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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Mar. Sci.</journal-id>
<journal-title>Frontiers in Marine Science</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Mar. Sci.</abbrev-journal-title>
<issn pub-type="epub">2296-7745</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta><article-meta>
<article-id pub-id-type="doi">10.3389/fmars.2022.911819</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Marine Science</subject>
<subj-group>
<subject>Original Research</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Role of Aerosols in Spring Blooms in the Central Yellow Sea During the COVID-19 Lockdown by China</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name><surname>Baek</surname><given-names>Ji-Yeon</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<uri xlink:href="https://loop.frontiersin.org/people/1752446"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Park</surname><given-names>Jinku</given-names></name>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>

</contrib>
<contrib contrib-type="author">
<name><surname>Kim</surname><given-names>Dae-Won</given-names></name>
<xref ref-type="aff" rid="aff3"><sup>3</sup></xref>
<uri xlink:href="https://loop.frontiersin.org/people/1752395"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Lee</surname><given-names>Jong-Seok</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<uri xlink:href="https://loop.frontiersin.org/people/1818541"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Lee</surname><given-names>Jae-Yong</given-names></name>
<xref ref-type="aff" rid="aff4"><sup>4</sup></xref>
<uri xlink:href="https://loop.frontiersin.org/people/1800431"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Lee</surname><given-names>Seung-Jae</given-names></name>
<xref ref-type="aff" rid="aff4"><sup>4</sup></xref>

</contrib>
<contrib contrib-type="author" corresp="yes">
<name><surname>Jo</surname><given-names>Young-Heon</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="author-notes" rid="fn001"><sup>*</sup></xref>
<uri xlink:href="https://loop.frontiersin.org/people/1321607"/>
</contrib>
</contrib-group>
<aff id="aff1"><sup>1</sup><institution>Brain Korea 21 School of Earth Environmental Systems, Pusan National University</institution>, <addr-line>Busan</addr-line>, <country>South Korea</country></aff>
<aff id="aff2"><sup>2</sup><institution>Center of Remote Sensing and Geographic Information System, Korea Polar Research Institute</institution>, <addr-line>Incheon</addr-line>, <country>South Korea</country></aff>
<aff id="aff3"><sup>3</sup><institution>Department of Oceanography, Pusan National University</institution>, <addr-line>Busan</addr-line>, <country>South Korea</country></aff>
<aff id="aff4"><sup>4</sup><institution>National Center for AgroMeteorology, Seoul National University</institution>, <addr-line>Seoul</addr-line>, <country>South Korea</country></aff>
<author-notes>
<fn fn-type="edited-by">
<p>Edited by: C&#xe9;dric Jamet, UMR8187 Laboratoire d&#x2019;oc&#xe9;anologie et de g&#xe9;osciences (LOG), France</p>
</fn>
<fn fn-type="edited-by">
<p>Reviewed by: Julien Brajard, Nansen Environmental and Remote Sensing Center (NERSC), Norway; Bing Han, National Marine Technology Center, China</p>
</fn>
<fn fn-type="corresp" id="fn001">
<p>*Correspondence: Young-Heon Jo, <email xlink:href="mailto:joyoung@pusan.ac.kr">joyoung@pusan.ac.kr</email></p>
</fn>
<fn fn-type="other" id="fn002">
<p>This article was submitted to Marine Biogeochemistry, a section of the journal Frontiers in Marine Science</p>
</fn>
</author-notes>
<pub-date pub-type="epub">
<day>23</day>
<month>09</month>
<year>2022</year></pub-date>
<pub-date pub-type="collection">
<year>2022</year>
</pub-date>
<volume>9</volume>
<elocation-id>911819</elocation-id>
<history>
<date date-type="received">
<day>03</day>
<month>04</month>
<year>2022</year>
</date>
<date date-type="accepted">
<day>08</day>
<month>06</month>
<year>2022</year>
</date></history>
<permissions>
<copyright-statement>Copyright &#xa9; 2022 Baek, Park, Kim, Lee, Lee, Lee and Jo</copyright-statement>
<copyright-year>2022</copyright-year>
<copyright-holder>Baek, Park, Kim, Lee, Lee, Lee and Jo</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/">
<p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</p>
</license>
</permissions>
<abstract>
<p>Reduced amounts of aerosols blowing into the Yellow Sea (YS), owing to the temporary lockdown of factories in China during COVID-19, resulted in a 15% decrease in spring chlorophyll-<italic>a</italic> concentration (CHL) in March 2020 compared to its mean March values from 2003 to 2021. Particularly, the effect of land-based AOD is insignificant compared with that of atmospheric aerosols flowing into the YS, as indicated by the currents and wind directions. Hence, the main objective of this study was to understand the relationship between atmospheric aerosols and CHL by quantitatively considering relevant environmental changes using a Random Forest (RF) algorithm. Various input physical forcing variables to RF were employed, including aerosol optical depth (AOD), sea surface temperature (SST), mixed layer depth (MLD), wind divergence (WD), and total precipitation (TP). From the RF-based analysis, we estimated the relative contribution of each physical forcing variable to the difference in CHL during and after the COVID-19 lockdown period. The sensitivity of the RF model to changes in aerosol levels indicated positive effects of increased amounts of aerosols during spring blooms. Additionally, we calculated the quantitative contribution of aerosols to CHL changes. When SST was warmer and TP was lower than their climatology in March 2020, CHL increased by 0.22 mg m<sup>-3</sup> and 0.02 mg m<sup>-3</sup>, respectively. Conversely, when MLD became shallower and AOD was lower than their climatology, CHL decreased as much as 0.01 mg m<sup>-3</sup> and 0.20 mg m<sup>-3</sup>. Variations in WD caused no significant change in CHL. Overall, the specific estimations for reduced spring blooms were caused by a reduction in aerosols during the COVID-19 lockdown period. Furthermore, the RF developed in this study can be used to examine CHL changes and the relative role of significant environmental changes in biological blooms in the ocean for any normal year.</p>
</abstract>
<kwd-group>
<kwd>COVID-19 lockdown</kwd>
<kwd>aerosol</kwd>
<kwd>spring bloom</kwd>
<kwd>random forest</kwd>
<kwd>Central Yellow Sea</kwd>
</kwd-group><contract-sponsor id="cn001">National Research Foundation of Korea<named-content content-type="fundref-id">10.13039/501100003725</named-content></contract-sponsor>
<counts>
<fig-count count="7"/>
<table-count count="3"/>
<equation-count count="6"/>
<ref-count count="79"/>
<page-count count="14"/>
<word-count count="8164"/>
</counts>
</article-meta>
</front>
<body>
<sec id="s1">
<title>1 Introduction</title>
<p>The outbreak of Coronavirus disease 2019 (COVID-19) in Wuhan, Hubei Province, China, was officially reported to the World Health Organization on December 31, 2019 (<ext-link ext-link-type="uri" xlink:href="https://covid19.who.int">https://covid19.who.int</ext-link>). At the end of January 2020, public transportation in Wuhan was closed to minimize the spread of the virus. Furthermore, industrial activities at manufacturing plants were temporarily shut down in most provinces in China, including Hubei, Zhejiang, Xinjiang, Hebei, Shannxi, and Henan. This lockdown was decontrolled in early April 2020, which is referred to as the COVID-19 lockdown period (<xref ref-type="bibr" rid="B3">Bauwens et al., 2020</xref>; <xref ref-type="bibr" rid="B57">Shakoor et al., 2020</xref>). Many studies have reported improved air quality from the reduced anthropogenic aerosol emissions, owing to the enforcement of the COVID-19 lockdown policy (<xref ref-type="bibr" rid="B20">He et al., 2020</xref>; <xref ref-type="bibr" rid="B66">Timmermann et al., 2020</xref>). Generally, aerosols in the atmosphere are anthropogenic in origin as they are mainly from emissions from Chinese factory operations, motor vehicle pollution, and seasonal dust such as Asian dust (<xref ref-type="bibr" rid="B75">Yu et al., 2013</xref>; <xref ref-type="bibr" rid="B50">Park et al., 2017</xref>). Aerosols from China can reach the North Pacific Ocean through the Korean Peninsula <italic>via</italic> the westerlies. Specifically, the region most affected by aerosols in the North Pacific Ocean is the Yellow Sea (YS), which is located on the western Korean Peninsula adjacent to northeastern China (<xref ref-type="bibr" rid="B30">Kim et al., 2009</xref>; <xref ref-type="bibr" rid="B56">Qi et al., 2013</xref>; <xref ref-type="bibr" rid="B77">Zhang et al., 2013</xref>; <xref ref-type="bibr" rid="B33">Lee et al., 2019</xref>). This is because this area of China has many industrial cities (<xref ref-type="bibr" rid="B37">Li et al., 2003</xref>; <xref ref-type="bibr" rid="B67">Wang and Su, 2020</xref>; <xref ref-type="bibr" rid="B73">Yoon et al., 2021</xref>). Aerosols can influence long-range transboundary air pollution (<xref ref-type="bibr" rid="B49">Oh et al., 2015</xref>; <xref ref-type="bibr" rid="B38">Lim et al., 2019</xref>) and ocean&#x2013;atmosphere interactions (<xref ref-type="bibr" rid="B65">Tao et al., 2012</xref>; <xref ref-type="bibr" rid="B41">Liu et al., 2013</xref>; <xref ref-type="bibr" rid="B32">Kripalani et al., 2022</xref>). In addition, aerosols scatter radiance from solar radiation in short wavelengths, which can disrupt the radiative energy balance of the earth&#x2013;atmosphere system. This process leads to low sea surface temperatures (<xref ref-type="bibr" rid="B74">Yue et al., 2011</xref>; Kripalani et al., 2022) or makes smaller cloud droplets, thereby reducing precipitation <xref ref-type="bibr" rid="B6">Cheng et al. (2021)</xref>. However, humid environments can also increase precipitation (<xref ref-type="bibr" rid="B28">Khain et al., 2008</xref>).</p>
<p>Anthropogenic nitrogen (NO<sub>x</sub> and NH<sub>y</sub>) in aerosols can be considered an important factor that can change the marine ecosystem when deposited into the ocean (<xref ref-type="bibr" rid="B63">Tan et al., 2011</xref>; <xref ref-type="bibr" rid="B41">Liu et al., 2013</xref>; <xref ref-type="bibr" rid="B69">Wei et al., 2015</xref>; <xref ref-type="bibr" rid="B48">Moon et al., 2021</xref>). The supply of nitrogen, a limiting factor, to the ocean temporarily promotes phytoplankton growth and increases primary production in the YS (<xref ref-type="bibr" rid="B68">Wang et al., 2003</xref>; <xref ref-type="bibr" rid="B45">Mahowald et al., 2005</xref>; <xref ref-type="bibr" rid="B78">Zhang et al., 2010</xref>; <xref ref-type="bibr" rid="B41">Liu et al., 2013</xref>; <xref ref-type="bibr" rid="B46">Mahowald et al., 2018</xref>). <xref ref-type="bibr" rid="B26">Kang et al. (2017)</xref> showed that phytoplankton&#x2019;s biochemical composition, including the carbohydrates, proteins, and lipids, may change upon exposure to the additional supply of nitrogen from the atmosphere (<xref ref-type="bibr" rid="B48">Moon et al., 2021</xref>). Additionally, changes in the biochemical composition of phytoplankton, which comprise the first trophic level of the food web, may be influenced by higher trophic levels (e.g., biomass and productivity of fishery resources) (<xref ref-type="bibr" rid="B26">Kang et al., 2017</xref>).</p>
<p><xref ref-type="bibr" rid="B41">Liu et al. (2013)</xref> and <xref ref-type="bibr" rid="B56">Qi et al. (2013)</xref> investigated the marine ecosystem using <italic>in-situ</italic> measurements after aerosols were imported into the ocean. Since then, many studies have used satellite data to monitor and evaluate the effects of continuous and long-range aerosol transport in near real-time and wide-area to complement the limitations of field observations. Using aerosol optical depth (AOD) from the MODerate Resolution Imaging Spectroradiometer (MODIS)-Terra, <xref ref-type="bibr" rid="B35">Lien et al. (2017)</xref> reported that phytoplankton blooms increase when Asian dust increases. <xref ref-type="bibr" rid="B72">Yoon et al. (2019)</xref> also used the aerosol index (AI) provided by the Visible Infrared Imaging Radiometer Suite (VIIRS) to investigate the increase in spring blooms in the North Pacific owing to the increase in Asian dust (<xref ref-type="bibr" rid="B63">Tan et al., 2011</xref>). Through many studies conducted over a long period of time, we attempted to confirm the effect of aerosols on marine ecosystems. However, previous studies have mainly focused on identifying the relative relationships among the contributing factors of the phytoplankton blooms, rather than on the quantitative contribution of each factor (<xref ref-type="bibr" rid="B61">Tan and Shi, 2012a</xref>; <xref ref-type="bibr" rid="B73">Yoon et al., 2021</xref>). As a result, previous studies have been limited in their ability to evaluate the quantitative contribution of aerosols to marine ecosystems in the YS.</p>
<p>In general, phytoplankton blooms can be estimated using the chlorophyll-<italic>a</italic> concentration (CHL), which indicates phytoplankton biomass (<xref ref-type="bibr" rid="B2">Arteaga et al., 2016</xref>). CHL is not only affected by aerosols, but also by physical forcing variables, such as sea surface temperature (SST) (<xref ref-type="bibr" rid="B79">Zhao et al., 2019</xref>) and mixed layer depth (MLD) (<xref ref-type="bibr" rid="B62">Tan and Shi, 2012b</xref>; <xref ref-type="bibr" rid="B44">Lu et al., 2021</xref>). An increase in photosynthetically active radiation (PAR) may increase SST, resulting in shallow MLD. The effects of each factor on CHL are as follows. Phytoplankton growth has a positive relationship with SST that reaches its highest peak when SST is between 9&#xb0;C and 13&#xb0;C; however, it has a negative relationship when SST is over 13&#xb0;C (<xref ref-type="bibr" rid="B71">Xu et al., 2013</xref>; <xref ref-type="bibr" rid="B79">Zhao et al., 2019</xref>; <xref ref-type="bibr" rid="B44">Lu et al., 2021</xref>). PAR also has a positive relationship with CHL because CHL increases as light intensity increases (<xref ref-type="bibr" rid="B62">Tan and Shi, 2012b</xref>); however, phytoplankton growth declines when it exceeds a threshold intensity level. Furthermore, the deepening of the MLD, owing to more intense wind speeds, increases the CHL (<xref ref-type="bibr" rid="B62">Tan and Shi, 2012b</xref>; <xref ref-type="bibr" rid="B44">Lu et al., 2021</xref>), whereas the decrease in anthropogenic aerosols is correlated with a reduction in spring phytoplankton biomass (<xref ref-type="bibr" rid="B73">Yoon et al., 2021</xref>). In addition, precipitation deposits aerosols directly into the ocean, thereby increasing phytoplankton growth (<xref ref-type="bibr" rid="B61">Tan and Shi, 2012a</xref>). However, some studies have reported that precipitation can inhibit phytoplankton growth through metal components, such as Cu and Pb, within rain drops (<xref ref-type="bibr" rid="B53">Paytan et al., 2009</xref>; <xref ref-type="bibr" rid="B41">Liu et al., 2013</xref>).</p>
<p>Thus, CHL changes relate to various physical parameters, as discussed. Hence, many studies have investigated the complex effects on CHL using machine learning (ML). ML is a technique that can solve nonlinear relationships and complex interactions between ecological factors, such as CHL and physical variables, rather than by using linear statistical methods (<xref ref-type="bibr" rid="B31">Kotsiantis et al., 2006</xref>; <xref ref-type="bibr" rid="B9">Cutler et al., 2007</xref>). <xref ref-type="bibr" rid="B6">Cheng et al. (2021)</xref> reported that the accuracy of the random forest (RF) model in predicting phytoplankton blooms, using multiple predictors, was higher than that of other the ML methods such as support vector machines and decision trees (<xref ref-type="bibr" rid="B42">Liu and Wu, 2017</xref>). <xref ref-type="bibr" rid="B52">Park et al. (2019)</xref> also found that the CHL reconstructed for multiple variables through the RF model more accurately simulated spatial patterns and CHL values when compared with other techniques. In addition, <xref ref-type="bibr" rid="B51">Park et al. (2020)</xref> qualitatively and quantitatively studied the effects of various factors on CHL through RF.</p>
<p>Anthropogenic aerosol emissions into the atmosphere have declined due to the COVID-19 lockdown policy in China. This phenomenon may provide a natural experimental environment that can facilitate the quantitative evaluation of changes in environmental conditions, including the effects of reducing anthropogenic aerosols, which can cause changes in the marine ecosystem. In doing so, we required an answer for the following scientific question: what happened during spring blooms in the YS under reduced aerosol levels (especially anthropogenic aerosols) during the COVID-19 lockdown? To answer this critical question, we examined the contributions of all relevant environmental changes to phytoplankton blooms in the YS based on the RF model using satellite ocean color data (Sections 3.1 to 3.3). Furthermore, we estimated the quantitative contribution of aerosols to CHL through partial dependence (PD) analysis of the RF model (Sections 3.4 to 3.5).</p>
</sec>
<sec id="s2">
<title>2 Data and Methodology</title>
<sec id="s2_1">
<title>2.1. Study Area</title>
<p>The YS, located between China and Korea, is a semi-enclosed marginal sea in the Pacific Northwest with an average depth of 44 m (<xref ref-type="bibr" rid="B25">Jin et al., 2013</xref>). The YS is predominantly affected by aerosols, as it is near the northeastern part of China where there is significant industrial activity. As a result, this area is influenced by atmospheric nitrogen deposition and it exhibits high primary productivity (<xref ref-type="bibr" rid="B73">Yoon et al., 2021</xref>). In addition, the YS is influenced by river inflows containing suspended sediment. This study examined the influence of aerosols on phytoplankton growth in an area that minimizes the effects of river discharge and suspended sediment. The central region of the YS (Central Yellow Sea [CYS]; 121.5&#x2013;125.5&#xb0;E, 34&#x2013;37&#xb0;N) was selected (<xref ref-type="fig" rid="f1"><bold>Figure&#xa0;1</bold></xref>) (<xref ref-type="bibr" rid="B59">Shi et al., 2017</xref>; <xref ref-type="bibr" rid="B14">Fu et al., 2018</xref>) because it was the region where spring blooms mainly occurred in the YS (<xref ref-type="bibr" rid="B71">Xu et al., 2013</xref>). In addition, the sources of land-based AOD in the study area did not make a substantial contribution to atmospheric aerosols in the CYS, as per the ocean currents and wind directions. Hence help intensively investigate the effect of aerosols on the CHL. According to <xref ref-type="bibr" rid="B71">Xu et al. (2013)</xref>, spring blooms in the CYS were defined as a CHL higher than 1.2 mg m<sup>-3</sup>.</p>
<fig id="f1" position="float">
<label>Figure&#xa0;1</label>
<caption>
<p>Central Yellow Sea (CYS), was analyzed to determine AOD <bold>(A&#x2013;C)</bold> and CHL <bold>(D&#x2013;F)</bold> anomalies in March 2019, 2020, and 2021.</p>
</caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fmars-09-911819-g001.tif"/>
</fig>
</sec>
<sec id="s2_2">
<title>2.2.Data</title>
<sec id="s2_2_1">
<title>2.2.1. AOD Data</title>
<p>The MODIS-Terra aerosol product provided daily observations for bright land surfaces based on the Deep Blue algorithm and daily observations of AOD at the global scale. This was performed at 0.55 &#x3bc;m over vegetated land (<xref ref-type="bibr" rid="B27">Kaufman et al., 1997</xref>; <xref ref-type="bibr" rid="B34">Levy et al., 2013</xref>) and ocean surfaces (<xref ref-type="bibr" rid="B60">Tanr&#xe9; et al., 1997</xref>; <xref ref-type="bibr" rid="B34">Levy et al., 2013</xref>) based on the Dark Target land and Dark Target ocean algorithms, respectively (<xref ref-type="bibr" rid="B22">Hsu et al., 2004</xref>; <xref ref-type="bibr" rid="B23">Hsu et al., 2006</xref>; <xref ref-type="bibr" rid="B21">Hsu et al., 2013</xref>). AOD datasets, combined with Deep Blue and Dark Target algorithms (<xref ref-type="bibr" rid="B21">Hsu et al., 2013</xref>; <xref ref-type="bibr" rid="B34">Levy et al., 2013</xref>), were obtained from Ocean Color (<ext-link ext-link-type="uri" xlink:href="https://lads-web.modaps.eosdis.nasa.gov">https://lads-web.modaps.eosdis.nasa.gov</ext-link>). Its temporal and spatial resolutions are daily and 10 km &#xd7; 10 km (at nadir), respectively, as provided by Level-2 MODIS-Terra. On comparing various satellite observations with AERONET around the CYS, the AOD from MODIS-Terra was more accurate than other sensor measurements.</p>
<p>Anthropogenic aerosols from northeastern China were considered to be the main factor influencing AOD during the lockdown because the emergence of Asian dust did not occur in March 2020. <xref ref-type="bibr" rid="B73">Yoon et al. (2021)</xref> found that the AOD in March 2020 was predominantly influenced by aerosols originating from northern China. In addition, it is worth noting that while there are strong coastal currents and thus very weak intrusion to the CYS in spring season (March to May), strong southwesterly winds toward the CYS usually transport aerosol in this season. Thus, aerosols transported from coastal regions into the CYS are likely minimal. Hence, this study considered only aerosols generated in the industrialized regions of China.</p>
</sec>
<sec id="s2_2_2">
<title>2.2.2. Ocean Color, Numerical Model and Reanalysis Data</title>
<p>The MODIS-Aqua phytoplankton biomass product provided daily and monthly CHL measurements. Monthly Level-3 MODIS-Aqua CHL datasets with a 4&#xa0;km spatial resolution were obtained from the NASA Ocean Biology Processing Group (<ext-link ext-link-type="uri" xlink:href="https://oceandata.sci.gsfc.nasa.gov">https://oceandata.sci.gsfc.nasa.gov</ext-link>). In addition, monthly Level-3 SST data provided by MODIS-Aqua were used and its spatial resolution was the same as that of the CHL data.</p>
<p>The Hybrid Coordinate Ocean Model provided temperature and salinity datasets at an ~8 km (1/12&#xb0;) spatial resolution with 3-hour intervals. The MLD was calculated using a density threshold of 0.03&#xa0;kg m<sup>-3</sup> from a depth of 10&#xa0;m, according to <xref ref-type="bibr" rid="B10">de Boyer Mont&#xe9;gut et al. (2004)</xref>. In addition, the European Center for Medium-range Weather Forecasts Reanalysis v5 (ERA5) provided the eastward component of the 10&#xa0;m wind (U<sub>10</sub>) and the northward component of the 10&#xa0;m wind (V<sub>10</sub>) datasets at ~25 km &#xd7; 25 km (1/4&#xb0; &#xd7; 1/4&#xb0;) with a monthly temporal resolution. Wind divergence (WD), &#x2202;<italic>u</italic>/&#x2202;<italic>x</italic>+&#x2202;<italic>v</italic>/&#x2202;<italic>y</italic> , which estimates the atmospheric inflow of aerosols into the ocean, was calculated using U<sub>10</sub> and V<sub>10</sub> (<xref ref-type="bibr" rid="B12">Freitas et al., 2017</xref>). The total precipitation (TP) data, provided at the same resolution in ERA5, were used to consider the effect of precipitation, which enables atmospheric aerosol information to enter the ocean directly.</p>
<p>We used re-mapped monthly mean data rather than daily or weekly due to missing measurement by cloud presence in ocean color satellite measurements (<xref ref-type="table" rid="T1"><bold>Table&#xa0;1</bold></xref>). Thus, we cannot address the specific lags of 5 to 14 days between aerosol sink to the sea surface and CHL, as reported by <xref ref-type="bibr" rid="B63">Tan et al. (2011)</xref>; <xref ref-type="bibr" rid="B58">Shi et al. (2012)</xref>; <xref ref-type="bibr" rid="B64">Tan and Wang (2014)</xref> , and <xref ref-type="bibr" rid="B72">Yoon et al. (2019)</xref>. In addition, we used data for March of each year from 2003 to 2021 because the COVID-19 lockdown period was from the end of February 2020 to the beginning of April 2020.</p>
<table-wrap id="T1" position="float">
<label>Table&#xa0;1</label>
<caption><p>Description of the dataset of using satellite, reanalysis, and model data.</p>
</caption>
<table frame="hsides">
<thead>
<tr>
<th valign="top" align="left">Variables</th>
<th valign="top" align="center">Abbreviation (Unit)</th>
<th valign="top" align="center">Spatial/Temporal Resolution</th>
<th valign="top" align="center">Dataset</th>
</tr>
</thead>
<tbody>
<tr>
<td valign="top" align="left">Aerosol optical depth</td>
<td valign="top" align="left">AOD (Non dimension)</td>
<td valign="top" align="left">10 km x 10&#xa0;km (at nadir), daily</td>
<td valign="top" align="left">MODIS-Terra</td>
</tr>
<tr>
<td valign="top" align="left">Sea surface temperature</td>
<td valign="top" align="left">SST (&#xb0;C)</td>
<td valign="top" align="left">4 km x 4 km, monthly</td>
<td valign="top" align="left">MODIS-Aqua</td>
</tr>
<tr>
<td valign="top" align="left">Mixed layer depth (Temperature, Salinity)</td>
<td valign="top" align="left">MLD (m)</td>
<td valign="top" align="left">~ 8&#xa0;km x ~ 8&#xa0;km, 3 hours</td>
<td valign="top" align="left">HYCOM</td>
</tr>
<tr>
<td valign="top" align="left">Wind divergence (U<sub>10</sub>, V<sub>10</sub>)</td>
<td valign="top" align="left">WD (sec<sup>-1</sup>)</td>
<td valign="top" align="left">~ 25&#xa0;km x ~ 25&#xa0;km, monthly</td>
<td valign="top" align="left">ERA5</td>
</tr>
<tr>
<td valign="top" align="left">Total precipitation</td>
<td valign="top" align="left">TP (mm)</td>
<td valign="top" align="left">~ 25&#xa0;km x ~ 25&#xa0;km, monthly</td>
<td valign="top" align="left">ERA5</td>
</tr>
<tr>
<td valign="top" align="left">Chlorophyll-<italic>a</italic> concentration</td>
<td valign="top" align="left">CHL (mg m<sup>-3</sup>)</td>
<td valign="top" align="left">4 km x 4&#xa0;km, monthly</td>
<td valign="top" align="left">MODIS-Aqua</td>
</tr>
</tbody>
</table>
</table-wrap>
</sec>
</sec>
<sec id="s2_3">
<title>2.3. Method</title>
<p>According to previous studies, among the ML techniques, the RF model simulates fairly well the complex effect of various factors on CHL (<xref ref-type="bibr" rid="B41">Liu et al., 2013</xref>; <xref ref-type="bibr" rid="B42">Liu and Wu, 2017</xref>; <xref ref-type="bibr" rid="B52">Park et al., 2019</xref>). Thus, we performed a regression analysis to evaluate the CHL response to AOD and other physical forcing variables (SST, MLD, WD, and TP) of the RF model. The RF model, an ensemble learning method, can perform classification and regression analyses to evaluate the CHL response to AOD and other physical forcing variables (SST, MLD, WD, and TP). Decision tree-based algorithms, such as RF, can measure the variable importance (VI) of the features used in model development (<xref ref-type="bibr" rid="B5">Breiman, 2001</xref>; <xref ref-type="bibr" rid="B1">Ali et al., 2012</xref>). After training, this score was calculated for each feature and the result was normalized such that the total sum of importance was 1. Thus, the VI, which indicates the effect of the predictors used in the RF model on CHL, could be evaluated (<xref ref-type="bibr" rid="B9">Cutler et al., 2007</xref>; <xref ref-type="bibr" rid="B51">Park et al., 2020</xref>; <xref ref-type="bibr" rid="B54">Pham et al., 2021</xref>).</p>
<p>Generally, the RF model sets the number of single decision trees (N<sub>trees</sub>) and the number of features (M<sub>try</sub>) to generate the best performance in each tree node. For regression, M<sub>try</sub> was set to the maximum number of features and for classification, it was set to the square root of the number of features (<xref ref-type="bibr" rid="B15">Geurts et al., 2006</xref>). Then, for the feature selected at each node, the node was divided into two child nodes based on the optimal partitioning condition (i.e., a small mean squared error, MSE) and a leaf node was calculated (<xref ref-type="bibr" rid="B51">Park et al., 2020</xref>). Finally, the results produced by each tree were ensembled on average to draw a conclusion. The critical parameters considered in the RF model were N<sub>trees</sub> and M<sub>try</sub>. N<sub>trees</sub> was set to 50 through an empirical trial and M<sub>try</sub> was set to 6 according to the convention.</p>
<p>Six predictors (variables) were used as the inputs for the RF model. The predictors used were the AOD, physical forcing variables (SST, MLD, WD, and TP), and climatology of the CHL (CHL<sub>c</sub>) during spring (March 1 to March 31) from 2003 to 2021. As inputs for the RF model, we used CHL<sub>c</sub> because it is considered the factor illustrating the environmental variables (<xref ref-type="bibr" rid="B51">Park et al., 2020</xref>). It is worth noting that PAR was not used; instead, we used AOD as input because both have directly inverse relations (<xref ref-type="bibr" rid="B36">Li et al., 2020</xref>). The target was the MODIS-Aqua CHL (CHL<sub>MODIS</sub>). The significance test of the predictors was conducted using the Boruta algorithm and all the data were normalized. In addition, for CHL<sub>c</sub> and CHL<sub>MODIS</sub>, which have skewed data, a logarithmic transformation was performed to approximate a normal distribution (<xref ref-type="bibr" rid="B17">Gregor et al., 2017</xref>; <xref ref-type="bibr" rid="B18">Hahm et al., 2019</xref>).</p>
<p>In Section 3.2, the performance of the RF models was evaluated using various statistical metrics, such as the determined coefficient (R<sup>2</sup>), root mean square error (RMSE), mean absolute error (MAE), and MSE (<xref ref-type="bibr" rid="B55">Popoola et al., 2019</xref>; <xref ref-type="bibr" rid="B51">Park et al., 2020</xref>). The R<sup>2</sup> indicates how well the estimated linear model fits the given data in statistics. RMSE is a measure commonly used when dealing with the difference between the <italic>in-situ</italic> data (X) and predicted value (Y). MAE means errors between paired observations expressing the same phenomenon. In other words, MAE is the mean absolute difference between the X and Y. MSE shows the mean of the squares of the error. The closer the MSE is to 0, the higher the accuracy is because the guessed value is closer to the original (<xref ref-type="bibr" rid="B8">Chicco et al., 2021</xref>). In addition, using the RF model, we determined whether CHL could increase when only AOD was additionally supplied to environmental conditions in March 2020 (Section 3.3). Subsequently, the quantitative contribution of each factor, including AOD to CHL in the RF model, was evaluated using a partial dependence (PD) plot (Section 3.4). A partial dependence (PD) plot depicts the relationship between input variables and predictions (Friedman. 2001). These results show how the predictions partially depend on the values of the input variables of interest. This method can be used to interpret a trained model that can identify linear, monotonic, or more complex relationships between predictors and targets (<xref ref-type="bibr" rid="B47">Molnar, 2020</xref>). Furthermore, the PD plot quantitatively describes the response probabilities of the predictors (<xref ref-type="bibr" rid="B13">Friedman, 2001</xref>; <xref ref-type="bibr" rid="B16">Greenwell, 2017</xref>; <xref ref-type="bibr" rid="B76">Zeng et al., 2017</xref>). In other words, the PD plot describes the dependence between the target and predictors of interest, marginalizing over the value of all other predictors. We considered that this PD analysis could represent the quantitative effect on the absolute contribution of each physical variable to CHL, that is, the amount of change in CHL (<xref ref-type="bibr" rid="B51">Park et al., 2020</xref>). PD analysis was performed as follows:</p>
<disp-formula>
<label>(1)</label><mml:math id="M1" display="block"><mml:mrow><mml:msub><mml:mi>f</mml:mi><mml:mi>s</mml:mi></mml:msub><mml:mrow><mml:mo>(</mml:mo><mml:mrow><mml:msub><mml:mi>X</mml:mi><mml:mi>s</mml:mi></mml:msub></mml:mrow><mml:mo>)</mml:mo></mml:mrow><mml:mo>=</mml:mo><mml:msub><mml:mi>E</mml:mi><mml:mrow><mml:msub><mml:mi>X</mml:mi><mml:mi>c</mml:mi></mml:msub></mml:mrow></mml:msub><mml:mrow><mml:mo>[</mml:mo><mml:mrow><mml:mover accent="true"><mml:mi>f</mml:mi><mml:mo>^</mml:mo></mml:mover><mml:mrow><mml:mo>(</mml:mo><mml:mrow><mml:msub><mml:mi>X</mml:mi><mml:mi>s</mml:mi></mml:msub><mml:mo>,</mml:mo><mml:msub><mml:mi>X</mml:mi><mml:mi>c</mml:mi></mml:msub></mml:mrow><mml:mo>)</mml:mo></mml:mrow></mml:mrow><mml:mo>]</mml:mo></mml:mrow><mml:mo>=</mml:mo><mml:mover><mml:mo>&#x222b;</mml:mo><mml:mo>&#x200b;</mml:mo></mml:mover><mml:mover accent="true"><mml:mi>f</mml:mi><mml:mo>^</mml:mo></mml:mover><mml:mrow><mml:mo>(</mml:mo><mml:mrow><mml:msub><mml:mi>X</mml:mi><mml:mi>s</mml:mi></mml:msub><mml:mo>,</mml:mo><mml:msub><mml:mi>X</mml:mi><mml:mi>c</mml:mi></mml:msub></mml:mrow><mml:mo>)</mml:mo></mml:mrow><mml:msub><mml:mi>p</mml:mi><mml:mi>c</mml:mi></mml:msub><mml:mrow><mml:mo>(</mml:mo><mml:mrow><mml:msub><mml:mi>X</mml:mi><mml:mi>c</mml:mi></mml:msub></mml:mrow><mml:mo>)</mml:mo></mml:mrow><mml:mi>d</mml:mi><mml:msub><mml:mi>X</mml:mi><mml:mi>c</mml:mi></mml:msub><mml:mo>,</mml:mo></mml:mrow></mml:math></disp-formula>
<p>where <inline-formula><mml:math id="im1" display="inline"><mml:mrow><mml:mover accent="true"><mml:mi>f</mml:mi><mml:mo>^</mml:mo></mml:mover><mml:mrow><mml:mo>(</mml:mo><mml:mi>x</mml:mi><mml:mo>)</mml:mo></mml:mrow><mml:mi>x</mml:mi><mml:mo>=</mml:mo><mml:mrow><mml:mo>{</mml:mo><mml:mrow><mml:msub><mml:mi>x</mml:mi><mml:mn>1</mml:mn></mml:msub><mml:msub><mml:mi>x</mml:mi><mml:mn>2</mml:mn></mml:msub><mml:mo>&#x22ef;</mml:mo><mml:msub><mml:mi>x</mml:mi><mml:mi>p</mml:mi></mml:msub></mml:mrow><mml:mo>}</mml:mo></mml:mrow></mml:mrow></mml:math></inline-formula> represents the number of features in the RF model (<italic>p</italic> = 6 in this study). In addition, when we divide <italic>x b</italic>y the set of selected <italic>X<sub>s</sub></italic> and complement (<italic>X<sub>c</sub></italic> ) the response variable in the PD plot for <italic>X<sub>a</sub></italic> is defined by Eq. (1). In other words, <italic>X<sub>s</sub></italic> is the feature (i.e., variables and inputs) to be calculated through the model and <italic>X<sub>C</sub></italic>is all variables except <italic>X<sub>s</sub></italic> used feature. <italic>p<sub>c</sub></italic>(<italic>X<sub>c</sub></italic>) represents the marginal probability density of <italic>X<sub>c</sub>.X<sub>s</sub></italic> is set to one variable, and <italic>X<sub>c</sub></italic> is the average value that the remaining inputs are affected by the change of <italic>X<sub>s</sub></italic> . This means that the effects of all the other predictors in the model were average. For more details, refer to <xref ref-type="bibr" rid="B51">Park et al. (2020)</xref>. Eq. (1) can be evaluated using the training set, as follows:</p>
<disp-formula>
<label>(2)</label><mml:math id="M2" display="block"><mml:mrow><mml:mover accent="true"><mml:mrow><mml:msub><mml:mi>f</mml:mi><mml:mi>s</mml:mi></mml:msub></mml:mrow><mml:mo stretchy="true">&#xaf;</mml:mo></mml:mover><mml:mrow><mml:mo>(</mml:mo><mml:mrow><mml:msub><mml:mi>X</mml:mi><mml:mi>s</mml:mi></mml:msub></mml:mrow><mml:mo>)</mml:mo></mml:mrow><mml:mo>=</mml:mo><mml:mfrac><mml:mn>1</mml:mn><mml:mi>n</mml:mi></mml:mfrac><mml:munderover><mml:mo>&#x2211;</mml:mo><mml:mrow><mml:mi>i</mml:mi><mml:mo>=</mml:mo><mml:mn>1</mml:mn></mml:mrow><mml:mi>n</mml:mi></mml:munderover><mml:mover accent="true"><mml:mi>f</mml:mi><mml:mo>^</mml:mo></mml:mover><mml:mrow><mml:mo>(</mml:mo><mml:mrow><mml:msub><mml:mi>X</mml:mi><mml:mi>s</mml:mi></mml:msub><mml:mo>,</mml:mo><mml:msub><mml:mi>X</mml:mi><mml:mrow><mml:mi>i</mml:mi><mml:mo>,</mml:mo><mml:mi>c</mml:mi></mml:mrow></mml:msub></mml:mrow><mml:mo>)</mml:mo></mml:mrow></mml:mrow></mml:math></disp-formula>
<p>where <italic>X<sub>i,c</sub></italic> (<italic>i=1, 2, ..., n</italic>) represents the value of <italic>X<sub>c</sub></italic> in the training samples.</p>
<p>The methodology of this study was based on that of <xref ref-type="bibr" rid="B51">Park et al. (2020)</xref> (<xref ref-type="bibr" rid="B52">Park et al., 2019</xref>). However, unlike the referenced papers on the RF approach, in this study, regression analysis was used among the RF model features to understand the effect of each factor on CHL. In addition, after quantitatively evaluating the impact of each element on spring blooms, the effect was formulated as an equation. Accordingly, this study attempted to extract critical information on how AOD was quantitatively related to spring blooms during the COVID-19 lockdown period.</p>
</sec>
</sec>
<sec id="s3">
<title>3 Results and Discussions</title>
<sec id="s3_1">
<title>3.1. Environmental Conditions of the COVID-19 Lockdown Period</title>
<p>First, we determined how much the aerosol decreased during the COVID-19 lockdown period compared to the other years; therefore, we compared AOD and CHL in March from 2019 to 2021 (<xref ref-type="fig" rid="f1"><bold>Figure&#xa0;1</bold></xref>). During the COVID-19 lockdown period in 2020, local patches were inferred to be small spring blooms (<xref ref-type="fig" rid="f1"><bold>Figure&#xa0;1E</bold></xref>). Especially, it was confirmed that the levels of both data in March 2020, during the COVID-19 lockdown period, decreased significantly compared to those of the other years (<xref ref-type="fig" rid="f1"><bold>Figures&#xa0;1B, E</bold></xref>). In 2019 and 2021, we observed that regions with high AOD distribution showed high CHL levels, confirming that both variables had similar spatial distributions (<xref ref-type="fig" rid="f1"><bold>Figures&#xa0;1A, C, D, F</bold></xref>). From <xref ref-type="fig" rid="f1"><bold>Figure&#xa0;1</bold></xref>, it can be inferred that the abnormally low CHL levels in 2020 was affected by low AOD. We also investigated the changes in other factors to determine whether the effect of reduced aerosol weakened spring blooms during the COVID-19 lockdown period.</p>
<p><xref ref-type="fig" rid="f2"><bold>Figure&#xa0;2</bold></xref> shows that AOD and CHL in March 2020 were lower than the average values from March 2003 to 2021, by approximately 50% (from 0.50 to 0.26) for AOD and approximately 15% (from 2.18 mg m<sup>-3</sup> to 1.90 mg m<sup>-3</sup>) for CHL (<xref ref-type="fig" rid="f2"><bold>Figures&#xa0;2A, F</bold></xref>). In contrast, <xref ref-type="fig" rid="f2"><bold>Figure&#xa0;2B</bold></xref> shows that SST increased by approximately 20% from 7.61&#xb0;C to 9.34&#xb0;C during the same period. This warmer SST is likely due to the reduced amounts of aerosols, which might have caused the increase in SST due to higher incoming solar radiation (<xref ref-type="bibr" rid="B74">Yue et al., 2011</xref>; Kripalani et al., 2022). Accordingly, an increased SST can induce strengthened thermal stratification and a shallower MLD (<xref ref-type="bibr" rid="B61">Tan and Shi, 2012a</xref>; <xref ref-type="bibr" rid="B44">Lu et al., 2021</xref>). Consequently, the MLD in 2020 became 25% more shallow, from 44.37&#xa0;m to 33.09&#xa0;m (<xref ref-type="fig" rid="f2"><bold>Figure&#xa0;2C</bold></xref>). In addition, phytoplankton biomass generally decreases as the MLD becomes more shallow (<xref ref-type="bibr" rid="B44">Lu et al., 2021</xref>). This was also seen for the CHL in 2020 and 2021. Additionally, the WD indicated that the airflow from the atmosphere to the ocean was slightly weakened by 13% (from -2.13 &#xd7; 10<sup>-6</sup> sec<sup>-1</sup> to -2.39 &#xd7; 10<sup>-6</sup> sec<sup>-1</sup>), but this value was not significantly different than that of other years. TP also decreased by 45%, from 7.38 &#xd7; 10<sup>-5</sup> mm to 3.92 &#xd7; 10<sup>-5</sup> mm, which is presumed to be an effect of aerosol reduction in humide environmental conditions (<xref ref-type="fig" rid="f2"><bold>Figures&#xa0;2D, E</bold></xref>) (<xref ref-type="bibr" rid="B28">Khain et al., 2008</xref>).</p>
<fig id="f2" position="float">
<label>Figure&#xa0;2</label>
<caption>
<p>Time series of monthly means of AOD <bold>(A)</bold>, SST <bold>(B)</bold>, MLD <bold>(C)</bold>, WD <bold>(D)</bold>, TP <bold>(E)</bold>, and CHL <bold>(F)</bold> from February (Feb.) 2003 to May 2021. Gray lines indicate the monthly mean predictor in each year from 2003 to 2019. Red lines show from February 2020 to May 2020 in the COVID-19 lockdown period (red shaded) and blue lines represent from February 2021 to May 2021.</p>
</caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fmars-09-911819-g002.tif"/>
</fig>
<p>In the case of 2021, many factors showed a significant change compared with the average values from March 2003 to 2021. AOD showed a sharp increase compared with the same period, and SST showed a similar increasing pattern in 2020. Therefore, the thermal stratification was strengthened owing to the increased SST, and the MLD became shallow, as in the COVID-19 lockdown period. In contrast, the WD and TP in 2021 showed much higher levels than the mean values throughout the period, and the increased WD strengthened the flow from the atmosphere into the ocean. The increase in TP may have been because of increased aerosols, and atmospheric aerosols may have possibly directly entered the ocean through precipitation. Consequently, in 2021, with an increase in aerosols, more aerosols could flow into the sea from the atmosphere due to the physical environment&#x2019;s conditions. We confirmed that 2021 showed a higher CHL than 2020 under different physical environmental conditions during the COVID-19 lockdown period (e.g., increased SST and decreased MLD). Accordingly, the spring blooms in the study area were mainly controlled by AOD changes, as shown in <xref ref-type="fig" rid="f1"><bold>Figures&#xa0;1</bold></xref>, <xref ref-type="fig" rid="f2"><bold>2</bold></xref>. Ultimately, we focused on the qualitative and quantitative effects of aerosol changes that significantly influenced spring blooms.</p>
</sec>
<sec id="s3_2">
<title>3.2. RF Model Performance to CHL</title>
<p>To identify the effect of each factor on CHL, we developed a RF model using the above-mentioned data. The performance of the training set with 80% of the total data (n = 94,480) showed R<sup>2</sup> = 0.98, RMSE = 0.22 mg m<sup>-3</sup>, MAE = 0.07 mg m<sup>-3</sup>, and MSE = 0.05 mg m<sup>-3</sup> with high accuracy and low RMSE (<xref ref-type="fig" rid="f3"><bold>Figure&#xa0;3A</bold></xref>; <xref ref-type="table" rid="T2"><bold>Table&#xa0;2</bold></xref>). It is worth noting that the splitting ratio of 80% to 20% for training and validation dataset shows slightly better results compared to other splitting ratios. According to <xref ref-type="bibr" rid="B11">Despotovic et al. (2016)</xref>, relative RMSE (RRMSE) evaluates model construction accuracy and is considered good when 10 % &#x2264; RRMSE &lt; 20 % (i.e., 10.49 % indicates a good level), excellent if RRMSE &lt; 10 %, fair if 20 % &#x2264; RRMSE &lt; 30 %, and poor if 30 % &#x2264; RRMSE (<xref ref-type="bibr" rid="B24">Jamieson et al., 1991</xref>; <xref ref-type="bibr" rid="B19">Heinemann et al., 2012</xref>; <xref ref-type="bibr" rid="B40">Li et al., 2013</xref>). Hence, the training set almost coincided with CHL<sub>MODIS</sub> and the reconstructed CHL derived from the RF model (CHL<sub>RF</sub>) (<xref ref-type="fig" rid="f3"><bold>Figure&#xa0;3A</bold></xref>). The performance of the validation set with 20 % of the total data (n = 23,620) had accuracy with R<sup>2 =</sup> 0.85, RMSE <sup>=</sup> 0.54 mg m<sup>-3</sup>, MAE = 0.17 mg m<sup>-3</sup>, and MSE = 0.29 mg m<sup>-3</sup>, and RRMSE = 25.37 %. Although the validation set had a lower R<sup>2</sup> and higher RMSE than those of the training set, thus, the reconstructed result was significant (<xref ref-type="fig" rid="f3"><bold>Figure&#xa0;3B</bold></xref>; <xref ref-type="table" rid="T2"><bold>Table&#xa0;2</bold></xref>). Additionally, we determined the relative contribution of each predictor to the RF model through the VI (<xref ref-type="fig" rid="f3"><bold>Figure&#xa0;3C</bold></xref>). The relative contributions of CHL<sub>c</sub>, TP, SST, WD, MLD, and AOD were 46.10 %, 14.42 %, 12.87 %, 9.64 %, 8.71 %, and 8.27 %, respectively. In addition, the standard deviations of CHL<sub>c</sub>, TP, SST, WD, MLD, and AOD were &#xb1;0.29 %, &#xb1;0.47 %, &#xb1;0.44 %, &#xb1;0.44 %, &#xb1;0.49 %, and &#xb1;0.39 %, respectively. CHLc, the average CHL from March 2003 to 2021, had the most significant effect on the CHL prediction because it reflects the CHL trend. Hence, CHL<sub>c</sub> was excluded from the physical forcing variables that directly influenced CHL variation.</p>
<fig id="f3" position="float">
<label>Figure&#xa0;3</label>
<caption>
<p>Performance evaluation of RF model for the training set <bold>(A)</bold> and validation set <bold>(B)</bold> between MODIS-Aqua CHL (<italic>CHL<sub>MODIS</sub></italic>) and the RF model-derived CHL (<italic>CHL<sub>RF</sub></italic>) The evaluation of variable importance (VI) of each predictor is also included here <bold>(C)</bold>.</p>
</caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fmars-09-911819-g003.tif"/>
</fig>
<table-wrap id="T2" position="float">
<label>Table&#xa0;2</label>
<caption><p>Evaluation of RF model performance.</p>
</caption>
<table frame="hsides">
<thead>
<tr>
<th valign="top" align="left"/>
<th valign="top" align="center">Training set</th>
<th valign="top" align="center">Validation set</th>
</tr>
</thead>
<tbody>
<tr>
<td valign="top" align="left"><bold>N</bold></td>
<td valign="top" align="left">94,480</td>
<td valign="top" align="left">23,620</td>
</tr>
<tr>
<td valign="top" align="left"><bold>R<sup>2</sup></bold></td>
<td valign="top" align="left">0.98</td>
<td valign="top" align="left">0.85</td>
</tr>
<tr>
<td valign="top" align="left"><bold>RMSE</bold></td>
<td valign="top" align="left">0.22 mg m<sup>-3</sup></td>
<td valign="top" align="left">0.54 mg m<sup>-3</sup></td>
</tr>
<tr>
<td valign="top" align="left"><bold>MAE</bold></td>
<td valign="top" align="left">0.07 mg m<sup>-3</sup></td>
<td valign="top" align="left">0.17 mg m<sup>-3</sup></td>
</tr>
<tr>
<td valign="top" align="left"><bold>MSE</bold></td>
<td valign="top" align="left">0.05 mg m<sup>-3</sup></td>
<td valign="top" align="left">0.29 mg m<sup>-3</sup></td>
</tr>
<tr>
<td valign="top" align="left"><bold>RRMSE</bold></td>
<td valign="top" align="left">10.49%</td>
<td valign="top" align="left">25.37%</td>
</tr>
</tbody>
</table>
</table-wrap>
<p>To determine whether the RF model could simulate the regional pattern, we compared the spatial distributions of CHL<sub>MODIS</sub> and CHL<sub>RF</sub> (<xref ref-type="fig" rid="f4"><bold>Figure&#xa0;4</bold></xref>). The locations and intensities of the spring blooms were also closely simulated each year. The CHL<sub>MODIS</sub> was 2.09 mg m<sup>-3</sup>, 1.89 mg m<sup>-3</sup>, and 2.71 mg m<sup>-3</sup>, and CHL<sub>RF</sub> was 2.01 mg m<sup>-3</sup>, 1.82 mg m<sup>-3</sup>, and 2.66 mg m<sup>-3</sup> in 2019, 2020, and 2021, respectively. If we estimated CHL<sub>RF</sub> without CHL<sub>c</sub>, the CHL<sub>RF</sub> predicted an overestimate (not shown). This result may be because CHL<sub>c</sub> reflects the CHL information trend. In particular, spring blooms in 2020, which occurred on a small scale and were weak compared to those in other years, were simulated reasonably well. Therefore, it was confirmed that the RF model was well-reconstructed based on the intensity and spatial pattern of CHL (<xref ref-type="fig" rid="f4"><bold>Figures&#xa0;4B, E</bold></xref>).</p>
<fig id="f4" position="float">
<label>Figure&#xa0;4</label>
<caption>
<p>Comparison of spatial patterns between the <italic>CHL<sub>MODIS</sub></italic><bold>(A&#x2013;C)</bold> and <italic>CHL<sub>RF</sub></italic><bold>(D&#x2013;F)</bold> from 2019 to 2021. The black boxes indicate the study area.</p>
</caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fmars-09-911819-g004.tif"/>
</fig>
<p>The established RF model simulated the spatial pattern and CHL value using six factors. The five factors that directly affect CHL had slight differences, but their relative contributions to the RF model were almost similar. Previous studies have shown that CHL is positively related to SST (<xref ref-type="bibr" rid="B79">Zhao et al., 2019</xref>) and negatively related to the MLD and TP (<xref ref-type="bibr" rid="B41">Liu et al., 2013</xref>; <xref ref-type="bibr" rid="B44">Lu et al., 2021</xref>). The influence of each factor (SST, MLD, WD, and TP), which changed as AOD decreased, was discussed in Section 3.1. Therefore, we concentrated more on the spring blooms based on CHL affected by AOD, which changed the most during the COVID-19 lockdown.</p>
</sec>
<sec id="s3_3">
<title>3.3. Relative Contribution of Aerosol to CHL</title>
<p>We focused on the relative effect of AOD on spring blooms, which contributed the least to the RF model but showed the most significant change in 2020 (Section 3.2). This section describes the sensitivity experiments for CHL<sub>RF</sub> to AOD variations under artificially changing aerosol levels (<xref ref-type="fig" rid="f4"><bold>Figures&#xa0;4</bold></xref>, <xref ref-type="fig" rid="f5"><bold>5</bold></xref>). CHL<sub>RF</sub> satisfactorily represents the spring blooms that occur each year. However, spring blooms had lessened in the COVID-19 lockdown period of 2020 compared to that in other years (<xref ref-type="fig" rid="f4"><bold>Figure&#xa0;4E</bold></xref>). Therefore, we attempted to confirm the change in spring blooms by artificially increasing and decreasing aerosols during the COVID-19 lockdown period through a sensitivity experiment using the RF model.</p>
<p>Two sensitivity experiment conditions were constructed to investigate changes in CHL variation by adjusting AOD. The two conditions are with AOD &#xb1; two sigma (2 &#x3c3; &#xb1; 95%), according to the empirical rule (three sigma rule) of statistics; where 2 &#x3c3; is derived by assuming the Gaussian fitting for the distribution of AOD climatology. Furthermore, the sensitivity experiments are conducted with AOD + &#x3c3; and AOD &#x2212; &#x3c3; while all other predictors remain unchanged. In other words, when only the AOD either increased or decreased, all other predictors except AOD are constant. The CHL changes to high (CHL<sub>HAOD</sub>) and low (CHL<sub>LAOD</sub>) AOD were estimated using the following equations:</p>
<disp-formula>
<label>(3)</label><mml:math id="M3" display="block"><mml:mrow><mml:mi>C</mml:mi><mml:mi>H</mml:mi><mml:msub><mml:mi>L</mml:mi><mml:mrow><mml:mi>H</mml:mi><mml:mi>A</mml:mi><mml:mi>O</mml:mi><mml:mi>D</mml:mi></mml:mrow></mml:msub><mml:mo>=</mml:mo><mml:mrow><mml:mo>(</mml:mo><mml:mrow><mml:mi>A</mml:mi><mml:mi>O</mml:mi><mml:mi>D</mml:mi><mml:mo>+</mml:mo><mml:mn>2</mml:mn><mml:mi>&#x3c3;</mml:mi><mml:msub><mml:mo>|</mml:mo><mml:mrow><mml:mi>a</mml:mi><mml:mi>l</mml:mi><mml:mi>l</mml:mi><mml:mtext>&#x2009;</mml:mtext><mml:mi>o</mml:mi><mml:mi>t</mml:mi><mml:mi>h</mml:mi><mml:mi>e</mml:mi><mml:mi>r</mml:mi><mml:mi>s</mml:mi><mml:mo>&#x2009;</mml:mo><mml:mtext>&#x2009;</mml:mtext><mml:mi>c</mml:mi><mml:mi>o</mml:mi><mml:mi>n</mml:mi><mml:mi>s</mml:mi><mml:mi>t</mml:mi><mml:mi>a</mml:mi><mml:mi>n</mml:mi><mml:mi>t</mml:mi></mml:mrow></mml:msub></mml:mrow><mml:mo>)</mml:mo></mml:mrow><mml:mo>&#x2212;</mml:mo><mml:mi>C</mml:mi><mml:mi>H</mml:mi><mml:msub><mml:mi>L</mml:mi><mml:mrow><mml:mi>R</mml:mi><mml:mi>F</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:math></disp-formula>
<disp-formula>
<label>(4)</label><mml:math id="M4" display="block"><mml:mrow><mml:mi>C</mml:mi><mml:mi>H</mml:mi><mml:msub><mml:mi>L</mml:mi><mml:mrow><mml:mi>L</mml:mi><mml:mi>A</mml:mi><mml:mi>O</mml:mi><mml:mi>D</mml:mi></mml:mrow></mml:msub><mml:mo>=</mml:mo><mml:mrow><mml:mo>(</mml:mo><mml:mrow><mml:mi>A</mml:mi><mml:mi>O</mml:mi><mml:mi>D</mml:mi><mml:mo>+</mml:mo><mml:mn>2</mml:mn><mml:mi>&#x3c3;</mml:mi><mml:msub><mml:mo>|</mml:mo><mml:mrow><mml:mi>a</mml:mi><mml:mi>l</mml:mi><mml:mi>l</mml:mi><mml:mtext>&#x2009;</mml:mtext><mml:mi>o</mml:mi><mml:mi>t</mml:mi><mml:mi>h</mml:mi><mml:mi>e</mml:mi><mml:mi>r</mml:mi><mml:mi>s</mml:mi><mml:mo>&#x2009;</mml:mo><mml:mtext>&#x2009;</mml:mtext><mml:mi>c</mml:mi><mml:mi>o</mml:mi><mml:mi>n</mml:mi><mml:mi>s</mml:mi><mml:mi>t</mml:mi><mml:mi>a</mml:mi><mml:mi>n</mml:mi><mml:mi>t</mml:mi></mml:mrow></mml:msub></mml:mrow><mml:mo>)</mml:mo></mml:mrow><mml:mo>&#x2212;</mml:mo><mml:mi>C</mml:mi><mml:mi>H</mml:mi><mml:msub><mml:mi>L</mml:mi><mml:mrow><mml:mi>R</mml:mi><mml:mi>F</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:math></disp-formula>
<p>The CHL<sub>HAOD</sub> increased by approximately 95% in AOD and showed an increased CHL in most areas when compared with the existing CHL<sub>RF</sub> (<xref ref-type="fig" rid="f5"><bold>Figures&#xa0;5A&#x2013;C</bold></xref>). When aerosols were artificially increased during the COVID-19 lockdown period (in March 2020), phytoplankton biomass increased rapidly in most regions compared with the biomass values from other years (<xref ref-type="fig" rid="f5"><bold>Figure&#xa0;5B</bold></xref>). In particular, although differences occur depending on the region, CHL<sub>RF</sub> increased by about 60% or more on average in 2019, 2020, and 2021. Based on this result, if the AOD had additional supplies, it could have generated intense spring blooms in March 2020. The CHL<sub>LAOD</sub> decreased by approximately 95% in AOD and also exhibited a decreased CHL in most areas when compared with CHL<sub>RF</sub> (<xref ref-type="fig" rid="f5"><bold>Figures&#xa0;5D&#x2013;F</bold></xref>). Furthermore, <xref ref-type="fig" rid="f5"><bold>Figures&#xa0;5D, 5F</bold></xref> show that the region had significantly lower CHL when the AOD was decreased by approximately 95%. However, the CHL<sub>LAOD</sub> in 2020 did not represent a significant decrease in most areas when compared to CHL<sub>RF</sub> because the AOD in March 2020 was already reduced by approximately 50% (0.50 to 0.26) (<xref ref-type="fig" rid="f5"><bold>Figure&#xa0;5E</bold></xref>). This result indicates that the effect of AOD on CHL during the COVID-19 lockdown period was analogous to that of CHL<sub>LAOD</sub>. This also proves that the experimental results suitably simulated the CHL response to the actual change in the aerosols in the environment.</p>
<fig id="f5" position="float">
<label>Figure&#xa0;5</label>
<caption>
<p>Result of <italic>CHL<sub>RF</sub></italic> according to changes in AOD. The upper panels <bold>(A&#x2013;C)</bold> represent the result of <italic>CHL<sub>RF</sub></italic> when AOD is increased by two sigma (2&#x3c3;, increasing about 95%) and the lower panels <bold>(D&#x2013;F)</bold> show when AOD is reduced by two sigma (2&#x3c3;,increasing about 95%) for a given year.</p>
</caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fmars-09-911819-g005.tif"/>
</fig>
<p>Therefore, in Section 3.3, we presented the experimental results for predicting CHL changes according to real environmental conditions through CHL reactions, based on artificial AOD fluctuations. These results suggest that AOD (i.e., atmospheric aerosol deposition) significantly affects spring blooms in the CYS.</p>
</sec>
<sec id="s3_4">
<title>3.4. PD Analysis for the Six Predictors</title>
<p>In Sections 3.2 and 3.3, we calculated the relative contribution of each factor to spring blooms. Relative contribution refers to the relative value that each factor can influence when various physical factors affect the CHL in combination. However, in Section 3.4, the quantitative contribution was considered as the absolute impact of each variable on CHL individually. This means that the relative contribution and quantitative contribution are different. Therefore, in this section we evaluated the quantitative contribution of each factor&#x2019;s absolute effect, including AOD, on spring blooms using a PD plot. The contribution of predictors to fluctuating CHL was expressed as the CHL<sub>&lt;predictor&gt;</sub>. The predictors included AOD (CHL<sub>AOD</sub>), SST (CHL<sub>SST</sub>), MLD (CHL<sub>MLD</sub>), TP (CHL<sub>TP</sub>), and CHL<sub>c</sub> (CHLCHL<sub>c</sub>). To quantitatively reveal the fluctuation of CHL according to the increase or decrease in AOD, we fixed the values of other predictors, except for AOD, during the entire period (i.e., an average of variables for March 2003 to 2021), as shown in Eq. (2). The fluctuating CHL according to the change in AOD was then determined using Eq. (1). For other predictors (e.g., SST, MLD, WD, TP, and CHL<sub>c</sub>), the fluctuating CHL was simulated using a method similar to that of AOD.</p>
<p><xref ref-type="fig" rid="f6"><bold>Figure&#xa0;6</bold></xref> shows the estimated CHL<sub>RF</sub> through the PD plots. This analysis can explain the fluctuating CHL<sub>RF</sub> responses to each variable. When AOD increased from 0 to 1, CHL<sub>AOD</sub> increased from 1.31 mg m<sup>-3</sup> to 1.76 mg m<sup>-3</sup> (<xref ref-type="fig" rid="f6"><bold>Figure&#xa0;6A</bold></xref>). When AOD was less than approximately 0.3, CHL<sub>AOD</sub> slowly increased. However, the peak value of CHL<sub>AOD</sub> appeared at 0.3 and the CHL fluctuation for AOD was approximately 1.40 mg m<sup>-3</sup>. Hence, a low AOD during the COVID-19 lockdown period induced a slight variation in CHL<sub>AOD</sub>. Therefore, through the PD plot for AOD, AOD reduction was presumed to cause weaker spring blooms in March 2020 than in other years. As a result, the AOD during the COVID-19 lockdown period (March 2020) recorded an abnormally low CHL (Section 3.1 and <xref ref-type="fig" rid="f2"><bold>Figure&#xa0;2</bold></xref>). CHL<sub>SST</sub> increased from 1.35 mg m<sup>-3</sup> to 2.20 mg m<sup>-3</sup> when SST changed from 5&#xb0;C to 11&#xb0;C (<xref ref-type="fig" rid="f6"><bold>Figure&#xa0;6B</bold></xref>). From approximately 7&#xb0;C to 8.5&#xb0;C , where SST was low, phytoplankton grew slowly and even decreased in abundance (<xref ref-type="bibr" rid="B70">Xuan et al., 2011</xref>). However, SST gradually increased and reached 8&#xb0;C to 12&#xb0;C (the average SST in the CYS ranges from 8&#xb0;C to 10&#xb0;C ), showing a spring bloom peak (<xref ref-type="bibr" rid="B44">Lu et al., 2021</xref>). Moreover, the changing CHL pattern influenced by SST matched the generated spring bloom pattern conditions in the CYS (<xref ref-type="bibr" rid="B71">Xu et al., 2013</xref>; <xref ref-type="bibr" rid="B79">Zhao et al., 2019</xref>).</p>
<fig id="f6" position="float">
<label>Figure&#xa0;6</label>
<caption>
<p>Partial dependence (PD) plots of the CHL for all predictors including AOD, SST, MLD, WD, TP, and <italic>CHL<sub>C</sub></italic>. The blue dotted lines show PD plots and red dashed lines represent the empirical polynomial regression.</p>
</caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fmars-09-911819-g006.tif"/>
</fig>
<p>When MLD changed from 15&#xa0;m to 85&#xa0;m, CHL<sub>MLD</sub> changed slightly from 1.57 mg m<sup>-3</sup> to 1.74 mg m<sup>-3</sup> (<xref ref-type="fig" rid="f6"><bold>Figure&#xa0;6C</bold></xref>), thereby reflecting the mean MLD (~ 60&#xa0;m) in the CYS. Furthermore, the CHL<sub>MLD</sub> increased with MLD depth. In the CYS, nutrients that affect phytoplankton growth accumulate in the bottom water during autumn and winter. The accumulated nutrients are then moved from the lower layer to the upper layer by vertical mixing in the spring (<xref ref-type="bibr" rid="B29">Kim et al., 2000</xref>). Additionally, the YS is affected by anthropogenic aerosols in the atmosphere (<xref ref-type="bibr" rid="B39">Lin et al., 2005</xref>; <xref ref-type="bibr" rid="B69">Wei et al., 2015</xref>). However, comparing <xref ref-type="fig" rid="f6"><bold>Figures&#xa0;6A, C</bold></xref>, the rate of increase in CHL by MLD was relatively weaker than that in the case of AOD. This result is supported by the data in <xref ref-type="fig" rid="f2"><bold>Figure&#xa0;2</bold></xref>. Both 2020 and 2021 showed a trend of shallower MLD than the average; however, CHL showed the opposite trend (Section 3.2 and <xref ref-type="fig" rid="f2"><bold>Figure&#xa0;2</bold></xref>) and AOD showed the same variability as CHL during the same period. Consequently, we could indirectly estimate that CHL was changed by AOD (<xref ref-type="fig" rid="f2"><bold>Figures&#xa0;2A, F</bold></xref>). These results are consistent with those of previous studies. According to <xref ref-type="bibr" rid="B48">Moon et al. (2021)</xref>, since 2010, the YS has been significantly affected by anthropogenic nitrogen deposition in the atmosphere. Further, <xref ref-type="bibr" rid="B73">Yoon et al. (2021)</xref> noted that most of the new nitrogen input in the YS was caused by atmospheric nitrogen deposition. Therefore, we found that the fluctuation in CHL was more affected by AOD than by MLD.</p>
<p>When WD ranged from &#x2212; 1.09 &#xd7; 10<sup>-5</sup> sec<sup>-1</sup> to 4.53 &#xd7; 10<sup>-6</sup> sec<sup>-1</sup>, CHL<sub>WD</sub> fluctuated from 1.53 mg m<sup>-3</sup> to 1.68 mg m<sup>-3</sup> (<xref ref-type="fig" rid="f6"><bold>Figure&#xa0;6D</bold></xref>). Negative divergence refers to the WD flow from the sea surface to the atmosphere. If the WD flow from the sea surface to the atmosphere decreases, WD flow from the atmosphere to the ocean (positive divergence) increases. As WD increased, CHL<sub>WD</sub> decreased and then gradually increased (<xref ref-type="fig" rid="f6"><bold>Figure&#xa0;6D</bold></xref>). The WD for March 2020 showed negative divergence. In addition, it revealed partially restricted industrial activities owing to the COVID-19 lockdown policy and showed that anthropogenic aerosol emissions decreased. As a result, the WD flow from the atmosphere to the sea surface weakened and the amount of aerosols deposited on the sea surface was quickly reduced. Conversely, in 2021, the flow from the atmosphere to the sea surface increased, which could have added abundant amounts of aerosols to the ocean. This process may act as a factor limiting the occurrence of spring blooms, thereby supporting the hypothesis that reducing AOD caused a decline in phytoplankton biomass. When TP increased from 0 mm to 0.15 mm, CHL<sub>TP</sub> decreased from 2.42 mg m<sup>-3</sup> to 1.28 mg m<sup>-3</sup> (<xref ref-type="fig" rid="f6"><bold>Figure&#xa0;6E</bold></xref>). These results suggest that phytoplankton growth decreased with precipitation. Furthermore, according to previous studies, phytoplankton growth is indirectly estimated to be limited due to the toxic effects of metal components, such as Cu and Pb, in precipitation (<xref ref-type="bibr" rid="B41">Liu et al., 2013</xref>). When CHL<sub>c</sub> increased from 1.29 mg m<sup>-3</sup> to 3.55 mg m<sup>-3</sup>, CHLCHL<sub>C</sub> increased from 1.24 mg m<sup>-3</sup> to 4.07 mg m<sup>-3</sup> (<xref ref-type="fig" rid="f6"><bold>Figure&#xa0;6F</bold></xref>). Because CHL<sub>c</sub> represents the climatology of CHL in the CYS, CHLCHL<sub>C</sub> increased with increasing CHL<sub>c</sub>.</p>
</sec>
<sec id="s3_5">
<title>3.5. Quantitative Contribution of Aerosol to CHL</title>
<p>Based on the results of the quantitative contributions in Section 3.4, we created an equation that can express the CHL fluctuation for each predictor. Thus, this equation can estimate the amount of CHL fluctuation exhibiting different responses to each factor by summing the amount of change by the deviation of each factor in a year. Section 3.5 reveals the quantitative contribution of each predictor to CHL under natural conditions. The resulting equations are as follows:</p>
<disp-formula>
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<disp-formula>
<label>(6)</label><mml:math id="M6" display="block"><mml:mrow><mml:msub><mml:mi>&#x3b1;</mml:mi><mml:mi>n</mml:mi></mml:msub><mml:mo>=</mml:mo><mml:mfrac><mml:mn>1</mml:mn><mml:mrow><mml:mi>C</mml:mi><mml:mi>H</mml:mi><mml:msub><mml:mi>L</mml:mi><mml:mi>c</mml:mi></mml:msub></mml:mrow></mml:mfrac><mml:mfrac><mml:mrow><mml:mo>&#x25b3;</mml:mo><mml:mi>C</mml:mi><mml:mi>H</mml:mi><mml:msub><mml:mi>L</mml:mi><mml:mrow><mml:mi>P</mml:mi><mml:mi>r</mml:mi><mml:mi>e</mml:mi><mml:mi>d</mml:mi><mml:mi>i</mml:mi><mml:mi>c</mml:mi><mml:mi>t</mml:mi><mml:mi>o</mml:mi><mml:msub><mml:mi>r</mml:mi><mml:mi>n</mml:mi></mml:msub></mml:mrow></mml:msub></mml:mrow><mml:mrow><mml:mo>&#x25b3;</mml:mo><mml:mi>P</mml:mi><mml:mi>r</mml:mi><mml:mi>e</mml:mi><mml:mi>d</mml:mi><mml:mi>i</mml:mi><mml:mi>c</mml:mi><mml:mi>t</mml:mi><mml:mi>o</mml:mi><mml:msub><mml:mi>r</mml:mi><mml:mi>n</mml:mi></mml:msub></mml:mrow></mml:mfrac><mml:msub><mml:mo>|</mml:mo><mml:mrow><mml:mi>a</mml:mi><mml:mi>l</mml:mi><mml:mi>l</mml:mi><mml:mi>o</mml:mi><mml:mi>t</mml:mi><mml:mi>h</mml:mi><mml:mi>e</mml:mi><mml:mi>r</mml:mi><mml:mi>s</mml:mi><mml:mtext>&#x2009;</mml:mtext><mml:mi>c</mml:mi><mml:mi>o</mml:mi><mml:mi>n</mml:mi><mml:mi>s</mml:mi><mml:mi>t</mml:mi><mml:mi>a</mml:mi><mml:mi>n</mml:mi><mml:mi>t</mml:mi></mml:mrow></mml:msub><mml:mo>,</mml:mo><mml:mi>n</mml:mi><mml:mo>=</mml:mo><mml:mn>1</mml:mn><mml:mo>,</mml:mo><mml:mn>2</mml:mn><mml:mo>,</mml:mo><mml:mn>...6</mml:mn><mml:mo>,</mml:mo></mml:mrow></mml:math></disp-formula>
<p>where &#x3b1;<italic><sub>n</sub></italic> is the empirically determined regression coefficient for each predictor (<xref ref-type="fig" rid="f6"><bold>Figure&#xa0;6</bold></xref>; <xref ref-type="table" rid="T3"><bold>Table&#xa0;3</bold></xref>). Additionally, &#x394; CHL<sub>&lt;predictor&gt;</sub> (difference CHL<sub>&lt;predictor&gt;</sub>) represents the difference between <italic>x</italic> and <italic>x</italic>&#x2212;1 , where <italic>x</italic> represents each year of the study periods 2021, 2020, 2019, &#x2026; and 2004. Hence, &#x394; CHL<sub>&lt;predictor&gt;</sub> was calculated for each variable variation simulated in the PD plot. Subsequently, the fluctuation CHL was calculated by summing the values of each &#x394; CHL<sub>&lt;predictor&gt;</sub>.</p>
<table-wrap id="T3" position="float">
<label>Table&#xa0;3</label>
<caption><p>Coefficient of the empirical polynomial regression for each predictor.</p></caption>
<table frame="hsides">
<thead>
<tr>
<th valign="top" align="left" rowspan="2">Predictor</th>
<th valign="top" align="center" colspan="2">Empirical polynomial coefficient (2a + b)</th>
</tr>
<tr>
<th valign="top" align="center"><italic>a</italic></th>
<th valign="top" align="center"><italic>b</italic></th>
</tr>
</thead>
<tbody>
<tr>
<td valign="top" align="left"><bold>AOD</bold></td>
<td valign="top" align="left">-0.9283</td>
<td valign="top" align="left">1.3340</td>
</tr>
<tr>
<td valign="top" align="left"><bold>SST</bold></td>
<td valign="top" align="left">0.0756</td>
<td valign="top" align="left">-1.2849</td>
</tr>
<tr>
<td valign="top" align="left"><bold>MLD</bold></td>
<td valign="top" align="left">3.7738&#xd7;10<sup>-5</sup></td>
<td valign="top" align="left">-0.0014</td>
</tr>
<tr>
<td valign="top" align="left"><bold>WD</bold></td>
<td valign="top" align="left">4.3302&#xd7;10<sup>9</sup></td>
<td valign="top" align="left">2.9383&#xd7;10<sup>4</sup></td>
</tr>
<tr>
<td valign="top" align="left"><bold>TP</bold></td>
<td valign="top" align="left">3.1281&#xd7;10<sup>6</sup></td>
<td valign="top" align="left">-827.8749</td>
</tr>
<tr>
<td valign="top" align="left"><bold>CHL<sub>c</sub></bold></td>
<td valign="top" align="left">-0.5207</td>
<td valign="top" align="left">3.2518</td>
</tr>
</tbody>
</table>
</table-wrap>
<p>Although the PD plot in <xref ref-type="fig" rid="f6"><bold>Figure 6</bold></xref> explains the responsive function of each predictor to CHL changes, we cannot estimate specific contributions of each predictor in different years. Subsequently, the  &#x3b1;n (empirical regression coefficients, 2aX + b, X is predictor) was defined by calculating the first derivation based on the empirical polynomial regression. The first derivative can represent the effect of a predictor on CHL (e.g., positive or negative linear trends) (<xref ref-type="bibr" rid="B4">Boelkins et al., 2018</xref>). All regression coefficients are listed in <xref ref-type="table" rid="T3"><bold>Table 3</bold></xref>. We calculated the quantitative contribution of each predictor to CHL under natural conditions only in March 2020 (during the COVID-19 lockdown period). The &#x3b1;<italic><sub>n</sub></italic> for each selected predictor was applied to Eq. (5). According to the variation in each predictor, the CHL variability was then calculated (<xref ref-type="table" rid="T3"><bold>Table&#xa0;3</bold></xref>). The difference in CHL with the variational predictor (&#x394; CHL<sub>&lt;predictor&gt;</sub>) was calculated as the difference between the COVID-19 lockdown period and the average from March 2003 to 2021 (climatology). &#x394; CHL<sub>AOD</sub> is the difference in CHL<sub>AOD</sub>, which indicates the change between the COVID-19 lockdown period and climatology after fixing the variable conditions, except AOD, as in Section 3.4. The other variables were calculated using the same process. Using the &#x3b1;<italic><sub>n</sub></italic> based on Eq. (5), &#x394; CHL<sub>&lt;predictor&gt;</sub> was quantitatively calculated for each predictor. <xref ref-type="fig" rid="f7"><bold>Figure&#xa0;7</bold></xref> shows the effects of each variable on &#x394; CHL<sub>&lt;predictor&gt;</sub> when it decreased by at least 90% and increased by 90% at most, compared to the climatology. The variation range for the predictor is the resulting value for all conditions in which each factor may change, including the COVID-19 lockdown period. Furthermore, <xref ref-type="fig" rid="f7"><bold>Figure&#xa0;7</bold></xref> shows the individual effect of the absolute contribution of each parameter to the CHL. As a result, &#x394; CHL<sub>AOD</sub> decreased by 0.20 mg m<sup>-3</sup> due to an AOD less than that of the climatology. However, &#x394; CHL<sub>SST</sub> increased by 0.22 mg m<sup>-3</sup> because SST was warmer than that measured in the same period in other years (<xref ref-type="fig" rid="f7"><bold>Figure&#xa0;7</bold></xref>). Moreover, MLD became more shallow than that of the climatology, reducing &#x394; CHL<sub>MLD</sub> by 0.01 mg m<sup>-3</sup>. Additionally, the negative WD yielded a stable &#x394; CHL<sub>WD</sub>, but less TP increased &#x394; CHL<sub>TP</sub> by 0.02 mg m<sup>-3</sup>. Similary, we estimated &#x394; CHLAOD in 2019 and 2021 using the linear model of the RF in <xref ref-type="fig" rid="f7"><bold>Figure 7</bold></xref>, showing as much as -0.05 mg m<sup>-3</sup> and + 0.13 mg m<sup>-3</sup>, respectively. However, &#x394; CHLSST increased by 0.07 mg m<sup>-3</sup> and 0.18 mg m<sup>-3</sup> in 2019 and 2021, respectively. Thus, the linear model allows us to estimate the CHL chages due to the various predictors</p>
<fig id="f7" position="float">
<label>Figure&#xa0;7</label>
<caption>
<p>Empirical variation coefficient of each predictor with the climatology of each variable from March 2003 to 2021. Red and black lines indicate the difference for CHL along variational AOD (&#x394;<italic>CHL<sub>AOD</sub></italic>) and SST (&#x394;<italic>CHL<sub>SST</sub></italic>), respectively. Blue, gray, and purple lines represent the &#x394;<italic>CHL<sub>MLD</sub></italic>, &#x394;<italic>CHL<sub>WD</sub></italic>, and &#x394;<italic>CHL<sub>TP</sub></italic>, respectively. Square boxes defined CHL according to the conditions of each predictor in the COVID-19 lockdown period. The green line and gray dot show CHL&#x2019;s zero and climatology condition for &#x394;<italic>CHL<sub>each predictor</sub></italic>, respectively.</p>
</caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fmars-09-911819-g007.tif"/>
</fig>
<p>From analyzing the individual effects of each factor, it was determined that the decreased AOD and shallower MLD, compared to those of climatology, affected the CHL reduction. Among them, the leading cause of the decreasing spring blooms during the COVID-19 lockdown period was the sharply reduced AOD from the shutdown policy in China. In addition, it was found that the increased SST and decreased TP effect on the increasing CHL. As a consequence, AOD and MLD were the causes that led to the decrease in CHL and, among them, the effect of AOD reduction was approximately 10 times greater than that of the shallower MLD. In addition, the quantitative (absolute) contribution of the individual factors to CHL, shown in <xref ref-type="fig" rid="f7"><bold>Figure&#xa0;7</bold></xref>, was largest in SST, followed by those in AOD, MLD, TP, and WD. For comparison, they are listed in absolute value order without mathematical symbols. This differs from the relative contributions presented in Section 3.2, suggesting that the strength of spring blooms in the YS can be controlled mainly by SST and AOD. In addition to the relationship already revealed in <xref ref-type="fig" rid="f7"><bold>Figure&#xa0;7</bold></xref>, the final results of this study, which is the quantitative relationship between CHL and each factor, which was limited in previous studies, are presented together.</p>
<p>Accordingly, we determined a causal relationship between AOD and CHL through time series analysis for each factor to investigate the cause of spring blooms that were weakened during the COVID-19 lockdown period. In addition, intense spring blooms were induced when additional AOD was supplied in March 2020 using the RF model. Finally, as a result of estimating the quantitative contribution of each factor to CHL, it was observed that the decrease in aerosols led to a decline in CHL. Overall, the weakened spring blooms during the COVID-19 lockdown period could have resulted from complex factors instigated by the temporary closure of industrial activities.</p>
</sec>
</sec>
<sec id="s4">
<title>4 Conclusions</title>
<p>The quantitative evaluation using the RF-based model and PD results was applied to understand the decrease of CHL in the CYS, which was mainly due to the reduction in aerosol during the COVID-19 lockdown period. Consequently, the following specific results were obtained:</p>
<p>1. We identified the aerosol effect on CHL by checking the spatial distribution of CHL, according to AOD &#xb1;&#xa0;2&#x3c3; , through the established RF model. In particular, as AOD decreased by about 95%, CHL also reduced by about 50% or more through sensitivity experiments. This result proves that decreased anthropogenic aerosol emissions due to the COVID-19 lockdown policy decreased spring blooms in the CYS. Therefore, aerosol must be considered essential to increasing spring blooms in the CYS (Section 3.3).</p>
<p>2. We performed the quantitative analysis in CHL according to the adjustment for each predictor using a PD plot and empirical polynomial regression analysis. These methods evaluated the quantitative effect of predictors affecting CHL reduction during the COVID-19 lockdown period in 2020. The CHL was affected by AOD (&#x2212; 0.20 mg m<sup>-3</sup>), MLD (&#x2212; 0.01 mg m<sup>-3</sup>), WD (&#xb1; 0.00 mg m<sup>-3</sup>), TP (+ 0.02 mg m<sup>-3</sup>), and SST (+ 0.22 mg m<sup>-3</sup>); among them, AOD had the predominant reduction effect (Section 3.5).</p>
<p>3. There, we elicited an abnormally low CHL during the COVID-19 lockdown period, affected by AOD, based on sensitivity tests for the RF model and various analysis methods. These results suggest that the effect of each factor, especially AOD, that affected the COVID-19 lockdown period could be quantitatively evaluated.</p>
<p>The limitations of this study are as follows: (1) Regarding aerosol sinking into the sea, <xref ref-type="bibr" rid="B41">Liu et al. (2013)</xref> showed the extent to which aerosols (including Asian dust) could indirectly induce CHL blooms in the YS. Furthermore, although the Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observation can provide aerosol subtype data, it cannot provide the amount of aerosol entering the ocean (e.g., <xref ref-type="bibr" rid="B64">Tan and Wang, 2014</xref>; <xref ref-type="bibr" rid="B72">Yoon et al., 2019</xref>; <xref ref-type="bibr" rid="B73">Yoon et al., 2021</xref>). Thus, we could not quantitatively estimate the amount of aerosol (anthropogenic aerosol) absorbed into the sea surface in the current analysis. (2) Regarding nutrient loads, AOD contains anthropogenic nitrogen (NO<sub>x</sub> and NH<sub>y</sub>) and minerals such as iron (Fe). Aerosols containing Fe (i.e., Asian dust) are also a significant factor that can cause spring blooms in the CYS (<xref ref-type="bibr" rid="B58">Shi et al., 2012</xref>; Yoo et al., 2018; <xref ref-type="bibr" rid="B72">Yoon et al., 2019</xref>). Thus, spring blooms can be accelerated by the nitrogen (excluding anthropogenic nitrogen) supplied by nearby rivers. Since there were no nutrient observations during the COVID-19 lockdown period in YS, the central area of the YS was selected as the study area to avoid the effects of nitrogen from the surrounding river. Additionally, we confirmed that Asian dust did not occur during that period, nor was any additionally supplied Fe (Section 2.2.1). Thus, further research may be needed to measure directly how much aerosol sinks into the sea and nutrient load through ocean currents from coastal regions.</p>
</sec>
<sec id="s5" sec-type="data-availability">
<title>Data Availability Statement</title>
<p>The original contributions presented in the study are included in the article/supplementary material. Further inquiries can be directed to the corresponding author.</p>
</sec>
<sec id="s6" sec-type="author-contributions">
<title>Author Contributions</title>
<p>Conceptualization: J-YB, JP, and Y-HJ. Data curation: J-YB, J-YL, and S-JL. Methodology: J-YB, JP, and Y-HJ. Formal analysis: J-YB, JP, D-WK, J-SL, and Y-HJ. Writing-original draft: J-YB. Writing&#x2014;review and editing: J-YB, JP, and Y-HJ. All authors have read and agreed to the published version of the manuscript.</p>
</sec>
<sec id="s7" sec-type="funding-information">
<title>Funding</title>
<p>This study was supported by a grant from the National Research Foundation of Korea (NRF) funded by the Korean government (MSIP) (NRF-2018R1A2B2006555). In addition, this research was part of the project &#x201c;Integrated management of marine environment and ecosystems around Saemangeum,&#x201d; funded by the Ministry of Oceans and Fisheries, Korea (grant number 20140257).</p>
</sec>
<sec id="s8" sec-type="COI-statement">
<title>Conflict of Interest</title>
<p>The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p>
</sec>
<sec id="s9" sec-type="disclaimer">
<title>Publisher&#x2019;s Note</title>
<p>All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

</p>
</sec>
</body>
<back>
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