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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Earth Sci.</journal-id>
<journal-title>Frontiers in Earth Science</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Earth Sci.</abbrev-journal-title>
<issn pub-type="epub">2296-6463</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="publisher-id">609058</article-id>
<article-id pub-id-type="doi">10.3389/feart.2020.609058</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Earth Science</subject>
<subj-group>
<subject>Original Research</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Classification of a Complexly Mixed Magnetic Mineral Assemblage in Pacific Ocean Surface Sediment by Electron Microscopy and Supervised Magnetic Unmixing</article-title>
<alt-title alt-title-type="left-running-head">Li et al.</alt-title>
<alt-title alt-title-type="right-running-head">Identification of Magnetic Minerals</alt-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Li</surname>
<given-names>Jinhua</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
<xref ref-type="aff" rid="aff4">
<sup>4</sup>
</xref>
<xref ref-type="corresp" rid="c001">&#x2a;</xref>
<uri xlink:href="http://loop.frontiersin.org/people/118398/overview"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Liu</surname>
<given-names>Yan</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
<xref ref-type="aff" rid="aff4">
<sup>4</sup>
</xref>
<uri xlink:href="http://loop.frontiersin.org/people/1094425/overview"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Liu</surname>
<given-names>Shuangchi</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff4">
<sup>4</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Roberts</surname>
<given-names>Andrew Philip</given-names>
</name>
<xref ref-type="aff" rid="aff5">
<sup>5</sup>
</xref>
<uri xlink:href="http://loop.frontiersin.org/people/116809/overview"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Pan</surname>
<given-names>Hongmiao</given-names>
</name>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
<xref ref-type="aff" rid="aff6">
<sup>6</sup>
</xref>
<uri xlink:href="http://loop.frontiersin.org/people600685/overview"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Xiao</surname>
<given-names>Tian</given-names>
</name>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
<xref ref-type="aff" rid="aff6">
<sup>6</sup>
</xref>
<uri xlink:href="http://loop.frontiersin.org/people/749094/overview"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Pan</surname>
<given-names>Yongxin</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
<xref ref-type="aff" rid="aff4">
<sup>4</sup>
</xref>
<uri xlink:href="http://loop.frontiersin.org/people/73631/overview"/>
</contrib>
</contrib-group>
<aff id="aff1">
<label>
<sup>1</sup>
</label>Key Laboratory of Earth and Planetary Physics, Institute of Geology and Geophysics, Innovation Academy for Earth Sciences, Chinese Academy of Sciences, <addr-line>Beijing</addr-line>, <country>China</country>
</aff>
<aff id="aff2">
<label>
<sup>2</sup>
</label>Laboratory for Marine Geology, Qingdao National Laboratory for Marine Science and Technology, <addr-line>Qingdao</addr-line>, <country>China</country>
</aff>
<aff id="aff3">
<label>
<sup>3</sup>
</label>International Associated Laboratory of Evolution and Development of Magnetotactic Multicellular Organisms (LIA-MagMC), CNRS-CAS, <addr-line>Beijing</addr-line>, <country>China</country>
</aff>
<aff id="aff4">
<label>
<sup>4</sup>
</label>College of Earth and Planetary Sciences, University of Chinese Academy of Sciences, <addr-line>Beijing</addr-line>, <country>China</country>
</aff>
<aff id="aff5">
<label>
<sup>5</sup>
</label>Research School of Earth Sciences, Australian National University, <addr-line>Canberra</addr-line>, <addr-line>ACT</addr-line>, <country>Australia</country>
</aff>
<aff id="aff6">
<label>
<sup>6</sup>
</label>Key Laboratory of Marine Ecology and Environmental Sciences, Institute of Oceanology, Chinese Academy of Sciences, <addr-line>Qingdao</addr-line>, <country>China</country>
</aff>
<author-notes>
<fn fn-type="edited-by">
<p>
<bold>Edited by:</bold> <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/217283/overview">Ricardo IF Trindade</ext-link>, University of S&#xe3;o Paulo, Brazil</p>
</fn>
<fn fn-type="edited-by">
<p>
<bold>Reviewed by:</bold> <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/405876/overview">Gary Dean Acton</ext-link>, Texas A&#x26;M University, United States</p>
<p>
<ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/201906/overview">Luis Manuel Alva Valdivia</ext-link>, National Autonomous University of Mexico, Mexico</p>
</fn>
<corresp id="c001">&#x2a;Correspondence: Jinhua Li, <email>lijinhua@mail.iggcas.ac.cn</email>
</corresp>
<fn fn-type="other">
<p>This article was submitted to Geomagnetism and Paleomagnetism, a section of the journal Frontiers in Earth Science</p>
</fn>
</author-notes>
<pub-date pub-type="epub">
<day>22</day>
<month>12</month>
<year>2020</year>
</pub-date>
<pub-date pub-type="collection">
<year>2020</year>
</pub-date>
<volume>8</volume>
<elocation-id>609058</elocation-id>
<history>
<date date-type="received">
<day>22</day>
<month>09</month>
<year>2020</year>
</date>
<date date-type="accepted">
<day>23</day>
<month>11</month>
<year>2020</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#x00A9; 2020 Li, Liu, Liu, Roberts, Pan, Xiao and Pan</copyright-statement>
<copyright-holder>Li, Liu, Liu, Roberts, PAN, XIAO and Pan</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>Unambiguous magnetic mineral identification in sediments is a prerequisite for reconstructing paleomagnetic and paleoenvironmental information from environmental magnetic parameters. We studied a deep-sea surface sediment sample from the Clarion Fracture Zone region, central Pacific Ocean, by combining magnetic measurements and scanning and transmission electron microscopic analyses. Eight titanomagnetite and magnetite particle types are recognized based on comprehensive documentation of crystal morphology, size, spatial arrangements, and compositions, which are indicative of their corresponding origins. Type-1 particles are detrital titanomagnetites with micron- and submicron sizes and irregular and angular shapes. Type-2 and -3 particles are well-defined octahedral titanomagnetites with submicron and nanometer sizes, respectively, which are likely related to local hydrothermal and volcanic activity. Type-4 particles are nanometer-sized titanomagnetites hosted within silicates, while type-5 particles are typical dendrite-like titanomagnetites that likely resulted from exsolution within host silicates. Type-6 particles are single domain magnetite magnetofossils related to local magnetotactic bacterial activity. Type-7 particles are superparamagnetic magnetite aggregates, while Type-8 particles are defect-rich single crystals composed of many small regions. Electron microscopy and supervised magnetic unmixing reveal that type-1 to -5 titanomagnetite and magnetite particles are the dominant magnetic minerals. In contrast, the magnetic contribution of magnetite magnetofossils appears to be small. Our work demonstrates that incorporating electron microscopic data removes much of the ambiguity associated with magnetic mineralogical interpretations in traditional rock magnetic measurements.</p>
</abstract>
<kwd-group>
<kwd>marine sediments</kwd>
<kwd>magnetic minerals</kwd>
<kwd>environmental magnetism</kwd>
<kwd>magnetic techniques</kwd>
<kwd>transmission electron microscopy</kwd>
<kwd>magnetofossils</kwd>
<kwd>titanomagnetite</kwd>
</kwd-group>
<counts>
<page-count count="0"/>
</counts>
</article-meta>
</front>
<body>
<sec id="s1">
<title>Introduction</title>
<p>Sedimentary sequences provide important geological records for understanding long-term variations of Earth&#x27;s magnetic field and paleoclimate (e.g., <xref ref-type="bibr" rid="B119">Valet and Meynadier, 1993</xref>; <xref ref-type="bibr" rid="B36">Guyodo and Valet, 1999</xref>; <xref ref-type="bibr" rid="B59">Kissel et al., 1999</xref>; <xref ref-type="bibr" rid="B27">Evans and Heller, 2001</xref>; <xref ref-type="bibr" rid="B28">Evans and Heller, 2003</xref>; <xref ref-type="bibr" rid="B130">Yamazaki, 2009</xref>; <xref ref-type="bibr" rid="B38">Hao et al., 2012</xref>; <xref ref-type="bibr" rid="B79">Liu et al., 2012</xref>; <xref ref-type="bibr" rid="B105">Roberts et al., 2013</xref>; <xref ref-type="bibr" rid="B60">Kissel et al., 2020</xref>; <xref ref-type="bibr" rid="B120">Valet et al., 2020</xref>). Magnetic mineral identification in sediments is fundamentally important for both paleomagnetic and environmental magnetic studies because the type, concentration, size and shape of magnetic minerals control their magnetic properties, including magnetic recording quality (e.g., <xref ref-type="bibr" rid="B17">Dunlop and &#xd6;zdemir, 1997</xref>; <xref ref-type="bibr" rid="B14">Dekkers, 2003</xref>; <xref ref-type="bibr" rid="B79">Liu et al., 2012</xref>; <xref ref-type="bibr" rid="B5">Chang et al., 2014a</xref>; <xref ref-type="bibr" rid="B68">Larrasoa&#xf1;a et al., 2014</xref>; <xref ref-type="bibr" rid="B109">Roberts et al., 2019</xref>). However, quantitative identification of individual magnetic mineral components is challenging because each component can have different origins, grain size, shape, mineralogy and stoichiometry. For example, four or five distinct magnetic mineral components are identified commonly in pelagic carbonate sediments, which might otherwise be considered to be among the simplest of magnetic mineral assemblages (e.g., <xref ref-type="bibr" rid="B105">Roberts et al., 2013</xref>). Quantitative identification of each magnetic mineral component and its magnetic contribution can be important in environmental and paleomagnetic studies (e.g., <xref ref-type="bibr" rid="B90">Ouyang et al., 2014</xref>; <xref ref-type="bibr" rid="B11">Chen et al., 2017</xref>).</p>
<p>Numerous magnetic techniques have been developed to measure the bulk magnetic properties of sediments to provide information about the concentration, domain state (a measure of magnetic grain size), and mineralogy of magnetic particles in a sample (e.g., <xref ref-type="bibr" rid="B122">Verosub and Roberts, 1995</xref>; <xref ref-type="bibr" rid="B28">Evans and Heller, 2003</xref>; <xref ref-type="bibr" rid="B69">Lascu et al., 2010</xref>; <xref ref-type="bibr" rid="B79">Liu et al., 2012</xref>; <xref ref-type="bibr" rid="B106">Roberts et al., 2014</xref>; <xref ref-type="bibr" rid="B133">Zhao et al., 2017</xref>; <xref ref-type="bibr" rid="B109">Roberts et al., 2019</xref>). Mathematical unmixing methods have also been developed to identify these magnetic mineral components quantitatively based on their bulk magnetic properties (e.g., <xref ref-type="bibr" rid="B49">Heslop, 2015</xref>). They generally involve fitting of functions to derivatives of isothermal remanent magnetization (IRM) acquisition or direct current demagnetization (DCD) curves (e.g., <xref ref-type="bibr" rid="B111">Robertson and France, 1994</xref>; <xref ref-type="bibr" rid="B66">Kruiver et al., 2001</xref>; <xref ref-type="bibr" rid="B47">Heslop et al., 2002</xref>; <xref ref-type="bibr" rid="B22">Egli, 2003</xref>, <xref ref-type="bibr" rid="B23">Egli, 2004a</xref>; <xref ref-type="bibr" rid="B25">Egli, 2004c</xref>; <xref ref-type="bibr" rid="B44">Heslop and Dillon, 2007</xref>; <xref ref-type="bibr" rid="B83">Maxbauer et al., 2016</xref>), alternating field demagnetization curves of an anhysteretic remanent magnetization or IRM (<xref ref-type="bibr" rid="B20">Egli and Lowrie, 2002</xref>; <xref ref-type="bibr" rid="B23">Egli, 2004a</xref>, <xref ref-type="bibr" rid="B24">Egli, 2004b</xref>, <xref ref-type="bibr" rid="B25">Egli, 2004c</xref>), or analysis of hysteresis loops (e.g., <xref ref-type="bibr" rid="B100">Roberts et al., 1995</xref>; <xref ref-type="bibr" rid="B18">Dunlop, 2002a</xref>, <xref ref-type="bibr" rid="B19">Dunlop, 2002b</xref>; <xref ref-type="bibr" rid="B117">Tauxe et al., 2002</xref>; <xref ref-type="bibr" rid="B45">Heslop and Roberts, 2012a</xref>; <xref ref-type="bibr" rid="B46">Heslop and Roberts, 2012b</xref>), ferromagnetic resonance (FMR) spectra (e.g., <xref ref-type="bibr" rid="B125">Weiss et al., 2004</xref>; <xref ref-type="bibr" rid="B62">Kopp et al., 2006a</xref>; <xref ref-type="bibr" rid="B63">Kopp et al., 2006b</xref>; <xref ref-type="bibr" rid="B33">Gehring et al., 2011</xref>; <xref ref-type="bibr" rid="B57">Kind et al., 2011</xref>; <xref ref-type="bibr" rid="B34">Gehring et al., 2013</xref>; <xref ref-type="bibr" rid="B6">Chang et al., 2014b</xref>), or first-order reversal curve (FORC) diagrams (e.g., <xref ref-type="bibr" rid="B106">Roberts et al., 2014</xref>; <xref ref-type="bibr" rid="B70">Lascu et al., 2015</xref>; <xref ref-type="bibr" rid="B10">Channell et al., 2016</xref>; <xref ref-type="bibr" rid="B42">Harrison et al., 2018</xref>; <xref ref-type="bibr" rid="B108">Roberts et al., 2018</xref>).</p>
<p>Nonuniqueness is a fundamental issue for bulk magnetic property analysis because 1) mathematical unmixing can produce an infinite number of solutions, and 2) magnetic minerals have variable magnetic properties that can overlap with those of other minerals (e.g., <xref ref-type="bibr" rid="B79">Liu et al., 2012</xref>). The combined presence of multiple magnetic mineral components produces a complicated relationship between the magnetic properties of magnetic minerals and their domain states, concentration, sizes, shapes and stoichiometry, which often frustrates component-specific magnetic diagnosis (e.g., <xref ref-type="bibr" rid="B126">Yamazaki and Ioka, 1997</xref>; <xref ref-type="bibr" rid="B48">Heslop, 2009</xref>; <xref ref-type="bibr" rid="B102">Roberts et al., 2011a</xref>; <xref ref-type="bibr" rid="B74">Li et al., 2012</xref>; <xref ref-type="bibr" rid="B79">Liu et al., 2012</xref>; <xref ref-type="bibr" rid="B75">Li et al., 2013a</xref>; <xref ref-type="bibr" rid="B109">Roberts et al., 2019</xref>). To minimize ambiguity for environmental and paleomagnetic interpretations, integration of multiple magnetic parameters and non-magnetic techniques is recommended to identify and quantify magnetic minerals in sediments (e.g., <xref ref-type="bibr" rid="B61">Kopp and Kirschvink, 2008</xref>; <xref ref-type="bibr" rid="B79">Liu et al., 2012</xref>; <xref ref-type="bibr" rid="B6">Chang et al., 2014b</xref>; <xref ref-type="bibr" rid="B49">Heslop, 2015</xref>; <xref ref-type="bibr" rid="B109">Roberts et al., 2019</xref>).</p>
<p>Transmission electron microscope (TEM) observations are among the most useful microscopic approaches because they can be used to characterize simultaneously mineralogy, stoichiometry, magnetism and crystallography of magnetic minerals at the micron and nanometer scales, even to the atomic level (e.g., <xref ref-type="bibr" rid="B41">Harrison et al., 2002</xref>; <xref ref-type="bibr" rid="B31">Galindo-Gonzalez et al., 2009</xref>; <xref ref-type="bibr" rid="B97">P&#xf3;sfai et al., 2013</xref>; <xref ref-type="bibr" rid="B72">Li and Pan, 2015</xref>; <xref ref-type="bibr" rid="B78">Li et al., 2020</xref>). TEM and scanning electron microscope (SEM) observations have been used in environmental magnetism and paleomagnetism for many years (e.g., <xref ref-type="bibr" rid="B29">Evans and Wayman, 1970</xref>; <xref ref-type="bibr" rid="B58">Kirschvink and Chang, 1984</xref>; <xref ref-type="bibr" rid="B41">Harrison et al., 2002</xref>; <xref ref-type="bibr" rid="B99">Roberts and Weaver, 2005</xref>; <xref ref-type="bibr" rid="B61">Kopp and Kirschvink, 2008</xref>; <xref ref-type="bibr" rid="B40">Harrison and Feinberg, 2009</xref>). Most recent studies emphasize the use of TEM in testing for the presence of biogenic magnetite particles produced by magnetotactic bacteria (MTB) (magnetofossils) from sediments (e.g., <xref ref-type="bibr" rid="B93">Petersen et al., 1986</xref>; <xref ref-type="bibr" rid="B114">Stolz et al., 1986</xref>; <xref ref-type="bibr" rid="B2">Chang and Kirschvink, 1989</xref>; <xref ref-type="bibr" rid="B121">Vali and Kirschvink, 1989</xref>; <xref ref-type="bibr" rid="B1">Akai et al., 1991</xref>; <xref ref-type="bibr" rid="B50">Hesse, 1994</xref>; <xref ref-type="bibr" rid="B113">Snowball, 1994</xref>; <xref ref-type="bibr" rid="B115">Tarduno et al., 1998</xref>; <xref ref-type="bibr" rid="B127">Yamazaki and Kawahata, 1998</xref>; <xref ref-type="bibr" rid="B92">Pan et al., 2005</xref>; <xref ref-type="bibr" rid="B52">Housen and Moskowitz, 2006</xref>; <xref ref-type="bibr" rid="B64">Kopp et al., 2007</xref>; <xref ref-type="bibr" rid="B82">Maloof et al., 2007</xref>; <xref ref-type="bibr" rid="B61">Kopp and Kirschvink, 2008</xref>; <xref ref-type="bibr" rid="B112">Schumann et al., 2008</xref>; <xref ref-type="bibr" rid="B65">Kopp et al., 2009</xref>; <xref ref-type="bibr" rid="B103">Roberts et al., 2011b</xref>; <xref ref-type="bibr" rid="B3">Chang et al., 2012</xref>; <xref ref-type="bibr" rid="B67">Larrasoa&#xf1;a et al., 2012</xref>; <xref ref-type="bibr" rid="B128">Yamazaki and Shimono, 2013</xref>; <xref ref-type="bibr" rid="B5">Chang et al., 2014a</xref>; <xref ref-type="bibr" rid="B6">Chang et al., 2014b</xref>; <xref ref-type="bibr" rid="B80">Liu et al., 2015</xref>; <xref ref-type="bibr" rid="B7">Chang et al., 2016a</xref>; <xref ref-type="bibr" rid="B16">Dong et al., 2016</xref>; <xref ref-type="bibr" rid="B9">Chang et al., 2018</xref>; <xref ref-type="bibr" rid="B118">Usui et al., 2019</xref>; <xref ref-type="bibr" rid="B43">He and Pan, 2020</xref>; <xref ref-type="bibr" rid="B55">Jiang et al., 2020</xref>; <xref ref-type="bibr" rid="B98">Qian et al., 2020</xref>; <xref ref-type="bibr" rid="B129">Yamazaki et al., 2020</xref>; <xref ref-type="bibr" rid="B131">Yuan et al., 2020</xref>). In contrast, relatively few studies have used TEM observations to study the mineralogy and chemistry of other magnetic mineral types in sediments (e.g., <xref ref-type="bibr" rid="B35">Gibbs-Eggar et al., 1999</xref>; <xref ref-type="bibr" rid="B30">Franke et al., 2007</xref>; <xref ref-type="bibr" rid="B8">Chang et al., 2016b</xref>; <xref ref-type="bibr" rid="B132">Zhang et al., 2018</xref>; <xref ref-type="bibr" rid="B77">Li et al., 2019</xref>). While magnetofossils are relatively easy to recognize in TEM observations due to their distinctive crystal morphologies and chain structures compared to other magnetic mineral types (e.g., <xref ref-type="bibr" rid="B61">Kopp and Kirschvink, 2008</xref>; <xref ref-type="bibr" rid="B56">Jimenez-Lopez et al., 2010</xref>; <xref ref-type="bibr" rid="B76">Li et al., 2013b</xref>), this can lead to bias in overestimating their magnetic contributions, and/or to ignoring contributions from, for example, weakly interacting or noninteracting single domain (SD) magnetite particles hosted by silicates (e.g., <xref ref-type="bibr" rid="B124">Wang et al., 2015</xref>; <xref ref-type="bibr" rid="B8">Chang et al., 2016b</xref>).</p>
<p>We combine rock magnetic measurements with SEM and TEM observations to characterize the magnetic mineralogy of a surface sediment from the central Pacific Ocean. We show that by incorporating detailed SEM and TEM characterizations, much of the ambiguity that is inherent to magnetic mineralogy interpretations when using only rock magnetic measurements is eliminated. This approach allows evaluation of the contribution of magnetic mineral components to paleomagnetic and rock magnetic signals and/or their environmental significance.</p>
</sec>
<sec sec-type="materials|methods" id="s2">
<title>Materials and Methods</title>
<sec id="s2-1">
<title>Sample and Preparation</title>
<p>Surface sediment was retrieved at station XTGC1311 (158.0485,917 W, 14.44244 N; 5,260&#xa0;m water depth; <xref ref-type="fig" rid="F1">Figure 1</xref>) during cruise DY29&#x2013;02 of R/V <italic>Haiyang Liuhao</italic> in 2013 to the Pacific Ocean (<xref ref-type="bibr" rid="B16">Dong et al., 2016</xref>). The station is adjacent to the Clarion Fracture Zone to the south, the Hawaiian Island Chain to the North, and Kiribati (Line Islands) to the West. The surrounding islands were formed by upper Jurassic to lower Cretaceous volcanic activity (<xref ref-type="bibr" rid="B13">Clouard and Bonneville, 2005</xref>). The seafloor between the Clarion Fracture Zone and the Clipperton Fracture Zone is characterized by long, north-south-trending hills, ridges, intervening valleys, and furrows (<xref ref-type="bibr" rid="B123">Vithana et al., 2019</xref>; <xref ref-type="bibr" rid="B81">Maci&#x105;g and Harff, 2020</xref>). Sediments in the area are characterized by organic carbon-starved siliceous clay (<xref ref-type="bibr" rid="B84">Mewes et al., 2016</xref>). Modern sedimentation at the sampled station consists of both Asian eolian dust transported by zonal westerlies and northeast trade winds and local hydrothermal and volcanic inputs (<xref ref-type="bibr" rid="B53">Hyeong et al., 2005</xref>; <xref ref-type="bibr" rid="B54">Hyeong et al., 2006</xref>; <xref ref-type="bibr" rid="B81">Maci&#x105;g and Harff, 2020</xref>). It is also possibly influenced by Antarctic Bottom Water (AABW), which is oxygen rich and migrates eastward and northward into this area (<xref ref-type="bibr" rid="B15">Deng et al., 2016</xref>; <xref ref-type="bibr" rid="B84">Mewes et al., 2016</xref>).</p>
<fig id="F1" position="float">
<label>FIGURE 1</label>
<caption>
<p>Location map with the position of sample station.</p>
</caption>
<graphic xlink:href="feart-08-609058-g001.tif"/>
</fig>
<p>Sediment samples were collected using a gravity corer. Surface sediments were subsampled immediately on the ship from the upper 1&#xa0;cm of the core (hereafter referred to as EPMNP-31) and were then stored at &#x2212;20&#xb0;C prior to analysis to minimize oxidation. Samples were vacuum dried at 30&#xb0;C for 12&#xa0;h and were then loaded into non-magnetic gelatin capsules for magnetic measurements.</p>
<p>For nanometer scale characterization, magnetic minerals were separated from the bulk sediment. Magnetic separation was carried out with the following procedure. First, about &#x223c;10&#xa0;mg of sediment was suspended into &#x223c;50&#xa0;ml of Milli-Q water in a &#x223c;100&#xa0;ml beaker and was then mixed by ultrasonication assisted by agitation with a glass stirring rod. Second, a 5 &#xd7; 5&#xa0;mm cylindrical neodymium magnet (surface field strength &#x3e; 100&#xa0;mT) was attached to the outside of the beaker &#x223c;2&#xa0;mm above the water-sediment surface. After &#x223c;4&#xa0;h of magnetic absorption, magnetic minerals that were concentrated adjacent to the magnet were transferred to a 10&#xa0;ml glass tube. To extract as much of the magnetic mineral content from the sediment as possible, the first and second steps were repeated several times until no obvious magnetic aggregates adjacent to the magnet were found. Third, extracted magnetic minerals were resuspended in &#x223c;5&#xa0;ml of Milli-Q water in a 10&#xa0;ml glass tube, mixed by ultrasonication, and then extracted magnetically again following a similar procedure as the second step above. To remove non-magnetic minerals from the extracts, the third step was repeated several times until non-magnetic particles were not observed at the bottom of the tube. The final three repeats were performed in 99.5% ethanol. Finally, extracted magnetic minerals were suspended in 50&#xa0;&#xb5;l of 99.5% ethanol and were stored at &#x2212;20&#xb0;C prior to TEM or SEM observations.</p>
</sec>
<sec id="s2-2">
<title>Magnetic Measurements</title>
<p>Low-temperature magnetic measurements were made with a Quantum Design Magnetic Property Measurement System (MPMS XP-5, 5.0 &#xd7; 10<sup>&#x2212;10</sup>&#xa0;Am<sup>2</sup> sensitivity). Zero-field-cooled (ZFC) and field-cooled (FC) curves were obtained by cooling the sample from 300 to 10&#xa0;K in a zero field and in a 2.5-T field, respectively, followed by imparting a saturation IRM (SIRM) to the sample in a 2.5-T field at 10&#xa0;K (hereafter SIRM<sub>10 K_2.5&#xa0;T</sub>), and then by measuring SIRM<sub>10 K_2.5&#xa0;T</sub> during warming back to 300&#xa0;K in zero field (<xref ref-type="bibr" rid="B85">Moskowitz et al., 1993</xref>). For low-temperature cycling (LTC) of a room temperature SIRM obtained in a 2.5-T field at 300&#xa0;K (hereafter SIRM<sub>300 K_2.5&#xa0;T</sub>), remanence was measured in zero field during a cooling-warming cycle (300 &#x2192; 10 &#x2192; 300&#xa0;K).</p>
<p>Room-temperature magnetic experiments were made using a Micromag Model 3,900 vibrating sample magnetometer (VSM) (Princeton Measurement Corporation; 5.0 &#xd7; 10<sup>&#x2212;11</sup>&#xa0;Am<sup>2</sup> sensitivity). A hysteresis loop was measured in a 1&#xa0;T maximum field with 500&#xa0;ms averaging time. The saturation magnetization (<italic>M</italic>
<sub>
<italic>s</italic>
</sub>), saturation remanence (<italic>M</italic>
<sub>
<italic>rs</italic>
</sub>), and coercivity (<italic>B</italic>
<sub>
<italic>c</italic>
</sub>), were determined after applying a high-field (0.7&#x2013;1&#xa0;T) slope correction. Static IRM acquisition and DCD curves were measured on an initially demagnetized and 1&#xa0;T-re-magnetized sample, respectively. The coercivity of remanence (<italic>B</italic>
<sub>
<italic>cr</italic>
</sub>) was determined from the DCD curve. IRM acquisition and DCD curves were measured to 1&#xa0;T using a logarithmic sweep mode with 1&#xa0;mT initial field and 120 measurement points. To simplify comparison of remanence results and to calculate the <italic>R</italic>-value of the Wohlfarth-Cisowski test (<xref ref-type="bibr" rid="B12">Cisowski, 1981</xref>), the IRM acquisition curve was normalized to the SIRM, and the DCD curve was rescaled as &#xbd; [1 &#x2b; IRM(&#x2212;H)/SIRM]. To quantify contributions from different coercivity families to the total IRM, the IRM curve was decomposed into cumulative log Gaussian (CLG) curves (<xref ref-type="bibr" rid="B111">Robertson and France, 1994</xref>) using the software of <xref ref-type="bibr" rid="B47">Heslop et al. (2002)</xref>. The different coercivity families are defined by their half saturation IRM (SIRM) field (<italic>B</italic>
<sub>1/2</sub>) and the percentage of their contribution to the total IRM.</p>
<p>FORCs (<xref ref-type="bibr" rid="B95">Pike et al., 1999</xref>; <xref ref-type="bibr" rid="B101">Roberts et al., 2000</xref>) were also measured with the VSM using the protocol described by <xref ref-type="bibr" rid="B21">Egli et al. (2010)</xref>. A total of 300 FORCs were measured with a positive saturation field of 1&#xa0;T, increasing field steps of 0.976&#xa0;mT, and a 600&#xa0;ms averaging time. A FORC diagram was calculated using the FORCinel v3.06 software (<xref ref-type="bibr" rid="B39">Harrison and Feinberg, 2008</xref>) and smoothed using the VARIFORC algorithm (<xref ref-type="bibr" rid="B26">Egli, 2013</xref>). The horizontal (<italic>B</italic>
<sub>
<italic>c</italic>
</sub>) and vertical (<italic>B</italic>
<sub>
<italic>i</italic>
</sub>) axes on a FORC diagram indicate the microcoercivity and interaction field distribution for SD particles, respectively (<xref ref-type="bibr" rid="B95">Pike et al., 1999</xref>; <xref ref-type="bibr" rid="B101">Roberts et al., 2000</xref>).</p>
</sec>
<sec id="s2-3">
<title>Scanning Electron Microscope and Transmission Electron Microscope Analyses</title>
<p>Extracted magnetic minerals were deposited onto carbon-based, double sided adhesive tape that was mounted onto the surface of an aluminum stub for SEM observations. The sample was carbon coated prior to imaging to create a conductive layer. Extracted magnetic minerals were deposited onto carbon-coated copper grids for TEM experiments. SEM and TEM experiments were carried out with a Nova NanoSEM 450 field-emission SEM (15&#xa0;kV accelerating voltage) and a JEM2100 TEM (200&#xa0;kV accelerating voltage), respectively, at the Institute of Geology and Geophysics, Chinese Academy of Sciences (IGGCAS, Beijing, China). Microchemical analyses were made by Energy-dispersive X-ray spectrometry (EDXS) elemental mapping in the SEM and point analysis in the TEM.</p>
</sec>
</sec>
<sec sec-type="results" id="s3">
<title>Results</title>
<sec id="s3-1">
<title>Room- and Low-Temperature Magnetic Properties</title>
<p>A hysteresis loop for the sample is closed at values well below &#x223c;400&#xa0;mT (<xref ref-type="fig" rid="F2">Figure 2A</xref>). Stepwise SIRM acquisition and demagnetization indicate that the sample is saturated and demagnetized largely below &#x223c;300&#xa0;mT, and completely at &#x223c;600&#xa0;mT (<xref ref-type="fig" rid="F2">Figure 2B</xref>). Hysteresis parameters after high-field slope correction are <italic>B</italic>
<sub>
<italic>c</italic>
</sub> &#x3d; 20.6&#xa0;mT, <italic>B</italic>
<sub>
<italic>cr</italic>
</sub> &#x3d; 44.9&#xa0;mT, <italic>B</italic>
<sub>
<italic>cr</italic>
</sub>/<italic>B</italic>
<sub>
<italic>c</italic>
</sub> &#x3d; 2.18, and <italic>M</italic>
<sub>
<italic>rs</italic>
</sub>/<italic>M</italic>
<sub>
<italic>s</italic>
</sub> &#x3d; 0.28. Normalized IRM acquisition and DCD curves are roughly symmetric with a calculated <italic>R</italic>-value of 0.45 for the Wohlfarth-Cisowski test (<xref ref-type="bibr" rid="B12">Cisowski, 1981</xref>).</p>
<fig id="F2" position="float">
<label>FIGURE 2</label>
<caption>
<p>
<bold>(A)</bold> Room-temperature hysteresis loop (solid and dashed lines are the original raw and high-field slope-corrected data, respectively. <bold>(B)</bold> Normalized IRM acquisition and DCD curves. <bold>(C)</bold> FC-SIRM<sub>10 K_2.5&#xa0;T</sub> and ZFC-SIRM<sub>10 K_2.5&#xa0;T</sub> warming curves. <bold>(D)</bold> SIRM<sub>300 K_2.5&#xa0;T</sub> cooling-warming cycle curves.</p>
</caption>
<graphic xlink:href="feart-08-609058-g002.tif"/>
</fig>
<p>Both ZFC and FC SIRM<sub>10 K_2.5&#xa0;T</sub> curves decrease gradually during warming from 10 to 300&#xa0;K (<xref ref-type="fig" rid="F2">Figure 2C</xref>). The LTC curve is humped. The SIRM<sub>300 K_2.5&#xa0;T</sub> cooling curve increases gradually from 300 to &#x223c;176&#xa0;K and then decreases gradually to 10&#xa0;K. The warming curve overlaps with the cooling curve below &#x223c;50&#xa0;K, and then increases slowly to 153&#xa0;K, and finally decreases gradually to 300&#xa0;K. The SIRM<sub>300 K_2.5&#xa0;T</sub> cooling-warming curves are roughly reversible with a &#x223c;6% remanence loss after cycling (<xref ref-type="fig" rid="F2">Figure 2D</xref>). The Verwey transition, which is characterized by an obvious remanence drop at &#x223c;100&#x2013;120&#xa0;K, is not clearly present in the ZFC/FC warming and LTC curves. This indicates that magnetite particles in this sample are nonstoichiometric, either due to surface oxidation or cation substitution (e.g., <xref ref-type="bibr" rid="B87">Muxworthy and McClelland, 2000</xref>; <xref ref-type="bibr" rid="B91">&#xd6;zdemir and Dunlop, 2010</xref>).</p>
</sec>
<sec id="s3-2">
<title>First-Order Reversal Curve Results</title>
<p>FORC measurements provide information about all magnetic particles in a sample in terms of their magnetization (magnitude), microcoercivity (horizontal distribution) and magnetic interaction field for SD particles (vertical distribution) (<xref ref-type="bibr" rid="B95">Pike et al., 1999</xref>; <xref ref-type="bibr" rid="B101">Roberts et al., 2000</xref>; <xref ref-type="bibr" rid="B106">Roberts et al., 2014</xref>). The FORC diagram in <xref ref-type="fig" rid="F3">Figure 3</xref> indicates the presence of non-interacting SD (<xref ref-type="bibr" rid="B89">Newell, 2005</xref>; <xref ref-type="bibr" rid="B21">Egli et al., 2010</xref>; <xref ref-type="bibr" rid="B106">Roberts et al., 2014</xref>), vortex state (<xref ref-type="bibr" rid="B94">Pike and Fernandez, 1999</xref>; <xref ref-type="bibr" rid="B86">Muxworthy and Dunlop, 2002</xref>; <xref ref-type="bibr" rid="B107">Roberts et al., 2017</xref>) and viscous particles near the superparamagnetic (SP)/SD threshold size (<xref ref-type="bibr" rid="B96">Pike et al., 2001</xref>). The non-interacting SD contribution produces a central ridge signal that can be extracted (<xref ref-type="fig" rid="F3">Figure 3B</xref>) following <xref ref-type="bibr" rid="B21">Egli et al. (2010)</xref> and separated into three components along a horizontal profile at <italic>B</italic>
<sub>
<italic>i</italic>
</sub> &#x3d; 0&#xa0;mT (<xref ref-type="fig" rid="F3">Figure 3D</xref>). The three SD components have peak coercivities of &#x223c;20.4, &#x223c;76.8, and 126.1&#xa0;mT. The remaining FORC distribution after central ridge extraction has a tri-lobate shape (<xref ref-type="fig" rid="F3">Figure 3C</xref>) associated with the vortex state (<xref ref-type="bibr" rid="B71">Lascu et al., 2018</xref>). The upper lobe intersects the vertical axis at higher values (<italic>B</italic>
<sub>
<italic>i</italic>
</sub> &#x3d; &#x223c;50&#xa0;mT) than the lower lobe, which intersects the vertical axis closer to the origin. The middle lobe is narrower and extends along the horizontal axis to <italic>B</italic>
<sub>
<italic>c</italic>
</sub> &#x3d; &#x223c;140&#xa0;mT (<xref ref-type="fig" rid="F3">Figure 3C</xref>). A narrow FORC distribution along the lower vertical axis is related to viscous magnetic particles near the SP/SD threshold size (<xref ref-type="fig" rid="F3">Figures 3A,C</xref>) (<xref ref-type="bibr" rid="B96">Pike et al., 2001</xref>; <xref ref-type="bibr" rid="B106">Roberts et al., 2014</xref>).</p>
<fig id="F3" position="float">
<label>FIGURE 3</label>
<caption>
<p>First-order reversal curve (FORC) results. <bold>(A)</bold> FORC diagram. <bold>(B)</bold> Central ridge component extracted from the FORC diagram. <bold>(C)</bold> Background FORC component after removal of the central ridge. <bold>(D)</bold> Horizontal profile <italic>&#x3c1;</italic>(<italic>B</italic>
<sub>
<italic>c</italic>
</sub>) of the FORC function (coercivity distribution at <italic>B</italic>
<sub>
<italic>i</italic>
</sub> &#x3d; 0&#xa0;mT). The black line indicates raw data, while blue, cyan and purple lines indicate three components decomposed from the raw data. The dashed red line indicates a sum of all three Gaussian components. <bold>(E)</bold> Vertical profiles <italic>&#x3c1;</italic>(<italic>B</italic>
<sub>
<italic>i</italic>
</sub>) of the FORC function (magnetostatic-interaction field distribution) at 20&#xa0;mT: the central ridge component (black), the background component with vertical spread (dashed black line), and the total of the two components (red line) are shown.</p>
</caption>
<graphic xlink:href="feart-08-609058-g003.tif"/>
</fig>
</sec>
<sec id="s3-3">
<title>Scanning Electron Microscope Analyses of Magnetic Minerals</title>
<p>SEM observations combined with EDXS elemental mapping reveal the overall microscale morphology and composition of sedimentary magnetic minerals. Minerals can be distinguished readily by combining analysis of particle morphologies and corresponding backscattered electron contrast and chemical composition (<xref ref-type="fig" rid="F4">Figure 4</xref>; <xref ref-type="sec" rid="s10">Supplementary Material S1</xref>). Most particles with dark contrast generally consist of Si, O and Fe (and/or Mn), which indicates that they are Fe/Mn silicates. In contrast, particles with bright contrast are often composed of Fe and O, some of which also contain Ti. They are titanomagnetite (with variable Ti contents) or magnetite, as confirmed by TEM analyses (see below). The particles are morphologically diverse with sizes ranging from tens of nm to tens of &#xb5;m.</p>
<fig id="F4" position="float">
<label>FIGURE 4</label>
<caption>
<p>Backscattered SEM images of magnetic mineral extracts. Fe-Mn silicate particles (yellow arrows), angular titanomagnetite particles (green arrows), octahedral or truncated octahedral titanomagnetite particles (red arrows), silicate-hosted magnetite particles (blue arrows), silicate-hosted dendritic magnetite particles (cyan arrows), and individual nanometer-sized magnetite particles (purple arrows) are recognized from SEM morphological observations and SEM-EDXS elemental mapping (<xref ref-type="sec" rid="s10">Supplementary Material S1</xref>).</p>
</caption>
<graphic xlink:href="feart-08-609058-g004.tif"/>
</fig>
<p>SEM observations reveal well-defined and uncorroded octahedral (<xref ref-type="fig" rid="F4">Figures 4G,I</xref>), truncated octahedral (<xref ref-type="fig" rid="F4">Figure 4H</xref>) and irregular and angular shapes for micron- and submicron magnetite particles (<xref ref-type="fig" rid="F4">Figures 4A&#x2013;I</xref>). Most nanometric magnetite particles are hosted within silicates (<xref ref-type="fig" rid="F4">Figures 4J&#x2013;O</xref>); a few are isolated or attached onto other particles (<xref ref-type="fig" rid="F4">Figures 4A&#x2013;4F</xref>). Two silicate-hosted titanomagnetite inclusion types are identified: randomly oriented, dispersed particles (<xref ref-type="fig" rid="F4">Figure 4J&#x2013;L</xref>) and dendritic particles (<xref ref-type="fig" rid="F4">Figures 4M&#x2013;O</xref>). Compared to the micron-sized titanomagnetite particles, the morphology and stoichiometry of these nanometric magnetite particles are difficult to characterize with SEM imaging and SEM-EDXS elemental mapping because of the &#x223c;1&#xa0;nm spatial resolution limit.</p>
</sec>
<sec id="s3-4">
<title>Transmission Electron Microscope Analyses of Magnetic Minerals</title>
<p>Systematic TEM and high-resolution TEM (HRTEM) observations were made on different magnetic particle types to identify their mineralogy and stoichiometry. Representative particles were further studied by selected area electron diffraction (SAED) and TEM-EDXS point analyses. Eight magnetic particle types were identified based on crystal morphology, size, composition and spatial arrangement (<xref ref-type="fig" rid="F5">Figures 5</xref>&#x2013;<xref ref-type="fig" rid="F9">9</xref>).</p>
<fig id="F5" position="float">
<label>FIGURE 5</label>
<caption>
<p>TEM analyses of <bold>(A&#x2013;F)</bold> Type-1, <bold>(G&#x2013;I)</bold> Type-2, and <bold>(J&#x2013;K)</bold> Type-3 magnetite particles. <bold>(A)</bold> Low-magnification TEM image of many micron-sized titanomagnetite particles. <bold>(B)</bold> TEM image of an individual titanomagnetite particle. <bold>(C)</bold> SAED pattern recorded from the [111] zone axis of the particle in <bold>(B)</bold>. <bold>(D)</bold> TEM image of an individual magnetite particle. <bold>(E)</bold> HRTEM image of a thin edge region of the particle in <bold>(D)</bold> (yellow dashed box). <bold>(F)</bold> SAED pattern recorded from the [112] zone axis of the particle in <bold>(D)</bold>. <bold>(G)</bold> TEM image of many octahedral magnetite particles [367.8 &#xb1; 44.9&#xa0;nm average size (n &#x3d; 18)]. <bold>(H)</bold> TEM image of a single octahedral magnetite particle recorded from the [111] zone axis [yellow dashed box in <bold>(G)</bold>]. The inset SEM image demonstrates an octahedral morphology. <bold>(I)</bold> SAED pattern of the particle in <bold>(H)</bold> recorded from the [111] zone axis of magnetite. <bold>(J)</bold> TEM image of many nanometer titanomagnetite particles. <bold>(K)</bold> HRTEM image of a single magnetite particle [yellow dashed box in <bold>(J)</bold>] recorded from the [0<inline-formula id="inf1">
<mml:math>
<mml:mrow>
<mml:mrow>
<mml:mover accent="true">
<mml:mn>1</mml:mn>
<mml:mo>&#xaf;</mml:mo>
</mml:mover>
</mml:mrow>
<mml:mn>1</mml:mn>
</mml:mrow>
</mml:math>
</inline-formula>] zone axis (the inset is the corresponding pattern). <bold>(L)</bold> EDXS spectra for individual particles (indicated by colored crosses and names in <bold>(B)</bold>, <bold>(D)</bold>, <bold>(G)</bold>, and <bold>(J)</bold>). The d-spacing values from HRTEM observations and indirectly calculated from SAED analyses, combined with corresponding TEM-EDXS point analyses, SAED and FFT patterns, match the crystal structure (Fd3m space group) of magnetite or titanomagnetite.</p>
</caption>
<graphic xlink:href="feart-08-609058-g005.tif"/>
</fig>
<p>Type-1 and type-2 particles are micron-or submicron-sized and generally occur as loose aggregates (<xref ref-type="fig" rid="F5">Figures 5A,D</xref>) or isolated particles (<xref ref-type="fig" rid="F5">Figure 5B</xref>). They are too thick to image lattice fringes directly by HRTEM. We generally tilted the sample stage to allow the incident electron beam to pass through large particles along a certain zone axis, and then selected thinner edge areas for HRTEM, SAED and TEM-EDXS point analyses. As shown in <xref ref-type="fig" rid="F5">Figures 5A&#x2013;F</xref>, TEM observations from one zone axis combined with SAED analyses on individual Type-1 particles reveal that they consist mainly of micron or submicron angular titanomagnetite (<xref ref-type="fig" rid="F5">Figures 5A,B,D</xref>), with Type-2 particles consisting of well-defined octahedral magnetite (<xref ref-type="fig" rid="F5">Figures 5G,H</xref>). Type-3 aggregates tend to consist of randomly organized nanometric titanomagnetite particles. HRTEM observations combined with corresponding Fast Fourier Transform (FFT) analyses reveal that these particles are elongated octahedral magnetite with average length of 52.9 &#xb1; 10.9&#xa0;nm, width of 43.9 &#xb1; 9.2&#xa0;nm and aspect ratio (length/width) of 1.22 &#xb1; 0.18 (n &#x3d; 30). TEM-EDXS point analyses reveal that Type-1 to Type-3 particles are titanomagnetite with variable Ti contents.</p>
<p>In contrast to Type-1 to Type-3 titanomagnetite, Type-4 and Type-5 magnetic particles are hosted within silicates (<xref ref-type="fig" rid="F6">Figures 6</xref> and <xref ref-type="fig" rid="F7">7</xref>). No preferred particle orientations are observed for the morphologically diverse Type-4 particles, which have sizes ranging from a few to several hundred nanometers. Some particles appear to have rounded or irregular 2D-projections in which crystal faces are difficult to define even from HRTEM lattice images (<xref ref-type="fig" rid="F6">Figures 6A&#x2013;D</xref>). In contrast, other particles likely have euhedral octahedral or cubo-octahedral shapes (<xref ref-type="fig" rid="F6">Figures 6E&#x2013;N</xref>). Type-5 particles are typical dendrite-like self-assembled magnetic nanoparticles (<xref ref-type="fig" rid="F7">Figure 7</xref>). Combined HRTEM, SAED and TEM-EDXS point analyses reveal that these silicate-hosted nanometer-sized particles are titanomagnetite with variable Ti contents (<xref ref-type="fig" rid="F6">Figures 6</xref> and <xref ref-type="fig" rid="F7">7</xref>).</p>
<fig id="F6" position="float">
<label>FIGURE 6</label>
<caption>
<p>TEM analyses of Type-4 magnetite inclusions hosted within silicates. <bold>(A)</bold> TEM image of a silicate particle hosting many dispersed titanomagnetite or magnetite inclusions. <bold>(B</bold>&#x2013;<bold>D)</bold> Titanomagnetite or magnetite particles likely attached to silicates: <bold>(B)</bold> low-magnification TEM image, <bold>(C)</bold> HRTEM image of part of the particle in the yellow dashed box in <bold>(B)</bold> and <bold>(D)</bold> the corresponding SAED pattern recorded from the [0<inline-formula id="inf2">
<mml:math>
<mml:mrow>
<mml:mrow>
<mml:mover accent="true">
<mml:mn>1</mml:mn>
<mml:mo>&#xaf;</mml:mo>
</mml:mover>
</mml:mrow>
<mml:mn>1</mml:mn>
</mml:mrow>
</mml:math>
</inline-formula>] zone axis. <bold>(E</bold>&#x2013;<bold>H)</bold> Silicate particle hosting many titanomagnetite or magnetite inclusions: <bold>(E)</bold> low-magnification TEM image, <bold>(F)</bold> TEM image of a single particle indicated by the yellow dashed box in <bold>(E)</bold>, <bold>(G)</bold> HRTEM image of a small region of the particle in <bold>(F)</bold> and <bold>(H)</bold> SAED pattern recorded from the [112] zone axis of the particle in <bold>(F)</bold>. <bold>(I</bold>&#x2013;<bold>K)</bold> TEM images of <bold>(I)</bold> a silicate particle hosting many titanomagnetite or magnetite inclusions and <bold>(J)</bold> of a small region indicated by the yellow dashed box in <bold>(I)</bold>, <bold>(K)</bold> HRTEM image (inset is the corresponding FFT pattern) of a particle indicated by the yellow dashed box in <bold>(J)</bold>. <bold>(L&#x2013;N)</bold> TEM images of <bold>(L)</bold> several titanomagnetite or magnetite inclusions that are likely embedded in, and attached to, silicates, and <bold>(M)</bold> a small region indicated by the yellow dashed box in <bold>(L)</bold>, and <bold>(N)</bold> HRTEM image (inset is the corresponding FFT pattern) of a particle indicated by the yellow dashed box in <bold>(M)</bold>. <bold>(O)</bold> EDXS spectra for different particles or regions of interest (indicated by colored crosses and names in <bold>(B)</bold>, <bold>(E)</bold>, <bold>(F)</bold> and <bold>(J)</bold>). The <italic>d</italic>-spacing values from HRTEM observations and indirectly calculated from SAED analyses, combined with corresponding TEM-EDXS point analyses, SAED and FFT patterns, match the crystal structure (<italic>Fd</italic>3<italic>m</italic> space group) of magnetite or titanomagnetite.</p>
</caption>
<graphic xlink:href="feart-08-609058-g006.tif"/>
</fig>
<fig id="F7" position="float">
<label>FIGURE 7</label>
<caption>
<p>TEM analyses of Type-5 magnetite dendrites hosted within silicates. <bold>(A)</bold> TEM image of a magnetite dendrite aggregate hosted within a silicate. <bold>(B)</bold> HRTEM image of a small region of the particle indicated by the yellow dashed box in <bold>(A)</bold>. <bold>(C)</bold> SAED pattern recorded from the [0<inline-formula id="inf3">
<mml:math>
<mml:mrow>
<mml:mrow>
<mml:mover accent="true">
<mml:mn>1</mml:mn>
<mml:mo>&#xaf;</mml:mo>
</mml:mover>
</mml:mrow>
<mml:mn>1</mml:mn>
</mml:mrow>
</mml:math>
</inline-formula>] zone axis of the particle in <bold>(B)</bold>. <bold>(D)</bold> EDXS spectra for dendrite magnetite and the host silicate [indicated by colored crosses in <bold>(A)</bold>].</p>
</caption>
<graphic xlink:href="feart-08-609058-g007.tif"/>
</fig>
<p>Consistent with SEM results, Type-1 to Type-5 particles dominate the magnetic mineral assemblage in TEM observations. With careful and extensive searching, we also found Type-6 particles, which clearly represent magnetite magnetofossils based on their well-defined crystal morphologies, nanometer sizes and chain organization (e.g., <xref ref-type="bibr" rid="B61">Kopp and Kirschvink, 2008</xref>; <xref ref-type="bibr" rid="B75">Li et al., 2013a</xref>). Three magnetofossil crystal morphologies are found in this sediment sample (<xref ref-type="fig" rid="F8">Figure 8</xref>): octahedral magnetofossils have an average length of 53.0 &#xb1; 5.7 nm, width of 50.6 &#xb1; 5.9&#xa0;nm and aspect ratio of 1.05 &#xb1; 0.05 (n &#x3d; 19), prismatic magnetofossils have an average length of 103.3 &#xb1; 21.2&#xa0;nm, width of 81.9 &#xb1; 15.8&#xa0;nm and aspect ratio of 1.26 &#xb1; 0.13 (n &#x3d; 13) and bullet-shaped magnetofossils have an average length of 116.5 &#xb1; 13.7&#xa0;nm, width of 41.1 &#xb1; 1.3&#xa0;nm and aspect ratio of 2.83 &#xb1; 0.3 (n &#x3d; 3). HRTEM observations confirm that they are single crystals without obvious twinning defects.</p>
<fig id="F8" position="float">
<label>FIGURE 8</label>
<caption>
<p>TEM analyses of Type-6 magnetite magnetofossils. <bold>(A)</bold> Three octahedral magnetite particles with chain structure. <bold>(B)</bold> Four elongated prismatic magnetite particles with chain structure. <bold>(C)</bold> Two bullet-shaped magnetite particles. <bold>(D)</bold> HRTEM image of an individual elongated prismatic particle recorded from the [001] zone axis. <bold>(E)</bold> Close-up image of the lower left-hand part of the particle in <bold>(D)</bold> (indicated by the yellow dashed box). <bold>(F)</bold> FFT pattern from the HRTEM image of the particle in <bold>(E)</bold>. <bold>(G)</bold> HRTEM image of a bullet-shaped magnetite particle recorded from the [0<inline-formula id="inf4">
<mml:math>
<mml:mrow>
<mml:mrow>
<mml:mover accent="true">
<mml:mn>1</mml:mn>
<mml:mo>&#xaf;</mml:mo>
</mml:mover>
</mml:mrow>
<mml:mn>1</mml:mn>
</mml:mrow>
</mml:math>
</inline-formula>] zone axis <bold>(H)</bold> Close-up image of the lower right-hand part of the particle in <bold>(G)</bold> (indicated by the yellow dashed box) <bold>(I)</bold> FFT pattern from the HRTEM image of the particle in <bold>(H)</bold>. <bold>(J)</bold> EDXS spectra for different individual particles (for positions of colored crosses in <bold>(A)</bold>, <bold>(D)</bold> and <bold>(G)</bold>). The <italic>d</italic>-spacing values from HRTEM observations and indirectly calculated from SAED analyses, combined with corresponding TEM-EDXS point analyses, SAED and FFT patterns, match the crystal structure (<italic>Fd3m</italic> space group) of magnetite.</p>
</caption>
<graphic xlink:href="feart-08-609058-g008.tif"/>
</fig>
<p>Type-7 and Type-8 particles have similar morphology in low-magnification TEM observations. Both appear to be tight aggregates of nanometer-sized magnetite (<xref ref-type="fig" rid="F9">Figures 9A,D</xref>). However, HRTEM observations and SAED analyses demonstrate that they are different. Type-7 magnetite aggregates are composed of many randomly oriented single crystals with sizes of about 10&#xa0;nm. As a result, SAED analysis of Type-7 magnetite aggregates have a typical ring-like diffraction pattern for polycrystalline samples (<xref ref-type="fig" rid="F9">Figures 9B,C</xref>). In contrast, Type-8 magnetite aggregates are single crystals with significant defects. Despite obvious boundaries that divide particles into different small regions, HRTEM observations reveal clearly that the same lattice fringes run intact through the particle, resulting in a typical spot-like single crystal diffraction pattern (<xref ref-type="fig" rid="F9">Figures 9E,F</xref>).</p>
<fig id="F9" position="float">
<label>FIGURE 9</label>
<caption>
<p>TEM analyses of Type-7 <bold>(A&#x2013;C)</bold> and Type-8 <bold>(D</bold>&#x2013;<bold>F)</bold> nanometer-sized magnetite aggregates. <bold>(A</bold>&#x2013;<bold>C)</bold> Randomly oriented magnetite crystal aggregates: <bold>(A)</bold> low-magnification TEM image, <bold>(B)</bold> HRTEM image of many particles with the corresponding SAED pattern (inset), and <bold>(C)</bold> HRTEM image of several particles with Miller indices. <bold>(D&#x2013;F)</bold> Uniformly oriented magnetite crystal aggregates: <bold>(D)</bold> low-magnification TEM image, <bold>(E)</bold> HRTEM image of many particles with the corresponding SAED pattern (inset) and <bold>(F)</bold> HRTEM image of several particles with Miller indices.</p>
</caption>
<graphic xlink:href="feart-08-609058-g009.tif"/>
</fig>
</sec>
</sec>
<sec sec-type="discussion" id="s4">
<title>Discussion</title>
<sec id="s4-1">
<title>Magnetic Mineral Assemblage in Surface Sediment Sample EPMNP-31</title>
<p>The generally low magnetic mineral concentration and mixture with non-magnetic minerals in sediments makes it necessary to pre-treat samples effectively to extract and enrich magnetic minerals for SEM and TEM analyses. Any magnetic mineral extraction process has inevitable biases, i.e., strongly magnetic minerals are relatively easy to extract from sediments (e.g., <xref ref-type="bibr" rid="B51">Hounslow and Maher, 1996</xref>; <xref ref-type="bibr" rid="B37">Han et al., 2016</xref>). The extraction process used here did not involve chemical treatment (e.g., dissolution by acid-ammonium oxalate) or mechanical treatment apart from ultrasonication to disperse the sediment slurry. It is, therefore, a relatively straightforward process. Our experimental results indicate that this extraction procedure has removed most non-magnetic minerals and that it has concentrated magnetic minerals, which is necessary for SEM and TEM analyses, although the procedure might miss weakly magnetic minerals (e.g., hematite, goethite). Five dominant (Type-1 to -5) and three minor (Type-6 to-8) titanomagnetite and magnetite particle types were identified from sample EPMNP-31 by combined use of SEM, SEM-EDXS elemental mapping, TEM, HRTEM, SAED and TEM-EDXS point analyses from micron to atomic scales. These microscopic observations provide direct evidence to help understand bulk sediment magnetic properties.</p>
<p>IRM decomposition indicates that the remanent magnetization in this sample is carried by four main coercivity components (<xref ref-type="fig" rid="F10">Figure 10</xref>). Component 1 has a 7% contribution and might represent the magnetic response from coarse vortex state grains (e.g., Type-1,-2 and some submicron Type-4 and-5 particles). Component 2 has a 56% contribution and may originate mainly from SD magnetite particles with low Ti contents (e.g., Type-4 and -5), and SD magnetite magnetofossils (i.e., Type-6). Component 3 has a 28% contribution, which may originate from SD titanomagnetite particles with relatively high Ti contents, good crystallinity and elongated Type-3 particles. Component 4 has a 9% contribution and may represent the magnetic response of weakly magnetic minerals that were missed by the magnetic extraction procedure. The Type-7 and -8 magnetite aggregates were missed by IRM decomposition possibly because they are likely to have SP properties. It should be noted that magnetic unmixing with CLG functions does not enable fitting of skewed distributions, which can result in solutions with more components (e.g., from three to five components) (<xref ref-type="fig" rid="F11">Figures 11A,B</xref>). When using skewed generalized Gaussian (SGG) functions (<xref ref-type="bibr" rid="B22">Egli, 2003</xref>), as few as two components can also give a good match (<xref ref-type="fig" rid="F11">Figures 11C,D</xref>). Therefore, we argue that precise magnetic mineral assemblage identification based on systematic electron microscopic observations is a prerequisite for supervised unmixing.</p>
<fig id="F10" position="float">
<label>FIGURE 10</label>
<caption>
<p>IRM component analysis based on supervised unmixing with information from magnetic mineral assemblages identified from SEM and TEM analyses. <bold>(A)</bold> Linear acquisition plot. <bold>(B)</bold> Gradient of acquisition plot. Four CLG components are required to fit the IRM acquisition curve: raw data (black circles), component 1 (blue), component 2 (cyan), component 3 (purple), component 4 (yellow), and the sum of the four components (red). <italic>B</italic>
<sub>
<italic>c,</italic>1/2</sub> values (the acquisition field at which 50% of the IRM is reached) for each coercivity fraction are indicated in parentheses in <bold>(A)</bold>. The dispersion parameter (DP, i.e., IRM coercivity distribution width) and remanence contribution for each coercivity fraction are indicated in the pie chart in <bold>(B)</bold>.</p>
</caption>
<graphic xlink:href="feart-08-609058-g010.tif"/>
</fig>
<fig id="F11" position="float">
<label>FIGURE 11</label>
<caption>
<p>Alternative IRM component analysis based on unsupervized fitting of coercivity distributions with <bold>(A</bold>,<bold>B)</bold> CLG functions (e.g., <xref ref-type="bibr" rid="B66">Kruiver et al., 2001</xref>) and <bold>(C,D)</bold> SGG functions (<xref ref-type="bibr" rid="B22">Egli, 2003</xref>). Left-hand column: linear acquisition plots; right-hand column: gradient of acquisition plots.</p>
</caption>
<graphic xlink:href="feart-08-609058-g011.tif"/>
</fig>
<p>Magnetic mineral types and their corresponding domain states were further identified by linking IRM, FORC and electron microscope analyses. Coarse-grained titanomagnetite or magnetite particles (e.g., IRM component 1) occur in the vortex state, as indicated by a tri-lobate FORC distribution after central ridge extraction (<xref ref-type="fig" rid="F3">Figure 3C</xref>). A strong central ridge FORC signal can be divided into three components with distinctive peak coercivities, which correspond to the other three IRM components. The lowest coercivity SD FORC component is dominant and corresponds to IRM component 2 and likely corresponds to Type-4 and -5 fine magnetite and low-Ti titanomagnetite particles. The intermediate coercivity SD FORC component corresponds to IRM component 3 and may be carried by Type-3 high-Ti titanomagnetite particles. The highest coercivity SD FORC component corresponds to IRM component 4 and likely represents weakly magnetic minerals that were missed by the magnetic extraction procedure. The magnetic minerals responsible for IRM component 2 are non-interacting (e.g., Type-4 and -5). For IRM component 3, individual titanomagnetite particles may be separated by non-magnetic sediment matrix, and therefore behave as non-interacting SD particles (e.g., Type-3; particles aggregate relatively easily during magnetic extraction). IRM measurements cannot detect SP particles because they do not carry a remanence at room temperature. However, as shown in <xref ref-type="fig" rid="F3">Figures 3</xref> and <xref ref-type="fig" rid="F9">9</xref>, small particles (Type-7, -8 and some Type-4 particles) near the SP/SD threshold size (&#x223c;25&#x2013;30&#xa0;nm for equidimensional magnetite; <xref ref-type="bibr" rid="B88">Muxworthy and Williams (2009)</xref>) produce a clear FORC signal, which is confirmed by TEM observations.</p>
<p>Magnetite magnetofossils (Type-6 particles) should also contribute to the central ridge FORC signal and IRM component 2. However, the magnetofossil contribution within the studied sample appears to be small. First, both SEM and TEM analyses reveal that Type-1 to -5 titanomagnetite or magnetite particles are the dominant magnetic minerals within the magnetic extract. Magnetofossil chain structures should be observed readily by SEM if they are as abundant in the magnetic mineral assemblage as they are in silicate-hosted nanometric magnetite particles. They were found only occasionally after much searching under TEM. Second, although magnetite magnetofossils may have comparable coercivities to IRM component 2, they generally produce two typical IRM components between &#x223c;30 and &#x223c;80&#xa0;mT with DP values &#x3c;0.2 due to their narrow grain size distributions (e.g., <xref ref-type="bibr" rid="B66">Kruiver et al., 2001</xref>; <xref ref-type="bibr" rid="B24">Egli, 2004b</xref>; <xref ref-type="bibr" rid="B49">Heslop, 2015</xref>). IRM component 2 has DP &#x3d; 0.3, which matches well with the silicate-hosted magnetite particles with diverse grain sizes ranging from a few to several hundred nanometers. Third, the chain structure of magnetite particles produced by modern MTB or preserved within sediments as magnetofossils generally produces significant shape anisotropy, which can be enhanced by elongation of prismatic and bullet-shaped magnetite particles (e.g., <xref ref-type="bibr" rid="B85">Moskowitz et al., 1993</xref>; <xref ref-type="bibr" rid="B92">Pan et al., 2005</xref>; <xref ref-type="bibr" rid="B52">Housen and Moskowitz, 2006</xref>; <xref ref-type="bibr" rid="B73">Li et al., 2010</xref>; <xref ref-type="bibr" rid="B74">Li et al., 2012</xref>; <xref ref-type="bibr" rid="B75">Li et al., 2013a</xref>; <xref ref-type="bibr" rid="B8">Chang et al., 2016b</xref>). Such shape anisotropy results in an apparent bifurcation of FC and ZFC warming curves below the Verwey transition temperature (i.e., &#x223c;90&#x2013;110&#xa0;K) (e.g., <xref ref-type="bibr" rid="B85">Moskowitz et al., 1993</xref>; <xref ref-type="bibr" rid="B76">Li et al., 2013b</xref>). Despite detection of chain structures for octahedral and prismatic magnetofossils and elongated bullet-shaped magnetofossils in TEM observations, FC and ZFC warming curves do not bifurcate; the former is slightly higher than the latter throughout warming, possibly due to the presence of particles that undergo thermal activation and remanence gain/loss during cooling/warming. Despite magnetite magnetofossils being found in the studied sediment, both bulk magnetic measurements and electron microscope observations reveal that they are much less abundant than other SD particle types, and that their magnetic contributions are small.</p>
</sec>
<sec id="s4-2">
<title>Combined Use of Magnetic and Microscopic Analyses: Importance and Necessity</title>
<p>Precise sedimentary magnetic mineral identification is a prerequisite for many paleomagnetic and environmental magnetic studies. In practice, bulk sediment samples are generally screened using bulk magnetic measurements to provide indications of the possible presence of certain magnetic minerals, which are then confirmed by direct SEM or TEM observations. Such a strategy enables efficient identification of targeted magnetic minerals, which has been used widely to identify magnetofossils in marine and lake sediments (e.g., <xref ref-type="bibr" rid="B61">Kopp and Kirschvink, 2008</xref>; <xref ref-type="bibr" rid="B104">Roberts et al., 2012</xref>; <xref ref-type="bibr" rid="B5">Chang et al., 2014a</xref>). Of the available magnetic measurements, combined use of FORC diagrams and FMR analyses is powerful for detecting magnetofossil chain structures because these methods are sensitive to the SD properties and strong shape anisotropy of magnetofossil chains and less sensitive to surface magnetite oxidation, which can compromise low-temperature remanence warming tests (e.g., <xref ref-type="bibr" rid="B57">Kind et al., 2011</xref>; <xref ref-type="bibr" rid="B4">Chang et al., 2013</xref>). However, like all other magnetic magnetofossil identification methods, FORC and FMR analyses also have limitations because neither method gives unique indications of a single magnetic mineral (e.g., <xref ref-type="bibr" rid="B79">Liu et al., 2012</xref>) and sediments tend to contain mixed magnetic mineral assemblages. Each component may have different origins and magnetic responses that can carry useful paleomagnetic and paleoenvironmental information. This is why so much effort has been expended in recent decades to identify magnetic minerals precisely and quantitatively in sediments by developing magnetic, mathematical, microscopic and non-magnetic methods (e.g., <xref ref-type="bibr" rid="B79">Liu et al., 2012</xref>; <xref ref-type="bibr" rid="B49">Heslop, 2015</xref>; <xref ref-type="bibr" rid="B109">Roberts et al., 2019</xref>).</p>
<p>Based on systematic analysis of a marine surface sediment sample, we emphasize the importance and necessity of combined use of bulk magnetic and electron microscopic approaches to precisely and comprehensively identify sedimentary magnetic minerals. First, direct SEM and TEM observations provide important constraints on supervising IRM curve unmixing, which allows quantification of four major remanence-bearing components. FORC analysis then enables association of each magnetic component with its respective domain state. FORC diagrams also indicate the presence of particles near the SP/SD threshold size, which cannot be detected by IRM measurements. IRM and FORC analyses also indicate that the sediment contains weakly magnetic high-coercivity minerals (e.g., hematite, goethite) that were not extracted or detected by SEM and TEM observations. Second, metagenomic analyses have shown that this sample contains 16S rRNA genes affiliated with MTB (<xref ref-type="bibr" rid="B16">Dong et al., 2016</xref>). A strong central ridge FORC component might be interpreted to indicate the presence of magnetofossils. However, careful comparative SEM and TEM analyses, along with IRM decomposition, demonstrate that magnetite magnetofossils are not abundant in this sample and that their contribution to remanence may be small or even negligible compared to abiotic SD magnetite and titanomagnetite. Third, systematic analyses of magnetic mineral morphology, mineralogy and composition by combined SEM and TEM approaches allow identification of at least eight magnetite and titanomagnetite particle types from central Pacific Ocean surface sediment. Each magnetic particle type may have its own origin that reflects local or remote environmental processes. Irregular angular shapes for Type-1 titanomagnetite or magnetite particles indicate that they have a detrital origin related to erosion of magnetite-bearing igneous rocks from elevated submarine volcanic sources, of which there are nearby sources (<xref ref-type="bibr" rid="B13">Clouard and Bonneville, 2005</xref>). Submicron (Type-2) and nanometer-sized (Type-3) octahedral titanomagnetite particles may have formed from local hydrothermal and volcanic activity in the Clarion Fracture Zone region (e.g., <xref ref-type="bibr" rid="B84">Mewes et al., 2016</xref>; <xref ref-type="bibr" rid="B32">Gartman and Hein, 2019</xref>). Dendritic titanomagnetite particles (Type-5) are generally self-assembled and embedded within silicates, which indicates that they are exsolved microstructures that formed by phase separation in an originally homogenous solid solution during igneous rock cooling. In contrast, nanometer-sized titanomagnetite and magnetite particles occur as randomly oriented inclusions within silicates. They may have formed prior to the host silicate minerals and were incorporated into the silicate during its subsequent crystallization (e.g., <xref ref-type="bibr" rid="B116">Tarduno et al., 2006</xref>; <xref ref-type="bibr" rid="B7">Chang et al., 2016a</xref>). Magnetite magnetofossils (Type-6) represent local MTB activity (e.g., <xref ref-type="bibr" rid="B16">Dong et al., 2016</xref>). Weakly magnetic high-coercivity minerals likely result from remote westerly-transported input from the Asian interior (e.g., <xref ref-type="bibr" rid="B53">Hyeong et al., 2005</xref>; <xref ref-type="bibr" rid="B54">Hyeong et al., 2006</xref>). Despite their unknown origin, two types of SP magnetite particles were found, which indicates that reductive dissolution of fine-grained magnetite is limited in this area. Two oxygen sources, i.e., diffusive oxygen transfer from underlying seamount basaltic basement and oxygen rich AABW (e.g., <xref ref-type="bibr" rid="B15">Deng et al., 2016</xref>; <xref ref-type="bibr" rid="B84">Mewes et al., 2016</xref>), produce a fully oxic sediment column at the study site. Such an oxic environment will produce surficial titanomagnetite and magnetite oxidation, while limiting reductive diagenetic modification of fine-grained titanomagnetite and magnetite (e.g., <xref ref-type="bibr" rid="B110">Roberts, 2015</xref>).</p>
</sec>
</sec>
<sec sec-type="conclusions" id="s5">
<title>Conclusions</title>
<p>We have studied systematically a deep-sea surface sediment from the Clarion Fracture Zone region in the central Pacific Ocean by combining bulk magnetic analyses and electron microscope observations. Eight titanomagnetite and magnetite particle types with different magnetic properties were identified, and their corresponding origins are discussed (<xref ref-type="table" rid="T1">Table 1</xref>). Type-1 particles are micron- and submicron-sized titanomagnetite with irregular and angular shapes, which are likely to be detrital particles that originated from erosion of magnetite-bearing igneous rocks in surrounding submarine volcanic highlands. Type-2 and-3 particles are well-defined octahedral titanomagnetite with submicron and nanometer sizes, respectively, which indicates that their formation may have been related to local hydrothermal and volcanic activity along the Clarion Fracture Zone region. Type-4 and-5 particles are silicate-hosted nanometer-sized titanomagnetite inclusions with diverse crystal morphologies and sizes that range from a few to a hundred nanometers. Type-4 particles are randomly assembled, while Type-5 particles are typical dendritic titanomagnetite. The inclusions would have resulted from exsolution within host silicates.</p>
<table-wrap id="T1" position="float">
<label>TABLE 1</label>
<caption>
<p>Magnetic mineral types identified in sample EPMNP-31.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th>Type</th>
<th align="center">Morphology</th>
<th align="center">Size</th>
<th align="center">Spatial arrangement</th>
<th align="center">Chemistry</th>
<th align="center">Domain state</th>
<th align="center">Origin</th>
</tr>
</thead>
<tbody>
<tr>
<td>Type 1</td>
<td>Irregular, angular</td>
<td>Several hundred nm to a few microns</td>
<td>Loose aggregates, isolated</td>
<td>Titanomagnetite, magnetite</td>
<td>Vortex state</td>
<td>Detrital</td>
</tr>
<tr>
<td>Type 2</td>
<td>Well-defined octahedral</td>
<td>367.8 &#xb1; 44.9&#xa0;nm</td>
<td>Loose aggregates, isolated</td>
<td>Titanomagnetite</td>
<td>Vortex state</td>
<td>Hydrothermal or igneous</td>
</tr>
<tr>
<td>Type 3</td>
<td>Elongated octahedral</td>
<td>52.9 &#xb1; 10.9&#xa0;nm (length); 43.9 &#xb1; 9.2&#xa0;nm (width)</td>
<td>Random aggregates</td>
<td>Titanomagnetite, magnetite</td>
<td>Single domain</td>
<td>Hydrothermal or igneous</td>
</tr>
<tr>
<td>Type 4</td>
<td>Irregular, octahedral, cubo-octahedral</td>
<td>Tens to hundreds of nanometers</td>
<td>Hosted within silicates</td>
<td>Titanomagnetite, magnetite</td>
<td>Single domain, vortex state, superparamagnetic</td>
<td>Exsolved microstructures from precursor minerals</td>
</tr>
<tr>
<td>Type 5</td>
<td>Dendrite-like</td>
<td>Tens to hundreds of nanometers</td>
<td>Hosted within silicates</td>
<td>Titanomagnetite</td>
<td>Vortex state, single domain</td>
<td>Formed early and incorporated into host silicates</td>
</tr>
<tr>
<td rowspan="3">Type 6</td>
<td>Octahedral magnetofossils</td>
<td>53.0 &#xb1; 5.7&#xa0;nm (length); 50.6 &#xb1; 5.9&#xa0;nm (width)</td>
<td>Short chain</td>
<td>Magnetite</td>
<td>Single domain</td>
<td>Local magnetotactic bacteria</td>
</tr>
<tr>
<td>Prismatic magnetofossils</td>
<td>103.3 &#xb1; 21.2&#xa0;nm (length); 81.9 &#xb1; 15.8&#xa0;nm (width)</td>
<td>Short chain</td>
<td>Magnetite</td>
<td>Single domain</td>
<td>Local magnetotactic bacteria</td>
</tr>
<tr>
<td>Bullet-shaped magnetofossils</td>
<td>116.5 &#xb1; 13.7&#xa0;nm (length); 41.1 &#xb1; 1.3&#xa0;nm (width)</td>
<td>Loose aggregates, isolated</td>
<td>Magnetite</td>
<td>Single domain</td>
<td>Local magnetotactic bacteria</td>
</tr>
<tr>
<td>Type 7</td>
<td>Irregular</td>
<td>A few nanometers</td>
<td>Random aggregates of many single crystals</td>
<td>Magnetite</td>
<td>Superparamagnetic</td>
<td>Unknown</td>
</tr>
<tr>
<td>Type 8</td>
<td>Irregular</td>
<td>A few nanometers</td>
<td>Aggregates of single crystals with defects</td>
<td>Magnetite</td>
<td>Superparamagnetic</td>
<td>Unknown</td>
</tr>
</tbody>
</table>
</table-wrap>
<p>The above five magnetic particle types dominate the magnetization of the studied sediment. In contrast, Type-6 to-8 magnetic particles are much less abundant. Type-6 particles are magnetite magnetofossils, which are related to local MTB activity. Type-7 comprises SP magnetite aggregates that consist of many randomly oriented single crystals. Type-8 consists of single crystals with significant defects in which obvious boundaries divide particles into many small (SP-like) regions. The well-preserved nature of the fine-grained magnetite indicates that surface sediments in this area are fully oxic.</p>
<p>Electron microscope results are consistent with bulk magnetic properties. They also provide a basis to constrain supervised IRM unmixing to identify quantitatively each magnetic component in the sediment. Coarse-grained titanomagnetite (e.g., Type-1, -2, and some submicron Type-4 and-5 titanomagnetite particles) are in the vortex state and contribute 7% of the remanence. Noninteracting SD titanomagnetite particles of Type-4 and -5 contribute 56% of the remanence. Noninteracting SD titanomagnetite particles of Type-3 contribute 28% of the remanence. A fourth IRM component due to weakly magnetic high-coercivity minerals was not extracted successfully by our extraction method and was not documented in TEM observations; it contributes 9% of the remanence.</p>
<p>Our work demonstrates that diagenetically unmodified natural surface sediments host diverse detrital magnetic mineral assemblages. Magnetic methods are used widely to identify magnetic minerals within such assemblages, although unsupervized interpretation is unlikely to accurately represent the complexity of natural magnetic mineral assemblages. Electron microscopic observations of the type presented here are time-consuming but essential for ground truthing of supervised magnetic unmixing. Nevertheless, the diversity of observed magnetic mineral types means that we aggregated different particle types to explain identified magnetic components. This demonstrates the complexity of producing consistent supervised magnetic data interpretations.</p>
</sec>
<sec id="s6">
<title>Data Availability Statement</title>
<p>The original contributions presented in the study are included in the article/<xref ref-type="sec" rid="s10">Supplementary Material</xref>, further inquiries can be directed to the corresponding author.</p>
</sec>
<sec id="s7">
<title>Author Contributions</title>
<p>JL designed and initiated the study, interpreted the measurements, and prepared the manuscript. JL and YL performed electron microscopic experiments and data analyses. JL, YL, and SL performed magnetic experiments and data analyses. AR and YP participated in data interpretation and manuscript refinement. HP and TX helped with sampling.</p>
</sec>
<sec id="s8">
<title>Funding</title>
<p>This study was supported financially by the National Natural Science Foundation of China (Grant Nos. 41920104009, 41890843, and 41621004), The Senior User Project of RVKEXUE2019GZ06 (Center for Ocean Mega-Science, Chinese Academy of Sciences), and the Australian Research Council (Grant Nos. DP160100805 and DP200100765).</p>
</sec>
<sec sec-type="COI-statement" id="s9">
<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>
</body>
<back>
<ack>
<p>We thank Dr Qingsong Liu and two reviewers for constructive comments that helped to improve the manuscript significantly. We thank Mr. Tang Xu for assistance with TEM experiments and the people from cruise DY29&#x2013;02 on R/V <italic>Haiyang Liuhao</italic> in 2013 for assistance with sampling.</p>
</ack>
<sec id="s10">
<title>Supplementary Material</title>
<p>The Supplementary Material for this article can be found online at: <ext-link ext-link-type="uri" xlink:href="https://www.frontiersin.org/articles/10.3389/feart.2020.609058/full#supplementary-material">https://www.frontiersin.org/articles/10.3389/feart.2020.609058/full&#x23;supplementary-material</ext-link>.</p>
<supplementary-material xlink:href="datasheet1.pdf" id="SM1" mimetype="application/pdf" xmlns:xlink="http://www.w3.org/1999/xlink"/>
</sec>
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