http://lod.bco-dmo.org/id/dataset/779688
eng; USA
utf8
dataset
Highest level of data collection, from a common set of sensors or instrumentation, usually within the same research project
Biological and Chemical Oceanography Data Management Office (BCO-DMO)
Unavailable
508-289-2009
WHOI MS#36
Woods Hole
MA
02543
USA
info@bco-dmo.org
http://www.bco-dmo.org
Monday - Friday 8:00am - 5:00pm
For questions regarding this resource, please contact BCO-DMO via the email address provided.
pointOfContact
2019-10-24
ISO 19115-2 Geographic Information - Metadata - Part 2: Extensions for Imagery and Gridded Data
ISO 19115-2:2009(E)
Coarse aerosol iron (Fe) collected on the US GEOTRACES Arctic cruise (HLY1502, GN01) from August to October 2015
2019-10-24
publication
2019-10-24
revision
BCO-DMO Linked Data URI
2019-10-24
creation
http://lod.bco-dmo.org/id/dataset/779688
Yuan Gao
Rutgers University
principalInvestigator
Biological and Chemical Oceanography Data Management Office (BCO-DMO)
Unavailable
508-289-2009
WHOI MS#36
Woods Hole
MA
02543
USA
info@bco-dmo.org
http://www.bco-dmo.org
Monday - Friday 8:00am - 5:00pm
For questions regarding this resource, please contact BCO-DMO via the email address provided.
publisher
Cite this dataset as: Gao, Y. (2019) Coarse aerosol iron (Fe) collected on the US GEOTRACES Arctic cruise (HLY1502, GN01) from August to October 2015. Biological and Chemical Oceanography Data Management Office (BCO-DMO). (Version 1) Version Date 2019-10-24 [if applicable, indicate subset used]. http://lod.bco-dmo.org/id/dataset/779688 [access date]
Aerosol Iron (Fe) (Coarse) collected on the US GEOTRACES Arctic cruise (HLY1502, GN01) from August to October 2015 Dataset Description: <p>These data are associated with the following publication:<br />
Gao, Y., Marsay, C., Yu, S., Fan, S., Mukherjee, P., Buck, C.S., &amp; Landing, W.M. (in press). Particle-Size Variability of Aerosol Iron and Impact on Iron Solubility and Dry Deposition Fluxes to the Arctic Ocean. Scientific Reports.</p> Methods and Sampling: <p><strong>Sampling:</strong><br />
Aerosol samples were collected by a MICRO ORIFIFICE UNIFORM DEPOSIT IMPACTOR (MOUDI) (MSP Corporation, MN, USA) which was installed on the forward rail of Healy's flying bridge, ~23 m above sea level, to minimize the influence of sea spray. To minimize the potential for contamination from the stack exhaust, samplers were forward of the ship's stack and sampling was controlled by wind speed and direction, through a Campbell Scientific CR800 data-logger interfaced with an anemometer and wind vane set up near the samplers. Aerosol sampling was restricted to periods when in-sector conditions (defined as a relative wind direction from within ±60° of the ship's bow and a relative wind speed of &gt;0.5 m s-1) persisted for at least five continuous minutes. The MOUDI impactor used Teflon filters for particle collection (Pall Corp., 47 mm diameter, 1 µm pore size), with a sampling flowrate of 30 L min-1. Both the MOUDI impactor and its pump were housed in enclosures to protect them from rain and sea-spray with an extension tube connected to the MOUDI inlet and extending from the enclosure. A rain shield was installed above the inlet. Due to the anticipated low dust conditions during GN01, and the relatively low frequency of in-sector wind conditions, sample collections lasted for an average of seven days.</p>
<p>Clean polyethylene gloves were worn for loading and unloading of sample filters, which were carried out underneath a high-efficiency particulate air (HEPA) filter blower within a plastic "bubble" clean area constructed in the ship's main laboratory. Filters were loaded onto the MOUDI impactor from labeled petri dishes using pre-cleaned Teflon tweezers and were transferred back to the same petri dishes after sample recovery. Filter holders were double-bagged for transfer between the ship's laboratory and the samplers. Deployment blanks were carried out using the same protocols, but with the pumps turned off. All sample and field blank filters were subsequently double-bagged and stored frozen until analysis.</p>
<p>Sampler Location: Flying deck, forward railings<br />
Sampler Type: MICRO ORIFIFICE UNIFORM DEPOSIT IMPACTOR (MOUDI) (MSP CORP.,MN, USA)<br />
Sampler Flow: 0.030 m3/min<br />
Substrate Type: Pall corp. Teflon Filter, 47 mm discs (Teflon, 1um pore size)<br />
Size Segregation Method: Size-segregated sample; 1um is used as a cut off size for COARSE and FINE particle sizes</p>
<p><strong>Aerosol Sample Analyses:</strong><br />
Total aerosol Fe in this study was measured following the detailed procedures in Morton et al. (2013) and Gao et al. (2013).</p>
<p><strong>Total Fe: </strong>Aerosol samples were analyzed for the total concentrations of atmospheric Fe by a sector field inductively coupled plasma-mass spectrometer (SF-ICPMS) in Rutgers Inorganic Analytical Laboratory, following a previously described digestion protocol (Gao et al., 2013). Briefly, a portion of each sample filter was placed in a 15 mL Teflon vial with a mixture of concentrated HNO3 (0.8 ml) and HF (0.1 ml) (Optima, Fisher Sci.) and digested for 4 hours on a hot plate at 160°C. Each digestion solution was evaporated to dryness, followed by the addition of 2 ml 3% HNO3 and 1 ppb Indium (In) for ICP-MS drift correction. Both field blanks and procedure blanks were treated in the same way as samples. All Teflon vials were acid-cleaned, and all procedures were carried out in a class-100 clean-room hood in the lab. The sample digestion procedures were assessed using Standard Reference Material (SRM) 1648a (National Institute of Standards and Technology, NIST, Gaithersburg, MD), subsamples of which were treated under the same conditions as for samples. The digest recoveries based on SRM1648a ranged between 89-99% for Fe (n=7) which was close enough to the measured quantities that no yield correction needed to be applied, and the precision determined from sample splits and duplicate digest aliquots ranged between 93-106% for Fe (n=10). The method detection limits were 0.691 pmol m-3 for Fe, which was obtained based on three times the standard deviation of a total of 14 filter blanks and a nominal 100 m3 sampling volume. A series of external calibration standards were run at the beginning and then at the end of the analyses.&nbsp; More details on the ICP-MS instrument settings can be found in Annett et al. (2017).</p>
<p><strong>Dissolvable Fe: </strong>The concentrations of dissolvable Fe in aerosol samples were obtained using UV/Visible spectroscopy with a modified Ferrozine method (Gao et al., 2013). The leaching solution for samples was 0.5 mM ammonium acetate that was filtered through a Nuclepore® track-etch membrane filter (47 mm, 0.2 μm) and adjusted to ~pH 5.3. The leaching conditions were chosen to simulate cloud water conditions for marine aerosols. A brief description of the procedures is as follows: a portion of each sample filter was first placed into a leaching solution of ammonium acetate (0.5 mM) for 1 h, and then the leachate was split into two parts, one for Fe(II) determination and the other for total dissolvable Fe. A solution of 0.01 M hydroxylamine hydrochloride solution (1%) was added to the total dissolvable Fe filtrate portion to reduce Fe(III) to Fe(II), and the sample solution was set aside for 1 h to ensure complete reduction before adding the same ferrozine solution as for the Fe(II) filtrate portion. The Fe(II) measured in this way was considered as total dissolvable Fe. After these procedures, each sample leaching solution was filtered through a 13 mm polytetrafluorethylene syringe filter of 0.2 μm pore size. All field blanks were treated in the same way as samples. The concentrations of Fe(II) in sample solutions were determined at 562 nm using a TIDAS-1 spectrometer module with a 200 cm liquid waveguide capillary flow cell (World Precision Instruments Inc., FL, USA). The detection limit of the method for Fe(II) was 0.30 nM, calculated as three times the standard deviation of the measured blank values (n=5). A total of 8 sets of size-segregated aerosol samples were analyzed with this procedure.</p>
Funding provided by NSF Division of Ocean Sciences (NSF OCE) Award Number: OCE-1438047 Award URL: https://www.nsf.gov/awardsearch/show-award?AWD_ID=1438047
Funding provided by NSF Division of Ocean Sciences (NSF OCE) Award Number: OCE-1435871 Award URL: https://www.nsf.gov/awardsearch/show-award?AWD_ID=1435871
Funding provided by NSF Division of Ocean Sciences (NSF OCE) Award Number: OCE-1437266 Award URL: https://www.nsf.gov/awardsearch/show-award?AWD_ID=1437266
onGoing
Yuan Gao
Rutgers University
973-353-1139
101 Warren Street 135 Smith Hall
Newark
NJ
07102
USA
yuangaoh@newark.rutgers.edu
pointOfContact
asNeeded
Dataset Version: 1
Unknown
Cruise_id
GEOTRC_EVENTNO
SAMPLE_ID
Julian_Day
Start_Day
Start_Month
Start_Year
Start_Time_UTC
Start_Lat
Start_Long
End_Day
End_Month
End_Year
End_Time
End_Lat
End_Long
Air_Vol_Total
Fe_A_T_CONC_COARSE_IMPACTOR
Fe_A_SSLNH4AC_CONC_COARSE_IMPACTOR
Fe_II_A_SSLNH4AC_CONC_COARSE_IMPACTOR
Micro-orifice uniform deposit impactor (MOUDI)
anemometer
Campbell Scientific CR800 data-logger
Element-1 sector field ICP-MS
TIDAS-1 spectrometer
theme
None, User defined
cruise id
event
sample identification
Julian day as a decimal (time elapsed in days from 00:00 on January 1st 4713 BC)
day of month
month of year
year
time of day
latitude
longitude
volume
metal concentration in atmosphere
featureType
BCO-DMO Standard Parameters
Aerosol Sampler
Anemometer
Data Logger
Inductively Coupled Plasma Mass Spectrometer
Spectrometer
instrument
BCO-DMO Standard Instruments
HLY1502
service
Deployment Activity
Western Arctic Ocean
place
Locations
otherRestrictions
otherRestrictions
Access Constraints: none. Use Constraints: Please follow guidelines at: http://www.bco-dmo.org/terms-use Distribution liability: Under no circumstances shall BCO-DMO be liable for any direct, incidental, special, consequential, indirect, or punitive damages that result from the use of, or the inability to use, the materials in this data submission. If you are dissatisfied with any materials in this data submission your sole and exclusive remedy is to discontinue use.
U.S. GEOTRACES
http://www.geotraces.org/
U.S. GEOTRACES
GEOTRACES is a SCOR sponsored program; and funding for program infrastructure development is provided by the U.S. National Science Foundation.
GEOTRACES gained momentum following a special symposium, S02: Biogeochemical cycling of trace elements and isotopes in the ocean and applications to constrain contemporary marine processes (GEOSECS II), at a 2003 Goldschmidt meeting convened in Japan. The GEOSECS II acronym referred to the Geochemical Ocean Section Studies To determine full water column distributions of selected trace elements and isotopes, including their concentration, chemical speciation, and physical form, along a sufficient number of sections in each ocean basin to establish the principal relationships between these distributions and with more traditional hydrographic parameters;
* To evaluate the sources, sinks, and internal cycling of these species and thereby characterize more completely the physical, chemical and biological processes regulating their distributions, and the sensitivity of these processes to global change; and
* To understand the processes that control the concentrations of geochemical species used for proxies of the past environment, both in the water column and in the substrates that reflect the water column.
GEOTRACES will be global in scope, consisting of ocean sections complemented by regional process studies. Sections and process studies will combine fieldwork, laboratory experiments and modelling. Beyond realizing the scientific objectives identified above, a natural outcome of this work will be to build a community of marine scientists who understand the processes regulating trace element cycles sufficiently well to exploit this knowledge reliably in future interdisciplinary studies.
Expand "Projects" below for information about and data resulting from individual US GEOTRACES research projects.
U.S. GEOTRACES
largerWorkCitation
program
U.S. Arctic GEOTRACES Study (GN01)
https://www.geotraces.org/
U.S. Arctic GEOTRACES Study (GN01)
<p><em>Description from NSF award abstract:</em><br />
In pursuit of its goal "to identify processes and quantify fluxes that control the distributions of key trace elements and isotopes in the ocean, and to establish the sensitivity of these distributions to changing environmental conditions", in 2015 the International GEOTRACES Program will embark on several years of research in the Arctic Ocean. In a region where climate warming and general environmental change are occurring at amazing speed, research such as this is important for understanding the current state of Arctic Ocean geochemistry and for developing predictive capability as the regional ecosystem continues to warm and influence global oceanic and climatic conditions. The three investigators funded on this award, will manage a large team of U.S.scientists who will compete through the regular NSF proposal process to contribute their own unique expertise in marine trace metal, isotopic, and carbon cycle geochemistry to the U.S. effort. The three managers will be responsible for arranging and overseeing at-sea technical services such as hydrographic measurements, nutrient analyses, and around-the-clock management of on-deck sampling activites upon which all participants depend, and for organizing all pre- and post-cruise technical support and scientific meetings. The management team will also lead educational outreach activities for the general public in Nome and Barrow, Alaska, to explain the significance of the study to these communities and to learn from residents' insights on observed changes in the marine system. The project itself will provide for the support and training of a number of pre-doctoral students and post-doctoral researchers. Inasmuch as the Arctic Ocean is an epicenter of global climate change, findings of this study are expected to advance present capability to forecast changes in regional and globlal ecosystem and climate system functioning.</p>
<p>As the United States' contribution to the International GEOTRACES Arctic Ocean initiative, this project will be part of an ongoing multi-national effort to further scientific knowledge about trace elements and isotopes in the world ocean. This U.S. expedition will focus on the western Arctic Ocean in the boreal summer of 2015. The scientific team will consist of the management team funded through this award plus a team of scientists from U.S. academic institutions who will have successfully competed for and received NSF funds for specific science projects in time to participate in the final stages of cruise planning. The cruise track segments will include the Bering Strait, Chukchi shelf, and the deep Canada Basin. Several stations will be designated as so-called super stations for intense study of atmospheric aerosols, sea ice, and sediment chemistry as well as water-column processes. In total, the set of coordinated international expeditions will involve the deployment of ice-capable research ships from 6 nations (US, Canada, Germany, Sweden, UK, and Russia) across different parts of the Arctic Ocean, and application of state-of-the-art methods to unravel the complex dynamics of trace metals and isotopes that are important as oceanographic and biogeochemical tracers in the sea.</p>
U.S. GEOTRACES Arctic
largerWorkCitation
project
Collaborative Research: GEOTRACES Arctic Section: Sampling and Analysis of Atmospheric Deposition
https://osprey.bco-dmo.org/project/779338
Collaborative Research: GEOTRACES Arctic Section: Sampling and Analysis of Atmospheric Deposition
<p><em>NSF Award Abstract:</em><br />
In this project, a group of investigators participating in the 2015 U.S. GEOTRACES Arctic Ocean expedition will study the distribution of a variety of trace elements in seawater, sea ice, and marine air. It is important to understand where they are and how they move in the Arctic because some trace elements are essential to life, others are known biological toxins, and still others are important because they can be used as tracers of a variety of physical, chemical, and biological processes in the sea. In common with other multinational initiatives in the International GEOTRACES Program, the goals of the U.S. Arctic expedition are to identify processes and quantify fluxes that control the distributions of key trace elements and isotopes in the ocean, and to establish the sensitivity of these distributions to changing environmental conditions. This multi-institutional team of ocean trace element experts will focus its attention on the importance of aerosol, precipitation, and sea ice melt water in trace element cycling. Results from this work will be disseminated through public educational initiatives, such as web communications and outreach to members of the public, including indigenous populations in Alaska. The project will also provide training for graduate and undergraduate students in biology and chemistry.</p>
<p>Atmospheric deposition is an important pathway and transport mechanism of both natural aerosols and contaminants to the ocean. Relative to other regions, atmospheric deposition rates in the Arctic are low and aerosols and dissolved chemicals in precipitation may be deposited directly to the sea surface or, unique to polar regions, onto sea ice. Given the unique biogeochemical processes of the region and its rapid changes in response to global climate change, quantifying the current atmospheric deposition of trace elements and isotopes to differing catchments (ocean, sea ice, and melt ponds) in the Arctic is critical to our ability to predict how their distribution may evolve over time. In this study, aerosol, precipitation, and melt water samples will be collected and analyzed for trace elements and isotopes in order to evaluate the impacts on the surface ocean and sea ice chemistry from natural and anthropogenic aerosols. Through this project, collected atmospheric samples from the Arctic will also be made available for distribution to the broader scientific community.</p>
GEOTRACES Arctic Atmospheric Deposition
largerWorkCitation
project
eng; USA
oceans
Western Arctic Ocean
-170.7498
176.7522
56.0743
88.4088
2015-08-10
2015-10-09
Arctic Ocean; Sailing from Dutch Harbor to Dutch Harbor (GN01)
0
BCO-DMO catalogue of parameters from Coarse aerosol iron (Fe) collected on the US GEOTRACES Arctic cruise (HLY1502, GN01) from August to October 2015
Biological and Chemical Oceanography Data Management Office (BCO-DMO)
Unavailable
508-289-2009
WHOI MS#36
Woods Hole
MA
02543
USA
info@bco-dmo.org
http://www.bco-dmo.org
Monday - Friday 8:00am - 5:00pm
For questions regarding this resource, please contact BCO-DMO via the email address provided.
pointOfContact
http://lod.bco-dmo.org/id/dataset-parameter/779704.rdf
Name: Cruise_id
Units: unitless
Description: <p>Cruise identifier</p>
http://lod.bco-dmo.org/id/dataset-parameter/779705.rdf
Name: GEOTRC_EVENTNO
Units: unitless
Description: <p>GEOTRACES Event Number</p>
http://lod.bco-dmo.org/id/dataset-parameter/779706.rdf
Name: SAMPLE_ID
Units: unitless
Description: <p>GEOTRACES Sample Number</p>
http://lod.bco-dmo.org/id/dataset-parameter/779707.rdf
Name: Julian_Day
Units: unitless
Description: <p>Sampling start Julian day</p>
http://lod.bco-dmo.org/id/dataset-parameter/779708.rdf
Name: Start_Day
Units: unitless
Description: <p>Sampling start day</p>
http://lod.bco-dmo.org/id/dataset-parameter/779709.rdf
Name: Start_Month
Units: unitless
Description: <p>Sampling start month</p>
http://lod.bco-dmo.org/id/dataset-parameter/779710.rdf
Name: Start_Year
Units: unitless
Description: <p>Sampling start year; format: yyyy</p>
http://lod.bco-dmo.org/id/dataset-parameter/779711.rdf
Name: Start_Time_UTC
Units: unitless
Description: <p>Sampling start time; format: HH:MM</p>
http://lod.bco-dmo.org/id/dataset-parameter/779712.rdf
Name: Start_Lat
Units: decimal degrees N
Description: <p>Sampling start Latitude</p>
http://lod.bco-dmo.org/id/dataset-parameter/779713.rdf
Name: Start_Long
Units: decimal degrees E
Description: <p>Sampling start Longitude</p>
http://lod.bco-dmo.org/id/dataset-parameter/779714.rdf
Name: End_Day
Units: unitless
Description: <p>Sampling end day</p>
http://lod.bco-dmo.org/id/dataset-parameter/779715.rdf
Name: End_Month
Units: unitless
Description: <p>Sampling end month</p>
http://lod.bco-dmo.org/id/dataset-parameter/779716.rdf
Name: End_Year
Units: unitless
Description: <p>Sampling end year; format: yyyy</p>
http://lod.bco-dmo.org/id/dataset-parameter/779717.rdf
Name: End_Time
Units: unitless
Description: <p>Sampling end time; format: HH:MM</p>
http://lod.bco-dmo.org/id/dataset-parameter/779718.rdf
Name: End_Lat
Units: decimal degrees N
Description: <p>Sampling end Latitude</p>
http://lod.bco-dmo.org/id/dataset-parameter/779719.rdf
Name: End_Long
Units: decimal degrees E
Description: <p>Sampling end Longitude</p>
http://lod.bco-dmo.org/id/dataset-parameter/779720.rdf
Name: Air_Vol_Total
Units: cubic meters (m^3)
Description: <p>Total volume of air sampled</p>
http://lod.bco-dmo.org/id/dataset-parameter/779721.rdf
Name: Fe_A_T_CONC_COARSE_IMPACTOR
Units: pmol/m^3
Description: <p>larger size fraction of total Fe concentration in aerosols (no preliminary leaching) collected with size fractionation</p>
http://lod.bco-dmo.org/id/dataset-parameter/779722.rdf
Name: Fe_A_SSLNH4AC_CONC_COARSE_IMPACTOR
Units: pmol/m^3
Description: <p>?</p>
http://lod.bco-dmo.org/id/dataset-parameter/779723.rdf
Name: Fe_II_A_SSLNH4AC_CONC_COARSE_IMPACTOR
Units: pmol/m^3
Description: <p>?</p>
GB/NERC/BODC > British Oceanographic Data Centre, Natural Environment Research Council, United Kingdom
Biological and Chemical Oceanography Data Management Office (BCO-DMO)
Unavailable
508-289-2009
WHOI MS#36
Woods Hole
MA
02543
USA
info@bco-dmo.org
http://www.bco-dmo.org
Monday - Friday 8:00am - 5:00pm
For questions regarding this resource, please contact BCO-DMO via the email address provided.
pointOfContact
1632
https://datadocs.bco-dmo.org/file/nGGl0GRC77D4go/Fe_Coarse.csv
Fe_Coarse.csv
Primary data file for dataset ID 779688
download
https://osprey.bco-dmo.org/dataset/779688/data/download
download
onLine
dataset
<p><strong>Sampling:</strong><br />
Aerosol samples were collected by a MICRO ORIFIFICE UNIFORM DEPOSIT IMPACTOR (MOUDI) (MSP Corporation, MN, USA) which was installed on the forward rail of Healy's flying bridge, ~23 m above sea level, to minimize the influence of sea spray. To minimize the potential for contamination from the stack exhaust, samplers were forward of the ship's stack and sampling was controlled by wind speed and direction, through a Campbell Scientific CR800 data-logger interfaced with an anemometer and wind vane set up near the samplers. Aerosol sampling was restricted to periods when in-sector conditions (defined as a relative wind direction from within ±60° of the ship's bow and a relative wind speed of &gt;0.5 m s-1) persisted for at least five continuous minutes. The MOUDI impactor used Teflon filters for particle collection (Pall Corp., 47 mm diameter, 1 µm pore size), with a sampling flowrate of 30 L min-1. Both the MOUDI impactor and its pump were housed in enclosures to protect them from rain and sea-spray with an extension tube connected to the MOUDI inlet and extending from the enclosure. A rain shield was installed above the inlet. Due to the anticipated low dust conditions during GN01, and the relatively low frequency of in-sector wind conditions, sample collections lasted for an average of seven days.</p>
<p>Clean polyethylene gloves were worn for loading and unloading of sample filters, which were carried out underneath a high-efficiency particulate air (HEPA) filter blower within a plastic "bubble" clean area constructed in the ship's main laboratory. Filters were loaded onto the MOUDI impactor from labeled petri dishes using pre-cleaned Teflon tweezers and were transferred back to the same petri dishes after sample recovery. Filter holders were double-bagged for transfer between the ship's laboratory and the samplers. Deployment blanks were carried out using the same protocols, but with the pumps turned off. All sample and field blank filters were subsequently double-bagged and stored frozen until analysis.</p>
<p>Sampler Location: Flying deck, forward railings<br />
Sampler Type: MICRO ORIFIFICE UNIFORM DEPOSIT IMPACTOR (MOUDI) (MSP CORP.,MN, USA)<br />
Sampler Flow: 0.030 m3/min<br />
Substrate Type: Pall corp. Teflon Filter, 47 mm discs (Teflon, 1um pore size)<br />
Size Segregation Method: Size-segregated sample; 1um is used as a cut off size for COARSE and FINE particle sizes</p>
<p><strong>Aerosol Sample Analyses:</strong><br />
Total aerosol Fe in this study was measured following the detailed procedures in Morton et al. (2013) and Gao et al. (2013).</p>
<p><strong>Total Fe: </strong>Aerosol samples were analyzed for the total concentrations of atmospheric Fe by a sector field inductively coupled plasma-mass spectrometer (SF-ICPMS) in Rutgers Inorganic Analytical Laboratory, following a previously described digestion protocol (Gao et al., 2013). Briefly, a portion of each sample filter was placed in a 15 mL Teflon vial with a mixture of concentrated HNO3 (0.8 ml) and HF (0.1 ml) (Optima, Fisher Sci.) and digested for 4 hours on a hot plate at 160°C. Each digestion solution was evaporated to dryness, followed by the addition of 2 ml 3% HNO3 and 1 ppb Indium (In) for ICP-MS drift correction. Both field blanks and procedure blanks were treated in the same way as samples. All Teflon vials were acid-cleaned, and all procedures were carried out in a class-100 clean-room hood in the lab. The sample digestion procedures were assessed using Standard Reference Material (SRM) 1648a (National Institute of Standards and Technology, NIST, Gaithersburg, MD), subsamples of which were treated under the same conditions as for samples. The digest recoveries based on SRM1648a ranged between 89-99% for Fe (n=7) which was close enough to the measured quantities that no yield correction needed to be applied, and the precision determined from sample splits and duplicate digest aliquots ranged between 93-106% for Fe (n=10). The method detection limits were 0.691 pmol m-3 for Fe, which was obtained based on three times the standard deviation of a total of 14 filter blanks and a nominal 100 m3 sampling volume. A series of external calibration standards were run at the beginning and then at the end of the analyses.&nbsp; More details on the ICP-MS instrument settings can be found in Annett et al. (2017).</p>
<p><strong>Dissolvable Fe: </strong>The concentrations of dissolvable Fe in aerosol samples were obtained using UV/Visible spectroscopy with a modified Ferrozine method (Gao et al., 2013). The leaching solution for samples was 0.5 mM ammonium acetate that was filtered through a Nuclepore® track-etch membrane filter (47 mm, 0.2 μm) and adjusted to ~pH 5.3. The leaching conditions were chosen to simulate cloud water conditions for marine aerosols. A brief description of the procedures is as follows: a portion of each sample filter was first placed into a leaching solution of ammonium acetate (0.5 mM) for 1 h, and then the leachate was split into two parts, one for Fe(II) determination and the other for total dissolvable Fe. A solution of 0.01 M hydroxylamine hydrochloride solution (1%) was added to the total dissolvable Fe filtrate portion to reduce Fe(III) to Fe(II), and the sample solution was set aside for 1 h to ensure complete reduction before adding the same ferrozine solution as for the Fe(II) filtrate portion. The Fe(II) measured in this way was considered as total dissolvable Fe. After these procedures, each sample leaching solution was filtered through a 13 mm polytetrafluorethylene syringe filter of 0.2 μm pore size. All field blanks were treated in the same way as samples. The concentrations of Fe(II) in sample solutions were determined at 562 nm using a TIDAS-1 spectrometer module with a 200 cm liquid waveguide capillary flow cell (World Precision Instruments Inc., FL, USA). The detection limit of the method for Fe(II) was 0.30 nM, calculated as three times the standard deviation of the measured blank values (n=5). A total of 8 sets of size-segregated aerosol samples were analyzed with this procedure.</p>
Specified by the Principal Investigator(s)
<p>Data processing followed standard protocols that was included in sample analyses section; no specific software was used.</p>
<p>BCO-DMO Processing:<br />
- modified parameter names (replaced spaces w/ underscores);<br />
- formatted time to HH:MM;<br />
- formatted months and days to two-digits;<br />
- added ISO Date/Time fields.</p>
Specified by the Principal Investigator(s)
asNeeded
7.x-1.1
Biological and Chemical Oceanography Data Management Office (BCO-DMO)
Unavailable
508-289-2009
WHOI MS#36
Woods Hole
MA
02543
USA
info@bco-dmo.org
http://www.bco-dmo.org
Monday - Friday 8:00am - 5:00pm
For questions regarding this resource, please contact BCO-DMO via the email address provided.
pointOfContact
Micro-orifice uniform deposit impactor (MOUDI)
Micro-orifice uniform deposit impactor (MOUDI)
PI Supplied Instrument Name: Micro-orifice uniform deposit impactor (MOUDI) PI Supplied Instrument Description:Aerosol samples were collected by a MICRO ORIFiCE UNIFORM DEPOSIT IMPACTOR (MOUDI) (MSP Corporation, MN, USA) which was installed on the forward rail of Healy's flying bridge. Instrument Name: Aerosol Sampler Instrument Short Name: Instrument Description: A device that collects a sample of aerosol (dry particles or liquid droplets) from the atmosphere. Community Standard Description: http://vocab.nerc.ac.uk/collection/L05/current/13/
anemometer
anemometer
PI Supplied Instrument Name: anemometer Instrument Name: Anemometer Instrument Short Name:Anemometer Instrument Description: An anemometer is a device for measuring the velocity or the pressure of the wind. It is commonly used to measure wind speed. Aboard research vessels, it is often mounted with other meteorological instruments and sensors. Community Standard Description: http://vocab.nerc.ac.uk/collection/L05/current/101/
Campbell Scientific CR800 data-logger
Campbell Scientific CR800 data-logger
PI Supplied Instrument Name: Campbell Scientific CR800 data-logger Instrument Name: Data Logger Instrument Short Name: Instrument Description: Electronic devices that record data over time or in relation to location either with a built-in instrument or sensor or via external instruments and sensors.
Element-1 sector field ICP-MS
Element-1 sector field ICP-MS
PI Supplied Instrument Name: Element-1 sector field ICP-MS PI Supplied Instrument Description:Element-1 sector field ICP-MS (Thermo-Finnigan, Bremen, Germany) for total aerosol Fe Instrument Name: Inductively Coupled Plasma Mass Spectrometer Instrument Short Name:ICP Mass Spec Instrument Description: An ICP Mass Spec is an instrument that passes nebulized samples into an inductively-coupled gas plasma (8-10000 K) where they are atomized and ionized. Ions of specific mass-to-charge ratios are quantified in a quadrupole mass spectrometer. Community Standard Description: http://vocab.nerc.ac.uk/collection/L05/current/LAB15/
TIDAS-1 spectrometer
TIDAS-1 spectrometer
PI Supplied Instrument Name: TIDAS-1 spectrometer PI Supplied Instrument Description:TIDAS-1 spectrometer module with a 200 cm liquid waveguide capillary flow cell (World Precision Instruments Inc., FL, USA) for dissolvable Fe. Instrument Name: Spectrometer Instrument Short Name:Spectrometer Instrument Description: A spectrometer is an optical instrument used to measure properties of light over a specific portion of the electromagnetic spectrum. Community Standard Description: http://vocab.nerc.ac.uk/collection/L22/current/TOOL0460/
Cruise: HLY1502
HLY1502
USCGC Healy
Community Standard Description
International Council for the Exploration of the Sea
USCGC Healy
vessel
HLY1502
David C. Kadko
Florida International University
https://datadocs.bco-dmo.org/docs/302/geotraces/GEOTRACES_ARCTIC/data_docs/cruise_reports/healy1502.pdf
Report describing HLY1502
USCGC Healy
Community Standard Description
International Council for the Exploration of the Sea
USCGC Healy
vessel