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Nitrogen is an essential element for life, and its availability can limit the growth of phytoplankton in the surface waters of the oceans. One source of nitrogen to surface waters is deposition from the atmosphere, which is the result of reactive nitrogen emissions from both human (anthropogenic) activities and natural processes. Anthropogenic nitrogen emissions to the atmosphere and nitrogen deposition to the oceans have increased exponentially since preindustrial times. In fact, global modeling studies have suggested that as much as 80% of total nitrogen deposition to the oceans is anthropogenic in origin, and that the magnitude of input to the global oceans rivals estimates of biological nitrogen fixation. The impacts associated with this increased nitrogen deposition are clear in both terrestrial and coastal systems, but the implications for open ocean biogeochemistry are less well studied. Recent work in the North Pacific Ocean (NPO) has suggested that increased nitrogen due to anthropogenic atmospheric deposition is detectable even in the open ocean, while other work can explain nutrient dynamics based upon natural biological and physical processes. The investigators propose to study the influence of both anthropogenic and natural sources on the deposition of nitrogen (as nitrate, ammonium, and organic nitrogen) in the NPO. This will be based on collection of aerosol and rainwater samples year-round at two sites: (1) Chang-Dao Island, China where they expect high anthropogenic nitrogen inputs; and (2) Oahu, Hawaii where they expect marine sources to dominate. They will also collect ship-based samples in the marine boundary layer via already planned short-term research cruises in each season. In addition to the scientific outcomes, this project will provide for human resources and professional development of the team members (faculty members, a graduate student, undergraduate student, and technicians), advance international collaborations, and contribute to education and public outreach. Identifying the sources of nitrogen deposition to the open ocean is crucial for understanding anthropogenic impacts on biogeochemical cycles. A primary question is, is nitrogen deposition the result of external, anthropogenic processes or does it represent recycled nitrogen from the ocean's point of view? The specific objectives of this project are to: characterize the atmospheric composition and sources of inorganic (ammonium and nitrate) and organic nitrogen with an emphasis on seasonality; diagnose the influence of air-sea exchange versus anthropogenic sources of nitrogen on atmospheric deposition; and determine the isotopic composition of gaseous and particulate inorganic nitrogen in the marine boundary layer via ship-based sample collections in the NPO. Using concentration and isotopic measurements of reactive nitrogen species, in addition to transport and chemical box modeling, the study aims to characterize nitrogen deposition in two locations with very different source influences. This study will provide the first comprehensive, seasonal analysis of the isotopic values of reactive nitrogen species in the NPO atmosphere where nitrogen deposition is considered intense. Ultimately this project will lead to a better understanding of how anthropogenic changes in the atmospheric nitrogen cycle may influence the biogeochemistry of the surface ocean as well as the composition of the marine atmosphere.This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the Foundation's intellectual merit and broader impacts review criteria.&lt;/p&gt;</gco:CharacterString>
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                <gco:CharacterString>&amp;lt;p&amp;gt;Aerosol sampling was conducted from September 22, 2019 to September 5, 2020. A high-volume aerosol sampler (model 2031, Qingdao Laoying Environmental Technology Co) operating at 1.0 m&amp;lt;sup&amp;gt;3&amp;lt;/sup&amp;gt; min &amp;lt;sup&amp;gt;-1&amp;lt;/sup&amp;gt; with 25 × 20 cm filters was used. Aerosol samples were for 24-72 h for each filter, with a total of 108 samples collected.&amp;lt;/p&amp;gt;</gco:CharacterString>
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                <gco:CharacterString>&amp;lt;p&amp;gt;We measured the concentrations of total nitrogen (TN), nitrate isotopes (&amp;lt;sup&amp;gt;15&amp;lt;/sup&amp;gt;N), ammonium isotopes (&amp;lt;sup&amp;gt;15&amp;lt;/sup&amp;gt;N), oxygen isotope (&amp;lt;sup&amp;gt;17&amp;lt;/sup&amp;gt;O and &amp;lt;sup&amp;gt;18&amp;lt;/sup&amp;gt;O), and a suite of ion concentrations (calcium (Ca&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt;), magnesium (Mg&amp;lt;sup&amp;gt;2+&amp;lt;/sup&amp;gt;), sodium (Na&amp;lt;sup&amp;gt;+&amp;lt;/sup&amp;gt;), and potassium (K&amp;lt;sup&amp;gt;+&amp;lt;/sup&amp;gt;), Chloride (Cl&amp;lt;sup&amp;gt;-&amp;lt;/sup&amp;gt;) and sulfate (SO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;&amp;lt;sup&amp;gt;2-&amp;lt;/sup&amp;gt;)). TN measurements were conducted at the Center for Isotope Geochemistry and Geochronology (CIGG) at the Qingdao National Laboratory for Marine Science and Technology (QNLM) in Qingdao, China. All other measurements were conducted at the Department of Earth, Environmental, and Planetary Sciences at Brown University in Providence, RI (USA).&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;TN was measured using an elemental analyzer (Elementar vario Isotope select) with an analytical standard deviation of ± 0.04 % for TN (n = 6). After the frozen samples were received at Brown University, a 5 × 5 cm square was cut from the center of the filter at room temperature and extracted in a pre-cleaned bottle with ~100 mL of MQ water (exact amounts were recorded via weight) and then sonicated for 1 h. After sonication, the filters were removed, and the samples were frozen at 20 ◦C until further analyses.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;&amp;amp;nbsp;The concentration of ammonium, nitrate, and nitrite were determined colorimetrically (indophenol blue) using a discrete UV–Vis analyzer (Westco Smartchem 200). U.S. EPA Compliant Methods 350.1 (O’Dell, 1993), 353.2 (Revision 2.0), and 354.1 were followed for ammonium, nitrate, and nitrite, respectively. Standard lab protocols were followed, including calibration to standards as well as blanks and in-house quality control measurements. The pooled standard deviation (1σ) for ammonium was 0.6 μmol L &amp;lt;sup&amp;gt;-1&amp;lt;/sup&amp;gt;, and 0.3 μmol L &amp;lt;sup&amp;gt;-1&amp;lt;/sup&amp;gt; for nitrate and nitrite.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;The denitrifier method (Casciotti et al., 2002; Sigman et al., 2001) was used to complete nitrate (&amp;lt;sup&amp;gt;15&amp;lt;/sup&amp;gt;N /&amp;lt;sup&amp;gt;14&amp;lt;/sup&amp;gt;N) and oxygen (&amp;lt;sup&amp;gt;18&amp;lt;/sup&amp;gt;O /&amp;lt;sup&amp;gt;16&amp;lt;/sup&amp;gt;O) isotope analyses on a continuous flow isotope ratio mass spectrometer. Values were reported in ‰ relative to standards. The azide method (Zhang et al., 2007) was used to complete ammonium (&amp;lt;sup&amp;gt;15&amp;lt;/sup&amp;gt;N /&amp;lt;sup&amp;gt;14&amp;lt;/sup&amp;gt;N) isotope analyses on a continuous flow isotope ratio mass spectrometer. Values were reported in ‰ relative to standards (IAEA-N&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; and USGS-25) and the pooled standard deviation for duplicates(n = 13 pairs) and replicates (n = 20) was 0.3 ‰ and 0.5 ‰, respectively.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Concentrations of calcium, magnesium, sodium, and potassium were measured on an Inductively Coupled Plasma (ICP) atomic emission spectrometer. Samples were filtered with 0.45-μm filters and an aliquot of each sample solution was made 2% acidic with nitric acid. A commercial standard (IV-4) for each specific element was run roughly every 10 samples. The relative standard deviation for the standards was ≤3.3% for all four elements. Chloride and sulfate concentrations were measured on an Ion Chromatography (IC) instrument (Dionex Integrion HPIC) using suppressed conductivity detection. Anions were determined using a Dionex AS19-4 μm guard (4 × 50 mm) and analytical column (4× 250 mm) with 20 mM KOH as eluent with a flow rate of 1 mL min&amp;lt;sup&amp;gt;-1&amp;lt;/sup&amp;gt;. All samples were filtered with 0.45-μm filters before being analyzed. In-house quality control standards were run approximately every six samples. The pooled standard deviation for duplicates was 2.0 μmol for both chloride and sulfate (n = 13 pairs and 12 pairs, respectively). The relative standard deviation for the low and high concentration QCs were ≤6.4% and &amp;amp;lt;3.4%, respectively.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Instruments:&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;High-volume aerosol sampler (model 2031, Qingdao Laoying Environmental Technology Co) operating at 1.0 m&amp;lt;sup&amp;gt;3&amp;lt;/sup&amp;gt; min &amp;lt;sup&amp;gt;-1&amp;lt;/sup&amp;gt; with 25 × 20 cm filters.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Elemental analyzer: the concentrations of TN were measured using an elemental analyzer (Elementar vario Isotope select).&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Discrete UV–Vis analyzer (Westco Smartchem 200): for ammonium, nitrate, and nitrite concentrations.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Continuous Flow Isotope Ratio Mass Spectrometer: for ammonium, nitrate, and oxygen isotope values.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Inductively Coupled Plasma (ICP) atomic emission spectrometer: to measure concentrations of calcium, magnesium, sodium, and potassium.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Ion Chromatography (IC) (Dionex Integrion HPIC): to measure chloride and sulfate concentrations.&amp;lt;/p&amp;gt;</gco:CharacterString>
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* Converted sampling latitude and longitude notation from decimal, minute, seconds to decimal degrees. Rounded these fields to 5 decimals
* Converted date to ISO notation (Y-m-d)</gco:CharacterString>
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                <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/instrument/691.rdf" xlink:title="Aerosol Sampler" xlink:actuate="onRequest">model 2031, Qingdao Laoying Environmental Technology Co</gmx:Anchor>
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            <gco:CharacterString>PI Supplied Instrument Name: model 2031, Qingdao Laoying Environmental Technology Co PI Supplied Instrument Description:High-volume aerosol sampler (model 2031, Qingdao Laoying Environmental Technology Co) operating at 1.0 m3 min -1 with 25 × 20 cm filters. 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/</gco:CharacterString>
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            <gco:CharacterString>PI Supplied Instrument Name:  PI Supplied Instrument Description:Inductively Coupled Plasma (ICP) atomic emission spectrometer: to measure concentrations of calcium, magnesium, sodium, and potassium. 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/</gco:CharacterString>
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                <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/instrument/662.rdf" xlink:title="Ion Chromatograph" xlink:actuate="onRequest">Dionex Integrion HPIC</gmx:Anchor>
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            <gco:CharacterString>PI Supplied Instrument Name: Dionex Integrion HPIC PI Supplied Instrument Description:Ion Chromatography (IC) (Dionex Integrion HPIC): to measure chloride and sulfate concentrations. Instrument Name: Ion Chromatograph Instrument Short Name:Ion Chromatograph   Instrument Description: Ion chromatography is a form of liquid chromatography that measures concentrations of ionic species by separating them based on their interaction with a resin. Ionic species separate differently depending on species type and size. Ion chromatographs are able to measure concentrations of major anions, such as fluoride, chloride, nitrate, nitrite, and sulfate, as well as major cations such as lithium, sodium, ammonium, potassium, calcium, and magnesium in the parts-per-billion (ppb) range. (from http://serc.carleton.edu/microbelife/research_methods/biogeochemical/ic.html)</gco:CharacterString>
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                <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/instrument/469.rdf" xlink:title="Isotope-ratio Mass Spectrometer" xlink:actuate="onRequest"></gmx:Anchor>
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            <gco:CharacterString>PI Supplied Instrument Name:  PI Supplied Instrument Description:Continuous Flow Isotope Ratio Mass Spectrometer: for ammonium, nitrate, and oxygen isotope values. Instrument Name: Isotope-ratio Mass Spectrometer Instrument Short Name:IR Mass Spec; IRMS   Instrument Description: The Isotope-ratio Mass Spectrometer is a particular type of mass spectrometer used to measure the relative abundance of isotopes in a given sample (e.g. VG Prism II Isotope Ratio Mass-Spectrometer). Community Standard Description: http://vocab.nerc.ac.uk/collection/L05/current/LAB16/</gco:CharacterString>
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                <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/instrument/707.rdf" xlink:title="Spectrophotometer" xlink:actuate="onRequest">Westco Smartchem 200</gmx:Anchor>
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            <gco:CharacterString>PI Supplied Instrument Name: Westco Smartchem 200 PI Supplied Instrument Description:Discrete UV–Vis analyzer (Westco Smartchem 200): for ammonium, nitrate, and nitrite concentrations. Instrument Name: Spectrophotometer Instrument Short Name:Spectrophotometer   Instrument Description: An instrument used to measure the relative absorption of electromagnetic radiation of different wavelengths in the near infra-red, visible and ultraviolet wavebands by samples. Community Standard Description: http://vocab.nerc.ac.uk/collection/L05/current/LAB20/</gco:CharacterString>
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