Pollution Aerosol in the Northeast: Northeastern-Midwestern Contributions
In recent years, atmospheric scientists have been endeavoring to determine the relative contributions of local and distant sources to pollution aerosol in eastern North America. Elemental analysis of aerosol from various sites in the northeastern United States has revealed a persistent northeastern...
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description | In recent years, atmospheric scientists have been endeavoring to determine the relative contributions of local and distant sources to pollution aerosol in eastern North America. Elemental analysis of aerosol from various sites in the northeastern United States has revealed a persistent northeastern ``foreground'' upon which pulses of midwestern aerosol are superimposed every few days, in response to large-scale meteorological features. Regional apportionment of tracer elements and sulfate in summer and winter samples from Narragansett, Rhode Island, and Underhill, Vermont, shows that most of the elements come predominantly from northeastern sources. Notable exceptions include arsenic and indium, for which Canadian nonferrous smelters are important sources, and sulfur and selenium, for which the Midwest is an important source. During 1982 and 1983, the Northeast and the Midwest contributed comparably to aerosol sulfate at Narragansett and Underhill, in spite of the fact that the emissions of sulfur dioxide in the Midwest were ten times those in the Northeast; Canadian smelters accounted for less than 10 percent of the total sulfate. During a major pollution episode in July 1982, northeastern and midwestern sources produced comparable sulfate concentrations in Rhode Island, whereas midwestern sources dominated northeastern sources in Vermont. Thus, although distant midwestern sources affect the quantity of pollution aerosol in the Northeast and may dominate episodically, nearer northeastern sources are comparably important on the long term. The regional elemental tracer system has shown that pollution aerosol in the Northeast is composed of a northeastern ``foreground'' plus superimposed pulses from the Midwest. When these pulses are strong enough, they form the classical episodes of midwestern aerosol. During periods of stagnation in the Northeast, however, aerosol produced locally can reach concentrations that rival or exceed those coming from the Midwest, even for sulfate. These two types of episodes can be distinguished clearly with elemental tracers. Over the long term, the Northeast is its most important source for elements that are distributed broadly over eastern North America or enriched in northeastern emissions (vanadium, antimony, zinc, manganese, and probably many other elements not part of our tracer system). For elements enriched in distant sources, such as arsenic and indium from the Canadian nonferrous smelters and selenium and sulfur from t |
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Elemental analysis of aerosol from various sites in the northeastern United States has revealed a persistent northeastern ``foreground'' upon which pulses of midwestern aerosol are superimposed every few days, in response to large-scale meteorological features. Regional apportionment of tracer elements and sulfate in summer and winter samples from Narragansett, Rhode Island, and Underhill, Vermont, shows that most of the elements come predominantly from northeastern sources. Notable exceptions include arsenic and indium, for which Canadian nonferrous smelters are important sources, and sulfur and selenium, for which the Midwest is an important source. During 1982 and 1983, the Northeast and the Midwest contributed comparably to aerosol sulfate at Narragansett and Underhill, in spite of the fact that the emissions of sulfur dioxide in the Midwest were ten times those in the Northeast; Canadian smelters accounted for less than 10 percent of the total sulfate. During a major pollution episode in July 1982, northeastern and midwestern sources produced comparable sulfate concentrations in Rhode Island, whereas midwestern sources dominated northeastern sources in Vermont. Thus, although distant midwestern sources affect the quantity of pollution aerosol in the Northeast and may dominate episodically, nearer northeastern sources are comparably important on the long term. The regional elemental tracer system has shown that pollution aerosol in the Northeast is composed of a northeastern ``foreground'' plus superimposed pulses from the Midwest. When these pulses are strong enough, they form the classical episodes of midwestern aerosol. During periods of stagnation in the Northeast, however, aerosol produced locally can reach concentrations that rival or exceed those coming from the Midwest, even for sulfate. These two types of episodes can be distinguished clearly with elemental tracers. Over the long term, the Northeast is its most important source for elements that are distributed broadly over eastern North America or enriched in northeastern emissions (vanadium, antimony, zinc, manganese, and probably many other elements not part of our tracer system). For elements enriched in distant sources, such as arsenic and indium from the Canadian nonferrous smelters and selenium and sulfur from the Midwest, the contributions of these distant sources may equal or exceed those from the Northeast. For sulfate, which is perhaps the most environmentally significant of these elements, transport models and other measurement programs confirm our basic conclusion that the Northeast and the Midwest contribute comparably to ambient levels in the Northeast. This amounts to a tenfold discrimination against midwestern sources, which emit approximately 20 million tons of SO$_{2}$ annually versus 2 million tons for north-eastern sources. A similar degree of discrimination with distance has been built into the MOI transport models (20). More data are needed to refine our understanding of sources and transport of pollution aerosol in eastern North America. The elemental tracer system can and should be extended to other elements, to source regions farther from the Northeast, to additional seasons and years, and to precipitation. But the basic picture seems clear: even though strong pulses of transported aerosol reach the Northeast regularly from the Midwest, over the long term the Northeast is a major or dominant source of its pollution aerosol.</description><identifier>ISSN: 0036-8075</identifier><identifier>EISSN: 1095-9203</identifier><identifier>DOI: 10.1126/science.228.4697.275</identifier><identifier>PMID: 17790213</identifier><identifier>CODEN: SCIEAS</identifier><language>eng</language><publisher>Washington, DC: The American Association for the Advancement of Science</publisher><subject>500200 - Environment, Atmospheric- Chemicals Monitoring & Transport- (-1989) ; AEROSOL MONITORING ; AEROSOLS ; Air pollution ; AIR POLLUTION MONITORING ; Antimony ; Applied sciences ; ARSENIC ; Atmospheric pollution ; COLLOIDS ; DATA ; DISPERSIONS ; ELEMENTS ; Environmental aspects ; ENVIRONMENTAL SCIENCES ; ENVIRONMENTAL TRANSPORT ; Exact sciences and technology ; FEDERAL REGION I ; INDIUM ; INFORMATION ; LONG-RANGE TRANSPORT ; MASS TRANSFER ; METALS ; MONITORING ; NONMETALS ; NORTH AMERICA ; NUMERICAL DATA ; OXYGEN COMPOUNDS ; Pollutants physicochemistry study: properties, effects, reactions, transport and distribution ; Pollution ; REGIONAL ANALYSIS ; SEASONAL VARIATIONS ; SELENIUM ; SEMIMETALS ; Signatures ; Smelters ; SOLS ; STATISTICAL DATA ; SULFATES ; SULFUR ; SULFUR COMPOUNDS ; Summer ; USA ; VARIATIONS ; Winter ; Zinc</subject><ispartof>Science (American Association for the Advancement of Science), 1985-04, Vol.228 (4697), p.275-284</ispartof><rights>Copyright 1985 The American Association for the Advancement of Science</rights><rights>1986 INIST-CNRS</rights><rights>COPYRIGHT 1985 American Association for the Advancement of Science</rights><rights>COPYRIGHT 1985 American Association for the Advancement of Science</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c679t-b879c3754a9853c7a4396377300bfeea35ad51b98b7880bdaeb22906f80ed1623</citedby><cites>FETCH-LOGICAL-c679t-b879c3754a9853c7a4396377300bfeea35ad51b98b7880bdaeb22906f80ed1623</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/1694830$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/1694830$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,776,780,799,881,2871,2872,27901,27902,57992,58225</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=8459053$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17790213$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/5154568$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Rahn, Kenneth A.</creatorcontrib><creatorcontrib>Lowenthal, Douglas H.</creatorcontrib><creatorcontrib>Univ. of Rhode Island, Narragansett</creatorcontrib><title>Pollution Aerosol in the Northeast: Northeastern-Midwestern Contributions</title><title>Science (American Association for the Advancement of Science)</title><addtitle>Science</addtitle><description>In recent years, atmospheric scientists have been endeavoring to determine the relative contributions of local and distant sources to pollution aerosol in eastern North America. Elemental analysis of aerosol from various sites in the northeastern United States has revealed a persistent northeastern ``foreground'' upon which pulses of midwestern aerosol are superimposed every few days, in response to large-scale meteorological features. Regional apportionment of tracer elements and sulfate in summer and winter samples from Narragansett, Rhode Island, and Underhill, Vermont, shows that most of the elements come predominantly from northeastern sources. Notable exceptions include arsenic and indium, for which Canadian nonferrous smelters are important sources, and sulfur and selenium, for which the Midwest is an important source. During 1982 and 1983, the Northeast and the Midwest contributed comparably to aerosol sulfate at Narragansett and Underhill, in spite of the fact that the emissions of sulfur dioxide in the Midwest were ten times those in the Northeast; Canadian smelters accounted for less than 10 percent of the total sulfate. During a major pollution episode in July 1982, northeastern and midwestern sources produced comparable sulfate concentrations in Rhode Island, whereas midwestern sources dominated northeastern sources in Vermont. Thus, although distant midwestern sources affect the quantity of pollution aerosol in the Northeast and may dominate episodically, nearer northeastern sources are comparably important on the long term. The regional elemental tracer system has shown that pollution aerosol in the Northeast is composed of a northeastern ``foreground'' plus superimposed pulses from the Midwest. When these pulses are strong enough, they form the classical episodes of midwestern aerosol. During periods of stagnation in the Northeast, however, aerosol produced locally can reach concentrations that rival or exceed those coming from the Midwest, even for sulfate. These two types of episodes can be distinguished clearly with elemental tracers. Over the long term, the Northeast is its most important source for elements that are distributed broadly over eastern North America or enriched in northeastern emissions (vanadium, antimony, zinc, manganese, and probably many other elements not part of our tracer system). For elements enriched in distant sources, such as arsenic and indium from the Canadian nonferrous smelters and selenium and sulfur from the Midwest, the contributions of these distant sources may equal or exceed those from the Northeast. For sulfate, which is perhaps the most environmentally significant of these elements, transport models and other measurement programs confirm our basic conclusion that the Northeast and the Midwest contribute comparably to ambient levels in the Northeast. This amounts to a tenfold discrimination against midwestern sources, which emit approximately 20 million tons of SO$_{2}$ annually versus 2 million tons for north-eastern sources. A similar degree of discrimination with distance has been built into the MOI transport models (20). More data are needed to refine our understanding of sources and transport of pollution aerosol in eastern North America. The elemental tracer system can and should be extended to other elements, to source regions farther from the Northeast, to additional seasons and years, and to precipitation. But the basic picture seems clear: even though strong pulses of transported aerosol reach the Northeast regularly from the Midwest, over the long term the Northeast is a major or dominant source of its pollution aerosol.</description><subject>500200 - Environment, Atmospheric- Chemicals Monitoring & Transport- (-1989)</subject><subject>AEROSOL MONITORING</subject><subject>AEROSOLS</subject><subject>Air pollution</subject><subject>AIR POLLUTION MONITORING</subject><subject>Antimony</subject><subject>Applied sciences</subject><subject>ARSENIC</subject><subject>Atmospheric pollution</subject><subject>COLLOIDS</subject><subject>DATA</subject><subject>DISPERSIONS</subject><subject>ELEMENTS</subject><subject>Environmental aspects</subject><subject>ENVIRONMENTAL SCIENCES</subject><subject>ENVIRONMENTAL TRANSPORT</subject><subject>Exact sciences and technology</subject><subject>FEDERAL REGION I</subject><subject>INDIUM</subject><subject>INFORMATION</subject><subject>LONG-RANGE TRANSPORT</subject><subject>MASS TRANSFER</subject><subject>METALS</subject><subject>MONITORING</subject><subject>NONMETALS</subject><subject>NORTH AMERICA</subject><subject>NUMERICAL DATA</subject><subject>OXYGEN COMPOUNDS</subject><subject>Pollutants physicochemistry study: properties, effects, reactions, transport and distribution</subject><subject>Pollution</subject><subject>REGIONAL ANALYSIS</subject><subject>SEASONAL VARIATIONS</subject><subject>SELENIUM</subject><subject>SEMIMETALS</subject><subject>Signatures</subject><subject>Smelters</subject><subject>SOLS</subject><subject>STATISTICAL DATA</subject><subject>SULFATES</subject><subject>SULFUR</subject><subject>SULFUR COMPOUNDS</subject><subject>Summer</subject><subject>USA</subject><subject>VARIATIONS</subject><subject>Winter</subject><subject>Zinc</subject><issn>0036-8075</issn><issn>1095-9203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1985</creationdate><recordtype>article</recordtype><recordid>eNqN0l2LEzEUBuBBFLe7-g8WKSLuxTo1H5NJ4l0tWgt1K_hxGzKZM90s02RNUlb_vem22BWKlFwkJM85hOQtinOMRhiT-m00FpyBESFiVNWSjwhnj4oBRpKVkiD6uBggROtSIM5OitMYbxDKZ5I-LU4w5xIRTAfF7Ivv-3Wy3g3HEHz0_dC6YbqG4ZUPedIxvdsvIbjys23v4H45nHiXgm3uy-Oz4kmn-wjPd_NZ8f3jh2-TT-V8MZ1NxvPS1FymshFcGspZpaVg1HBdUVlTzilCTQegKdMtw40UDRcCNa2GhhCJ6k4gaHFN6FnxctvXx2RVfoUE5tp458AkxTCrWC0yutii2-B_rvN11cpGA32vHfh1VJxSggghPMvX_5Wk4piQmmZ4uYVL3YOyrvMpaLMEB0H33kFn8_aYcloJhLN-c0Dn0cLKmgP84h-eRYJfaanXMarZ16tj5eLHsfL99EgppvOH8vKQNDlEsASVP3qyeKirrTY5WTFAp26DXenwW2GkNiFWuxCrHGK1CbHKIc5lL3Zfsm5W0O6LdqnN4NUO6Gh03wXtjI1_naiYRGzDzrfsJiYf9m1qWQmK6B_oCgBW</recordid><startdate>19850419</startdate><enddate>19850419</enddate><creator>Rahn, Kenneth A.</creator><creator>Lowenthal, Douglas H.</creator><general>The American Association for the Advancement of Science</general><general>American Association for the Advancement of Science</general><scope>IQODW</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8GL</scope><scope>IBG</scope><scope>IOV</scope><scope>ISN</scope><scope>8FD</scope><scope>H8D</scope><scope>L7M</scope><scope>7X8</scope><scope>OTOTI</scope></search><sort><creationdate>19850419</creationdate><title>Pollution Aerosol in the Northeast: Northeastern-Midwestern Contributions</title><author>Rahn, Kenneth A. ; Lowenthal, Douglas H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c679t-b879c3754a9853c7a4396377300bfeea35ad51b98b7880bdaeb22906f80ed1623</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1985</creationdate><topic>500200 - Environment, Atmospheric- Chemicals Monitoring & Transport- (-1989)</topic><topic>AEROSOL MONITORING</topic><topic>AEROSOLS</topic><topic>Air pollution</topic><topic>AIR POLLUTION MONITORING</topic><topic>Antimony</topic><topic>Applied sciences</topic><topic>ARSENIC</topic><topic>Atmospheric pollution</topic><topic>COLLOIDS</topic><topic>DATA</topic><topic>DISPERSIONS</topic><topic>ELEMENTS</topic><topic>Environmental aspects</topic><topic>ENVIRONMENTAL SCIENCES</topic><topic>ENVIRONMENTAL TRANSPORT</topic><topic>Exact sciences and technology</topic><topic>FEDERAL REGION I</topic><topic>INDIUM</topic><topic>INFORMATION</topic><topic>LONG-RANGE TRANSPORT</topic><topic>MASS TRANSFER</topic><topic>METALS</topic><topic>MONITORING</topic><topic>NONMETALS</topic><topic>NORTH AMERICA</topic><topic>NUMERICAL DATA</topic><topic>OXYGEN COMPOUNDS</topic><topic>Pollutants physicochemistry study: properties, effects, reactions, transport and distribution</topic><topic>Pollution</topic><topic>REGIONAL ANALYSIS</topic><topic>SEASONAL VARIATIONS</topic><topic>SELENIUM</topic><topic>SEMIMETALS</topic><topic>Signatures</topic><topic>Smelters</topic><topic>SOLS</topic><topic>STATISTICAL DATA</topic><topic>SULFATES</topic><topic>SULFUR</topic><topic>SULFUR COMPOUNDS</topic><topic>Summer</topic><topic>USA</topic><topic>VARIATIONS</topic><topic>Winter</topic><topic>Zinc</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rahn, Kenneth A.</creatorcontrib><creatorcontrib>Lowenthal, Douglas H.</creatorcontrib><creatorcontrib>Univ. of Rhode Island, Narragansett</creatorcontrib><collection>Pascal-Francis</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: High School</collection><collection>Gale In Context: Biography</collection><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Canada</collection><collection>Technology Research Database</collection><collection>Aerospace Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><collection>OSTI.GOV</collection><jtitle>Science (American Association for the Advancement of Science)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rahn, Kenneth A.</au><au>Lowenthal, Douglas H.</au><aucorp>Univ. of Rhode Island, Narragansett</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pollution Aerosol in the Northeast: Northeastern-Midwestern Contributions</atitle><jtitle>Science (American Association for the Advancement of Science)</jtitle><addtitle>Science</addtitle><date>1985-04-19</date><risdate>1985</risdate><volume>228</volume><issue>4697</issue><spage>275</spage><epage>284</epage><pages>275-284</pages><issn>0036-8075</issn><eissn>1095-9203</eissn><coden>SCIEAS</coden><abstract>In recent years, atmospheric scientists have been endeavoring to determine the relative contributions of local and distant sources to pollution aerosol in eastern North America. Elemental analysis of aerosol from various sites in the northeastern United States has revealed a persistent northeastern ``foreground'' upon which pulses of midwestern aerosol are superimposed every few days, in response to large-scale meteorological features. Regional apportionment of tracer elements and sulfate in summer and winter samples from Narragansett, Rhode Island, and Underhill, Vermont, shows that most of the elements come predominantly from northeastern sources. Notable exceptions include arsenic and indium, for which Canadian nonferrous smelters are important sources, and sulfur and selenium, for which the Midwest is an important source. During 1982 and 1983, the Northeast and the Midwest contributed comparably to aerosol sulfate at Narragansett and Underhill, in spite of the fact that the emissions of sulfur dioxide in the Midwest were ten times those in the Northeast; Canadian smelters accounted for less than 10 percent of the total sulfate. During a major pollution episode in July 1982, northeastern and midwestern sources produced comparable sulfate concentrations in Rhode Island, whereas midwestern sources dominated northeastern sources in Vermont. Thus, although distant midwestern sources affect the quantity of pollution aerosol in the Northeast and may dominate episodically, nearer northeastern sources are comparably important on the long term. The regional elemental tracer system has shown that pollution aerosol in the Northeast is composed of a northeastern ``foreground'' plus superimposed pulses from the Midwest. When these pulses are strong enough, they form the classical episodes of midwestern aerosol. During periods of stagnation in the Northeast, however, aerosol produced locally can reach concentrations that rival or exceed those coming from the Midwest, even for sulfate. These two types of episodes can be distinguished clearly with elemental tracers. Over the long term, the Northeast is its most important source for elements that are distributed broadly over eastern North America or enriched in northeastern emissions (vanadium, antimony, zinc, manganese, and probably many other elements not part of our tracer system). For elements enriched in distant sources, such as arsenic and indium from the Canadian nonferrous smelters and selenium and sulfur from the Midwest, the contributions of these distant sources may equal or exceed those from the Northeast. For sulfate, which is perhaps the most environmentally significant of these elements, transport models and other measurement programs confirm our basic conclusion that the Northeast and the Midwest contribute comparably to ambient levels in the Northeast. This amounts to a tenfold discrimination against midwestern sources, which emit approximately 20 million tons of SO$_{2}$ annually versus 2 million tons for north-eastern sources. A similar degree of discrimination with distance has been built into the MOI transport models (20). More data are needed to refine our understanding of sources and transport of pollution aerosol in eastern North America. The elemental tracer system can and should be extended to other elements, to source regions farther from the Northeast, to additional seasons and years, and to precipitation. But the basic picture seems clear: even though strong pulses of transported aerosol reach the Northeast regularly from the Midwest, over the long term the Northeast is a major or dominant source of its pollution aerosol.</abstract><cop>Washington, DC</cop><pub>The American Association for the Advancement of Science</pub><pmid>17790213</pmid><doi>10.1126/science.228.4697.275</doi><tpages>10</tpages></addata></record> |
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source | American Association for the Advancement of Science; Jstor Complete Legacy |
subjects | 500200 - Environment, Atmospheric- Chemicals Monitoring & Transport- (-1989) AEROSOL MONITORING AEROSOLS Air pollution AIR POLLUTION MONITORING Antimony Applied sciences ARSENIC Atmospheric pollution COLLOIDS DATA DISPERSIONS ELEMENTS Environmental aspects ENVIRONMENTAL SCIENCES ENVIRONMENTAL TRANSPORT Exact sciences and technology FEDERAL REGION I INDIUM INFORMATION LONG-RANGE TRANSPORT MASS TRANSFER METALS MONITORING NONMETALS NORTH AMERICA NUMERICAL DATA OXYGEN COMPOUNDS Pollutants physicochemistry study: properties, effects, reactions, transport and distribution Pollution REGIONAL ANALYSIS SEASONAL VARIATIONS SELENIUM SEMIMETALS Signatures Smelters SOLS STATISTICAL DATA SULFATES SULFUR SULFUR COMPOUNDS Summer USA VARIATIONS Winter Zinc |
title | Pollution Aerosol in the Northeast: Northeastern-Midwestern Contributions |
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