Spatial and seasonal variations of elemental composition in Mt. Everest (Qomolangma) snow/firn

In May 2005, a total of 14 surface snow (0–10 cm) samples were collected along the climbing route from the advanced base camp to the summit (6500–8844 m a.s.l.) on the northern slope of Mt. Everest (Qomolangma). A 108 m firn/ice core was retrieved from the col of the East Rongbuk Glacier (28.03°N, 86.96°E, 6518 m a.s.l.) on the north eastern saddle of Mt. Everest in September 2002. Surface snow and the upper 3.5 m firn samples from the core were analyzed for major and trace elements by inductively coupled plasma mass spectroscopy (ICP-MS). Measurements show that crustal elements dominated both surface snow and the firn core, suggesting that Everest snow chemistry is mainly influenced by crustal aerosols from local rock or prevalent spring dust storms over southern/central Asia.There are no clear trends for element variations with elevation due to local crustal aerosol inputs or redistribution of surface snow by strong winds during the spring. Seasonal variability in snow/firn elements show that high elemental concentrations occur during the non-monsoon season and low values during the monsoon season. Ca, Cr, Cs, and Sr display the most distinct seasonal variations. Elemental concentrations (especially for heavy metals) at Mt. Everest are comparable with polar sites, generally lower than in suburban areas, and far lower than in large cities. This indicates that anthropogenic activities and heavy metal pollution have little effect on the Mt. Everest atmospheric environment. Everest firn core REE concentrations are the first reported in the region and seem to be comparable with those measured in modern and Last Glacial Maximum snow/ice samples from Greenland and Antarctica, and with precipitation samples from Japan and the East China Sea. This suggests that REE concentrations measured at Everest are representative of the background atmospheric environment.     

Organochlorine pesticides (DDTs and HCHs) in soils from the outskirts of Beijing, China

Concentrations of HCH (hexachlorocyclohexane) and DDT (Dichlorodiphenyltrichloroethane) were determined in shallow subsurface (5-30 cm depth) and deep soil layers (150-180 cm depth) from the outskirts of Beijing, China. Concentrations of total HCHs (including alpha, beta, gamma, delta-isomers) and total DDTs (including p,p'-DDT, p,p'-DDE, p,p'-DDD, o,p'-DDT) in shallow subsurface soils ranged from 1.36 to 56.61 ng/g dw (median 5.25 ng/g), and from 0.77 to 2178 ng/g (median 38.66 ng/g), respectively, and those in the deeper layers were approximately an order of magnitude less. The spatial distribution of HCHs and DDTs reflected the known historical usage of these pesticides. No correlation between the concentrations of pesticides and soil organic matter content or clay content can be found. The factors affecting residue levels and compositions of DDT and HCH were discussed. The contour maps of beta/gamma ratios and DDT/DDE ratios for both the shallow subsurface and deep layer soils were drawn.     

The levels and distribution of organochlorine pesticides (OCPs) in sediments from the Haihe River, China

The levels and distribution patterns of the selected organochlorine pesticides (OCPs=p,p'-DDT, o,p'-DDT, p,p'-DDE, p,p'-DDD, alpha-, beta-, gamma- and delta-HCH) in surficial sediments from the Haihe River and Dagu Drainage River of Tianjin were investigated by means of gas chromatography coupled with micro-electronic capture detector (GC-microECD). Concentrations of OCPs in the sediments from the Haihe River ranged from 1.88 to 18.76ng g(-1) (mean 7.33ng g(-1)) for sum HCH, 0.32-80.18ng g(-1) (mean 15.94ng g(-1)) for sum DDT. Compared with the Haihe River, the Dagu Drainage River was much more contaminated by HCHs and DDTs, wherein sum HCH ranged from 33.24 to 141.03ng g(-1) (mean 87.74ng g(-1)) and sum DDT ranged from 3.60 to 83.49ng g(-1) with a mean value of 35.52ng g(-1). The concentration distribution of sum DDT and sum HCH was different indicated their different contamination sources. Composition analyses indicated that a recent usage or discharge of HCH and DDT into the Dagu Drainage River.     

Residues of organochlorine pesticides in Hong Kong soils

It was short of research on the organochlorine pesticides (OCPs) residues in the soils of Hong Kong. Sixty-six representative soil samples were collected from the 46 sites covering five types of land uses in Hong Kong. Hexachlorohexanes (HCH) and 7 Stockholm Convention OCPs were analyzed by gas chromatograph (GC) equipped with a Nickel 63 electronic capture detector (muECD). The results presented that HCH and 5 Stockholm Convention pesticides were detected in Hong Kong soils although the detectable ratio varies to a great extent. The concentration sequence of the five detectable OCPs was HCH > dichlorodiphenyltrichloroethane (DDT) > hexachlorobenzene (HCB) approximately = Endrin > alpha-endosulfan. Among the OCPs and their homologues or isomers, beta-HCH and p,p'-DDE were the two predominant substances according to the concentrations and detectable ratios, concentrations of which in soils were averagely 6.12 microg kg(-1) and 0.41 microg kg(-1) respectively. Soil horizon samples of 0-10 cm, 10-30 cm and >30 cm depth were selected from nine soil profiles to demonstrate the depth distributions of DDT and HCH in soil profiles. Concentrations of HCH tended to increase gradually from the topsoil to bottom layer while the lowest concentration of DDT is usually found in the subsoil (10-30 cm) in most sampling sites. In addition, close correlations of pH(KCl) and total organic carbon (TOC) with HCH indicated an effect on the residues of HCH caused by these two soils properties, but such relationships were not found with DDT or other OCPs.     

Large-scale spatial pollution patterns around the North Sea indicated by coastal bird eggs within an EcoQO programme

To categorize the marine environmental health status, the Oslo and Paris commissions have recently formulated Ecological Quality Objectives (EcoQOs) for many ecological features including the contamination of coastal bird eggs with mercury and organochlorines. In this study, we describe spatial and temporal patterns of egg contamination around the North Sea and compared them to the EcoQOs. Concentrations of mercury, polychlorinated biphenyl (??PCB) congeners, dichlorodiphenyltrichloroethane (??DDT) and derivatives, hexachlorobenzene (HCB) and hexachlorocyclohexane (??HCH) isomers were analysed in two tern species (Sterna hirundo and Sterna paradisaea) and Oystercatcher (Haematopus ostralegus) eggs collected between 2008 and 2010 in a total of 21 sites in seven countries surrounding the North Sea. Hg, ??PCB and HCB were highest in the southern sites, while ??DDT and ??HCH concentrations were greatest in eggs from the western North Sea and the Elbe estuary. There were rarely any consistent decreases over time for any compounds. In the terns, Hg, HCB and ??HCH increased at most sites, ??PCB and ??DDT in Sweden and Norway. In the Oystercatcher, HCB and ??HCH increased at more than the half of the sites, ??PCB, ??DDT and Hg at several German sites. In the terns, Hg, ??PCB and ??DDT exceeded the EcoQO in all, HCB in most years and sites. At most sites, ??HCH fulfilled the EcoQO in some study years. In the Oystercatcher, Hg, ??PCB and ??DDT exceeded the EcoQO in all or most years and sites. HCB and ??HCH fulfilled the EcoQO in some or all years at most sites. The EcoQO was exceeded most frequently in estuaries. We conclude that EcoQOs are suitable for drawing contamination patterns of the coastal North Sea in an easily understandable manner, offering the opportunity to harmonize the EcoQOs with coordinated environmental monitoring programmes.     

Glaciochemical records from a Mt. Everest ice core: relationship to atmospheric circulation over Asia

Glaciochemical records recovered from an 80.4 m ice core in the East Rongbuk (ER) Glacier (elevation: 6450 m) on the northern slope of Mt. Everest provide a reconstructing of past climate for the period AD 1846–1997. Empirical orthogonal function (EOF) analysis on the eight major ion (SO₄²⁻, Mg²⁺, Ca²⁺, Na⁺, Cl⁻, NH₄⁺, K⁺, and NO₃⁻) time-series reveals inter-species relations and common structure within the ER glaciochemical data. The first two EOF series (EOF1-ions and EOF2-ions) are compared with instrumental data of sea level pressure (SLP) to demonstrate that the EOF-ions series display strong connections to winter (January) and summer (July) SLP over the Mongolian region. The positive relationship between EOF1-ions and the Mongolian High (MongHi) series suggests that enhanced winter MongHi strengthens the transport of dust aerosols southward from arid regions over central Asia to Mt. Everest. The close correspondence between EOF2-ions and the summer Mongolian Low (MongLow) indicates that the deeper MongLow, which is related to the stronger Indian Monsoon, contributes to a decrease in summer dust aerosols. Therefore, the ER ice core record comprises two assemblages of crustal species, each transported from different source regions during different seasons. EOF1-ions represents the majority of the crustal species and is related to winter atmospheric circulation patterns. These species are mainly transported from arid regions of central Asia during the winter dry season. EOF2-ions represents crustal species transported by summer atmospheric circulation from local/regional sources in the northern and southern Himalayas.     

Impacts of Asian dust storm associated with the stratosphere-to-troposphere transport in the spring of 2001 and 2002 on dust and tritium variations in Mount Wrangell ice core,Alaska

The relation of interannual connection between Asian dust outbreaks and stratosphere-to-troposphere transport (STT) in spring was suggested by the dust and tritium variations in the Mount Wrangell ice core, Alaska in [Yasunari, T.J., Shiraiwa, T., Kanamori, S., Fujii, Y., Igarashi, M., Yamazaki, K., Benson, C.S., Hondoh, T., 2007. Intra-annual variations in atmospheric dust and tritium in the North Pacific region detected from an ice core from Mount Wrangell, Alaska. J. Geophys. Res., 112, D10208. doi: 10.1029/2006JD008121]. However, these impacts on the ice core site in each event scale have not been investigated. Hence, the present paper focuses on the material transport and deposition processes for further understanding these impacts on the ice core. The variations in dust and tritium concentrations in spring in an ice core taken at Mt. Wrangell, Alaska are explained by meteorological analysis and simulation of trajectories associated with Asian dust outbreaks and STT. Material transport and deposition at Mt. Wrangell are examined in two contrasting years (2001 and 2002). Dust and tritium concentrations both reached peak values in the early spring of 2002, while the dust peak occurred in early spring and the tritium peak occurred in late spring in 2001. Six severe East Asian transpacific dust storms over this period are modeled by forward trajectory and meteorologically analyzed. It is found that 5 of 6 events contributed to the ice core record in Alaska. Stratospheric air is also transported to the ice core site in most cases. Tritium deposition is found to have been suppressed in the cases of the 2001 dust storms due to lack of snowfall at appropriate times. Taken the detailed transport and deposition processes after the severe dust storms with atmospheric circulations into account, we can well explain spring dust and tritium variations in the Mount Wrangell ice core.     

Northern hemisphere concentrations of methane and nitrous oxide since 1800: Results from the Mt. Logan and 20D ice cores

Concentrations of CH₄ and N₂O have been determined in bubbles extracted from the Mt. Logan (Yukon) and 20D (south Greenland) ice cores. The enclosure dates of the trapped gas samples range from 1802 to 1960; thus these data help to document the anthropogenic increases of these two greenhouse gases in the Northen Hemisphere atmosphere. In general, the new data are in accord with previous ice core studies showing accelerating increases in concentration of both gases since 1900. The Mt. Logan records appear to be the first for any trace gases from alpine glacial ice. The present data set is too sparse to be conclusive, but suggests generally higher CH₄ concentrations over south Greenland than Mt. Logan, particularly for the 1850 - 1900 period.     

Seasonal variations of organochlorine insecticide residues in air from Porto Novo, South India

Air samples collected from Porto Novo (11 degrees 29' N, 79 degrees 46' E), Tamil Nadu State, South India from December, 1987 to January, 1989 were analysed to determine the seasonal variations of the levels of organochlorine insecticides such as HCH (BHC) and DDT. Both these insecticides showed higher levels from August to January, although this trend was more marked in HCH than DDT, reflecting the application of HCH largely, and probably small quantities of DDT during the flowering season of rice. The alpha-HCH was detected as a dominant isomer for all seasons monitored followed by gamma-HCH. Among DDT compounds, p,p'-DDT was the highest except in dry season (January to April) when p,p-DDE showed higher percentage. The levels and percentage composition of these insecticides recorded in the present study may aid in interpreting the role of a 'point source' area since India is one of the countries still using the persistent organochlorine pesticides in large quantities.     

Organochlorine pesticides and PCBs in fish from lakes of the Tibetan Plateau and the implications

High mountains may play significant roles in the global transport of persistent organic pollutants (POPs). This work aims to investigate the levels, patterns and distribution of semi-volatile organoclorine pollutants and to improve the understanding of the long-range atmospheric transport and fate of contaminants on the Tibetan Plateau. A total of 60 fish samples were collected from eight lakes located between 2813 and 4718 m above sea level across the Plateau. Concentrations of polychlorinated biphenyls (PCBs), organochlorine pesticides (OCPs) including dichlorodiphenyltrichloroethane and its metabolites (DDTs), hexachlorocyclohexanes (HCHs) and hexachlorobenzene (HCB) were measured in fish muscle. The results showed that concentrations of DDT, HCH and HCB were comparable to or lower than those found in remote mountains of Europe, Canada and US, while PCB concentrations in fish were, on average, about 4-150 times lower on Tibet than at other mountain areas. The transport and fate of contaminants in the Plateau are significantly influenced by the unique climatological and meteorological conditions, particularly by the summer Indian monsoon and winter westerly jet stream.     

Organo-chlorine pesticide (DDT and HCH) residues in the Taihu Lake Region and its movement in soil-water system I. Field survey of DDT and HCH residues in ecosystem of the region

The use of organo-chlorine (DDT and HCH) has been banned in China for 20 years. A field survey was carried out during 1999-2000 in the Taihu Lake Region. Organo-chlorine pesticide (OCP) residues in soil, water, fish and sediment samples were investigated. DDT was detected in 5 out of 10 samples with concentration ranging from 0.3 to 5.3 microg/kg in the surface (0-15 cm) layer, 6 out of 10 with 0.5 to 4.0 microg/kg in the subsoil layer (16-30 cm), and 4 of 10 with 0 to 2.7 microg/ kg in the deep soil layer (31-50 cm). Results for HCH residues in soil samples were similar to those of DDT. These results indicate that OCP residues in 0-50 cm profile had been leached out or degraded to safe level. In river water DDT was detected in 10 out of 13 samples ranging from 0.2 to 9.3 microg/l, with an average of 1.0 microg/l. While HCH was detected in 12 out of 13 samples ranging from 0.02 to 36.1 microg/l, with an average 5.6 microg/l. DDT residues in sediment ranged from 0.1 to 8.8 microg/kg, while HCH ranged from 0.3 to 66.5 microg/kg. DDT residues in fish body ranged from 3.7 to 23.5 microg/kg and HCH ranged from 3.7 to 132 microg/kg. These results demonstrate an accumulation through food chain (from soil-water-sediment-microbes-crop-fish-... etc.), also that HCH residues are generally more persistent than DDT residues. However, all these data are well below than the state warning standard limit.     

Chlorinated hydrocarbons in coastal bottom sediments of the Japan Sea

Data on distribution of chlorinated hydrocarbons in coastal bottom sediments of different areas of the Japan Sea are presented. Results obtained during the autumn 1994 expedition in Peter-the-Great Bay were compared with the data of previous surveys in the D.P.R. Korea coastal zone and Tatarsky Strait (Sakhalin Island). Concentrations of DDT metabolites and HCH isomers appear to be related mainly to pesticide usage in agriculture. Mean concentrations of total DDTs decreased from 12.5 ng g(-1) in the D.P.R.K. coastal zone to 2.2 ng g(-1) at Sakhalin Island shelf, whereas total HCH concentrations decreased from 3.4 to 0.4 ng g(-1). Differences in chemical composition of pesticides used in the D.P.R.K. and Russia were evident. The importance of further monitoring of persistent organochlorines in bottom sediments and the need for regulation of wastewater discharges is stressed.     

Organochlorine pollutants in human blood and their relation with age, gender and habitat from North-east India

Organochlorine pesticides (OCPs) have been beneficial to man and environment but their inadvertent use has caused considerable harm to human health. Despite the proliferation of different types of pesticides, organochlorines such as HCH and DDT still account for two third of the total consumption in India because of their low cost and versatility in action again various pests. Since, Assam, a state in North-eastern part of India is an endemic area with perennial transmission where mosquito borne diseases are serious health problems; these pesticides are still being used in huge quantities in vector control as well as in agriculture. A total of 331 human blood samples were collected from district Nagaon and Dibrugarh of Assam to determine the residue levels of DDT and HCH in human blood. The concentrations of selected persistent organochlorine pollutants were measured with gas chromatography-electron capture detector. The results demonstrated that the mean levels of total DDT and HCH were 743 μg L(-1) and 627 μg L(-1) for district Nagaon while 417 μg L(-1) and 348 μg L(-1) for district Dibrugarh. The difference of total HCH and total DDT between these two districts was found to be highly significant (P<0.0001). Among DDT metabolites, the same trend was observed for both the districts as p,p-DDT was the principal component contributed 41% for Nagaon and 58% for Dibrugarh. In case of HCH residues, for Nagaon, β-HCH was the predominant contaminant comprised more than 34% while for Dibrugarh, it was α-HCH that was contributing 43% of total HCH concentration.     

Distribution and ecotoxicological concerns of persistent organic pollutants in sediment from creek ecosystem

In order to study the distribution and ecotoxicological concerns of persistent organic pollutants, grab sediment samples were collected from different locations across Thane creek, India. Analyses of samples were carried out using gas chromatography (GC)–electron capture detector and GC–mass spectrometry techniques. In organochlorine pesticides (OCPs), DDT (1,1,1,-trichloro-2,2-bis(p-chlorophenyl) ethane), DDE (1,1-dichloro-2,2-bis(p-chlorophenyl) ethylene), DDD (1-chloro-4-(2,2-dichloro-1-(4-chlorophenyl)ethyl) benzene) and α, β, and γ conformer of hexachlorocyclohexane (HCH), and 9 polychlorinated biphenyls (PCBs) congeners were analyzed in surface sediment samples. Concentrations of these pollutants in grab sediment samples may indicate their current use and impact on marine ecosystem. Average concentrations of total DDT (including DDD and DDE), HCH, and Σ₉PCBs were found to be 4.9, 12.5, and 2.9 µg kg^?1(dry weight) respectively. High concentrations of OCPs and PCBs were found at discharge locations in creek compared to other locations. Location-wise distribution of OCPs and PCBs indicates their high concentrations at the waste water receiving point. Data were compared for ecotoxicological impacts based on the levels specified in the sediment quality standards of the US Environmental Protection Agency and the Canadian Council of Ministers of the Environment. γ-HCH was found to have maximum potential to induce ecotoxicological impacts.     

PCBs and chlorinated hydrocarbon pesticides in Antarctic atmosphere and hydrosphere

PCBs and chlorinated hydrocarbon pesticides such as DDTs and HCHs (BHCs) were measured in air, water, ice and snow samples collected around the Japanese research stations in Antarctica and adjacent oceans during December 1980 to March 1982. The atmospheric concentrations of chlorinated hydrocarbons decreased in the transport process from northern lands to Antarctica, but the compositions of PCBs, DDT compounds and HCH isomers were relatively uniform throughout this process. Regional and seasonal variations were found in aerial concentrations of these pollutants at Syowa Station and adjacent seas in Antarctica. Chlorinated hydrocarbons were also detected in snow, ice, lake water and sea water samples, in which rather high concentrations were found in snow and ice samples. This suggests that snow and ice serve as media of supply of these pollutants into Antarctic marine environment. Most interestingly, the concentrations of DDTs and higher chlorinated biphenyls were much lower in sea water under fast ice than in that from outer margin of pack ice. This indicates that the active removal of these pollutants is occurred in the sea under fast ice, and that is strongly associated with high primary productivity. It is, therefore, presumed that the concentrations of PCBs and DDTs in marine organisms living under fast ice in Antarctica could be lower than those in other oceans.     

Contamination of bovine milk with DDT and HCH residues in relation to their usage in malaria control programme

The contribution of spraying DDT and HCH for malaria control towards the contamination of bovine milk was investigated by analysing milk samples collected from preselected localities sprayed with either DDT or HCH in the Punjab. A direct correlation was found between the amounts of residues of these insecticides in milk and their typical usage pattern for the mosquito control programme. It is considered that these results may have significant bearing on the regulatory control of DDT and HCH residues in milk.     

Chlorinated pesticide residues in surface sediments from the River Kaveri, south India

Chlorinated compounds have preferential attraction for organic phases found in sediments. Usage of chlorinated pesticides in agriculture and vector control is more in developing countries. The residue levels of HCH isomers, and DDT, and its metabolites were quantified in surface sediments from the River kaveri and Coleroon in Tamil Nadu state, South India. The concentration of HCH ranged from 4.35 to 158.4 ng g-1 (dry wt.). Among the isomers of HCH, alpha-HCH is predominant followed by beta and gamma-HCH. The levels of DDT varied from 0.69 to 4.85 ng g-1 (dry wt.). Among the DDT compounds, p,p'-DDE quantified more (> 40%) in all the sites. This suggests that p,p'-DDE is a major breakdown (dehydrochlorination) product of DDT in the sediment compartment. Higher concentration of HCH residues reveals its large usage in agriculture. The flux of pesticide residues from land to river including downward flux to sediment is less.     

Atmospheric nitrous oxide: patterns of global change during recent decades and centuries

Data from weekly global measurements of nitrous oxide from 1981 to the end of 1996 are presented. The results show that there is more N2O in the northern hemisphere by about 0.7 +/- 0.04 ppbv, and the Arctic to Antarctic difference is about 1.2 +/- 0.1 ppbv. Concentrations at locations influenced by continental air are higher than at marine sites, showing the existence of large land-based emissions. For the period studied, N2O increased at an average rate of about 0.6 ppbv/year (approximately 0.2%/year) although there were periods when the rates were substantially different. Using ice core data, a record of N2O can be put together that goes back about 1000 years. It shows pre-industrial levels of about 287 +/- 1 ppbv and that concentrations have now risen by about 27 ppbv or 9.4% over the last century. The ice core data show that N2O started increasing only during the 20th century. The data presented here represent a comprehensive view of the present global distribution of N20 and its historical and recent trends.     

Organochlorine contaminants in seven species of Arctic seabirds from northern Baffin Bay

Organochlorine contaminants (OCs) were determined in liver and fat of seven species of seabirds (Alle alle, Uria lomvia, Cepphus grylle, Rissa tridactyla, Pagophila eburnea, Larus hyperboreus, and Fulmaris glacialis) collected in May/June 1998 from the Northwater Polynya in northern Baffin Bay. OC concentrations ranged over an order of magnitude between seabird species and OC groups, with PCBs having the highest concentrations followed by DDT, chlordane, HCH and ClBz. Positive relationships between delta15N (estimator of trophic level) and OC concentrations (lipid basis) were found for all OC groups, showing that trophic position and biomagnification significantly influence OC concentrations in Arctic seabirds. Concentrations of a number of OCs in particular species (e.g., HCH in P. eburnean) were lower than expected based on delta15N and was attributed to biotransformation. P. eburnea and F. glacialis, which scavenge, and R. tridactyla, which migrate from the south, were consistently above the delta15N-OC regression providing evidence that these variables can elevate OC concentrations. Stable isotope measurements in muscle may not be suitable for identifying past scavenging events by seabirds. OC relative proportions were related to trophic position and phylogeny, showing that OC biotransformation varies between seabird groups. Trophic level, migration, scavenging and biotransformation all play important roles in the OCs found in Arctic seabirds.     

北京城市雨水、树冠水和地表径流中有机氯农药的污染特征

对北京降雨过程中雨水、树冠水、地表径流等介质中有机氯农药(OCPs)的污染特征进行了研究,研究的污染物包括六氯苯(HCB)、六六六(HCH)和滴滴涕(DDT)。结果显示,在雨水、树冠水和地表径流中,HCH含量最高(几何平均浓度分别为11.1、21.6和25.1 ng/L),其次是HCB(几何平均浓度分别为3.71、3.54和5.91 ng/L)和DDT(几何平均浓度分别为2.64、4.66和10.6 ng/L)。对地表径流样品中所测的OCPs组分浓度与径流水质参数和气象参数的相关分析显示,所测各OCPs组分浓度与pH呈显著负相关,与径流的溶解性有机碳含量呈显著正相关,降雨量和雨前晴天数对不同组分OCPs的影响并不完全相同。平均贡献率的计算表明,雨水是城市地表径流中OCPs的一个重要来源,树冠水的贡献也不可忽视。