-ESI-MS-MS) was used to study the estuarine behaviour of the polar pesticides, atrazine, chloridazon, diuron and metolachlor, and their transformation products (TPs), hydroxyatrazine (HA), desisopropylatrazine (DIA), desethylatrazine (DEA), 3,4-dichlorophenylmethylurea (DPMU) and monuron. The compounds were identified by comparing their LC retention times and product-ion spectra with those of standard solutions. In all but one case the detection limits of the method were sufficient to determine the compounds of interest over the entire salinity range in the estuary. The concentrations of the dissolved pesticides ranged from 70 ng l-1 for chloridazon to 1350 ng l-1 for diuron. The levels of TPs were 3-8% of the levels of their parent pesticide. The mixing plots of polar pesticides and their TPs indicated that TPs, which are present in fresh river water, are conservatively transported to the sea and that no additional amounts of TPs are formed during their transport through the estuary. The one exception was HA, of which approximately 10% of the amount transported to the North Sea is formed in the lower part of the estuary by photochemical oxidation of atrazine. The latter was concluded from the ratios of each analyte over the sum total of the parent pesticide and all TPs along the salinity gradient, which proved to be a useful tool for identifying such estuarine transformations. 相似文献
107.
Rice WE 《Environmental monitoring and assessment》2004,99(1-3):251-257
A sub-surface desert water harvester was constructed in the sagebrush steppe habitat of south-central Idaho, U.S.A. The desert
water harvester utilizes a buried micro-catchment and three buried storage tanks to augment water for wildlife during the
dry season. In this region, mean annual precipitation (MAP) ranges between about 150–250 mm (6″–10″), 70% of which falls during
the cold season, November to May. Mid-summer through early autumn, June through October, is the dry portion of the year. During
this period, the sub-surface water harvester provides supplemental water for wildlife for 30–90 days, depending upon the precipitation
that year. The desert water harvester is constructed with commonly available, “over the counter” materials. The micro-catchment
is made of a square-shaped, 20 mL. “PERMALON” polyethylene pond liner (approximately 22.9 m × 22.9 m = 523 m2) buried at a depth of about 60 cm. A PVC pipe connects the harvester with two storage tanks and a drinking trough. The total
capacity of the water harvester is about 4777 L (1262 U.S. gallons) which includes three underground storage tanks, a trough
and pipes. The drinking trough is refined with an access ramp for birds and small animals. The technology is simple, cheap,
and durable and can be adapted to other uses, e.g. drip irrigation, short-term water for small livestock, poultry farming
etc. The desert water harvester can be used to concentrate and collect water from precipitation and run-off in semi-arid and
arid regions. Water harvested in such a relatively small area will not impact the ground water table but it should help to
grow small areas of crops or vegetables to aid villagers in self-sufficiency. 相似文献
108.
Rattanachongkiat S Millward GE Foulkes ME 《Journal of environmental monitoring : JEM》2004,6(4):254-261
Suitable techniques have been developed for the extraction of arsenic species in a variety of biological and environmental samples from the Pak Pa-Nang Estuary and catchment, located in Southern Thailand, and for their determination using HPLC directly coupled with ICP-MS. The estuary catchment comprises a tin mining area and inhabitants of the region can suffer from various stages of arsenic poisoning. The important arsenic species, AsB, DMA, MMA, and inorganic arsenic (As III and V) have been determined in fish and crustacean samples to provide toxicological information on those fauna which contribute to the local diet. A Hamilton PRP-X100 anion-exchange HPLC system employing a step elution has been used successfully to achieve separation of the arsenic species. A nitric acid microwave digestion procedure, followed by carrier gas nitrogen addition- (N2)-ICP-MS analysis was used to measure total arsenic in sample digests and extracts. The arsenic speciation of the biological samples was preserved using a Trypsin enzymatic extraction procedure. Extraction efficiencies were high, with values of 82-102%(As) for fish and crustacean samples. Validation for these procedures was carried out using certified reference materials. Fish and crustacean samples from the Pak Pa-Nang Estuary showed a range for total arsenic concentration, up to 17 microg g(-1) dry mass. The major species of arsenic in all fauna samples taken was AsB, together with smaller quantities of DMA and, more importantly, inorganic As. For sediment samples, arsenic species were determined following phosphoric acid (1 M H3PO4) extraction in an open focused microwave system. A phosphate-based eluant, pH 6-7.5, with anion exchange HPLC coupled with ICP-MS was used for separation and detection of AsIII, AsV, MMA and DMA. The optimum conditions, identified using an estuarine sediment reference material (LGC), were achieved using 45 W power and a 20 minute heating period for extraction of 0.5 g sediment. The stability and recovery of arsenic species under the extraction conditions were also determined by a spiking procedure which included the estuarine sediment reference material. The results show good stability for all species after extraction with a variability of less than 10%. Total concentrations of arsenic in the sediments from the Pak Pa-Nang river catchment and the estuary covered the ranges 7-269 microg g(-1)and 4-20 [micro sign]g g(-1)(dry weight), respectively. AsV was the major species found in all the sediment samples with smaller quantities of AsIII. The presence of the more toxic inorganic forms of arsenic in both sediments and biota samples has implications for human health, particularly as they are readily 'available'. 相似文献
109.
Givelet N Le Roux G Cheburkin A Chen B Frank J Goodsite ME Kempter H Krachler M Noernberg T Rausch N Rheinberger S Roos-Barraclough F Sapkota A Scholz C Shotyk W 《Journal of environmental monitoring : JEM》2004,6(5):481-492
For detailed reconstructions of atmospheric metal deposition using peat cores from bogs, a comprehensive protocol for working with peat cores is proposed. The first step is to locate and determine suitable sampling sites in accordance with the principal goal of the study, the period of time of interest and the precision required. Using the state of the art procedures and field equipment, peat cores are collected in such a way as to provide high quality records for paleoenvironmental study. Pertinent field observations gathered during the fieldwork are recorded in a field report. Cores are kept frozen at -18 degree C until they can be prepared in the laboratory. Frozen peat cores are precisely cut into 1 cm slices using a stainless steel band saw with stainless steel blades. The outside edges of each slice are removed using a titanium knife to avoid any possible contamination which might have occurred during the sampling and handling stage. Each slice is split, with one-half kept frozen for future studies (archived), and the other half further subdivided for physical, chemical, and mineralogical analyses. Physical parameters such as ash and water contents, the bulk density and the degree of decomposition of the peat are determined using established methods. A subsample is dried overnight at 105 degree C in a drying oven and milled in a centrifugal mill with titanium sieve. Prior to any expensive and time consuming chemical procedures and analyses, the resulting powdered samples, after manual homogenisation, are measured for more than twenty-two major and trace elements using non-destructive X-Ray fluorescence (XRF) methods. This approach provides lots of valuable geochemical data which documents the natural geochemical processes which occur in the peat profiles and their possible effect on the trace metal profiles. The development, evaluation and use of peat cores from bogs as archives of high-resolution records of atmospheric deposition of mineral dust and trace elements have led to the development of many analytical procedures which now permit the measurement of a wide range of elements in peat samples such as lead and lead isotope ratios, mercury, arsenic, antimony, silver, molybdenum, thorium, uranium, rare earth elements. Radiometric methods (the carbon bomb pulse of (14)C, (210)Pb and conventional (14)C dating) are combined to allow reliable age-depth models to be reconstructed for each peat profile. 相似文献
110.
Yafa C Farmer JG Graham MC Bacon JR Barbante C Cairns WR Bindler R Renberg I Cheburkin A Emons H Handley MJ Norton SA Krachler M Shotyk W Li XD Martinez-Cortizas A Pulford ID MacIver V Schweyer J Steinnes E Sjøbakk TE Weiss D Dolgopolova A Kylander M 《Journal of environmental monitoring : JEM》2004,6(5):493-501
Given the increasing interest in using peat bogs as archives of atmospheric metal deposition, the lack of validated sample preparation methods and suitable certified reference materials has hindered not only the quality assurance of the generated analytical data but also the interpretation and comparison of peat core metal profiles from different laboratories in the international community. Reference materials play an important role in the evaluation of the accuracy of analytical results and are essential parts of good laboratory practice. An ombrotrophic peat bog reference material has been developed by 14 laboratories from nine countries in an inter-laboratory comparison between February and October 2002. The material has been characterised for both acid-extractable and total concentrations of a range of elements, including Al, As, Ca, Cd, Cr, Cu, Fe, Hg, Mg, Mn, Na, Ni, P, Pb, Ti, V and Zn. The steps involved in the production of the reference material (i.e. collection and preparation, homogeneity and stability studies, and certification) are described in detail. 相似文献