<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd">
<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article">
 <front>
  <journal-meta>
   <journal-id journal-id-type="publisher-id">
    ijg
   </journal-id>
   <journal-title-group>
    <journal-title>
     International Journal of Geosciences
    </journal-title>
   </journal-title-group>
   <issn pub-type="epub">
    2156-8359
   </issn>
   <issn publication-format="print">
    2156-8367
   </issn>
   <publisher>
    <publisher-name>
     Scientific Research Publishing
    </publisher-name>
   </publisher>
  </journal-meta>
  <article-meta>
   <article-id pub-id-type="doi">
    10.4236/ijg.2024.156026
   </article-id>
   <article-id pub-id-type="publisher-id">
    ijg-133914
   </article-id>
   <article-categories>
    <subj-group subj-group-type="heading">
     <subject>
      Articles
     </subject>
    </subj-group>
    <subj-group subj-group-type="Discipline-v2">
     <subject>
      Earth 
     </subject>
     <subject>
       Environmental Sciences
     </subject>
    </subj-group>
   </article-categories>
   <title-group>
    A Review on Diagnostic Phytoliths for the Application in Paleovegetation Reconstruction and Environmental Archaeology in East Asia
   </title-group>
   <contrib-group>
    <contrib contrib-type="author" xlink:type="simple">
     <name name-style="western">
      <surname>
       Weiyu
      </surname>
      <given-names>
       Chen
      </given-names>
     </name> 
     <xref ref-type="aff" rid="aff1"> 
      <sup>1</sup>
     </xref> 
     <xref ref-type="aff" rid="aff2"> 
      <sup>2</sup>
     </xref>
    </contrib>
   </contrib-group> 
   <aff id="aff1">
    <addr-line>
     aKey Laboratory of Land Surface Pattern and Simulation, Institute of Geographic Sciences and Natural Resources Research, Chinese Academy of Sciences, Beijing, China
    </addr-line> 
   </aff> 
   <aff id="aff2">
    <addr-line>
     aCollege of Resources and Environment, University of Chinese Academy of Sciences, Beijing, China
    </addr-line> 
   </aff> 
   <pub-date pub-type="epub">
    <day>
     20
    </day> 
    <month>
     06
    </month>
    <year>
     2024
    </year>
   </pub-date> 
   <volume>
    15
   </volume> 
   <issue>
    06
   </issue>
   <fpage>
    479
   </fpage>
   <lpage>
    492
   </lpage>
   <history>
    <date date-type="received">
     <day>
      10,
     </day>
     <month>
      May
     </month>
     <year>
      2024
     </year>
    </date>
    <date date-type="published">
     <day>
      17,
     </day>
     <month>
      May
     </month>
     <year>
      2024
     </year> 
    </date> 
    <date date-type="accepted">
     <day>
      17,
     </day>
     <month>
      June
     </month>
     <year>
      2024
     </year> 
    </date>
   </history>
   <permissions>
    <copyright-statement>
     © Copyright 2014 by authors and Scientific Research Publishing Inc. 
    </copyright-statement>
    <copyright-year>
     2014
    </copyright-year>
    <license>
     <license-p>
      This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/
     </license-p>
    </license>
   </permissions>
   <abstract>
    Phytoliths are extensively utilized as an archaeobotanical indicator in paleovegetation reconstruction and environmental archaeology. Over the past two decades, numerous phytolith morphotypes, particularly those exhibiting diagnostic morphological features and over representative of source plants at the genus and species levels, were discovered and reported. These advancements have significantly contributed to phytolith-based vegetation reconstruction on different timescales, enhanced our understanding of prehistoric plant utilization, and elucidated cultivation and domestication processes of key crops in ancient agriculture. However, there are still inconsistencies and misunderstandings regarding the morphological characteristics of diagnostic phytoliths in various plant groups. This review highlighted the standardization in the classification and description of phytolith morphotypes, and summarized the advancements in phytolith morphology research over the past two decades. Morphological illustrations of diagnostic phytoliths from various plant groups, particularly key crops and their relatives from dryland and rice agriculture in East Asia, were presented as references for phytolith identification and application. Finally, this review proposes future directions for phytolith morphological studies, emphasizing the comprehensive consideration of anatomical structure and morphometric parameters, as well as the need for extensive research on modern plant phytoliths and control experiments on phytolith growth.
   </abstract>
   <kwd-group> 
    <kwd>
     Diagnostic Phytolith
    </kwd> 
    <kwd>
      Paleovegetation Reconstruction
    </kwd> 
    <kwd>
      Environmental Archaeology
    </kwd>
   </kwd-group>
  </article-meta>
 </front>
 <body>
  <sec id="s1">
   <title>1. Introduction</title>
   <p>Phytoliths are amorphous silica gel concretions (opal) formed in the cells and intercellular spaces of plant tissues such as stems, leaves, seeds and fruits <xref ref-type="bibr" rid="scirp.133914-1">
     [1]
    </xref> <xref ref-type="bibr" rid="scirp.133914-2">
     [2]
    </xref>. Their grain size is mostly around 20 - 200 µm, with a large specific gravity of 2.1 - 2.3 <xref ref-type="bibr" rid="scirp.133914-2">
     [2]
    </xref>. Phytoliths have characteristics of corrosion resistance and in-situ deposition <xref ref-type="bibr" rid="scirp.133914-2">
     [2]
    </xref>. Phytoliths can directly inherit the morphology of source plant cells (e.g., epidermal cell, bulliform cell, hair cell) and intercellular spaces. Consequently, they have strong taxonomic significance for identification of source plant groups <xref ref-type="bibr" rid="scirp.133914-1">
     [1]
    </xref>. In some cases, phytolith types of diagnostic features can be classified into plant genera or even species <xref ref-type="bibr" rid="scirp.133914-1">
     [1]
    </xref> <xref ref-type="bibr" rid="scirp.133914-2">
     [2]
    </xref> <xref ref-type="bibr" rid="scirp.133914-3">
     [3]
    </xref> <xref ref-type="bibr" rid="scirp.133914-4">
     [4]
    </xref> <xref ref-type="bibr" rid="scirp.133914-5">
     [5]
    </xref>. Therefore, phytoliths are widely utilized to reconstruct paleovegetation changes <xref ref-type="bibr" rid="scirp.133914-6">
     [6]
    </xref> <xref ref-type="bibr" rid="scirp.133914-7">
     [7]
    </xref> <xref ref-type="bibr" rid="scirp.133914-8">
     [8]
    </xref> <xref ref-type="bibr" rid="scirp.133914-9">
     [9]
    </xref>, early plant use in the Neolithic and Paleolithic Periods <xref ref-type="bibr" rid="scirp.133914-1">
     [1]
    </xref> <xref ref-type="bibr" rid="scirp.133914-10">
     [10]
    </xref> <xref ref-type="bibr" rid="scirp.133914-11">
     [11]
    </xref> <xref ref-type="bibr" rid="scirp.133914-12">
     [12]
    </xref> <xref ref-type="bibr" rid="scirp.133914-13">
     [13]
    </xref>, prehistoric crop cultivation and domestication <xref ref-type="bibr" rid="scirp.133914-14">
     [14]
    </xref> <xref ref-type="bibr" rid="scirp.133914-15">
     [15]
    </xref> <xref ref-type="bibr" rid="scirp.133914-16">
     [16]
    </xref> <xref ref-type="bibr" rid="scirp.133914-17">
     [17]
    </xref>, plant diet of ancient animal <xref ref-type="bibr" rid="scirp.133914-18">
     [18]
    </xref>, <sup>14</sup>C dating in the Late Quaternary <xref ref-type="bibr" rid="scirp.133914-19">
     [19]
    </xref> <xref ref-type="bibr" rid="scirp.133914-20">
     [20]
    </xref>, and estimation of carbon sink potential <xref ref-type="bibr" rid="scirp.133914-21">
     [21]
    </xref> <xref ref-type="bibr" rid="scirp.133914-22">
     [22]
    </xref>, etc.</p>
   <p>Phytolith morphology research is an important basis for application of phytolith analysis <xref ref-type="bibr" rid="scirp.133914-1">
     [1]
    </xref>. Up to now, there are about 260 types of phytolith morphological types that can be distinguished by their morphological characteristics, among which about 110 types come from grasses, and more than 50 types from angiosperm woody taxa and ferns <xref ref-type="bibr" rid="scirp.133914-23">
     [23]
    </xref>. Generally, common phytolith morphotypes are those widely existing in plants of different taxonomic groups, such as Rodel and Acute <xref ref-type="bibr" rid="scirp.133914-1">
     [1]
    </xref> <xref ref-type="bibr" rid="scirp.133914-2">
     [2]
    </xref>. Diagnostic phytolith morphotypes are those with specific features and over representative of source families, genera or species <xref ref-type="bibr" rid="scirp.133914-24">
     [24]
    </xref>, such as Saddle of Bambusoideae <xref ref-type="bibr" rid="scirp.133914-25">
     [25]
    </xref>, Stipa Bilobate <xref ref-type="bibr" rid="scirp.133914-26">
     [26]
    </xref>, Saddle of Chloridoideae <xref ref-type="bibr" rid="scirp.133914-27">
     [27]
    </xref>, Spheroid echinate of Arecaceae <xref ref-type="bibr" rid="scirp.133914-28">
     [28]
    </xref>, as well as those with unique features from some key crops and their relatives (e.g., millets crops <xref ref-type="bibr" rid="scirp.133914-5">
     [5]
    </xref>, wild and cultivated rice <xref ref-type="bibr" rid="scirp.133914-29">
     [29]
    </xref>) in ancient dryland and rice agriculture that have been intensively studied in East Asia <xref ref-type="bibr" rid="scirp.133914-3">
     [3]
    </xref> <xref ref-type="bibr" rid="scirp.133914-4">
     [4]
    </xref> <xref ref-type="bibr" rid="scirp.133914-5">
     [5]
    </xref> <xref ref-type="bibr" rid="scirp.133914-12">
     [12]
    </xref> <xref ref-type="bibr" rid="scirp.133914-29">
     [29]
    </xref>-<xref ref-type="bibr" rid="scirp.133914-35">
     [35]
    </xref>. Along with the development of phytolith analysis, the standardization of phytolith morphology nomenclature and description became increasingly important. In 2005, the International Phytolith Society (IPS) guided the release of the first version of the International Code for Phytolith Nomenclature (ICPN 1.0) <xref ref-type="bibr" rid="scirp.133914-24">
     [24]
    </xref>, which made a primary attempt to standardize phytolith nomenclature and terminology <xref ref-type="bibr" rid="scirp.133914-36">
     [36]
    </xref> <xref ref-type="bibr" rid="scirp.133914-37">
     [37]
    </xref>. And then, the International Committee for Phytolith Taxonomy officially released the second version ICPN 2.0 in the year 2019 <xref ref-type="bibr" rid="scirp.133914-38">
     [38]
    </xref>.</p>
   <p>In the last 20 years, numerous phytolith morphotypes from various plant taxa have been reported, based on a large number of modern phytolith investigations <xref ref-type="bibr" rid="scirp.133914-3">
     [3]
    </xref> <xref ref-type="bibr" rid="scirp.133914-5">
     [5]
    </xref> <xref ref-type="bibr" rid="scirp.133914-25">
     [25]
    </xref>-<xref ref-type="bibr" rid="scirp.133914-35">
     [35]
    </xref> <xref ref-type="bibr" rid="scirp.133914-39">
     [39]
    </xref>-<xref ref-type="bibr" rid="scirp.133914-46">
     [46]
    </xref>. However, there are still great inconsistency in the naming and classification of phytolith morphology, and difficulties and disagreements in the identification of diagnostic phytolith morphotypes <xref ref-type="bibr" rid="scirp.133914-24">
     [24]
    </xref> <xref ref-type="bibr" rid="scirp.133914-36">
     [36]
    </xref>. This review briefly outlines the updated scheme in the ICPN 2.0, and presents illustrative plates of diagnostic phytolith morphotypes, particularly focusing on those in East Asia. The aims of this review are to provide illustrated material for identification and application of diagnostic phytolith morphotypes in vegetation reconstruction and environmental archaeology.</p>
  </sec><sec id="s2">
   <title>2. Progress in Phytolith Nomenclature Scheme</title>
   <p>The standardization of morphotype nomenclature and description for phytoliths plays an imprtant role in phytolith research <xref ref-type="bibr" rid="scirp.133914-38">
     [38]
    </xref>. The ICPN 1.0 suggested that the nomenclature of phytolith types should follow the sequence of shape (three- and two-dimensional descriptor), texture and/or ornamentation, and anatomical origin, and use standard morphological descriptors <xref ref-type="bibr" rid="scirp.133914-24">
     [24]
    </xref>. Subsequently, ICPN 2.0 revised phytolith nomenclature and morphological description <xref ref-type="bibr" rid="scirp.133914-38">
     [38]
    </xref>. The ICPN 2.0 scheme specifies 7 principles for the morphological nomenclature of phytolith types in detailed, including unique and concise phytolith naming, hierarchical naming order from taxonomic to anatomical to morphological (with an exception of short cell phytoliths from grass), using standard descriptors in the given glossary, use of combined name for closely related morphotypes, capitalizing only the first descriptor, an unique code for each morphotype, and rationale for a new name or retained one <xref ref-type="bibr" rid="scirp.133914-38">
     [38]
    </xref>.</p>
   <p>Here, comparison of ICPN schemes and former used names were made for reference (<xref ref-type="table" rid="table1">
     Table 1
    </xref>). Following the above guidelines, ICPN 2.0 scheme retained names with clear and unique characteristics, such as Papillate, Saddle, Bilobate, Polylobate, Cross, Rondel and so on <xref ref-type="bibr" rid="scirp.133914-24">
     [24]
    </xref> <xref ref-type="bibr" rid="scirp.133914-38">
     [38]
    </xref>. Phytolith types that were difficult to distinguish by morphological characteristics, should be classified according to the principles <xref ref-type="bibr" rid="scirp.133914-38">
     [38]
    </xref>. For example, Spheroid phytoliths could be divided into Spheroid psilate, Spheroid echinate and Spheroid ornate <xref ref-type="bibr" rid="scirp.133914-38">
     [38]
    </xref>. Elongate long cells could be classified into Elongate entire, Elongate sinuate, Elongate dentate and Elongate dendritic <xref ref-type="bibr" rid="scirp.133914-38">
     [38]
    </xref>. Those of bulliform cells could be divided into Blocky and Bulliform flabellate (referring to curved edge on one side) <xref ref-type="bibr" rid="scirp.133914-38">
     [38]
    </xref>. Some morphotypes with similar feature under the microscope and few taxonomic significance were merged. For example, Acicular hair cells and Unciform hair cells were combined into Acute bulbosus <xref ref-type="bibr" rid="scirp.133914-38">
     [38]
    </xref>.</p>
   <p>Compared with former schemes, the description glossary of shape, texture and ornamentation were revised in the ICPN 2.0 <xref ref-type="bibr" rid="scirp.133914-38">
     [38]
    </xref>. For example, the changes in shape descriptors included new descriptors of amoeboid (i.e., an irregular plate shape with several small rounded projections), bulbous and prismatic, and substitution of globular with spheroidal and fan-shaped with flabellate, and combination of descriptors lanceolate and unciform, and so on <xref ref-type="bibr" rid="scirp.133914-38">
     [38]
    </xref>. Terms of velloate and dentate were added into the margin descriptors <xref ref-type="bibr" rid="scirp.133914-38">
     [38]
    </xref>. Besides, ICPN 2.0 classified meanings of rugulate into descriptors plicate and rugose, and combined cavate and lacunose into descriptor scrobiculate <xref ref-type="bibr" rid="scirp.133914-38">
     [38]
    </xref>.</p>
  </sec><sec id="s3">
   <title>3. Typical Illustrations of Diagnostic Phytoliths</title>
   <p>Based on a wide range of investigations on modern phytolith morphology, many advances were achieved in phytolith morphotypes, particularly in the field of</p>
   <table-wrap id="table1">
    <label>
     <xref ref-type="table" rid="table1">
      Table 1
     </xref></label>
    <caption>
     <title>
      <xref ref-type="bibr" rid="scirp.133914-"></xref>Table 1. Comparison of different schemes for phytolith naming.Table 1. Comparison of different schemes for phytolith naming.</title>
    </caption>
    <table class="MsoTableGrid custom-table" border="0" cellspacing="0" cellpadding="0"> 
     <tr> 
      <td class="custom-bottom-td acenter" width="20.98%"><p style="text-align:center">ICPN 2.0 <xref ref-type="bibr" rid="scirp.133914-38">
         [38]
        </xref></p></td> 
      <td class="custom-bottom-td acenter" width="13.57%"><p style="text-align:center">Code <xref ref-type="bibr" rid="scirp.133914-38">
         [38]
        </xref></p></td> 
      <td class="custom-bottom-td acenter" width="36.03%"><p style="text-align:center">ICPN 1.0 <xref ref-type="bibr" rid="scirp.133914-24">
         [24]
        </xref></p></td> 
      <td class="custom-bottom-td acenter" width="29.42%"><p style="text-align:center">Former name <xref ref-type="bibr" rid="scirp.133914-1">
         [1]
        </xref> <xref ref-type="bibr" rid="scirp.133914-2">
         [2]
        </xref> <xref ref-type="bibr" rid="scirp.133914-24">
         [24]
        </xref></p></td> 
     </tr> 
     <tr> 
      <td class="custom-top-td acenter" width="20.98%"><p style="text-align:center">Spheroid psilate</p></td> 
      <td class="custom-top-td acenter" width="13.57%"><p style="text-align:center">SPH_PSI</p></td> 
      <td class="custom-top-td acenter" width="36.03%"><p style="text-align:center">Globular psilate</p></td> 
      <td class="custom-top-td acenter" width="29.42%"><p style="text-align:center">Spherical smooth</p></td> 
     </tr> 
     <tr> 
      <td class="acenter" width="20.98%"><p style="text-align:center">Spheroid echinate</p></td> 
      <td class="acenter" width="13.57%"><p style="text-align:center">SPH_ECH</p></td> 
      <td class="acenter" width="36.03%"><p style="text-align:center">Globular echinate</p></td> 
      <td class="acenter" width="29.42%"><p style="text-align:center">Spherical crenate</p></td> 
     </tr> 
     <tr> 
      <td class="acenter" width="20.98%"><p style="text-align:center">Spheroid ornate</p></td> 
      <td class="acenter" width="13.57%"><p style="text-align:center">SPH_ORN</p></td> 
      <td class="acenter" width="36.03%"><p style="text-align:center">Globular granulate</p></td> 
      <td class="acenter" width="29.42%"><p style="text-align:center">Spherical rugose</p></td> 
     </tr> 
     <tr> 
      <td class="acenter" width="20.98%"><p style="text-align:center">Acute bulbosus</p></td> 
      <td class="acenter" width="13.57%"><p style="text-align:center">ACU_BUL</p></td> 
      <td class="acenter" width="36.03%"><p style="text-align:center">Acicular hair cell/Unciform hair cell</p></td> 
      <td class="acenter" width="29.42%"><p style="text-align:center">Point-shaped</p></td> 
     </tr> 
     <tr> 
      <td class="acenter" width="20.98%"><p style="text-align:center">Blocky</p></td> 
      <td class="acenter" width="13.57%"><p style="text-align:center">BLO</p></td> 
      <td class="acenter" width="36.03%"><p style="text-align:center">Parallelepipedal bulliform</p></td> 
      <td class="acenter" width="29.42%"><p style="text-align:center">Bulliform/Square/Rectangle</p></td> 
     </tr> 
     <tr> 
      <td class="acenter" width="20.98%"><p style="text-align:center">Bulliform flabellate</p></td> 
      <td class="acenter" width="13.57%"><p style="text-align:center">BUL_FLA</p></td> 
      <td class="acenter" width="36.03%"><p style="text-align:center">Cuneiform bulliform cell</p></td> 
      <td class="acenter" width="29.42%"><p style="text-align:center">Bulliform/Fan-shaped</p></td> 
     </tr> 
     <tr> 
      <td class="acenter" width="20.98%"><p style="text-align:center">Elongate entire</p></td> 
      <td class="acenter" width="13.57%"><p style="text-align:center">ELO_ENT</p></td> 
      <td class="acenter" width="36.03%"><p style="text-align:center">Elongate psilate</p></td> 
      <td class="acenter" width="29.42%"><p style="text-align:center">Smooth elongate</p></td> 
     </tr> 
     <tr> 
      <td class="acenter" width="20.98%"><p style="text-align:center">Elongate sinuate</p></td> 
      <td class="acenter" width="13.57%"><p style="text-align:center">ELO_SIN</p></td> 
      <td class="acenter" width="36.03%"><p style="text-align:center">/</p></td> 
      <td class="acenter" width="29.42%"><p style="text-align:center">/</p></td> 
     </tr> 
     <tr> 
      <td class="acenter" width="20.98%"><p style="text-align:center">Elongate dentate</p></td> 
      <td class="acenter" width="13.57%"><p style="text-align:center">ELO_DET</p></td> 
      <td class="acenter" width="36.03%"><p style="text-align:center">Elongate echinate long cell</p></td> 
      <td class="acenter" width="29.42%"><p style="text-align:center">Elongate spiny/Elongate sinuous</p></td> 
     </tr> 
     <tr> 
      <td class="acenter" width="20.98%"><p style="text-align:center">Elongate dendritic</p></td> 
      <td class="acenter" width="13.57%"><p style="text-align:center">ELO_DEN</p></td> 
      <td class="acenter" width="36.03%"><p style="text-align:center">Dendritic/Dentritic</p></td> 
      <td class="acenter" width="29.42%"><p style="text-align:center">Dendriform</p></td> 
     </tr> 
     <tr> 
      <td class="acenter" width="20.98%"><p style="text-align:center">Papillate</p></td> 
      <td class="acenter" width="13.57%"><p style="text-align:center">PAP</p></td> 
      <td class="acenter" width="36.03%"><p style="text-align:center">Papillate</p></td> 
      <td class="acenter" width="29.42%"><p style="text-align:center">Papillate</p></td> 
     </tr> 
     <tr> 
      <td class="acenter" width="20.98%"><p style="text-align:center">Stomata</p></td> 
      <td class="acenter" width="13.57%"><p style="text-align:center">STO</p></td> 
      <td class="acenter" width="36.03%"><p style="text-align:center">Stomata</p></td> 
      <td class="acenter" width="29.42%"><p style="text-align:center">Stomata</p></td> 
     </tr> 
     <tr> 
      <td class="acenter" width="20.98%"><p style="text-align:center">Tracheary</p></td> 
      <td class="acenter" width="13.57%"><p style="text-align:center">TRA</p></td> 
      <td class="acenter" width="36.03%"><p style="text-align:center">Cylindric sulcate tracheid</p></td> 
      <td class="acenter" width="29.42%"><p style="text-align:center">Tracheid</p></td> 
     </tr> 
     <tr> 
      <td class="acenter" width="20.98%"><p style="text-align:center">Saddle</p></td> 
      <td class="acenter" width="13.57%"><p style="text-align:center">SAD</p></td> 
      <td class="acenter" width="36.03%"><p style="text-align:center">Saddle</p></td> 
      <td class="acenter" width="29.42%"><p style="text-align:center">Saddle</p></td> 
     </tr> 
     <tr> 
      <td class="acenter" width="20.98%"><p style="text-align:center">Bilobate</p></td> 
      <td class="acenter" width="13.57%"><p style="text-align:center">BIL</p></td> 
      <td class="acenter" width="36.03%"><p style="text-align:center">Bilobate short cell</p></td> 
      <td class="acenter" width="29.42%"><p style="text-align:center">Dumbbell/Bilobate</p></td> 
     </tr> 
     <tr> 
      <td class="acenter" width="20.98%"><p style="text-align:center">Polylobate</p></td> 
      <td class="acenter" width="13.57%"><p style="text-align:center">POL</p></td> 
      <td class="acenter" width="36.03%"><p style="text-align:center">Cylindrical polylobate</p></td> 
      <td class="acenter" width="29.42%"><p style="text-align:center">Polylobate/Multilobate</p></td> 
     </tr> 
     <tr> 
      <td class="acenter" width="20.98%"><p style="text-align:center">Cross</p></td> 
      <td class="acenter" width="13.57%"><p style="text-align:center">CRO</p></td> 
      <td class="acenter" width="36.03%"><p style="text-align:center">Cross</p></td> 
      <td class="acenter" width="29.42%"><p style="text-align:center">Cross</p></td> 
     </tr> 
     <tr> 
      <td class="acenter" width="20.98%"><p style="text-align:center">Crenate</p></td> 
      <td class="acenter" width="13.57%"><p style="text-align:center">CRE</p></td> 
      <td class="acenter" width="36.03%"><p style="text-align:center">Trapeziform polylobate/Trapeziform sinuate</p></td> 
      <td class="acenter" width="29.42%"><p style="text-align:center">Wavy trapezoid/Tooth</p></td> 
     </tr> 
     <tr> 
      <td class="acenter" width="20.98%"><p style="text-align:center">Rondel</p></td> 
      <td class="acenter" width="13.57%"><p style="text-align:center">RON</p></td> 
      <td class="acenter" width="36.03%"><p style="text-align:center">Rondel</p></td> 
      <td class="acenter" width="29.42%"><p style="text-align:center">Hat-shaped/Tower-shaped</p></td> 
     </tr> 
     <tr> 
      <td class="acenter" width="20.98%"><p style="text-align:center">Trapezoid</p></td> 
      <td class="acenter" width="13.57%"><p style="text-align:center">TRZ</p></td> 
      <td class="acenter" width="36.03%"><p style="text-align:center">Trapeziform short cell</p></td> 
      <td class="acenter" width="29.42%"><p style="text-align:center">/</p></td> 
     </tr> 
    </table>
   </table-wrap>
   <p>diagnostic phytolith morphotypes and their taxonomic significance of different plant groups <xref ref-type="bibr" rid="scirp.133914-1">
     [1]
    </xref> <xref ref-type="bibr" rid="scirp.133914-2">
     [2]
    </xref> <xref ref-type="bibr" rid="scirp.133914-3">
     [3]
    </xref> <xref ref-type="bibr" rid="scirp.133914-4">
     [4]
    </xref> <xref ref-type="bibr" rid="scirp.133914-5">
     [5]
    </xref> <xref ref-type="bibr" rid="scirp.133914-25">
     [25]
    </xref>-<xref ref-type="bibr" rid="scirp.133914-35">
     [35]
    </xref> <xref ref-type="bibr" rid="scirp.133914-39">
     [39]
    </xref>-<xref ref-type="bibr" rid="scirp.133914-47">
     [47]
    </xref>. However, there are still some confusions in the definition and description of diagnostic phytolith morphotypes <xref ref-type="bibr" rid="scirp.133914-40">
     [40]
    </xref> <xref ref-type="bibr" rid="scirp.133914-47">
     [47]
    </xref>. Here, research progress and typical morphological illustrations of diagnostic phytolith morphotypes in the past 20 years were sorted out, focusing on the region of East Asia. The following naming and description of phytoliths refer to the ICPN 2.0 <xref ref-type="bibr" rid="scirp.133914-38">
     [38]
    </xref>.</p>
   <sec id="s3_1">
    <title>3.1. Diagnostic Phytoliths in Grasses</title>
    <p>Compared with traditional palaeoecological indicators such as pollen and spores, the herbaceous diagnostic phytolith morphotypes have more explicit representations for many plant groups, particularly for those in Poaceae including Bambusoideae, Oryzoideae, Arundiaceae, Chloridoideae and Panicoideae, and Cyperaceae <xref ref-type="bibr" rid="scirp.133914-48">
      [48]
     </xref>, etc. This advantage of herbaceous phytoliths has been widely applied to the reconstruction of grassland vegetation, and recovered details about the changes in vegetation composition and plant diversity of grassland at different geological time scales <xref ref-type="bibr" rid="scirp.133914-6">
      [6]
     </xref> <xref ref-type="bibr" rid="scirp.133914-8">
      [8]
     </xref>.</p>
    <p>Phytolith types from Bambusoideae included Saddle, Bulliform flabellate, Blocky, Rondel, Stomata, Acute bulbosus, Tracheary, etc., among which Saddle (length/width ratio &gt; 1) (<xref ref-type="fig" rid="fig1(a)">
      Figure 1(a)
     </xref>) and Bulliform flabellate (clavate margin) (<xref ref-type="fig" rid="fig1(b)">
      Figure 1(b)
     </xref>) were diagnostic morphotypes of Bambusoideae <xref ref-type="bibr" rid="scirp.133914-2">
      [2]
     </xref> <xref ref-type="bibr" rid="scirp.133914-25">
      [25]
     </xref>. Phytoliths from Oryzoideae included Bilobate, Bulliform flabellate, Rodel, Elongate sinuate, Acute bulbosus, Double-peaked glume, etc., among which Bulliform flabellate with scale-decoration (<xref ref-type="fig" rid="fig1(c)">
      Figure 1(c)
     </xref>) and Double-peaked glume (<xref ref-type="fig" rid="fig1(d)">
      Figure 1(d)
     </xref>) were diagnostic morphotypes <xref ref-type="bibr" rid="scirp.133914-31">
      [31]
     </xref> <xref ref-type="bibr" rid="scirp.133914-49">
      [49]
     </xref>-<xref ref-type="bibr" rid="scirp.133914-53">
      [53]
     </xref>. Phytolith from Arundiaceae included Saddle, Bulliform flabellate, Elongate sinuate, Trapzoid, Acute bulbosus, etc., among which Saddle (length/width ratio ≈ 1) (<xref ref-type="fig" rid="fig1(e)">
      Figure 1(e)
     </xref>) and Bulliform flabellate (shield margin) (<xref ref-type="fig" rid="fig1(f)">
      Figure 1(f)
     </xref>) were diagnostic <xref ref-type="bibr" rid="scirp.133914-2">
      [2]
     </xref> <xref ref-type="bibr" rid="scirp.133914-27">
      [27]
     </xref> <xref ref-type="bibr" rid="scirp.133914-41">
      [41]
     </xref>. Phytoliths from plants of Chloridoideae included Saddle, Bilobate, Elongate sinuate, Acute bulbosus, Bulliform flabellate, Tracheary, etc., among which Saddle with a length/width ratio &lt; 1 (<xref ref-type="fig" rid="fig1(g)">
      Figure 1(g)
     </xref>) was the diagnostic morphotype <xref ref-type="bibr" rid="scirp.133914-2">
      [2]
     </xref> <xref ref-type="bibr" rid="scirp.133914-21">
      [21]
     </xref>. Phytolith from Pooideae included Bilobate, Elongate dentate, Rodel, Acute bulbosus, blocky, Tracheary, etc., among which Bilobate trapeziform (<xref ref-type="fig" rid="fig1(h)">
      Figure 1(h)
     </xref>) and Elongate dentate (<xref ref-type="fig" rid="fig1(i)">
      Figure 1(i)
     </xref>) were diagnostic morphotypes <xref ref-type="bibr" rid="scirp.133914-2">
      [2]
     </xref> <xref ref-type="bibr" rid="scirp.133914-26">
      [26]
     </xref>. Phytolith from Panicoideae included Bilobate (including Cross), Polylobate, Blocky, Elongate sinuate/Elongate dendritic, Bulliform flabellate, Rodel, Acute bulbosus, Tracheary, etc., among which Bilobate (<xref ref-type="fig" rid="fig1(j)">
      Figure 1(j)
     </xref>), Polylobate (<xref ref-type="fig" rid="fig1(k">
      Figure 1(k
     </xref>)) <xref ref-type="bibr" rid="scirp.133914-2">
      [2]
     </xref> <xref ref-type="bibr" rid="scirp.133914-54">
      [54]
     </xref> and Elongate sinuate of lemma (<xref ref-type="fig" rid="fig1(l)">
      Figure 1(l)
     </xref>) <xref ref-type="bibr" rid="scirp.133914-3">
      [3]
     </xref> <xref ref-type="bibr" rid="scirp.133914-4">
      [4]
     </xref> <xref ref-type="bibr" rid="scirp.133914-5">
      [5]
     </xref> were diagnostic morphotypes. Cyperaceae phytoliths included Polygonal granulate (<xref ref-type="fig" rid="fig1(m)">
      Figure 1(m)
     </xref>), Papillate (<xref ref-type="fig" rid="fig1(n)">
      Figure 1(n)
     </xref>), Acute bulbosus, Elongate, Stomata, Tracheary, etc., among which the first two were the diagnostic morphotypes <xref ref-type="bibr" rid="scirp.133914-2">
      [2]
     </xref> <xref ref-type="bibr" rid="scirp.133914-42">
      [42]
     </xref> <xref ref-type="bibr" rid="scirp.133914-55">
      [55]
     </xref>. In addition, there were some other phytolith producers in herbaceous plants (e.g., Zingiberaceae <xref ref-type="bibr" rid="scirp.133914-39">
      [39]
     </xref>, Commelinaceae <xref ref-type="bibr" rid="scirp.133914-56">
      [56]
     </xref>).</p>
   </sec>
   <sec id="s3_2">
    <title>3.2. Diagnostic Phytoliths in Woody Plants and Ferns</title>
    <p>In recent years, phytolith morphological studies of woody plants have gradually established diagnostic phytolith morphotypes for the groups of broadleaved trees and conifer trees, which exhibit significant potential in the reconstruction of forest and woodland environment <xref ref-type="bibr" rid="scirp.133914-28">
      [28]
     </xref> <xref ref-type="bibr" rid="scirp.133914-40">
      [40]
     </xref> <xref ref-type="bibr" rid="scirp.133914-44">
      [44]
     </xref> <xref ref-type="bibr" rid="scirp.133914-46">
      [46]
     </xref> <xref ref-type="bibr" rid="scirp.133914-47">
      [47]
     </xref>. It was found that phytolith types in broadleaved trees included Stomata stellate, Elongate brachiate geniculate, Irregular sinuate, Polygonal tabular, Trichome irregular tubercule, Trichome bulbous irregular, Elongate facetate, Tracheary annulate/facetate geniculate, Tracheary annulate/facetate claviform, Tracheary helical, Spheroid favose, Elongate entire, Spheroid hollow, Irregular articulated granulate and so on <xref ref-type="bibr" rid="scirp.133914-44">
      [44]
     </xref>. Among these types, Elongate brachiate geniculate (<xref ref-type="fig" rid="fig2(a)">
      Figure 2(a)
     </xref>), Polygonal tabular (<xref ref-type="fig" rid="fig2(b)">
      Figure 2(b)
     </xref>), Elongate facetate (<xref ref-type="fig" rid="fig2(c)">
      Figure 2(c)
     </xref>), Tracheary annulate/facetate claviform (<xref ref-type="fig" rid="fig2(d)">
      Figure 2(d)
     </xref>) and Tracheary annulate/facetate geniculate (<xref ref-type="fig" rid="fig2(e)">
      Figure 2(e)
     </xref>) could be used as diagnostic phytolith morphotypes for broadleaved trees <xref ref-type="bibr" rid="scirp.133914-44">
      [44]
     </xref>. Besides, Spheroid echinate (<xref ref-type="fig" rid="fig2(f)">
      Figure 2(f)
     </xref>) was a diagnostic phytolith morphotype for Arecaceae <xref ref-type="bibr" rid="scirp.133914-28">
      [28]
     </xref> <xref ref-type="bibr" rid="scirp.133914-39">
      [39]
     </xref> <xref ref-type="bibr" rid="scirp.133914-46">
      [46]
     </xref>, whose diameter (6 - 25 µm) could be used</p>
    <fig id="fig1" position="float">
     <label>Figure 1</label>
     <caption>
      <title>Figure 1. Illustrations of diagnostic phytolith morphotypes from grasses. (a) Bambusoideae Saddle <xref ref-type="bibr" rid="scirp.133914-25">
        [25]
       </xref>, (b) Bulliform flabellate clavate <xref ref-type="bibr" rid="scirp.133914-25">
        [25]
       </xref>, (c) Bulliform flabellate with scale-decoration <xref ref-type="bibr" rid="scirp.133914-43">
        [43]
       </xref>, (d) Double-peaked glume <xref ref-type="bibr" rid="scirp.133914-53">
        [53]
       </xref>, (e) Arundiaceae Saddle <xref ref-type="bibr" rid="scirp.133914-41">
        [41]
       </xref>, (f) Bulliform flabellate <xref ref-type="bibr" rid="scirp.133914-41">
        [41]
       </xref> (g) Chloridoideae Saddle <xref ref-type="bibr" rid="scirp.133914-27">
        [27]
       </xref>, (h) Bilobate trapeziform <xref ref-type="bibr" rid="scirp.133914-26">
        [26]
       </xref>, (i) Elongate dentate <xref ref-type="bibr" rid="scirp.133914-26">
        [26]
       </xref>, (j) Bilobate <xref ref-type="bibr" rid="scirp.133914-23">
        [23]
       </xref>, (k) Polylobate <xref ref-type="bibr" rid="scirp.133914-23">
        [23]
       </xref>, (l) lemma Elongate dendritic <xref ref-type="bibr" rid="scirp.133914-5">
        [5]
       </xref>, (m) Polygonal granulate <xref ref-type="bibr" rid="scirp.133914-55">
        [55]
       </xref>, (n) Papillate <xref ref-type="bibr" rid="scirp.133914-55">
        [55]
       </xref>. Scale = 10 µm.</title>
     </caption>
     <graphic mimetype="image" position="float" xlink:type="simple" xlink:href="https://html.scirp.org/file/2802513-rId13.jpeg?20240620020509" />
    </fig>
    <fig id="fig2" position="float">
     <label>Figure 2</label>
     <caption>
      <title>Figure 2. Illustrations of diagnostic phytolith morphotypes from woody plants and ferns. (a) Elongate brachiate geniculate <xref ref-type="bibr" rid="scirp.133914-44">
        [44]
       </xref>, (b) Polygonal tabular <xref ref-type="bibr" rid="scirp.133914-44">
        [44]
       </xref>, (c) Elongate facetate <xref ref-type="bibr" rid="scirp.133914-44">
        [44]
       </xref>, (d) Tracheary annulate/facetate claviform <xref ref-type="bibr" rid="scirp.133914-44">
        [44]
       </xref>, (e) Tracheary annulate/facetate geniculate <xref ref-type="bibr" rid="scirp.133914-44">
        [44]
       </xref>, (f) Spheroid echinate <xref ref-type="bibr" rid="scirp.133914-46">
        [46]
       </xref>, (g) Blocky polyhedral <xref ref-type="bibr" rid="scirp.133914-40">
        [40]
       </xref>, (h) Elongate tabular cavate <xref ref-type="bibr" rid="scirp.133914-40">
        [40]
       </xref>, (i) Irregular anticlinal <xref ref-type="bibr" rid="scirp.133914-45">
        [45]
       </xref>, (j) Prismatic elongate <xref ref-type="bibr" rid="scirp.133914-45">
        [45]
       </xref>, (k) Elongate sinuate <xref ref-type="bibr" rid="scirp.133914-57">
        [57]
       </xref>, (l) Spheroidal cavate granulate <xref ref-type="bibr" rid="scirp.133914-45">
        [45]
       </xref>, (m) Silicified epidermis granulate <xref ref-type="bibr" rid="scirp.133914-45">
        [45]
       </xref>, (n) Amoeboid branchiate <xref ref-type="bibr" rid="scirp.133914-45">
        [45]
       </xref>, (o) Prismatic cubic <xref ref-type="bibr" rid="scirp.133914-45">
        [45]
       </xref>. Scale = 20 µm.</title>
     </caption>
     <graphic mimetype="image" position="float" xlink:type="simple" xlink:href="https://html.scirp.org/file/2802513-rId14.jpeg?20240620020509" />
    </fig>
    <p>to distinguish it from Spheroid echinate of Bromeliaceae (&lt;2 to 10 µmm) <xref ref-type="bibr" rid="scirp.133914-39">
      [39]
     </xref> <xref ref-type="bibr" rid="scirp.133914-46">
      [46]
     </xref>. The morphotypes of conifer phytoliths included Blocky polyhedral, Elongate tabular cavate, Elongate echinate, Elongate entire, Stomata, etc., among which Blocky polyhedral (<xref ref-type="fig" rid="fig2(g)">
      Figure 2(g)
     </xref>) and Elongate tabular cavate (<xref ref-type="fig" rid="fig2(h)">
      Figure 2(h)
     </xref>) were diagnostic morphotypes <xref ref-type="bibr" rid="scirp.133914-40">
      [40]
     </xref> <xref ref-type="bibr" rid="scirp.133914-47">
      [47]
     </xref>.</p>
    <p>In addition, studies on modern fern phytoliths have shown that there are mainly 12 types of fern phytoliths, including Acicular, Amoeboid branchiate, Elongate echinate, Elongate sinuate, Irregular anticlinal, Prismatic elongate, Prismatic cubic, Stomata, Spheroidal cavate granulate, Silicified epidermis granulate, Tracheary elongate, and Silicified epidermis/hypodermis <xref ref-type="bibr" rid="scirp.133914-45">
      [45]
     </xref> <xref ref-type="bibr" rid="scirp.133914-57">
      [57]
     </xref>. Among them, Irregular anticlinal (<xref ref-type="fig" rid="fig2(i)">
      Figure 2(i)
     </xref>), Prismatic elongate (<xref ref-type="fig" rid="fig2(j)">
      Figure 2(j)
     </xref>), Elongate sinuate (<xref ref-type="fig" rid="fig2(k)">
      Figure 2(k)
     </xref>), Spheroidal cavate granulate (<xref ref-type="fig" rid="fig2(l)">
      Figure 2(l)
     </xref>), Silicified epidermis granulate (<xref ref-type="fig" rid="fig2(m)">
      Figure 2(m)
     </xref>), Amoeboid branchiate (<xref ref-type="fig" rid="fig2(n)">
      Figure 2(n)
     </xref>) and Prismatic cubic (<xref ref-type="fig" rid="fig2(o)">
      Figure 2(o)
     </xref>) were diagnostic morphotypes for ferns <xref ref-type="bibr" rid="scirp.133914-45">
      [45]
     </xref>.</p>
   </sec>
   <sec id="s3_3">
    <title>3.3. Diagnostic Phytoliths in Key Crops and Their Relatives in East Asia</title>
    <p>Researches in environmental archaeology have promoted investigation and application of diagnostic phytoliths of crops and their relatives <xref ref-type="bibr" rid="scirp.133914-2">
      [2]
     </xref> <xref ref-type="bibr" rid="scirp.133914-3">
      [3]
     </xref> <xref ref-type="bibr" rid="scirp.133914-4">
      [4]
     </xref> <xref ref-type="bibr" rid="scirp.133914-5">
      [5]
     </xref> <xref ref-type="bibr" rid="scirp.133914-10">
      [10]
     </xref>-<xref ref-type="bibr" rid="scirp.133914-15">
      [15]
     </xref> <xref ref-type="bibr" rid="scirp.133914-53">
      [53]
     </xref>. Some phytolith morphotypes have the potential of identification precision and accuracy to genus or species <xref ref-type="bibr" rid="scirp.133914-3">
      [3]
     </xref> <xref ref-type="bibr" rid="scirp.133914-4">
      [4]
     </xref>. Therefore, they have been widely utilized in the study of domesticated and cultivated processes of key crops in dryland and rice agriculture in East Asia, such as rice, various types of millets and their relative plants <xref ref-type="bibr" rid="scirp.133914-4">
      [4]
     </xref> <xref ref-type="bibr" rid="scirp.133914-12">
      [12]
     </xref> <xref ref-type="bibr" rid="scirp.133914-14">
      [14]
     </xref> <xref ref-type="bibr" rid="scirp.133914-15">
      [15]
     </xref> <xref ref-type="bibr" rid="scirp.133914-16">
      [16]
     </xref>.</p>
    <p>Morphological studies of maize (Zea mays L.) phytolith confirmed that Cross (<xref ref-type="fig" rid="fig3(a)">
      Figure 3(a)
     </xref>) was the diagnostic morphotype, whose size and basal features could be used to distinguish it from other grasses <xref ref-type="bibr" rid="scirp.133914-1">
      [1]
     </xref> <xref ref-type="bibr" rid="scirp.133914-13">
      [13]
     </xref> <xref ref-type="bibr" rid="scirp.133914-58">
      [58]
     </xref> <xref ref-type="bibr" rid="scirp.133914-59">
      [59]
     </xref>. The diagnostic phytolith morphotype of cereals were Epidermis elongate dendritic and Papillate (<xref ref-type="fig" rid="fig3(b)">
      Figure 3(b)
     </xref>), whose size and margin shape could be used for identification of wheat and barley remains <xref ref-type="bibr" rid="scirp.133914-17">
      [17]
     </xref> <xref ref-type="bibr" rid="scirp.133914-60">
      [60]
     </xref>.</p>
    <p>Rice (Oryza sativa) is one of the most important crops in East Asia <xref ref-type="bibr" rid="scirp.133914-49">
      [49]
     </xref>. Rice phytolith of Double-peaked glume (<xref ref-type="fig" rid="fig1(d)">
      Figure 1(d)
     </xref>) and its morphological parameters could be used to distinguish between wild and domesticated rice <xref ref-type="bibr" rid="scirp.133914-31">
      [31]
     </xref>. The number of fish-scaled decoration on Bulliform flabellate (<xref ref-type="fig" rid="fig1(c)">
      Figure 1(c)
     </xref>) could also effectively distinguish between wild and domesticated rice <xref ref-type="bibr" rid="scirp.133914-50">
      [50]
     </xref>. The percentage of Bulliform flabellate with ≥ 9 scale decorations among all Bulliform flabellate phytoliths could be used as an indicator to evaluate whether ancient rice had developed domestication properties <xref ref-type="bibr" rid="scirp.133914-49">
      [49]
     </xref> <xref ref-type="bibr" rid="scirp.133914-50">
      [50]
     </xref> <xref ref-type="bibr" rid="scirp.133914-51">
      [51]
     </xref> <xref ref-type="bibr" rid="scirp.133914-52">
      [52]
     </xref> <xref ref-type="bibr" rid="scirp.133914-53">
      [53]
     </xref>, based on the finding that the lowest value of Bulliform flabellate with ≥9 scale decorations was ~40% in domesticated rice <xref ref-type="bibr" rid="scirp.133914-50">
      [50]
     </xref>.</p>
    <p>The glumes phytoliths of millets, typical crops of dryland agriculture in China, had important significance in identification of ancient millet plants <xref ref-type="bibr" rid="scirp.133914-12">
      [12]
     </xref>. The Ω-type (<xref ref-type="fig" rid="fig3(c)">
      Figure 3(c)
     </xref>) and η-type (<xref ref-type="fig" rid="fig3(d)">
      Figure 3(d)
     </xref>) margin shapes of Epidermis elongate dendritic on the outer and inner glumes were the most important</p>
    <fig id="fig3" position="float">
     <label>Figure 3</label>
     <caption>
      <title>Figure 3. Illustrations Illustrations of diagnostic phytolith morphotypes from key crops and related plants. (a) maize Cross <xref ref-type="bibr" rid="scirp.133914-58">
        [58]
       </xref>, (b) cereal Epidermis elongate dendritic and Papillate <xref ref-type="bibr" rid="scirp.133914-17">
        [17]
       </xref>, (c) Ω-type Epidermis elongate dendritic <xref ref-type="bibr" rid="scirp.133914-3">
        [3]
       </xref>, (d) η-type Epidermis elongate dendritic <xref ref-type="bibr" rid="scirp.133914-3">
        [3]
       </xref>, (e) foxtail millet Cross <xref ref-type="bibr" rid="scirp.133914-3">
        [3]
       </xref>, (f) common millet Bilobate <xref ref-type="bibr" rid="scirp.133914-3">
        [3]
       </xref>, (g) foxtail millet Papillate <xref ref-type="bibr" rid="scirp.133914-3">
        [3]
       </xref>, (h) cross-wavy ends of epidermal long cells from foxtail millet <xref ref-type="bibr" rid="scirp.133914-3">
        [3]
       </xref>, (i) cross-finger ends of epidermal long cells from common millet <xref ref-type="bibr" rid="scirp.133914-3">
        [3]
       </xref>, (j) silicon surface ridgy line sculpture in Ω-type Elongate dendritic from foxtail millet <xref ref-type="bibr" rid="scirp.133914-3">
        [3]
       </xref>, (k) β-type epidermis elongate dendritic from barnyard millet <xref ref-type="bibr" rid="scirp.133914-33">
        [33]
       </xref>, (l) Tabular sinuate verrucate <xref ref-type="bibr" rid="scirp.133914-35">
        [35]
       </xref>, (m) Tabular sinuate psilate <xref ref-type="bibr" rid="scirp.133914-35">
        [35]
       </xref>, (n) Trichome base calcium phytolith with regular cracks <xref ref-type="bibr" rid="scirp.133914-61">
        [61]
       </xref>, (o) Druse calcium phytolith <xref ref-type="bibr" rid="scirp.133914-61">
        [61]
       </xref>. Scale = 20 µm.</title>
     </caption>
     <graphic mimetype="image" position="float" xlink:type="simple" xlink:href="https://html.scirp.org/file/2802513-rId15.jpeg?20240620020509" />
    </fig>
    <p>features for identifying common millet and foxtail millet, respectively <xref ref-type="bibr" rid="scirp.133914-12">
      [12]
     </xref>. Furthermore, Lu et al. <xref ref-type="bibr" rid="scirp.133914-3">
      [3]
     </xref> demonstrated five identification criteria of diagnostic morphological features for these two groups: 1) foxtail millet had Cross phytolith (<xref ref-type="fig" rid="fig3(e)">
      Figure 3(e)
     </xref>) in glumes and lower lemma, while common millet had Bilobate (<xref ref-type="fig" rid="fig3(f)">
      Figure 3(f)
     </xref>); 2) only foxtail millet had Papillae in upper lemma and palea (<xref ref-type="fig" rid="fig3(g)">
      Figure 3(g)
     </xref>); 3) Elongate dendritic in upper lemma and palea of foxtail millet had Ω-type margins, while that of common millet had η-type margins, and these two margin types could be subdivided into three subtypes; 4) the ends of epidermal long cells of foxtail millet and common millet were cross-wavy type (<xref ref-type="fig" rid="fig3(h)">
      Figure 3(h)
     </xref>) and cross-finger type (<xref ref-type="fig" rid="fig3(i)">
      Figure 3(i)
     </xref>), respectively; 5) rippling feature developed on the surface keratose layer and long cells of the upper lemma in foxtail millet (<xref ref-type="fig" rid="fig3(j)">
      Figure 3(j)
     </xref>). Moreover, Zhang et al. <xref ref-type="bibr" rid="scirp.133914-30">
      [30]
     </xref> <xref ref-type="bibr" rid="scirp.133914-34">
      [34]
     </xref> found that morphological parameters of Elongate dendritic of ΩIII margin on inner and outer glume could discriminate between foxtail millet and green foxtail. Ge et al. <xref ref-type="bibr" rid="scirp.133914-33">
      [33]
     </xref> found that the diagnostic phytolith morphotype of barnyard grass was Elongate dendritic with β-type margins (<xref ref-type="fig" rid="fig3(k)">
      Figure 3(k)
     </xref>).</p>
    <p>In addition, Wang et al. <xref ref-type="bibr" rid="scirp.133914-35">
      [35]
     </xref> found that Tabular sinuate verrucate (<xref ref-type="fig" rid="fig3(l)">
      Figure 3(l)
     </xref>) and Tabular sinuate psilate (<xref ref-type="fig" rid="fig3(m)">
      Figure 3(m)
     </xref>) were the diagnostic phytoliths in bastfiber crops. Recently, a new kind of calcium phytoliths, with similar anatomical origin to silicified phytoliths, were successfully applied in the identification of ancient tea residues <xref ref-type="bibr" rid="scirp.133914-61">
      [61]
     </xref>-<xref ref-type="bibr" rid="scirp.133914-63">
      [63]
     </xref>. The diagnostic morphotypes of tea calcium phytoliths in Camellia sinensis L. were Trichome base calcium phytolith with regular cracks (<xref ref-type="fig" rid="fig3(n)">
      Figure 3(n)
     </xref>) and Druse calcium phytolith (<xref ref-type="fig" rid="fig3(o)">
      Figure 3(o)
     </xref>) <xref ref-type="bibr" rid="scirp.133914-61">
      [61]
     </xref> <xref ref-type="bibr" rid="scirp.133914-62">
      [62]
     </xref>.</p>
   </sec>
  </sec><sec id="s4">
   <title>4. Conclusions and Prospects</title>
   <p>Significant progress has been made in the study of phytolith morphology in recent 20 years. The morphotype nomenclature and description for phytoliths have been gradually standardized. Numerous diagnostic phytolith morphotypes, especially those with over-representative to plant groups, have been discovered and reported. Based on the ICPN 2.0 scheme, this review briefly summarized the research progress of diagnostic phytoliths of plants of grasses, woody plants, key crops and relatives in dryland agriculture and rice agriculture in East Asia, and presented typical illustrations as a reference for phytolith analysis in vegetation reconstruction and environmental archaeology. The prospects for phytolith morphology research could be that:</p>
   <p>1) Phytolith analysis should strictly follow the ICPN 2.0, and take comprehensive consideration of diagnostic morphotypes and their geometric parameters in identification process.</p>
   <p>2) Extensive analysis on the morphology of modern plants, especially woody plants, can improve the representative of phytolith and enhance the reliability and plant diversity of paleovegetation reconstruction.</p>
   <p>3) Control experiments of phytolith growth and morphological change under different environmental conditions and interventions will provide important modern evidences for the mechanism interpretation in the phytolith-based paleoenvironment reconstruction and understanding of management strategies in ancient crop domestication.</p>
  </sec>
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