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  <front>
    <journal-meta>
      <journal-id journal-id-type="publisher-id">103</journal-id>
      <journal-id journal-id-type="index">urn:lsid:arphahub.com:pub:77d0745d-c3a1-5248-81de-8cdc02bed84a</journal-id>
      <journal-id journal-id-type="aggregator">urn:lsid:zoobank.org:pub:F56F6CF9-7502-4001-A751-35D5F2EF6CA0</journal-id>
      <journal-title-group>
        <journal-title xml:lang="en">Arthropod Systematics &amp; Phylogeny</journal-title>
        <abbrev-journal-title xml:lang="en">ASP</abbrev-journal-title>
      </journal-title-group>
      <issn pub-type="ppub">1863-7221</issn>
      <issn pub-type="epub">1864-8312</issn>
      <publisher>
        <publisher-name>Senckenberg Gesellschaft für Naturforschung</publisher-name>
      </publisher>
    </journal-meta>
    <article-meta>
      <article-id pub-id-type="doi">10.3897/asp.84.e181309</article-id>
      <article-id pub-id-type="publisher-id">181309</article-id>
      <article-categories>
        <subj-group subj-group-type="heading">
          <subject>Research Article</subject>
        </subj-group>
        <subj-group subj-group-type="biological_taxon">
          <subject>Reduviidae</subject>
        </subj-group>
        <subj-group subj-group-type="scientific_subject">
          <subject>Identification key</subject>
          <subject>Molecular systematics</subject>
          <subject>Phylogeny</subject>
          <subject>Taxonomy</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>New species and novel mitochondrial gene rearrangements in the thread-legged bug genus <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part></tp:taxon-name></italic> (<tp:taxon-name><tp:taxon-name-part taxon-name-part-type="order" reg="Hemiptera">Hemiptera</tp:taxon-name-part></tp:taxon-name>: <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="family" reg="Reduviidae">Reduviidae</tp:taxon-name-part></tp:taxon-name>: <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily" reg="Emesinae">Emesinae</tp:taxon-name-part></tp:taxon-name>)</article-title>
      </title-group>
      <contrib-group content-type="authors">
        <contrib contrib-type="author" corresp="no">
          <name name-style="western">
            <surname>Chen</surname>
            <given-names>Zhuo</given-names>
          </name>
          <uri content-type="orcid">https://orcid.org/0000-0003-3393-0338</uri>
          <xref ref-type="aff" rid="A1">1</xref>
          <role content-type="http://credit.niso.org/contributor-roles/conceptualization/">Conceptualization</role>
          <role content-type="http://credit.niso.org/contributor-roles/writing-original-draft/">Writing - original draft</role>
          <role content-type="http://credit.niso.org/contributor-roles/data-curation/">Data curation</role>
          <role content-type="http://credit.niso.org/contributor-roles/formal-analysis/">Formal analysis</role>
          <role content-type="http://credit.niso.org/contributor-roles/funding-acquisition/">Funding acquisition</role>
          <role content-type="http://credit.niso.org/contributor-roles/investigation/">Investigation</role>
          <role content-type="http://credit.niso.org/contributor-roles/methodology/">Methodology</role>
          <role content-type="http://credit.niso.org/contributor-roles/software/">Software</role>
          <role content-type="http://credit.niso.org/contributor-roles/validation/">Validation</role>
          <role content-type="http://credit.niso.org/contributor-roles/visualization/">Visualization</role>
        </contrib>
        <contrib contrib-type="author" corresp="no">
          <name name-style="western">
            <surname>Li</surname>
            <given-names>Hu</given-names>
          </name>
          <uri content-type="orcid">https://orcid.org/0000-0001-8590-1753</uri>
          <xref ref-type="aff" rid="A1">1</xref>
          <role content-type="http://credit.niso.org/contributor-roles/writing-review-editing/">Writing - review and editing</role>
          <role content-type="http://credit.niso.org/contributor-roles/data-curation/">Data curation</role>
          <role content-type="http://credit.niso.org/contributor-roles/funding-acquisition/">Funding acquisition</role>
          <role content-type="http://credit.niso.org/contributor-roles/methodology/">Methodology</role>
          <role content-type="http://credit.niso.org/contributor-roles/project-administration/">Project administration</role>
          <role content-type="http://credit.niso.org/contributor-roles/supervision/">Supervision</role>
        </contrib>
        <contrib contrib-type="author" corresp="yes">
          <name name-style="western">
            <surname>Cai</surname>
            <given-names>Wanzhi</given-names>
          </name>
          <email xlink:type="simple">caiwz@cau.edu.cn</email>
          <uri content-type="orcid">https://orcid.org/0000-0002-8620-0446</uri>
          <xref ref-type="aff" rid="A1">1</xref>
          <role content-type="http://credit.niso.org/contributor-roles/conceptualization/">Conceptualization</role>
          <role content-type="http://credit.niso.org/contributor-roles/writing-review-editing/">Writing - review and editing</role>
          <role content-type="http://credit.niso.org/contributor-roles/funding-acquisition/">Funding acquisition</role>
          <role content-type="http://credit.niso.org/contributor-roles/project-administration/">Project administration</role>
          <role content-type="http://credit.niso.org/contributor-roles/resources/">Resources</role>
          <role content-type="http://credit.niso.org/contributor-roles/supervision/">Supervision</role>
        </contrib>
      </contrib-group>
      <aff id="A1">
        <label>1</label>
        <addr-line content-type="verbatim">State Key Laboratory of Agricultural and Forestry Biosecurity, MARA Key Lab of Pest Monitoring and Green Management, College of Plant Protection, China Agricultural University, Beijing 100193, China</addr-line>
        <institution>China Agricultural University</institution>
        <addr-line content-type="city">Beijing</addr-line>
        <country>China</country>
      </aff>
      <author-notes>
        <fn fn-type="corresp">
          <p>Corresponding author: Wanzhi Cai (<email xlink:type="simple">caiwz@cau.edu.cn</email>)</p>
        </fn>
      </author-notes>
      <pub-date pub-type="collection">
        <year>2026</year>
      </pub-date>
      <pub-date pub-type="epub">
        <day>09</day>
        <month>07</month>
        <year>2026</year>
      </pub-date>
      <volume>84</volume>
      <fpage>565</fpage>
      <lpage>581</lpage>
      <uri content-type="arpha" xlink:href="http://openbiodiv.net/B99B11C2-9832-5D4E-B26D-3985CD3028A9">B99B11C2-9832-5D4E-B26D-3985CD3028A9</uri>
      <uri content-type="zoobank" xlink:href="https://zoobank.org/11DE66E1-3B5B-43BF-80AE-E743832F2A4C">11DE66E1-3B5B-43BF-80AE-E743832F2A4C</uri>
      <history>
        <date date-type="received">
          <day>04</day>
          <month>12</month>
          <year>2025</year>
        </date>
        <date date-type="accepted">
          <day>02</day>
          <month>06</month>
          <year>2026</year>
        </date>
      </history>
      <permissions>
        <copyright-statement>Zhuo Chen, Hu Li, Wanzhi Cai</copyright-statement>
        <license license-type="creative-commons-attribution" xlink:href="http://creativecommons.org/licenses/by/4.0/" xlink:type="simple">
          <license-p>This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</license-p>
        </license>
      </permissions>
      <self-uri content-type="zoobank" xlink:type="simple">https://zoobank.org/11DE66E1-3B5B-43BF-80AE-E743832F2A4C</self-uri>
      <abstract>
        <p>
          <bold>Abstract</bold>
        </p>
        <p>The thread-legged bug genus <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part></tp:taxon-name></italic> Wygodzinsky, 1966 (<tp:taxon-name><tp:taxon-name-part taxon-name-part-type="order" reg="Hemiptera">Hemiptera</tp:taxon-name-part></tp:taxon-name>: <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="suborder" reg="Heteroptera">Heteroptera</tp:taxon-name-part></tp:taxon-name>: <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="family" reg="Reduviidae">Reduviidae</tp:taxon-name-part></tp:taxon-name>: <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily" reg="Emesinae">Emesinae</tp:taxon-name-part></tp:taxon-name>: <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="tribe" reg="Emesini">Emesini</tp:taxon-name-part></tp:taxon-name>) is a small group of five species endemic to the Oriental Region. However, the species diversity of this genus is still far from completely explored, especially in the mainland of Asia. Here we describe three new species, <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="ornata">ornata</tp:taxon-name-part></tp:taxon-name></italic><bold>sp. n</bold>., <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="pulchella">pulchella</tp:taxon-name-part></tp:taxon-name></italic><bold>sp. n</bold>. and <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="weilingfengi">weilingfengi</tp:taxon-name-part></tp:taxon-name></italic><bold>sp. n</bold>., from southern China. Based on the newly sequenced mitochondrial genomes of four <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part></tp:taxon-name></italic> species, we detected two gene rearrangement patterns in the genus: a translocation of <italic>trnI</italic> and <italic>trnQ</italic> in all four species, and a loss of <italic>trnW</italic> in <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="pulchella">pulchella</tp:taxon-name-part></tp:taxon-name></italic><bold>sp. n</bold>. Both gene rearrangements are novel within <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="family" reg="Reduviidae">Reduviidae</tp:taxon-name-part></tp:taxon-name> as well as <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="suborder" reg="Heteroptera">Heteroptera</tp:taxon-name-part></tp:taxon-name>, and can be explained by the tandem duplication-random loss (<abbrev xlink:title="tandem duplication-random loss">TDRL</abbrev>) model. Phylogenetic analyses based on mitogenomic datasets recovered the monophyly of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part></tp:taxon-name></italic>, with the translocation of <italic>trnI</italic>-<italic>trnQ</italic> as a potential molecular synapomorphy for the genus.</p>
      </abstract>
      <kwd-group>
        <label>Keywords</label>
        <kwd>
          <tp:taxon-name>
            <tp:taxon-name-part taxon-name-part-type="suborder" reg="Heteroptera">Heteroptera</tp:taxon-name-part>
          </tp:taxon-name>
        </kwd>
        <kwd>mitochondrial genome</kwd>
        <kwd>gene rearrangement</kwd>
        <kwd>phylogeny</kwd>
        <kwd>taxonomy</kwd>
        <kwd>Oriental Region</kwd>
      </kwd-group>
      <funding-group>
        <award-group>
          <funding-source>
            <named-content content-type="funder_name">China Postdoctoral Science Foundation</named-content>
            <named-content content-type="funder_identifier">501100002858</named-content>
            <named-content content-type="funder_ror">https://ror.org/0426zh255</named-content>
            <named-content content-type="funder_doi">http://doi.org/10.13039/501100002858</named-content>
          </funding-source>
        </award-group>
        <award-group>
          <funding-source>
            <named-content content-type="funder_name">China Scholarship Council</named-content>
            <named-content content-type="funder_identifier">501100004543</named-content>
            <named-content content-type="funder_ror">https://ror.org/04atp4p48</named-content>
            <named-content content-type="funder_doi">http://doi.org/10.13039/501100004543</named-content>
          </funding-source>
        </award-group>
        <award-group>
          <funding-source>
            <named-content content-type="funder_name">National Natural Science Foundation of China</named-content>
            <named-content content-type="funder_identifier">501100001809</named-content>
            <named-content content-type="funder_ror">https://ror.org/01h0zpd94</named-content>
            <named-content content-type="funder_doi">http://doi.org/10.13039/501100001809</named-content>
          </funding-source>
        </award-group>
        <funding-statement>2115 Talent Development Program of China Agricultural University</funding-statement>
      </funding-group>
    </article-meta>
  </front>
  <body>
    <sec sec-type="1. Introduction" id="sec1">
      <title>1. Introduction</title>
      <p><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily" reg="Emesinae">Emesinae</tp:taxon-name-part></tp:taxon-name>, commonly known as the thread-legged bugs, is the second most species-rich lineage within the assassin bug family <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="family" reg="Reduviidae">Reduviidae</tp:taxon-name-part></tp:taxon-name>. To date, it encompasses over 1,000 extant species distributed across seven tribes: <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="tribe" reg="Collartidini">Collartidini</tp:taxon-name-part></tp:taxon-name>, <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="tribe" reg="Emesini">Emesini</tp:taxon-name-part></tp:taxon-name>, <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="tribe" reg="Leistarchini">Leistarchini</tp:taxon-name-part></tp:taxon-name>, <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="tribe" reg="Oncerotrachelini">Oncerotrachelini</tp:taxon-name-part></tp:taxon-name>, <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="tribe" reg="Saicini">Saicini</tp:taxon-name-part></tp:taxon-name>, <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="tribe" reg="Saiciretini">Saiciretini</tp:taxon-name-part></tp:taxon-name> and <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="tribe" reg="Visayanocorini">Visayanocorini</tp:taxon-name-part></tp:taxon-name> (<xref ref-type="bibr" rid="B25">Maldonado-Capriles 1990</xref>; <xref ref-type="bibr" rid="B44">Standring et al. 2023</xref>; <xref ref-type="bibr" rid="B6">Castro-Huertas and Melo 2025</xref>). The thread-legged bugs are terrestrial predatory insects characterized by typically elongated body, slender antennae and legs, and raptorial forelegs (<xref ref-type="bibr" rid="B38">Schuh and Weirauch 2020</xref>). They inhabit diverse environments including grasslands, shrublands, forests, and even caves (<xref ref-type="bibr" rid="B51">Wygodzinsky 1966</xref>; <xref ref-type="bibr" rid="B14">Ishikawa and Miyamoto 2012</xref>). Many species exhibit close associations with spiderwebs, acting as obligate predators of web-building spiders or facultatively feeding on spiders and spider prey (<xref ref-type="bibr" rid="B51">Wygodzinsky 1966</xref>; <xref ref-type="bibr" rid="B50">Wignall and Taylor 2011</xref>; <xref ref-type="bibr" rid="B41">Soley and Taylor 2012</xref>; <xref ref-type="bibr" rid="B36">Resende et al. 2016</xref>). <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily" reg="Emesinae">Emesinae</tp:taxon-name-part></tp:taxon-name>, with its rich phenotypic diversity and natural history, represents an ideal subject for studying predatory behavior and its associated phenotypic evolution (<xref ref-type="bibr" rid="B40">Soley 2016</xref>; <xref ref-type="bibr" rid="B44">Standring et al. 2023</xref>; <xref ref-type="bibr" rid="B6">Castro-Huertas and Melo 2025</xref>). However, the phylogenetic relationships and evolutionary history of <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily" reg="Emesinae">Emesinae</tp:taxon-name-part></tp:taxon-name> have not yet been comprehensively investigated, and mitochondrial data from this subfamily remain largely unexplored and underutilized in the context of systematic and evolutionary studies.</p>
      <p>Mitochondrial genomes (mitogenomes), owing to their unique genetic characteristics and the presence of multiple copies within each cell, have been extensively utilized in studies of insect phylogenetics, population genetics, and adaptive evolution (<xref ref-type="bibr" rid="B45">Sterling-Montealegre and Prada 2024</xref>; <xref ref-type="bibr" rid="B3">Cameron 2025</xref>; <xref ref-type="bibr" rid="B54">Zhao et al. 2025</xref>; <xref ref-type="bibr" rid="B55">Zhu et al. 2025</xref>). Beyond sequence variation, current research highlights the remarkable diversity in mitogenome size and structure, including alterations in gene order, gene duplication, and gene loss (<xref ref-type="bibr" rid="B42">Song et al. 2019</xref>; <xref ref-type="bibr" rid="B48">Tyagi et al. 2020</xref>; <xref ref-type="bibr" rid="B31">Pei et al. 2024</xref>). Although most insect lineages retain the putative ancestral pancrustacean gene order, mitochondrial gene rearrangements have been observed in many orders such as <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="order" reg="Hymenoptera">Hymenoptera</tp:taxon-name-part></tp:taxon-name> (<xref ref-type="bibr" rid="B26">Mao et al. 2014</xref>; <xref ref-type="bibr" rid="B46">Tang et al. 2019</xref>), <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="order" reg="Hemiptera">Hemiptera</tp:taxon-name-part></tp:taxon-name> (<xref ref-type="bibr" rid="B47">Thao et al. 2004</xref>; <xref ref-type="bibr" rid="B23">Li et al. 2012</xref>), and <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="order" reg="Trichoptera">Trichoptera</tp:taxon-name-part></tp:taxon-name> (<xref ref-type="bibr" rid="B11">Ge et al. 2023</xref>; <xref ref-type="bibr" rid="B32">Peng et al. 2025</xref>). <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="order" reg="Hemiptera">Hemiptera</tp:taxon-name-part></tp:taxon-name> exhibits multiple types of mitochondrial gene rearrangements, some of which are inferred to be molecular synapomorphies for specific lineages (<xref ref-type="bibr" rid="B43">Song et al. 2016</xref>; <xref ref-type="bibr" rid="B24">Liu et al. 2019</xref>; <xref ref-type="bibr" rid="B52">Ye et al. 2021</xref>). Currently, only a limited number of <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily" reg="Emesinae">Emesinae</tp:taxon-name-part></tp:taxon-name> species have had their mitogenomes reported, with tRNA gene rearrangements found in a single species, <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Ischnobaenella">Ischnobaenella</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="hainana">hainana</tp:taxon-name-part></tp:taxon-name></italic> (Hsiao, 1965) (<xref ref-type="bibr" rid="B52">Ye et al. 2021</xref>).</p>
      <p>The thread-legged bug genus <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part></tp:taxon-name></italic> Wygodzinsky, 1966, belonging to the tribe <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="tribe" reg="Emesini">Emesini</tp:taxon-name-part></tp:taxon-name>, is a rarely-collected group of five extant species. Four species (<italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="feminata">feminata</tp:taxon-name-part></tp:taxon-name></italic> Wygodzinsky, 1966, <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="murudiana">murudiana</tp:taxon-name-part></tp:taxon-name></italic> Wygodzinsky, 1966, <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="poiana">poiana</tp:taxon-name-part></tp:taxon-name></italic> Wygodzinsky, 1966 and <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="uniannulata">uniannulata</tp:taxon-name-part></tp:taxon-name></italic> Rédei, 2007) are endemic to Borneo, while the fifth (<italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="chinensis">chinensis</tp:taxon-name-part></tp:taxon-name></italic> Chen, Li &amp; Cai, 2020) was recently discovered in southwestern China (<xref ref-type="bibr" rid="B51">Wygodzinsky 1966</xref>; <xref ref-type="bibr" rid="B35">Rédei 2007</xref>; <xref ref-type="bibr" rid="B7">Chen et al. 2020a</xref>). Members of this genus exhibit significant sexual dimorphism, with males being macropterous and all known females being apterous (<xref ref-type="bibr" rid="B51">Wygodzinsky 1966</xref>). <xref ref-type="bibr" rid="B7">Chen et al. (2020a)</xref> speculated that additional species of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part></tp:taxon-name></italic> may be discovered elsewhere in the Oriental Region including the Indochinese Peninsula. However, the species diversity of this genus is still poorly explored in the Asian continent, and no molecular data for this genus is currently available.</p>
      <p>In the present study, we further investigate the species diversity of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part></tp:taxon-name></italic>, describe three new species from southern China, and accordingly update the species-level key for the genus. Based on the newly sequenced mitogenomes, we reveal unique mitochondrial gene rearrangements within the genus, which are also novel within <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="family" reg="Reduviidae">Reduviidae</tp:taxon-name-part></tp:taxon-name>. The possible mechanism of the gene rearrangements is inferred, and their phylogenetic implication is also discussed.</p>
    </sec>
    <sec sec-type="2. Material and methods" id="sec2">
      <title>2. Material and methods</title>
      <sec sec-type="2.1. Material depository and morphological study" id="sec3">
        <title>2.1. Material depository and morphological study</title>
        <p>Specimens examined in this study are deposited in the following collections: <named-content content-type="dwc:institutional_code" xlink:title="China Agricultural University" xlink:href="https://scientific-collections.gbif.org/institution/c2e8bcb9-a67c-447f-a612-446f80743833">CAU</named-content> – Entomological Museum of China Agricultural University, Beijing, China; <abbrev content-type="institution" xlink:title="Naturalis Biodiversity Center, Leiden, Netherlands">RMNH</abbrev> – Naturalis Biodiversity Center, Leiden, Netherlands; <named-content content-type="dwc:institutional_code" xlink:title="Natural History Museum, London" xlink:href="https://scientific-collections.gbif.org/institution/1d808a7c-1f9e-4379-9616-edb749ecf10e">NHMUK</named-content> – Natural History Museum, London, UK. Details of specimens used for morphological comparison are shown in Table S1.</p>
        <p>External morphological characters were examined using a Nikon SMZ745 stereoscopic microscope. Male and female genitalia were soaked in a heated 10% KOH solution for approximately ten minutes to remove soft tissue, rinsed in distilled water, and dissected under a stereoscopic microscope. Dissected genitalia were placed in a plastic vial containing glycerol and, after examination, pinned under the corresponding specimen. Photographs were taken using a Canon 7D Mark II digital camera with a Canon macro lens EF 100 mm f/2.8L IS USM and MP-E 65 mm f/2.8 1-5X for habitus, and a Nikon Z7 II digital camera with an Olympus BX51 microscope for dissected body parts. Figures were stacked with Helicon Focus v.5.3 and assembled using Adobe Photoshop 2020. The distribution map was constructed using the online version of SimpleMappr (<xref ref-type="bibr" rid="B39">Shorthouse 2010</xref>).</p>
        <p>Morphological terminology mainly follows <xref ref-type="bibr" rid="B51">Wygodzinsky (1966)</xref> and <xref ref-type="bibr" rid="B44">Standring et al. (2023)</xref>. Measurements were obtained using a calibrated micrometer.</p>
      </sec>
      <sec sec-type="2.2. Taxon sampling for molecular analysis" id="sec4">
        <title>2.2. Taxon sampling for molecular analysis</title>
        <p>Seven specimens belonging to four species of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part></tp:taxon-name></italic> were used for DNA extraction and mitogenome sequencing. Voucher information of the sampled specimens is listed in Table S2.</p>
        <p>Five species from other genera of <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily" reg="Emesinae">Emesinae</tp:taxon-name-part></tp:taxon-name>, as well as 29 non-emesine <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="family" reg="Reduviidae">Reduviidae</tp:taxon-name-part></tp:taxon-name> were included in the present phylogenetic analysis. Three species from <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="family" reg="Miridae">Miridae</tp:taxon-name-part></tp:taxon-name>, <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="family" reg="Nabidae">Nabidae</tp:taxon-name-part></tp:taxon-name> and <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="family" reg="Pachynomidae">Pachynomidae</tp:taxon-name-part></tp:taxon-name> were selected as outgroups. GenBank accession numbers of the newly-sequenced and published data used in this study are listed in Table S3.</p>
      </sec>
      <sec sec-type="2.3. DNA extraction, sequencing and data processing" id="sec5">
        <title>2.3. DNA extraction, sequencing and data processing</title>
        <p>Total genomic DNA was extracted nondestructively from the right foreleg using the Qiagen DNeasy Blood and Tissue Kit following the manufacturer's protocol. Each sample was soaked in tissue lysis buffer for about twenty hours to improve the quality of DNA extraction. An Illumina TruSeq library with a 350 bp average insert size was prepared for each sample. All libraries were sequenced using the Illumina NovaSeq 6000 platform with 150 bp paired-end reads. Raw reads were trimmed of adapters with Trimmomatic (<xref ref-type="bibr" rid="B1">Bolger et al. 2014</xref>) and removed of short and low-quality reads (&gt;15 bp Ns, or &gt;75 bp bases with a quality score ≤3) with Prinseq 0.20.4 (<xref ref-type="bibr" rid="B37">Schmieder and Edwards 2011</xref>). Clean reads were assembled de novo using IDBA-UD (<xref ref-type="bibr" rid="B33">Peng et al. 2012</xref>) with minimum and maximum <italic>k</italic> values of 41 and 141 bp, respectively. The mitogenome sequences were initially annotated by MitoZ 2.4 (<xref ref-type="bibr" rid="B28">Meng et al. 2019</xref>). The resultant gene boundaries were checked in Geneious Prime 2023 (<xref ref-type="bibr" rid="B17">Kearse et al. 2012</xref>) by alignment with homologous genes of the published <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily" reg="Emesinae">Emesinae</tp:taxon-name-part></tp:taxon-name> mitogenomes (GenBank accession numbers <ext-link xlink:href="PV626514" ext-link-type="gen">PV626514</ext-link> and <ext-link xlink:href="PV626532" ext-link-type="gen">PV626532</ext-link>).</p>
        <p>Thirteen protein-coding genes (<abbrev xlink:title="protein-coding genes">PCGs</abbrev>) and two ribosomal RNA genes (<italic>12S</italic> and <italic>16S</italic>) were used in phylogenetic analysis. Each gene was aligned using MAFFT 7.450 (<xref ref-type="bibr" rid="B16">Katoh and Standley 2013</xref>) with the L-INS-i algorithm. The alignment of the thirteen <abbrev xlink:title="protein-coding genes">PCGs</abbrev> was based on amino acid sequences translated with the invertebrate mitochondrial genetic codon table. All alignments were trimmed with trimAl 1.4.1 (<xref ref-type="bibr" rid="B5">Capella-Gutiérrez et al. 2009</xref>) and concatenated with FASConCAT-g 1.04 (<xref ref-type="bibr" rid="B19">Kück and Longo 2014</xref>). Two datasets were generated for phylogenetic analysis: the PCGRNA matrix, which includes all three codon positions of the <abbrev xlink:title="protein-coding genes">PCGs</abbrev>, and the two rRNA genes (12,622 bp); the PCG12RNA matrix, which includes the first and second codon positions of the <abbrev xlink:title="protein-coding genes">PCGs</abbrev>, and the two rRNA genes (9,068 bp).</p>
      </sec>
      <sec sec-type="2.4. Phylogenetic analysis" id="sec6">
        <title>2.4. Phylogenetic analysis</title>
        <p>Phylogenetic relationships were reconstructed using Bayesian inference (<abbrev xlink:title="Bayesian inference">BI</abbrev>) and Maximum-likelihood (<abbrev xlink:title="Maximum-likelihood">ML</abbrev>) methods. <abbrev xlink:title="Bayesian inference">BI</abbrev> analyses were conducted using PhyloBayes-MPI 1.8 (<xref ref-type="bibr" rid="B21">Lartillot et al. 2013</xref>) with the site-heterogeneous mixture CAT-GTR model. Two independent Markov Chain Monte Carlo (<abbrev xlink:title="Markov Chain Monte Carlo">MCMC</abbrev>) runs of 100,000 generations each were executed. Convergence was evaluated with the “bpcomp” and “tracecomp” procedure in the PhyloBayes package with a burn-in of initial 25% by the recommended criterion of maximum discrepancy &lt;0.1. A consensus tree was generated simultaneously by pooling the remaining <abbrev xlink:title="Markov Chain Monte Carlo">MCMC</abbrev> trees of both runs, with Bayesian posterior probabilities (<abbrev xlink:title="Bayesian posterior probabilities">PP</abbrev>) on each node. <abbrev xlink:title="Maximum-likelihood">ML</abbrev> partitioned analyses were conducted in IQ-TREE 2.1.2 (<xref ref-type="bibr" rid="B29">Minh et al. 2020</xref>). The best partitioning schemes and substitution models were selected using ModelFinder (<xref ref-type="bibr" rid="B15">Kalyaanamoorthy et al. 2017</xref>) based on the Bayesian information criterion (<abbrev xlink:title="Bayesian information criterion">BIC</abbrev>). The node support was evaluated with 1,000 SH-aLRT (<xref ref-type="bibr" rid="B12">Guindon et al. 2010</xref>) and 1,000 UFBoot2 (<xref ref-type="bibr" rid="B13">Hoang et al. 2018</xref>) replicates. The resulting trees were visualized and edited in Figtree 1.4.4 (<xref ref-type="bibr" rid="B34">Rambaut 2018</xref>) and iTOL 6.8.1 (<xref ref-type="bibr" rid="B22">Letunic and Bork 2021</xref>). Genetic distances of the standard <italic>COX1</italic> barcoding region (658 bp) were calculated using MEGA 7.0 (<xref ref-type="bibr" rid="B20">Kumar et al. 2016</xref>) with the Kimura 2 Parameter (<abbrev xlink:title="Kimura 2 Parameter">K2P</abbrev>) model (<xref ref-type="bibr" rid="B18">Kimura 1980</xref>).</p>
      </sec>
    </sec>
    <sec sec-type="3. Results" id="sec7">
      <title>3. Results</title>
      <sec sec-type="3.1. General structure and gene rearrangements in mitogenomes of Chinemesa" id="sec8">
        <title>3.1. General structure and gene rearrangements in mitogenomes of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part></tp:taxon-name></italic></title>
        <p>The complete mitogenomes of the four newly sequenced species of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part></tp:taxon-name></italic> ranged from 15,604 to 15,655 bp in length. Except for <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="pulchella">pulchella</tp:taxon-name-part></tp:taxon-name></italic><bold>sp. n</bold>. which lacks the <italic>trnW</italic> gene, all species possessed the entire set of 37 genes (13 <abbrev xlink:title="protein-coding genes">PCGs</abbrev>, 22 tRNA genes, and two rRNA genes) typically present in insect mitogenomes, along with a putative control region. These mitogenomes exhibited the typical A + T biased composition (73.5%–74.8%), with positive AT-skew (0.22–0.23) and negative GC-skew (-0.26–-0.18).</p>
        <p>A unique tRNA gene rearrangement was observed in all four species: the <italic>trnI</italic> and <italic>trnQ</italic> have translocated between <italic>trnW</italic> and <italic>trnC</italic> (Fig. <xref ref-type="fig" rid="F1">1</xref>). Although the <italic>trnW</italic> was absent in the mitogenome of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="pulchella">pulchella</tp:taxon-name-part></tp:taxon-name></italic><bold>sp. n</bold>., a 17-bp region was identified sharing 91.8% similarity with the homologue sequences of <italic>trnW</italic> in the other three species.</p>
        <fig id="F1">
          <object-id content-type="doi">10.3897/asp.84.e181309.figure1</object-id>
          <object-id content-type="arpha">A22A3CD1-9EE1-5C50-A2EE-09E13F23021F</object-id>
          <label>Figure 1.</label>
          <caption>
            <p>Phylogenetic tree of <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="family" reg="Reduviidae">Reduviidae</tp:taxon-name-part></tp:taxon-name> inferred from the Bayesian inference (<abbrev xlink:title="Bayesian inference">BI</abbrev>) analysis based on the PCGRNA dataset. Colour-coded circles at nodes indicate support values as specified in the bottom-left legends. Asterisks denote new mitogenomes generated in this study.</p>
          </caption>
          <graphic xlink:href="arthropod-systematics-84-565-g001.jpg" id="oo_1712254.jpg">
            <uri content-type="original_file">https://binary.pensoft.net/fig/1712254</uri>
          </graphic>
        </fig>
      </sec>
      <sec sec-type="3.2. Phylogenetic analysis" id="sec9">
        <title>3.2. Phylogenetic analysis</title>
        <p>ModelFinder merged the original 15 partitions of the PCGRNA and PCG12RNA datasets into six partitions, with the best-fitting model for each partition shown in Tables S4, S5. All analyses recovered the monophyly of <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="family" reg="Reduviidae">Reduviidae</tp:taxon-name-part></tp:taxon-name> and the sister relationship between the Phymatine Complex and the Trichobothrial Clade (formerly termed “Higher <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="family" reg="Reduviidae">Reduviidae</tp:taxon-name-part></tp:taxon-name>”), but the internal relationships within the Trichobothrial Clade varied across analyses (Figs <xref ref-type="fig" rid="F1">1</xref>, S1–S4). All subfamilies with two or more representatives were supported as monophyletic in <abbrev xlink:title="Maximum-likelihood">ML</abbrev> analyses. However, in <abbrev xlink:title="Bayesian inference">BI</abbrev> analyses, <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily" reg="Reduviinae">Reduviinae</tp:taxon-name-part></tp:taxon-name> was recovered as paraphyletic (PCG12RNA) or polyphyletic (PCGRNA). All analyses generated an identical topology within <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily" reg="Emesinae">Emesinae</tp:taxon-name-part></tp:taxon-name>. Our results support the monophyly of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part></tp:taxon-name></italic>, with <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Gardena">Gardena</tp:taxon-name-part></tp:taxon-name></italic> + <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Ghilianella">Ghilianella</tp:taxon-name-part></tp:taxon-name></italic> recovered as its sister group. <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="ornata">ornata</tp:taxon-name-part></tp:taxon-name></italic><bold>sp. n</bold>. is sister to <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="weilingfengi">weilingfengi</tp:taxon-name-part></tp:taxon-name></italic><bold>sp. n</bold>., together forming a sister clade to <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="chinensis">chinensis</tp:taxon-name-part></tp:taxon-name></italic> + <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="pulchella">pulchella</tp:taxon-name-part></tp:taxon-name></italic><bold>sp. n</bold>.</p>
        <p>The interspecific genetic distances among the four <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part></tp:taxon-name></italic> species ranged from 11.6% to 22.8%, with the maximum value between <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="chinensis">chinensis</tp:taxon-name-part></tp:taxon-name></italic> and <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="ornata">ornata</tp:taxon-name-part></tp:taxon-name></italic><bold>sp. n</bold>., while the minimum value is between <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="chinensis">chinensis</tp:taxon-name-part></tp:taxon-name></italic> and <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="pulchella">pulchella</tp:taxon-name-part></tp:taxon-name></italic><bold>sp. n</bold>. The intraspecific distance within each species ranged from 0 to 0.2% (Table S6).</p>
      </sec>
      <sec sec-type="3.3. Taxonomy" id="sec10">
        <title>3.3. Taxonomy</title>
        <p>
          <bold>Family <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="family" reg="Reduviidae">Reduviidae</tp:taxon-name-part></tp:taxon-name> Latreille, 1807</bold>
        </p>
        <p>
          <bold>Subfamily <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily" reg="Emesinae">Emesinae</tp:taxon-name-part></tp:taxon-name> Amyot &amp; Serville, 1843</bold>
        </p>
        <p>
          <bold>Tribe <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="tribe" reg="Emesini">Emesini</tp:taxon-name-part></tp:taxon-name> Amyot &amp; Serville, 1843</bold>
        </p>
        <tp:taxon-treatment>
          <tp:treatment-meta>
            <kwd-group>
              <label>Taxon classification</label>
              <kwd>
                <named-content content-type="kingdom">
                  <tp:taxon-name>
                    <tp:taxon-name-part taxon-name-part-type="kingdom" reg="Animalia">Animalia</tp:taxon-name-part>
                  </tp:taxon-name>
                </named-content>
              </kwd>
              <kwd>
                <named-content content-type="order">Hemiptera</named-content>
              </kwd>
              <kwd>
                <named-content content-type="family">Reduviidae</named-content>
              </kwd>
            </kwd-group>
          </tp:treatment-meta>
          <tp:nomenclature>
            <label>Genus</label>
            <tp:taxon-name><object-id content-type="arpha">08E00DA0-7E88-56F2-B855-0D57462FA45B</object-id>
                    		<tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part>
                    	</tp:taxon-name>
            <tp:taxon-authority>Wygodzinsky, 1966</tp:taxon-authority>
            <tp:nomenclature-citation-list>
              <tp:nomenclature-citation>
                <tp:taxon-name>
                  <tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part>
                </tp:taxon-name>
                <comment><xref ref-type="bibr" rid="B51">Wygodzinsky 1966</xref>: 225; <xref ref-type="bibr" rid="B25">Maldonado-Capriles 1990</xref>: 83; <xref ref-type="bibr" rid="B35">Rédei 2007</xref>: 213; <xref ref-type="bibr" rid="B7">Chen et al. 2020a</xref>: 20; <xref ref-type="bibr" rid="B53">Yi and He 2025</xref>: 270. Type species by original designation: <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="poiana">poiana</tp:taxon-name-part></tp:taxon-name> Wygodzinsky, 1966.</comment>
              </tp:nomenclature-citation>
            </tp:nomenclature-citation-list>
          </tp:nomenclature>
          <tp:treatment-sec sec-type="Diagnosis">
            <title>Diagnosis.</title>
            <p>Recognized within <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="tribe" reg="Emesini">Emesini</tp:taxon-name-part></tp:taxon-name> by the following combination of character states: anteocular region of head longer than postocular; labium conspicuously curved between visible segments I and II; mesonotum bearing long, erect, spine-like process; profemur armed ventrally with two series of small to medium-sized spines, posteroventral series beginning near base of segment, anteroventral series beginning at some distance from base; protarsus three-segmented; protarsal claws asymmetrical; hemelytron with pentagonal basal cell in addition to large discal cell, M and Cu veins extending basad from basal cell with M free-ending proximally; hind wing with m-cu crossvein and 2A vein present.</p>
          </tp:treatment-sec>
          <tp:treatment-sec sec-type="Diversity and distribution">
            <title>Diversity and distribution.</title>
            <p>Including the three new species described herein, the genus comprises eight species, four distributed in Borneo and the other four in southern China (Fig. <xref ref-type="fig" rid="F8">8</xref>).</p>
          </tp:treatment-sec>
        </tp:taxon-treatment>
        <tp:taxon-treatment>
          <tp:treatment-meta>
            <kwd-group>
              <label>Taxon classification</label>
              <kwd>
                <named-content content-type="kingdom">
                  <tp:taxon-name>
                    <tp:taxon-name-part taxon-name-part-type="kingdom" reg="Animalia">Animalia</tp:taxon-name-part>
                  </tp:taxon-name>
                </named-content>
              </kwd>
              <kwd>
                <named-content content-type="order">Hemiptera</named-content>
              </kwd>
              <kwd>
                <named-content content-type="family">Reduviidae</named-content>
              </kwd>
            </kwd-group>
          </tp:treatment-meta>
          <tp:nomenclature>
            <tp:taxon-name><object-id content-type="arpha">8011F9F1-6D41-52FD-8FA8-FE89523F842B</object-id>
                    		<tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="ornata">ornata</tp:taxon-name-part>
                    	
                    		<object-id content-type="zoobank" xlink:type="simple">https://zoobank.org/1AB25846-FAD9-4ABB-910B-23F08626BFCE</object-id>
                    	</tp:taxon-name>
            <tp:taxon-status>sp. n.</tp:taxon-status>
            <xref ref-type="fig" rid="F2">Figures 2</xref>
            <xref ref-type="fig" rid="F3">, 3</xref>
          </tp:nomenclature>
          <tp:treatment-sec sec-type="Type material">
            <title>Type material.</title>
            <p>Holotype: ♀, CHINA, Fujian, Sanming, Youxi, Banmian Tw. [坂面镇], Luohanshan [罗汉山], 3.vi.2024 (<named-content content-type="dwc:institutional_code" xlink:title="China Agricultural University" xlink:href="https://scientific-collections.gbif.org/institution/c2e8bcb9-a67c-447f-a612-446f80743833">CAU</named-content>).</p>
            <fig id="F2">
              <object-id content-type="doi">10.3897/asp.84.e181309.figure2</object-id>
              <object-id content-type="arpha">3C4DC2F7-9970-5A4B-9DB3-D345C45711CD</object-id>
              <label>Figure 2.</label>
              <caption>
                <p>Habitus and morphological details of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="ornata">ornata</tp:taxon-name-part></tp:taxon-name></italic><bold>sp. n</bold>.: <bold>A</bold> Apterous female, holotype, dorsal view; <bold>B</bold> apterous female, holotype, ventral view; <bold>C</bold> anterior part of body of apterous female, dorsal view; <bold>D</bold> anterior part of body of apterous female, lateral view; <bold>E</bold> foreleg of apterous female, ventral view; <bold>F</bold> abdomen of apterous female, dorsal view. Scale bar 5 mm (A, B), 1.5 mm (C–F).</p>
              </caption>
              <graphic xlink:href="arthropod-systematics-84-565-g002.jpg" id="oo_1712255.jpg">
                <uri content-type="original_file">https://binary.pensoft.net/fig/1712255</uri>
              </graphic>
            </fig>
            <fig id="F3">
              <object-id content-type="doi">10.3897/asp.84.e181309.figure3</object-id>
              <object-id content-type="arpha">3A7F75B7-5F2B-5D4B-8D71-F28A72D2AD0C</object-id>
              <label>Figure 3.</label>
              <caption>
                <p>Female genitalia of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="ornata">ornata</tp:taxon-name-part></tp:taxon-name></italic><bold>sp. n</bold>.: <bold>A</bold> Dorsal view; <bold>B</bold> lateral view; <bold>C</bold> ventral view. Scale bar 0.5 mm.</p>
              </caption>
              <graphic xlink:href="arthropod-systematics-84-565-g003.jpg" id="oo_1712256.jpg">
                <uri content-type="original_file">https://binary.pensoft.net/fig/1712256</uri>
              </graphic>
            </fig>
          </tp:treatment-sec>
          <tp:treatment-sec sec-type="Diagnosis">
            <title>Diagnosis.</title>
            <p>Body medium-sized, 11.4 mm; anterior lobe of pronotum nearly as long as head (Fig. <xref ref-type="fig" rid="F2">2C, D</xref>); profemur with two light-colored annuli and one subapical light-colored spot (Fig. <xref ref-type="fig" rid="F2">2E</xref>); mesofemur with six alternating dark and light annuli in apical half (Fig. <xref ref-type="fig" rid="F2">2A, B</xref>); metafemur with 17 alternating dark and light annuli (Fig. <xref ref-type="fig" rid="F2">2A, B</xref>); femorotibial articulations of mid and hind legs broadly whitish and tinged with red (Fig. <xref ref-type="fig" rid="F2">2A, B</xref>); female abdominal tergite IX 1.3 times as long as tergite VIII (Fig. <xref ref-type="fig" rid="F3">3A</xref>); posterior margin of styloides weakly incised at midpoint (Fig. <xref ref-type="fig" rid="F3">3C</xref>).</p>
          </tp:treatment-sec>
          <tp:treatment-sec sec-type="Description">
            <title>Description.</title>
            <p>Apterous female (Fig. <xref ref-type="fig" rid="F2">2A, B</xref>). <bold>Colouration</bold>: Generally reddish-brown. Lateral and ventral surfaces of head dark brown; lateral and ventral surfaces of thorax and abdomen blackish-brown. Anteclypeus dark brown; labrum whitish-yellow. Antenna blackish-brown; extreme base and apex of scape and extreme apex of pedicel whitish-yellow. Labium blackish-brown, with base and apex of visible segment III yellowish-brown (Fig. <xref ref-type="fig" rid="F2">2D</xref>). Spine-like process on mesonotum blackish-brown (Fig. <xref ref-type="fig" rid="F2">2D</xref>). Profemur reddish-brown to dark brown, with two whitish-yellow annuli at midportion and one small whitish-yellow spot subapically (Fig. <xref ref-type="fig" rid="F2">2E</xref>); protibia dark brown (Fig. <xref ref-type="fig" rid="F2">2E</xref>); protarsus brown (Fig. <xref ref-type="fig" rid="F2">2E</xref>). Mid and hind legs yellowish-brown; meso- and metafemora each with three indistinct, broad, dark brown annuli and two narrow whitish-yellow annuli in apical half, apically broadly whitish and tinged with red (Fig. <xref ref-type="fig" rid="F2">2A, B</xref>); metafemur with five indistinct, narrow, dark brown annuli in basal half (Fig. <xref ref-type="fig" rid="F2">2A, B</xref>); meso- and metatibiae each with two indistinct dark brown annuli in basal third, basally broadly whitish and tinged with red (Fig. <xref ref-type="fig" rid="F2">2A, B</xref>); meso- and metatarsi pale brown. Abdominal tergites IV–VII each with one pair of submedian, longitudinal, yellowish-brown stripes (Fig. <xref ref-type="fig" rid="F2">2F</xref>); tergites VIII and IX yellowish-brown at midportion (Fig. <xref ref-type="fig" rid="F2">2F</xref>); tergite X yellowish-brown (Fig. <xref ref-type="fig" rid="F2">2F</xref>); connexival segments IV–VII each with one small yellowish-brown spot at anterolateral angle (Fig. <xref ref-type="fig" rid="F2">2F</xref>); sternites IV–VI each with one indistinct, small, yellowish-brown spot on both sides, and one indistinct, small, yellowish-brown spot before spiracle. — <bold>Vestiture</bold>: Body surface smooth, strongly polished, covered with dense, very short, decumbent to suberect pubescence and sparse, long, erect pubescence. Meso- and metapleura gently wrinkled. Profemur with several long, erect, strong setae ventrally; protibia with short, erect, strong setae ventrally. Connexivum gently wrinkled. — <bold>Structure</bold>: Head (Fig. <xref ref-type="fig" rid="F2">2C, D</xref>) subfusiform, 1.9 times as long as width across eyes; width across eyes twice as broad as interocular space. Eye (Fig. <xref ref-type="fig" rid="F2">2C, D</xref>) small, far remote from dorsal and ventral margins of head in lateral view. Antennal scape 1.15 times as long as pedicel, four times as long as head; basiflagellomere slightly longer than distiflagellomere. Labium (Fig. <xref ref-type="fig" rid="F2">2D</xref>) with visible segment I 1.25 times as long as visible segment II; visible segment III 1.7 times as long as visible segment I. Pronotum (Fig. <xref ref-type="fig" rid="F2">2C, D</xref>) subcylindrical, 1.8 times as long as its maximum width; anterior lobe nearly as long as head, gradually narrowed posteriorly; posterior lobe short, collar-like. Mesonotum (Fig. <xref ref-type="fig" rid="F2">2C, D</xref>) slightly convex dorsally, with faint longitudinal carina along midline, posteriorly with erect spine-like process; metanotum (Fig. <xref ref-type="fig" rid="F2">2C, D</xref>) 0.45 times as long as mesonotum, flattened dorsally; meso- and metasterna with longitudinal carina along midline. Foreleg (Fig. <xref ref-type="fig" rid="F2">2E</xref>) robust; procoxa 1.5 times as long as pronotum; profemur gently curved, 11.5 times as long as its maximum width, 1.8 times as long as procoxa; posteroventral series composed of eight long spines and many smaller ones inserted on distinct basal processes, and of some small, denticle-like spines apically; protibia 0.75 times as long as profemur, armed ventrally with two irregular rows of small denticles. Meso- and metatibiae 1.45 and 1.5 times as long as respective femur. Abdomen (Fig. <xref ref-type="fig" rid="F2">2F</xref>) elongate, 4.6 times as long as its maximum width. Female genitalia: tergite VIII (Fig. <xref ref-type="fig" rid="F3">3A, B</xref>) transverse, subsemicircular; tergite IX (Fig. <xref ref-type="fig" rid="F3">3A, B</xref>) trapezoidal, 1.3 times as long as tergite VIII; tergite X (Fig. <xref ref-type="fig" rid="F3">3A, B</xref>) clearly exposed; valvifer I (Fig. <xref ref-type="fig" rid="F3">3B, C</xref>) broad, with rounded posterolateral margin and nearly straight posteromedial margin; valvula I (Fig. <xref ref-type="fig" rid="F3">3B, C</xref>) small, apically obtuse; posterior margin of styloides weakly incised at midpoint (Fig. <xref ref-type="fig" rid="F3">3C</xref>). — <bold>Measurements</bold>: [in mm, ♀ (n = 1)]. Length of body: to apex of abdomen 11.40; length of head 1.50; length of anteocular region 0.60; length of postocular region 0.90; width across eyes 0.80; interocular space 0.40; length of antennal segments 5.95, 5.10, 1.05, 1.00; length of visible labial segments 0.50, 0.40, 0.85; length of anterior pronotal lobe 1.30; length of posterior pronotal lobe 0.25; maximum width of anterior pronotal lobe 0.86; maximum width of posterior pronotal lobe 0.70; length of procoxa, femur, tibia, tarsus 2.35, 4.25, 3.20, 0.50; maximum width of profemur 0.35; length of mid femur, tibia, tarsus 7.05, 10.30, 0.40; length of metafemur, tibia, tarsus 9.20, 13.80, 0.45; length of abdomen 6.40; maximum width of abdomen 1.40.</p>
          </tp:treatment-sec>
          <tp:treatment-sec sec-type="Distribution">
            <title>Distribution.</title>
            <p>China – Fujian: Youxi (Fig. <xref ref-type="fig" rid="F8">8</xref>).</p>
          </tp:treatment-sec>
          <tp:treatment-sec sec-type="Etymology">
            <title>Etymology.</title>
            <p>The specific epithet is derived from Latin ornata (meaning ornated or decorated), referring to the impressive color patterns of this new species.</p>
          </tp:treatment-sec>
          <tp:treatment-sec sec-type="Comparative notes">
            <title>Comparative notes.</title>
            <p><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="ornata">ornata</tp:taxon-name-part></tp:taxon-name></italic><bold>sp. n</bold>. and <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="feminata">feminata</tp:taxon-name-part></tp:taxon-name></italic> are known only from the apterous female. However, these two species are not conspecific because the new species possesses completely different body size and colouration. The anterior lobe of the pronotum is nearly as long as the head in <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="ornata">ornata</tp:taxon-name-part></tp:taxon-name></italic><bold>sp. n</bold>. but much longer in <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="feminata">feminata</tp:taxon-name-part></tp:taxon-name></italic>.</p>
            <p>Based on our phylogenetic results, <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="ornata">ornata</tp:taxon-name-part></tp:taxon-name></italic><bold>sp. n</bold>. is closely related to <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="weilingfengi">weilingfengi</tp:taxon-name-part></tp:taxon-name></italic><bold>sp. n</bold>. (see below). It is distinguished from the latter by the longer anterior lobe of the pronotum which is subequal in length of the head, and the reddish femorotibial articulations of mid and hind legs. In <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="weilingfengi">weilingfengi</tp:taxon-name-part></tp:taxon-name></italic><bold>sp. n</bold>., the anterior lobe of the pronotum is distinctly shorter than the head, the femorotibial articulations of mid and hind legs are whitish, and the extreme base of the meso- and metatibiae is dark brown. The <italic>COX1</italic> genetic distance between <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="ornata">ornata</tp:taxon-name-part></tp:taxon-name></italic><bold>sp. n</bold>. and <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="weilingfengi">weilingfengi</tp:taxon-name-part></tp:taxon-name></italic><bold>sp. n</bold>. is 13.6%, falling within the range of interspecific distances among the sampled <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part></tp:taxon-name></italic> species (11.6%–22.8%), indicating that they should be treated as distinct species.</p>
          </tp:treatment-sec>
        </tp:taxon-treatment>
        <tp:taxon-treatment>
          <tp:treatment-meta>
            <kwd-group>
              <label>Taxon classification</label>
              <kwd>
                <named-content content-type="kingdom">
                  <tp:taxon-name>
                    <tp:taxon-name-part taxon-name-part-type="kingdom" reg="Animalia">Animalia</tp:taxon-name-part>
                  </tp:taxon-name>
                </named-content>
              </kwd>
              <kwd>
                <named-content content-type="order">Hemiptera</named-content>
              </kwd>
              <kwd>
                <named-content content-type="family">Reduviidae</named-content>
              </kwd>
            </kwd-group>
          </tp:treatment-meta>
          <tp:nomenclature>
            <tp:taxon-name><object-id content-type="arpha">D3B66FD7-B1B7-54F8-8A81-37870056948A</object-id>
                    		<tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="pulchella">pulchella</tp:taxon-name-part>
                    	
                    		<object-id content-type="zoobank" xlink:type="simple">https://zoobank.org/196F6BF7-DC6C-4147-A129-CD9531A27AC4</object-id>
                    	</tp:taxon-name>
            <tp:taxon-status>sp. n.</tp:taxon-status>
            <xref ref-type="fig" rid="F4">Figures 4</xref>
            <xref ref-type="fig" rid="F5">, 5</xref>
          </tp:nomenclature>
          <tp:treatment-sec sec-type="Type material">
            <title>Type material.</title>
            <p>Holotype: ♂, CHINA, Xizang, Nyingchi, Medog, Damu Tw. [达木乡], 1420 m, 11.vi.2017, Chufei Tang (<named-content content-type="dwc:institutional_code" xlink:title="China Agricultural University" xlink:href="https://scientific-collections.gbif.org/institution/c2e8bcb9-a67c-447f-a612-446f80743833">CAU</named-content>). Paratype: 1♂, CHINA, Xizang, Nyingchi, Medog, Damu Tw. [达木乡], 1814 m, 22.vi.2017, Chufei Tang (<named-content content-type="dwc:institutional_code" xlink:title="China Agricultural University" xlink:href="https://scientific-collections.gbif.org/institution/c2e8bcb9-a67c-447f-a612-446f80743833">CAU</named-content>).</p>
            <fig id="F4">
              <object-id content-type="doi">10.3897/asp.84.e181309.figure4</object-id>
              <object-id content-type="arpha">8957B930-B513-587E-9444-AED3E5384707</object-id>
              <label>Figure 4.</label>
              <caption>
                <p>Habitus and morphological details of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="pulchella">pulchella</tp:taxon-name-part></tp:taxon-name></italic><bold>sp. n</bold>.: <bold>A</bold> Macropterous male, holotype, dorsal view; <bold>B</bold> macropterous male, holotype, lateral view; <bold>C</bold> macropterous male, holotype, ventral view; <bold>D</bold> foreleg of macropterous female, ventral view. Scale bar 2 mm (A–C), 1.5 mm (D).</p>
              </caption>
              <graphic xlink:href="arthropod-systematics-84-565-g004.jpg" id="oo_1712257.jpg">
                <uri content-type="original_file">https://binary.pensoft.net/fig/1712257</uri>
              </graphic>
            </fig>
            <fig id="F5">
              <object-id content-type="doi">10.3897/asp.84.e181309.figure5</object-id>
              <object-id content-type="arpha">FDA01FE4-DA17-5307-83C5-96933CB0A87E</object-id>
              <label>Figure 5.</label>
              <caption>
                <p>Male genitalia of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="pulchella">pulchella</tp:taxon-name-part></tp:taxon-name></italic><bold>sp. n</bold>.: <bold>A</bold> Pygophore, dorsal view; <bold>B</bold> pygophore, lateral view; <bold>C</bold> pygophore, caudal view; <bold>D</bold> paramere, dorsal view; <bold>E</bold> paramere, lateral view; <bold>F</bold> phallus, dorsal view; <bold>G</bold> phallus, lateral view; <bold>H</bold> phallus, ventral view. Scale bar 0.5 mm.</p>
              </caption>
              <graphic xlink:href="arthropod-systematics-84-565-g005.jpg" id="oo_1712258.jpg">
                <uri content-type="original_file">https://binary.pensoft.net/fig/1712258</uri>
              </graphic>
            </fig>
          </tp:treatment-sec>
          <tp:treatment-sec sec-type="Diagnosis">
            <title>Diagnosis.</title>
            <p>Body medium-sized, 11–12 mm; head bicolorous, blackish anterior lobe and reddish posterior lobe (Fig. <xref ref-type="fig" rid="F4">4A, B</xref>); anterior lobe of pronotum slightly shorter than head (Fig. <xref ref-type="fig" rid="F4">4A, B</xref>); posterior lobe of pronotum with one pair of submedian, oblique, yellowish-brown stripes in basal half (Fig. <xref ref-type="fig" rid="F4">4A</xref>); procoxa with one median light-colored annulus (Fig. <xref ref-type="fig" rid="F4">4D</xref>); profemur with three light-colored annuli (Fig. <xref ref-type="fig" rid="F4">4D</xref>); meso- and metafemora with two indistinct, pale brown annuli and two broad, dark brown annuli in apical half, and one apical whitish annulus; hemelytron with indistinct reticulate patterns (Fig. <xref ref-type="fig" rid="F4">4A</xref>); connexivum bicolorous (Fig. <xref ref-type="fig" rid="F4">4B, C</xref>); abdomen ventrally with light-colored spots on both sides (Fig. <xref ref-type="fig" rid="F4">4B, C</xref>); phallosoma with paired lateral sclerites and one pair of dorsolateral lobes near apex (Fig. <xref ref-type="fig" rid="F5">5F–H</xref>).</p>
          </tp:treatment-sec>
          <tp:treatment-sec sec-type="Description">
            <title>Description.</title>
            <p>Macropterous male (Fig. <xref ref-type="fig" rid="F4">4A–C</xref>): <bold>Colouration</bold>: Generally blackish-brown. Anterior lobe of head with one pair of triangular, whitish-yellow spots behind antennal insertions (Fig. <xref ref-type="fig" rid="F4">4A</xref>); posterior lobe reddish-brown (Fig. <xref ref-type="fig" rid="F4">4A, B</xref>); apex and lateral margins of anteclypeus yellowish-brown; labrum whitish-yellow. Extreme apex of antennal scape whitish. Labium with base and apex of visible segment III yellowish-brown (Fig. <xref ref-type="fig" rid="F4">4B</xref>). Anterior lobe of pronotum tinged with brown along midline (Fig. <xref ref-type="fig" rid="F4">4A</xref>); posterior lobe with one pair of submedian, oblique, yellowish-brown stripes in anterior half (Fig. <xref ref-type="fig" rid="F4">4A</xref>). Procoxa with broad, pale brown annulus at midpoint (Fig. <xref ref-type="fig" rid="F4">4D</xref>); profemur dark brown to blackish-brown, with two whitish-yellow annuli at midportion and one small whitish-yellow spot subbasally (Fig. <xref ref-type="fig" rid="F4">4D</xref>); protibia with narrow whitish-yellow annulus at midpoint (Fig. <xref ref-type="fig" rid="F4">4D</xref>); protarsus brown (Fig. <xref ref-type="fig" rid="F4">4D</xref>). Mid and hind legs yellowish-brown; meso- and metafemora each with one indistinct, narrow, whitish-yellow annulus at base, two indistinct, pale brown annuli and two broad, dark brown annuli in apical half, apically broadly whitish; mesotibia with two broad, dark brown annuli in basal third, basally broadly whitish. Hemelytron brown, with indistinct reticulate patterns (Fig. <xref ref-type="fig" rid="F4">4A</xref>); veins partially yellowish-brown. Abdomen dark brown to blackish-brown; connexival segments III–VII yellowish-brown in basal half (Fig. <xref ref-type="fig" rid="F4">4B, C</xref>); sternite III with one small yellowish-brown spot posteriorly on both sides (Fig. <xref ref-type="fig" rid="F4">4B, C</xref>); sternites IV–VI each with two small yellowish-brown spots on both sides (Fig. <xref ref-type="fig" rid="F4">4B, C</xref>). — <bold>Vestiture</bold>: Body surface smooth, strongly polished, covered with dense, very short, decumbent to suberect pubescence and sparse, long, erect pubescence. Posterior lobe of pronotum transversely wrinkled. Meso- and metapleura gently wrinkled. Profemur with several long, erect, strong setae ventrally; protibia with short, erect, strong setae ventrally. — <bold>Structure</bold>: Head (Fig. <xref ref-type="fig" rid="F4">4A–C</xref>) elongate oval, 1.1 times as long as width across eyes; width across eyes 2.15 times as broad as interocular space. Eye (Fig. <xref ref-type="fig" rid="F4">4A–C</xref>) medium-sized, remote from dorsal and ventral margins of head in lateral view. Labium (Fig. <xref ref-type="fig" rid="F4">4B, C</xref>) with visible segments I and II subequal in length; visible segment III 1.65–1.75 times as long as visible segment I. Pronotum (Fig. <xref ref-type="fig" rid="F4">4A, B</xref>) 1.35 times as long as width across humeral angles; anterior lobe 0.9 times as long as head, with shallow longitudinal furrow along midline; posterior lobe bell-like, with shallow, triangular, median impression on disc, humeral angles rounded and slightly elevated, posterior margin gently concave. Scutellum (Fig. <xref ref-type="fig" rid="F4">4A, B</xref>) semicircular, with erect spine-like process. Metanotum with short spine-like process; meso- and metasterna (Fig. <xref ref-type="fig" rid="F4">4C</xref>) with longitudinal carina along midline. Foreleg (Fig. <xref ref-type="fig" rid="F4">4D</xref>) robust; procoxa 0.9 times as long as pronotum; profemur gently curved, 14.5 times as long as its maximum width, twice as long as procoxa; posteroventral series composed of nine long spines and many smaller ones inserted on distinct basal processes, and of some small, denticle-like spines apically; protibia 0.8 times as long as profemur, armed ventrally with two irregular rows of small denticles. Mesotibia 1.55 times as long as mesofemur. Hemelytron (Fig. <xref ref-type="fig" rid="F4">4A</xref>) narrow at proximal portion and widest at subapical portion; M basad of subbasal cell less than half of length of Cu; subbasal cell acuminate. Abdomen (Fig. <xref ref-type="fig" rid="F4">4B, C</xref>) elongate, 3.5–3.6 times as long as its maximum width. Male genitalia: pygophore (Fig. <xref ref-type="fig" rid="F5">5A–C</xref>) oblong, with narrow transverse bridge and wide, flattened, deeply incised apical projection; paramere (Fig. <xref ref-type="fig" rid="F4">4D, E</xref>) short, curved, with subacute apex; phallus as shown in Fig. <xref ref-type="fig" rid="F5">5F–H</xref>; articulatory apparatus thick, with basal plate arms widely separated; phallosoma membranous, with one pair of narrow lateral sclerites and one pair of dorsolateral lobes near apex; struts long and slender, apically widened and flattened; endosoma tube-like. — <bold>Measurements</bold>: [in mm, ♂ (n = 2)]. Length of body: to apex of hemelytron 12.00, to apex of abdomen 11.00–11.30; length of head 1.10–1.30; length of anteocular region 0.50; length of postocular region 0.40; width across eyes 1.05–1.10; interocular space 0.50; length of antennal segments 6.20, ? (missing), ? (missing), ? (missing); length of visible labial segments 0.40–0.45, 0.40–0.45, 0.70–0.75; length of anterior pronotal lobe 1.05–1.10; length of posterior pronotal lobe 1.15–1.40; maximum width of anterior pronotal lobe 0.80–0.90; maximum width of posterior pronotal lobe 1.70–1.80; length of procoxa, femur, tibia, tarsus 2.10, 4.30–4.40, 3.40, 0.50; maximum width of profemur 0.30; length of mesofemur, tibia, tarsus 6.30, 9.70, 0.50; length of metafemur, tibia, tarsus 9.50, ? (missing), ? (missing); length of hemelytron 7.90; length of abdomen 6.10–6.50; maximum width of abdomen 1.75–1.80.</p>
          </tp:treatment-sec>
          <tp:treatment-sec sec-type="Distribution">
            <title>Distribution.</title>
            <p>China – Xizang: Medog (Fig. <xref ref-type="fig" rid="F8">8</xref>).</p>
          </tp:treatment-sec>
          <tp:treatment-sec sec-type="Etymology">
            <title>Etymology.</title>
            <p>The specific epithet is derived from Latin pulchella (meaning beautiful), referring to the peculiar markings on the head, pronotum, and abdomen of this new species.</p>
          </tp:treatment-sec>
          <tp:treatment-sec sec-type="Comparative notes">
            <title>Comparative notes.</title>
            <p><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="pulchella">pulchella</tp:taxon-name-part></tp:taxon-name></italic><bold>sp. n</bold>. can be distinguished from its other congeners by the remarkable color patterns first of all: body generally blackish (vs reddish-brown to dark brown in other species); head bicolorous, with anterior lobe blackish and posterior lobe reddish (vs head concolorous in other species); abdomen ventrally with whitish-yellow spots on both sides (vs lacking such spots in other species).</p>
            <p>This new species is morphologically similar to <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="chinensis">chinensis</tp:taxon-name-part></tp:taxon-name></italic> and <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="murudiana">murudiana</tp:taxon-name-part></tp:taxon-name></italic>. These species share the medium body size, the relatively short anterior lobe of the pronotum (shorter than the head), and the bicolorous connexivum. The new species can be readily separated from the latter two species by: procoxa about half as long as profemur (vs much longer than half of length in <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="murudiana">murudiana</tp:taxon-name-part></tp:taxon-name></italic>); meso- and metafemora each with four alternating light and dark annuli, and one apical whitish annulus (vs with 15 alternating light and dark annuli in <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="murudiana">murudiana</tp:taxon-name-part></tp:taxon-name></italic>; mesofemur with two broad and one narrow light annuli, metafemur with six dark annuli and one apical whitish annulus in <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="chinensis">chinensis</tp:taxon-name-part></tp:taxon-name></italic>); hemelytron with indistinct reticulate patterns (vs with distinct reticulate patterns in <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="murudiana">murudiana</tp:taxon-name-part></tp:taxon-name></italic>); subbasal cell of hemelytron acuminate (vs broad in <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="chinensis">chinensis</tp:taxon-name-part></tp:taxon-name></italic>); pygophore oblong (vs elongate oval in <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="chinensis">chinensis</tp:taxon-name-part></tp:taxon-name></italic>); phallosoma with paired lateral sclerites near apex (vs without such sclerites in <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="murudiana">murudiana</tp:taxon-name-part></tp:taxon-name></italic>).</p>
          </tp:treatment-sec>
        </tp:taxon-treatment>
        <tp:taxon-treatment>
          <tp:treatment-meta>
            <kwd-group>
              <label>Taxon classification</label>
              <kwd>
                <named-content content-type="kingdom">
                  <tp:taxon-name>
                    <tp:taxon-name-part taxon-name-part-type="kingdom" reg="Animalia">Animalia</tp:taxon-name-part>
                  </tp:taxon-name>
                </named-content>
              </kwd>
              <kwd>
                <named-content content-type="order">Hemiptera</named-content>
              </kwd>
              <kwd>
                <named-content content-type="family">Reduviidae</named-content>
              </kwd>
            </kwd-group>
          </tp:treatment-meta>
          <tp:nomenclature>
            <tp:taxon-name><object-id content-type="arpha">1EEA0727-1940-5DDC-AA39-694C34D7C0D4</object-id>
                    		<tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="weilingfengi">weilingfengi</tp:taxon-name-part>
                    	
                    		<object-id content-type="zoobank" xlink:type="simple">https://zoobank.org/FC6C691B-D1C9-433A-85A7-0D50CA161952</object-id>
                    	</tp:taxon-name>
            <tp:taxon-status>sp. n.</tp:taxon-status>
            <xref ref-type="fig" rid="F6">Figures 6</xref>
            <xref ref-type="fig" rid="F7">, 7</xref>
          </tp:nomenclature>
          <tp:treatment-sec sec-type="Type material">
            <title>Type material.</title>
            <p>Holotype: ♂, CHINA, Yunnan, Xishuangbanna, Mengla, Wangtianshu [望天树], 19.xi.2022, Lingfeng Wei (<named-content content-type="dwc:institutional_code" xlink:title="China Agricultural University" xlink:href="https://scientific-collections.gbif.org/institution/c2e8bcb9-a67c-447f-a612-446f80743833">CAU</named-content>).</p>
            <fig id="F6">
              <object-id content-type="doi">10.3897/asp.84.e181309.figure6</object-id>
              <object-id content-type="arpha">037FE106-F7B6-5E9E-90C2-2FD9B1BC2B91</object-id>
              <label>Figure 6.</label>
              <caption>
                <p>Habitus and morphological details of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="weilingfengi">weilingfengi</tp:taxon-name-part></tp:taxon-name></italic><bold>sp. n</bold>.: <bold>A</bold> Macropterous male, holotype, dorsal view; <bold>B</bold> macropterous male, holotype, ventral view; <bold>C</bold> anterior part of body of macropterous male, dorsal view; <bold>D</bold> anterior part of body of macropterous male, lateral view; <bold>E</bold> foreleg of macropterous male, ventral view; <bold>F</bold> hemelytron of macropterous male, dorsal view. Scale bar 5 mm (A, B), 1.5 mm (C–F).</p>
              </caption>
              <graphic xlink:href="arthropod-systematics-84-565-g006.jpg" id="oo_1712259.jpg">
                <uri content-type="original_file">https://binary.pensoft.net/fig/1712259</uri>
              </graphic>
            </fig>
            <fig id="F7">
              <object-id content-type="doi">10.3897/asp.84.e181309.figure7</object-id>
              <object-id content-type="arpha">758E09B8-1B4F-54EC-81B1-0F85236DFA37</object-id>
              <label>Figure 7.</label>
              <caption>
                <p>Male genitalia of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="weilingfengi">weilingfengi</tp:taxon-name-part></tp:taxon-name></italic><bold>sp. n</bold>.: <bold>A</bold> Pygophore, dorsal view; <bold>B</bold> pygophore, lateral view; <bold>C</bold> pygophore, caudal view; <bold>D</bold> paramere, dorsal view; <bold>E</bold> paramere, lateral view; <bold>F</bold> phallus, dorsal view; <bold>G</bold> phallus, lateral view; <bold>H</bold> phallus, ventral view. Scale bar 1 mm.</p>
              </caption>
              <graphic xlink:href="arthropod-systematics-84-565-g007.jpg" id="oo_1712260.jpg">
                <uri content-type="original_file">https://binary.pensoft.net/fig/1712260</uri>
              </graphic>
            </fig>
          </tp:treatment-sec>
          <tp:treatment-sec sec-type="Diagnosis">
            <title>Diagnosis.</title>
            <p>Body small-sized, 9.5 mm; anterior lobe of pronotum distinctly shorter than head (Fig. <xref ref-type="fig" rid="F6">6C, D</xref>); posterior lobe of pronotum with one pair of submedian, oblique, yellowish-brown stripes, humeral angle yellowish-brown (Fig. <xref ref-type="fig" rid="F6">6C, D</xref>); profemur with two light-colored annuli and one subapical light-colored spot (Fig. <xref ref-type="fig" rid="F6">6E</xref>); meso- and metafemora with 15 and 17 alternating dark and light annuli, respectively (Fig. <xref ref-type="fig" rid="F6">6A, B</xref>); extreme base of meso- and metatibiae dark brown (Fig. <xref ref-type="fig" rid="F6">6A, B</xref>); hemelytron with distinct reticulate patterns (Fig. <xref ref-type="fig" rid="F6">6F</xref>); connexivum bicolorous (Fig. <xref ref-type="fig" rid="F6">6B</xref>); phallosoma with paired lateral sclerites near apex (Fig. <xref ref-type="fig" rid="F7">7F–H</xref>).</p>
          </tp:treatment-sec>
          <tp:treatment-sec sec-type="Description">
            <title>Description.</title>
            <p>Macropterous male (Fig. <xref ref-type="fig" rid="F6">6A, B</xref>). <bold>Colouration</bold>: Generally dark brown. Head reddish-brown, with portion before antennal insertions darker (Fig. <xref ref-type="fig" rid="F6">6C, D</xref>); labrum pale brown. Antenna blackish-brown; extreme apex of scape and pedicel whitish-yellow. Labium with intersegmental portions yellowish-brown (Fig. <xref ref-type="fig" rid="F6">6D</xref>). Pronotum blackish-brown; dorsal surface of anterior lobe reddish-brown (Fig. <xref ref-type="fig" rid="F6">6C, D</xref>); posterior lobe with one pair of submedian, oblique, yellowish-brown stripes reaching posterior margin, humeral angle yellowish-brown (Fig. <xref ref-type="fig" rid="F6">6C, D</xref>). Meso- and metapleura and sterna blackish-brown. Procoxa and trochanter reddish-brown (Fig. <xref ref-type="fig" rid="F6">6E</xref>); profemur reddish-brown to blackish-brown, with two whitish-yellow annuli at midportion and one small whitish-yellow spot subapically (Fig. <xref ref-type="fig" rid="F6">6E</xref>); protibia blackish-brown (Fig. <xref ref-type="fig" rid="F6">6E</xref>); protarsus brown (Fig. <xref ref-type="fig" rid="F6">6E</xref>). Mid and hind legs yellowish-brown; meso- and metafemora each with four or five narrow dark brown annuli in basal half, three broad dark brown annuli and two narrow whitish-yellow annuli in apical half, apically broadly whitish (Fig. <xref ref-type="fig" rid="F6">6A, B</xref>); meso- and metatibiae each with two broad dark brown annuli in basal third, basally broadly whitish with extreme base dark brown (Fig. <xref ref-type="fig" rid="F6">6A, B</xref>). Hemelytron brown, with distinct reticulate patterns; veins yellowish-brown (Fig. <xref ref-type="fig" rid="F6">6F</xref>). Abdomen with connexival segments IV–VII yellowish-brown in basal half (Fig. <xref ref-type="fig" rid="F6">6B</xref>). — <bold>Vestiture</bold>: Body surface smooth, strongly polished, covered with dense, very short, decumbent to suberect pubescence and sparse, long, erect pubescence. Antennal scape densely covered with long erect setae about three times as long as diameter of segment. Posterior lobe of pronotum transversely wrinkled. Meso- and metapleura gently wrinkled. Profemur with several long, erect, strong setae ventrally; protibia with short, erect, strong setae ventrally. — <bold>Structure</bold>: Head (Fig. <xref ref-type="fig" rid="F6">6C, D</xref>) subfusiform, 1.3 times as long as width across eyes; width across eyes 2.4 times as broad as interocular space. Eye (Fig. <xref ref-type="fig" rid="F6">6C, D</xref>) large, reaching dorsal and ventral margins of head in lateral view. Antennal scape 1.05 times as long as pedicel, 5.3 times as long as head; basiflagellomere slightly shorter than distiflagellomere. Labium (Fig. <xref ref-type="fig" rid="F6">6D</xref>) with visible segment I 1.3 times as long as visible segment II; visible segment III 1.75 times as long as visible segment I. Pronotum (Fig. <xref ref-type="fig" rid="F6">6C, D</xref>) 1.5 times as long as width across humeral angles; anterior lobe 0.7 times as long as head, with shallow longitudinal furrow along midline; posterior lobe bell-like, with shallow, triangular, median impression on disc, humeral angles rounded and slightly elevated, posterior margin concave. Scutellum (Fig. <xref ref-type="fig" rid="F6">6C, D</xref>) semicircular, with erect spine-like process. Metanotum with short spine-like process; meso- and metasterna with longitudinal carina along midline. Foreleg (Fig. <xref ref-type="fig" rid="F6">6E</xref>) robust; procoxa 1.05 times as long as pronotum; profemur gently curved, 13 times as long as its maximum width, 1.7 times as long as procoxa; posteroventral series composed of eight long spines and many smaller ones inserted on distinct basal processes, and of some small, denticle-like spines apically; protibia 0.85 times as long as profemur, armed ventrally with two irregular rows of small denticles. Meso- and metatibiae 1.55 and 1.7 times as long as respective femur. Hemelytron (Fig. <xref ref-type="fig" rid="F6">6F</xref>) narrow at proximal portion and widest at subapical portion; M basad of subbasal cell about one-third as long as Cu; subbasal cell acuminate. Abdomen elongate, 4.4 times as long as its maximum width. Male genitalia: pygophore (Fig. <xref ref-type="fig" rid="F7">7A–C</xref>) oblong, with narrow transverse bridge and wide, flattened, weakly incised apical projection; paramere (Fig. <xref ref-type="fig" rid="F7">7D, E</xref>) short, curved, with obtuse apex; phallus as shown in Fig. <xref ref-type="fig" rid="F7">7F–H</xref>; articulatory apparatus thick, with basal plate arms widely separated; phallosoma membranous, with one pair of narrow lateral sclerites near apex; struts long and slender, apically widened and flattened. — <bold>Measurements</bold> [in mm, ♂ (n = 1)]. Length of body: to apex of hemelytron 9.10, to apex of abdomen 9.50; length of head 1.10; length of anteocular region 0.40; length of postocular region 0.25; width across eyes 0.85; interocular space 0.35; length of antennal segments 5.80, 5.50, 1.00, 1.50; length of visible labial segments 0.40, 0.30, 0.70; length of anterior pronotal lobe 0.80; length of posterior pronotal lobe 1.00; maximum width of anterior pronotal lobe 0.60; maximum width of posterior pronotal lobe 1.20; length of procoxa, femur, tibia, tarsus 1.90, 3.30, 2.80, 0.40; maximum width of profemur 0.25; length of mesofemur, tibia, tarsus 6.10, 9.50, 0.40; length of metafemur, tibia, tarsus 8.40, 14.60, 0.40; length of hemelytron 5.90; length of abdomen 5.30; maximum width of abdomen 1.20.</p>
          </tp:treatment-sec>
          <tp:treatment-sec sec-type="Distribution">
            <title>Distribution.</title>
            <p>China – Yunnan: Mengla (Fig. <xref ref-type="fig" rid="F8">8</xref>).</p>
            <fig id="F8">
              <object-id content-type="doi">10.3897/asp.84.e181309.figure8</object-id>
              <object-id content-type="arpha">9597AAF1-D19E-5049-B1B0-CFAE9D572353</object-id>
              <label>Figure 8.</label>
              <caption>
                <p>Known distribution of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part></tp:taxon-name></italic> spp.</p>
              </caption>
              <graphic xlink:href="arthropod-systematics-84-565-g008.jpg" id="oo_1712261.jpg">
                <uri content-type="original_file">https://binary.pensoft.net/fig/1712261</uri>
              </graphic>
            </fig>
          </tp:treatment-sec>
          <tp:treatment-sec sec-type="Etymology">
            <title>Etymology.</title>
            <p>This new species is dedicated to Mr. Lingfeng Wei (Forest City Studio, Shanghai, China), the collector of the holotype of this rare species, for his kind support to our study of <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="family" reg="Reduviidae">Reduviidae</tp:taxon-name-part></tp:taxon-name>.</p>
          </tp:treatment-sec>
          <tp:treatment-sec sec-type="Comparative notes">
            <title>Comparative notes.</title>
            <p><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="weilingfengi">weilingfengi</tp:taxon-name-part></tp:taxon-name></italic><bold>sp. n</bold>. is morphologically similar to <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="murudiana">murudiana</tp:taxon-name-part></tp:taxon-name></italic> in the similar color patterns of the mid and hind legs, the distinct reticular patterns on the hemelytron, and the bicolored connexivum. This new species can be easily distinguished from the latter by: body small-sized, 9.5 mm in length (vs 14 mm in <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="murudiana">murudiana</tp:taxon-name-part></tp:taxon-name></italic>); anterior lobe of pronotum distinctly shorter than head (vs slightly shorter than head in <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="murudiana">murudiana</tp:taxon-name-part></tp:taxon-name></italic>); extreme base of meso- and metatibiae dark brown (vs broadly whitish in <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="murudiana">murudiana</tp:taxon-name-part></tp:taxon-name></italic>); phallosoma with paired lateral sclerites near apex (vs without such sclerites in <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="murudiana">murudiana</tp:taxon-name-part></tp:taxon-name></italic>).</p>
          </tp:treatment-sec>
        </tp:taxon-treatment>
      </sec>
      <sec sec-type="Key to species of Chinemesa modified after Chen et al. (2020a)" id="sec11">
        <title>Key to species of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part></tp:taxon-name></italic> modified after <xref ref-type="bibr" rid="B7">Chen et al. (2020a)</xref></title>
        <table-wrap content-type="key" position="anchor" orientation="portrait">
          <table>
            <tbody>
              <tr>
                <td>
                  <bold>1</bold>
                </td>
                <td>Macropterous male</td>
                <td>
                  <bold>2</bold>
                </td>
              </tr>
              <tr>
                <td>
                  <bold>1’</bold>
                </td>
                <td>Apterous female</td>
                <td>
                  <bold>7</bold>
                </td>
              </tr>
              <tr>
                <td>
                  <bold>2</bold>
                </td>
                <td>Anterior lobe of pronotum longer than head; hemelytron without reticulate patterns; connexivum unicolored</td>
                <td>
                  <bold>3</bold>
                </td>
              </tr>
              <tr>
                <td>
                  <bold>2’</bold>
                </td>
                <td>Anterior lobe of pronotum shorter than head; hemelytron with distinct or indistinct reticulate patterns; connexivum bicolored</td>
                <td>
                  <bold>4</bold>
                </td>
              </tr>
              <tr>
                <td>
                  <bold>3</bold>
                </td>
                <td>Body about 16.5 mm in length; profemur with four reddish-brown annuli; meso- and metafemora each with about nine reddish-brown annuli and one broad apical whitish annulus</td>
                <td>
                  <bold><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="poiana">poiana</tp:taxon-name-part></tp:taxon-name></italic> Wygodzinsky, 1966</bold>
                </td>
              </tr>
              <tr>
                <td>
                  <bold>3’</bold>
                </td>
                <td>Body about 7.8 mm in length; profemur with two whitish annuli; mesofemur with one narrow subapical whitish annulus, metafemur with one broad apical whitish annulus</td>
                <td>
                  <bold><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="uniannulata">uniannulata</tp:taxon-name-part></tp:taxon-name></italic> Rédei, 2007</bold>
                </td>
              </tr>
              <tr>
                <td>
                  <bold>4</bold>
                </td>
                <td>Head bicolored, with blackish anterior lobe and reddish posterior lobe; abdomen ventrally with distinct light-colored spots; phallosoma with one pair of dorsolateral lobes near apex</td>
                <td><bold><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="pulchella">pulchella</tp:taxon-name-part></tp:taxon-name></italic> sp. n</bold>.</td>
              </tr>
              <tr>
                <td>
                  <bold>4’</bold>
                </td>
                <td>Head unicolored, reddish-brown or dark brown; abdomen ventrally without light-colored spots; phallosoma without dorsolateral lobes near apex</td>
                <td>
                  <bold>5</bold>
                </td>
              </tr>
              <tr>
                <td>
                  <bold>5</bold>
                </td>
                <td>Profemur twice as long as procoxa; mesofemur with one narrow subapical whitish annulus; hemelytron with indistinct reticulate patterns and broad basal cell</td>
                <td>
                  <bold><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="chinensis">chinensis</tp:taxon-name-part></tp:taxon-name></italic> Chen, Li &amp; Cai, 2020</bold>
                </td>
              </tr>
              <tr>
                <td>
                  <bold>5’</bold>
                </td>
                <td>Profemur less than twice as long as procoxa; mesofemur with one broad apical whitish annulus; hemelytron with distinct reticulate patterns and acuminate basal cell</td>
                <td>
                  <bold>6</bold>
                </td>
              </tr>
              <tr>
                <td>
                  <bold>6</bold>
                </td>
                <td>Body about 9.5 mm in length; anterior lobe of pronotum distinctly shorter than head; extreme base of meso- and metatibiae dark brown; phallosoma with paired lateral sclerites near apex</td>
                <td><bold><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="weilingfengi">weilingfengi</tp:taxon-name-part></tp:taxon-name></italic> sp. n</bold>.</td>
              </tr>
              <tr>
                <td>
                  <bold>6’</bold>
                </td>
                <td>Body about 14 mm in length; anterior lobe of pronotum slightly shorter than head; base of meso- and metafemora broadly whitish; phallosoma without paired lateral sclerites near apex</td>
                <td>
                  <bold><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="murudiana">murudiana</tp:taxon-name-part></tp:taxon-name></italic> Wygodzinsky, 1966</bold>
                </td>
              </tr>
              <tr>
                <td>
                  <bold>7</bold>
                </td>
                <td>Body about 17 mm in length; anterior lobe of pronotum distinctly longer than head; metafemur reddish-brown, with three light-colored annuli</td>
                <td>
                  <bold><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="feminata">feminata</tp:taxon-name-part></tp:taxon-name></italic> Wygodzinsky, 1966</bold>
                </td>
              </tr>
              <tr>
                <td>
                  <bold>7’</bold>
                </td>
                <td>Body about 11.4 mm in length; anterior lobe of pronotum slightly shorter than head; metafemur yellowish-brown, with 17 alternating dark and light annuli</td>
                <td><bold><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="ornata">ornata</tp:taxon-name-part></tp:taxon-name></italic> sp. n</bold>.</td>
              </tr>
            </tbody>
          </table>
        </table-wrap>
      </sec>
    </sec>
    <sec sec-type="4. Discussion" id="sec12">
      <title>4. Discussion</title>
      <sec sec-type="4.1. Mitochondrial gene rearrangements of Chinemesa and phylogenetic implication" id="sec13">
        <title>4.1. Mitochondrial gene rearrangements of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part></tp:taxon-name></italic> and phylogenetic implication</title>
        <p>Gene rearrangement has long been considered a key aspect of mitogenome evolution. Mitochondrial gene rearrangements can be classified in several ways: (i) by gene type, into major (protein-coding and/or rRNA genes) and minor rearrangements (tRNA genes); (ii) by whether the transcription direction changes, into translocations and inversions; and (iii) by the gene clusters involved, into local and remote rearrangements (<xref ref-type="bibr" rid="B4">Cameron et al. 2007</xref>). Different types of gene rearrangements can occur in combination, with some types being more prevalent than others (<xref ref-type="bibr" rid="B9">Dowton et al. 2009</xref>). At least 23 rearranged gene orders have been observed in <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="suborder" reg="Heteroptera">Heteroptera</tp:taxon-name-part></tp:taxon-name>, distributed across twelve different families (<xref ref-type="bibr" rid="B8">Chen et al. 2020b</xref>; <xref ref-type="bibr" rid="B52">Ye et al. 2021</xref>; <xref ref-type="bibr" rid="B54">Zhao et al. 2025</xref>). <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="family" reg="Reduviidae">Reduviidae</tp:taxon-name-part></tp:taxon-name> represents a “hot-spot group” of mitochondrial gene rearrangement in <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="suborder" reg="Heteroptera">Heteroptera</tp:taxon-name-part></tp:taxon-name>, with ten distinct types previously reported in the family (<xref ref-type="bibr" rid="B52">Ye et al. 2021</xref>; <xref ref-type="bibr" rid="B10">Du et al. 2023</xref>).</p>
        <p>The mitogenomes of the four <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part></tp:taxon-name></italic> species reported here reveal two novel gene orders that differ from all known gene orders of <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="family" reg="Reduviidae">Reduviidae</tp:taxon-name-part></tp:taxon-name> (Fig. <xref ref-type="fig" rid="F1">1</xref>). In all four species, <italic>trnI</italic> and <italic>trnQ</italic> are translocated from their ancestral position between the control region and <italic>trnM</italic> to a new position between <italic>trnW</italic> and <italic>trnC</italic>. An additional loss of <italic>trnW</italic> occurs in <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="pulchella">pulchella</tp:taxon-name-part></tp:taxon-name></italic><bold>sp. n</bold>. The translocation of <italic>trnI</italic>-<italic>trnQ</italic> and the loss of <italic>trnW</italic> can be explained using the tandem duplication-random loss (<abbrev xlink:title="tandem duplication-random loss">TDRL</abbrev>) model (<xref ref-type="bibr" rid="B2">Boore 2000</xref>; <xref ref-type="bibr" rid="B49">Wei et al. 2010</xref>). With a common <abbrev xlink:title="tandem duplication-random loss">TDRL</abbrev> process, the tandem duplication of <italic>trnI</italic>-<italic>trnQ</italic>-<italic>trnM</italic>-<italic>ND2</italic>-<italic>trnW</italic> generated an intermediate sequence (<italic>trnI</italic>-<italic>trnQ</italic>-<italic>trnM</italic>-<italic>ND2</italic>-<italic>trnW</italic>-<italic>trnI</italic>-<italic>trnQ</italic>-<italic>trnM</italic>-<italic>ND2</italic>-<italic>trnW</italic>), followed by the deletion of <italic>trnI</italic> and <italic>trnQ</italic> in the first copy and <italic>trnM</italic>, <italic>ND2</italic> and <italic>trnW</italic> in the second copy, yielding the current gene order (Fig. <xref ref-type="fig" rid="F9">9A</xref>). The non-coding region (3–19 bp) between <italic>trnQ</italic> and <italic>trnC</italic> may represent a residual sequence of the gene deletion process. In the mitogenome of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="pulchella">pulchella</tp:taxon-name-part></tp:taxon-name></italic><bold>sp. n</bold>., <italic>trnW</italic> in the first copy is also deleted, leaving a 27-bp remnant between <italic>ND2</italic> and <italic>trnI</italic> (Fig. <xref ref-type="fig" rid="F9">9B</xref>).</p>
        <fig id="F9">
          <object-id content-type="doi">10.3897/asp.84.e181309.figure9</object-id>
          <object-id content-type="arpha">BC7CB362-6DF9-57F1-891C-6C144371AF6D</object-id>
          <label>Figure 9.</label>
          <caption>
            <p>The hypothetical process of gene rearrangements of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part></tp:taxon-name></italic> spp. based on the <abbrev xlink:title="tandem duplication-random loss">TDRL</abbrev> model: A. the translocation of <italic>trnI</italic> and <italic>trnQ</italic> in <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part></tp:taxon-name></italic> spp.; B. the translocation of <italic>trnI</italic> and <italic>trnQ</italic> and loss of <italic>trnW</italic> in <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="pulchella">pulchella</tp:taxon-name-part></tp:taxon-name></italic><bold>sp. n</bold>. Different types of genes are labeled with different color blocks: <abbrev xlink:title="protein-coding genes">PCGs</abbrev>, blue; rearranged tRNAs, orange; unrearranged tRNAs, pink; control region (CR), brown; deleted genes, light grey; non-coding region (NCR), dark grey.</p>
          </caption>
          <graphic xlink:href="arthropod-systematics-84-565-g009.jpg" id="oo_1712262.jpg">
            <uri content-type="original_file">https://binary.pensoft.net/fig/1712262</uri>
          </graphic>
        </fig>
        <p>Including the two newly discovered gene rearrangements in this study, a total of twelve types of rearranged gene orders has been documented in <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="family" reg="Reduviidae">Reduviidae</tp:taxon-name-part></tp:taxon-name> (Fig. <xref ref-type="fig" rid="F1">1</xref>), all of which are minor rearrangements. The tRNA genes are observed to have the highest mobility, possibly due to their small size (<xref ref-type="bibr" rid="B30">Moritz and Brown 1987</xref>; <xref ref-type="bibr" rid="B32">Peng et al. 2025</xref>). Among these rearrangement cases, tRNA gene translocation involves at least seven genes, while gene duplication and gene loss occur in only three and two genes, respectively, indicating that tRNA gene translocation is the primary form of mitochondrial gene rearrangement in <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="family" reg="Reduviidae">Reduviidae</tp:taxon-name-part></tp:taxon-name>.</p>
        <p>From an evolutionary perspective, gene rearrangements may represent potential molecular synapomorphies for specific lineages. For instance, the gene order <italic>trnQ</italic>-<italic>trnI</italic>, present in all known <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="family" reg="Aradidae">Aradidae</tp:taxon-name-part></tp:taxon-name> mitogenomes, is regarded as a molecular synapomorphy of the family (<xref ref-type="bibr" rid="B43">Song et al. 2016</xref>). The transposition of <italic>trnT</italic> and <italic>trnP</italic> (<italic>trnP</italic>-<italic>trnT</italic>) is hypothesized as a potential molecular synapomorphy of the superfamily <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="superfamily" reg="Pyrrhocoroidea">Pyrrhocoroidea</tp:taxon-name-part></tp:taxon-name> (<xref ref-type="bibr" rid="B24">Liu et al. 2019</xref>; <xref ref-type="bibr" rid="B27">Men et al. 2019</xref>). However, previously reported gene rearrangements within <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="family" reg="Reduviidae">Reduviidae</tp:taxon-name-part></tp:taxon-name> were scattered across unrelated lineages and thus considered to have evolved independently (<xref ref-type="bibr" rid="B52">Ye et al. 2021</xref>). The newly discovered <italic>trnI</italic>-<italic>trnQ</italic> translocation exists in all sequenced <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part></tp:taxon-name></italic> mitogenomes, suggesting that this rearrangement event likely occurred at least in the most recent common ancestor of these species and was retained as a potential molecular synapomorphy during the subsequent evolution of the genus. The loss of <italic>trnW</italic> evolved independently in <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="pulchella">pulchella</tp:taxon-name-part></tp:taxon-name></italic><bold>sp. n</bold>.</p>
      </sec>
      <sec sec-type="4.2. Diversity and distribution of Chinemesa" id="sec14">
        <title>4.2. Diversity and distribution of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part></tp:taxon-name></italic></title>
        <p>For a long time, <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part></tp:taxon-name></italic> was considered endemic to Borneo (<xref ref-type="bibr" rid="B51">Wygodzinsky 1966</xref>; <xref ref-type="bibr" rid="B25">Maldonado-Capriles 1990</xref>; <xref ref-type="bibr" rid="B35">Rédei 2007</xref>). <xref ref-type="bibr" rid="B7">Chen et al. (2020a)</xref> described the first species of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part></tp:taxon-name></italic> from the mainland of Asia, extending the generic distribution range to the northern tropical boundary, and suggesting the possibility of finding new species elsewhere in the Oriental Region. The three new species described herein, all from southern China, further expand our understanding of the diversity of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part></tp:taxon-name></italic> in the Asian mainland, and extend the northern limit of the generic distribution to the edge of the Oriental Region at approximately 29.5°N.</p>
        <p>Males of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part></tp:taxon-name></italic> possess fully developed wings, and specimens of at least two species (<italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="pulchella">pulchella</tp:taxon-name-part></tp:taxon-name></italic><bold>sp. n</bold>. and <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">C.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="uniannulata">uniannulata</tp:taxon-name-part></tp:taxon-name></italic>) were collected using Malaise traps, indicating the flight capability of the males. However, all known females of this genus are apterous, suggesting that geographical isolation may act as an important driving force for the diversification of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part></tp:taxon-name></italic>. Judging from the present distribution of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part></tp:taxon-name></italic>, there are still large gaps in the Indochinese Peninsula and the Malay Peninsula, where further species are expected to be discovered. Future study should also focus on the natural history of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part></tp:taxon-name></italic> species to better understand the role of habitat partition in the speciation of this genus.</p>
      </sec>
    </sec>
    <sec sec-type="5. Funding" id="sec15">
      <title>5. Funding</title>
      <p>This work was supported by grants from the National Natural Science Foundation of China (Nos. 32400373, 32120103006), the China Postdoctoral Science Foundation (No. 2025M773789), the China Scholarship Council (No. 202106350082), and the 2115 Talent Development Program of China Agricultural University.</p>
    </sec>
    <sec sec-type="6. Declarations" id="sec16">
      <title>6. Declarations</title>
      <p><bold>Conflict of interests</bold>. The authors declare that they have no conflict of interests.</p>
      <p><bold>Data availability statement</bold>. The molecular data newly generated in this study have been deposited in GenBank with accession numbers listed in Table S3.</p>
    </sec>
  </body>
  <back>
    <ack>
      <title>7. Acknowledgements</title>
      <p>We sincerely appreciate Chufei Tang and Lingfeng Wei for providing us specimens used in the present study. We are very grateful to Michael D. Webb, Valérie A. Lemaître (<named-content content-type="dwc:institutional_code" xlink:title="Natural History Museum, London" xlink:href="https://scientific-collections.gbif.org/institution/1d808a7c-1f9e-4379-9616-edb749ecf10e">NHMUK</named-content>), Charlotte Hartong and Luc Willemse (<abbrev content-type="institution" xlink:title="Naturalis Biodiversity Center, Leiden, Netherlands">RMNH</abbrev>) for their kind help during our examination of <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="family" reg="Reduviidae">Reduviidae</tp:taxon-name-part></tp:taxon-name> specimens under their care. We thank Tadashi Ishikawa and an anonymous reviewer for their valuable comments on the manuscript, and Christiane Weirauch for her editorial work.</p>
    </ack>
    <ref-list>
      <title>8. References</title>
      <ref id="B1">
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    <sec sec-type="supplementary-material">
      <title>Supplementary materials</title>
      <supplementary-material id="S1" position="float" orientation="portrait" xlink:type="simple">
        <object-id content-type="doi">10.3897/asp.84.e181309.suppl1</object-id>
        <object-id content-type="arpha">47F865F5-916D-5580-B743-94303C5D3982</object-id>
        <label>Supplementary Material 1</label>
        <caption>
          <p>Tables S1–S6</p>
        </caption>
        <statement content-type="dataType">
          <label>Data type</label>
          <p><bold/>: .xlsx</p>
        </statement>
        <statement content-type="notes">
          <label>Explanation notes</label>
          <p><bold>Table S1</bold>. Information of specimens used for morphological comparison. — <bold>Table S2</bold>. Molecular sampling information of the present study. — <bold>Table S3</bold>. Molecular data used in the present study. The newly generated sequences are outlined in bold. — <bold>Table S4</bold>. The best-fitting partitioning scheme for the PCGRNA matrix. — <bold>Table S5</bold>. The best-fitting partitioning scheme for the PCG12RNA matrix. — <bold>Table S6</bold>. The <abbrev xlink:title="Kimura 2 Parameter">K2P</abbrev> genetic divergences among the sampled <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Chinemesa">Chinemesa</tp:taxon-name-part></tp:taxon-name></italic> specimens based on the standard <italic>COX1</italic> barcoding region.</p>
        </statement>
        <media xlink:href="arthropod-systematics-84-565-s001.xlsx" mimetype="application" mime-subtype="vnd.openxmlformats-officedocument.spreadsheetml.sheet" position="float" orientation="portrait" id="oo_1712263.xlsx">
          <uri content-type="original_file">https://binary.pensoft.net/file/1712263</uri>
        </media>
        <permissions>
          <license>
            <license-p>This dataset is made available under the Open Database License (<ext-link ext-link-type="uri" xlink:href="http://opendatacommons.org/licenses/odbl/1.0">http://opendatacommons.org/licenses/odbl/1.0</ext-link>). The Open Database License (ODbL) is a license agreement intended to allow users to freely share, modify, and use this dataset while maintaining this same freedom for others, provided that the original source and author(s) are credited.</license-p>
          </license>
        </permissions>
        <attrib specific-use="authors"> Chen Z, Li H, Cai W (2026)</attrib>
      </supplementary-material>
      <supplementary-material id="S2" position="float" orientation="portrait" xlink:type="simple">
        <object-id content-type="doi">10.3897/asp.84.e181309.suppl2</object-id>
        <object-id content-type="arpha">7B7D81CB-BD21-5837-9197-CED624AEF8DD</object-id>
        <label>Supplementary Material 2</label>
        <caption>
          <p>Figures S1–S4</p>
        </caption>
        <statement content-type="dataType">
          <label>Data type</label>
          <p><bold/>: .zip</p>
        </statement>
        <statement content-type="notes">
          <label>Explanation notes</label>
          <p><bold>Figure S1</bold>. Phylogenetic tree of <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="family" reg="Reduviidae">Reduviidae</tp:taxon-name-part></tp:taxon-name> inferred from the Bayesian inference (<abbrev xlink:title="Bayesian inference">BI</abbrev>) analysis based on the PCGRNA dataset. Support values on nodes indicate <abbrev xlink:title="Bayesian posterior probabilities">PP</abbrev>. — <bold>Figure S2</bold>. Phylogenetic tree of <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="family" reg="Reduviidae">Reduviidae</tp:taxon-name-part></tp:taxon-name> inferred from the maximum-likelihood (<abbrev xlink:title="Maximum-likelihood">ML</abbrev>) analysis based on the PCGRNA dataset. Support values on nodes indicate SH-aLRT (left) and UFBoot2 (right). — <bold>Figure S3</bold>. Phylogenetic tree of <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="family" reg="Reduviidae">Reduviidae</tp:taxon-name-part></tp:taxon-name> inferred from the Bayesian inference (<abbrev xlink:title="Bayesian inference">BI</abbrev>) analysis based on the PCG12RNA dataset. Support values on nodes indicate <abbrev xlink:title="Bayesian posterior probabilities">PP</abbrev>. — <bold>Figure S4</bold>. Phylogenetic tree of <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="family" reg="Reduviidae">Reduviidae</tp:taxon-name-part></tp:taxon-name> inferred from the maximum-likelihood (<abbrev xlink:title="Maximum-likelihood">ML</abbrev>) analysis based on the PCG12RNA dataset. Support values on nodes indicate SH-aLRT (left) and UFBoot2 (right).</p>
        </statement>
        <media xlink:href="arthropod-systematics-84-565-s002.zip" mimetype="application" mime-subtype="zip" position="float" orientation="portrait" id="oo_1712264.zip">
          <uri content-type="original_file">https://binary.pensoft.net/file/1712264</uri>
        </media>
        <permissions>
          <license>
            <license-p>This dataset is made available under the Open Database License (<ext-link ext-link-type="uri" xlink:href="http://opendatacommons.org/licenses/odbl/1.0">http://opendatacommons.org/licenses/odbl/1.0</ext-link>). The Open Database License (ODbL) is a license agreement intended to allow users to freely share, modify, and use this dataset while maintaining this same freedom for others, provided that the original source and author(s) are credited.</license-p>
          </license>
        </permissions>
        <attrib specific-use="authors"> Chen Z, Li H, Cai W (2026)</attrib>
      </supplementary-material>
    </sec>
  </back>
</article>
