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In situ measurements of bromine oxide at two high-latitude boundary layer sites: Implications of variability
Bromine oxide (BrO) was measured in situ during the Arctic Tropospheric Ozone Chemistry (ARCTOC) '96 campaign in Ny Ålesund, Spitsbergen (April–May 1996), and during the Alert 2000 Polar Sunrise Experiment in Alert, Nunavut, Canada (April–May 2000). Measurements were made in near‐surface air du...
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Published in: | Journal of Geophysical Research. D. Atmospheres 2003-02, Vol.108 (D3), p.ACH3.1-n/a |
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container_issue | D3 |
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container_title | Journal of Geophysical Research. D. Atmospheres |
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creator | Avallone, Linnea M. Toohey, Darin W. Fortin, Tara J. McKinney, Karena A. Fuentes, Jose D. |
description | Bromine oxide (BrO) was measured in situ during the Arctic Tropospheric Ozone Chemistry (ARCTOC) '96 campaign in Ny Ålesund, Spitsbergen (April–May 1996), and during the Alert 2000 Polar Sunrise Experiment in Alert, Nunavut, Canada (April–May 2000). Measurements were made in near‐surface air during low‐ozone events in early May at both sites. The average of the in situ concentrations of BrO at Ny Ålesund is consistent with the path average of near‐simultaneous long‐path differential optical absorption spectroscopy measurements, but there is considerable scatter in a point‐by‐point comparison. The differences between these observations are consistent with a strong surface influence on reactive bromine. We see similar variability of the in situ measurements at Alert, which reflects the real variability of both surface sources and sinks. The fluctuations of BrO abundances are used to assess the expected loss rates and associated lifetimes of ozone during depletion events. We show that ozone loss will be underpredicted by any temporal or spatial average of BrO. |
doi_str_mv | 10.1029/2002JD002843 |
format | article |
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Measurements were made in near‐surface air during low‐ozone events in early May at both sites. The average of the in situ concentrations of BrO at Ny Ålesund is consistent with the path average of near‐simultaneous long‐path differential optical absorption spectroscopy measurements, but there is considerable scatter in a point‐by‐point comparison. The differences between these observations are consistent with a strong surface influence on reactive bromine. We see similar variability of the in situ measurements at Alert, which reflects the real variability of both surface sources and sinks. The fluctuations of BrO abundances are used to assess the expected loss rates and associated lifetimes of ozone during depletion events. We show that ozone loss will be underpredicted by any temporal or spatial average of BrO.</description><identifier>ISSN: 0148-0227</identifier><identifier>EISSN: 2156-2202</identifier><identifier>DOI: 10.1029/2002JD002843</identifier><language>eng</language><publisher>Washington, DC: Blackwell Publishing Ltd</publisher><subject>Arctic ; boundary layer ozone ; bromine oxide ; Chemical composition and interactions. Ionic interactions and processes ; Earth, ocean, space ; Exact sciences and technology ; External geophysics ; halogens ; Meteorology ; ozone loss</subject><ispartof>Journal of Geophysical Research. D. Atmospheres, 2003-02, Vol.108 (D3), p.ACH3.1-n/a</ispartof><rights>Copyright 2003 by the American Geophysical Union.</rights><rights>2003 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4452-3f873a758acb81aa40080af911f6309412bbddddbf5376f22f1fa0529aca77f13</citedby><cites>FETCH-LOGICAL-c4452-3f873a758acb81aa40080af911f6309412bbddddbf5376f22f1fa0529aca77f13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1029%2F2002JD002843$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1029%2F2002JD002843$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,11514,27924,27925,46468,46892</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14747275$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Avallone, Linnea M.</creatorcontrib><creatorcontrib>Toohey, Darin W.</creatorcontrib><creatorcontrib>Fortin, Tara J.</creatorcontrib><creatorcontrib>McKinney, Karena A.</creatorcontrib><creatorcontrib>Fuentes, Jose D.</creatorcontrib><title>In situ measurements of bromine oxide at two high-latitude boundary layer sites: Implications of variability</title><title>Journal of Geophysical Research. D. Atmospheres</title><addtitle>J. Geophys. Res</addtitle><description>Bromine oxide (BrO) was measured in situ during the Arctic Tropospheric Ozone Chemistry (ARCTOC) '96 campaign in Ny Ålesund, Spitsbergen (April–May 1996), and during the Alert 2000 Polar Sunrise Experiment in Alert, Nunavut, Canada (April–May 2000). Measurements were made in near‐surface air during low‐ozone events in early May at both sites. The average of the in situ concentrations of BrO at Ny Ålesund is consistent with the path average of near‐simultaneous long‐path differential optical absorption spectroscopy measurements, but there is considerable scatter in a point‐by‐point comparison. The differences between these observations are consistent with a strong surface influence on reactive bromine. We see similar variability of the in situ measurements at Alert, which reflects the real variability of both surface sources and sinks. The fluctuations of BrO abundances are used to assess the expected loss rates and associated lifetimes of ozone during depletion events. We show that ozone loss will be underpredicted by any temporal or spatial average of BrO.</description><subject>Arctic</subject><subject>boundary layer ozone</subject><subject>bromine oxide</subject><subject>Chemical composition and interactions. Ionic interactions and processes</subject><subject>Earth, ocean, space</subject><subject>Exact sciences and technology</subject><subject>External geophysics</subject><subject>halogens</subject><subject>Meteorology</subject><subject>ozone loss</subject><issn>0148-0227</issn><issn>2156-2202</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><recordid>eNqFkEFvFCEUgImxiZvamz-Ai54chQcMM97M1l23bWpiNBov5M0sWJQZtjBju_9e6jbqSd8BEvJ9X8Ij5AlnLziD9iUwBmen5WikeEAWwFVdATB4SBaMy6ZiAPoROcn5GysjVS0ZX5CwGWn200wHi3lOdrDjlGl0tEtx8KOl8dZvLcWJTjeRXvmvV1XAqQjlsYvzuMW0pwH3Nt1lbH5FN8Mu-L4wcfwV-oHJY-eDn_aPyZHDkO3J_X1MPq7efFi-rS7erTfL1xdVL6WCSrhGC9Sqwb5rOKJkrGHoWs5dLVgrOXTdtkznlNC1A3DcIVPQYo9aOy6OybNDd5fi9WzzZAafexsCjjbO2YBumRC8_i_Im7oRwJoCPj-AfYo5J-vMLvmh_N1wZu7Wb_5ef8Gf3ncx9xhcwrH3-Y8jtdSgVeHEgbvxwe7_2TRn6_ennHEFxaoOls-Tvf1tYfpuai20Mp8u12a5-gz8fPXFnIufXrCjCA</recordid><startdate>20030216</startdate><enddate>20030216</enddate><creator>Avallone, Linnea M.</creator><creator>Toohey, Darin W.</creator><creator>Fortin, Tara J.</creator><creator>McKinney, Karena A.</creator><creator>Fuentes, Jose D.</creator><general>Blackwell Publishing Ltd</general><general>American Geophysical Union</general><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TG</scope><scope>KL.</scope><scope>8FD</scope><scope>H8D</scope><scope>L7M</scope></search><sort><creationdate>20030216</creationdate><title>In situ measurements of bromine oxide at two high-latitude boundary layer sites: Implications of variability</title><author>Avallone, Linnea M. ; Toohey, Darin W. ; Fortin, Tara J. ; McKinney, Karena A. ; Fuentes, Jose D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4452-3f873a758acb81aa40080af911f6309412bbddddbf5376f22f1fa0529aca77f13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Arctic</topic><topic>boundary layer ozone</topic><topic>bromine oxide</topic><topic>Chemical composition and interactions. Ionic interactions and processes</topic><topic>Earth, ocean, space</topic><topic>Exact sciences and technology</topic><topic>External geophysics</topic><topic>halogens</topic><topic>Meteorology</topic><topic>ozone loss</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Avallone, Linnea M.</creatorcontrib><creatorcontrib>Toohey, Darin W.</creatorcontrib><creatorcontrib>Fortin, Tara J.</creatorcontrib><creatorcontrib>McKinney, Karena A.</creatorcontrib><creatorcontrib>Fuentes, Jose D.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Meteorological & Geoastrophysical Abstracts - Academic</collection><collection>Technology Research Database</collection><collection>Aerospace Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Journal of Geophysical Research. D. Atmospheres</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Avallone, Linnea M.</au><au>Toohey, Darin W.</au><au>Fortin, Tara J.</au><au>McKinney, Karena A.</au><au>Fuentes, Jose D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In situ measurements of bromine oxide at two high-latitude boundary layer sites: Implications of variability</atitle><jtitle>Journal of Geophysical Research. D. Atmospheres</jtitle><addtitle>J. Geophys. Res</addtitle><date>2003-02-16</date><risdate>2003</risdate><volume>108</volume><issue>D3</issue><spage>ACH3.1</spage><epage>n/a</epage><pages>ACH3.1-n/a</pages><issn>0148-0227</issn><eissn>2156-2202</eissn><abstract>Bromine oxide (BrO) was measured in situ during the Arctic Tropospheric Ozone Chemistry (ARCTOC) '96 campaign in Ny Ålesund, Spitsbergen (April–May 1996), and during the Alert 2000 Polar Sunrise Experiment in Alert, Nunavut, Canada (April–May 2000). Measurements were made in near‐surface air during low‐ozone events in early May at both sites. The average of the in situ concentrations of BrO at Ny Ålesund is consistent with the path average of near‐simultaneous long‐path differential optical absorption spectroscopy measurements, but there is considerable scatter in a point‐by‐point comparison. The differences between these observations are consistent with a strong surface influence on reactive bromine. We see similar variability of the in situ measurements at Alert, which reflects the real variability of both surface sources and sinks. The fluctuations of BrO abundances are used to assess the expected loss rates and associated lifetimes of ozone during depletion events. We show that ozone loss will be underpredicted by any temporal or spatial average of BrO.</abstract><cop>Washington, DC</cop><pub>Blackwell Publishing Ltd</pub><doi>10.1029/2002JD002843</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Arctic boundary layer ozone bromine oxide Chemical composition and interactions. Ionic interactions and processes Earth, ocean, space Exact sciences and technology External geophysics halogens Meteorology ozone loss |
title | In situ measurements of bromine oxide at two high-latitude boundary layer sites: Implications of variability |
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