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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-title-group>
        <journal-title xml:lang="en">Arthropod Systematics &amp;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.79.e66321</article-id>
      <article-id pub-id-type="publisher-id">66321</article-id>
      <article-categories>
        <subj-group subj-group-type="heading">
          <subject>Research Article</subject>
        </subj-group>
        <subj-group subj-group-type="biological_taxon">
          <subject>Gonyleptidae</subject>
        </subj-group>
        <subj-group subj-group-type="scientific_subject">
          <subject>Cladistics</subject>
          <subject>Taxonomy</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>Harvestmen in the semiarid: a new genus and three new species of <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily">Pachylinae</tp:taxon-name-part></tp:taxon-name> (<tp:taxon-name><tp:taxon-name-part taxon-name-part-type="order">Opiliones</tp:taxon-name-part></tp:taxon-name>: <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="family">Gonyleptidae</tp:taxon-name-part></tp:taxon-name>) from Caatinga dry vegetation, with a cladistic analysis</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author" xlink:type="simple" corresp="yes">
          <name name-style="western">
            <surname>Saraiva</surname>
            <given-names>Nícolas Eugenio de Vasconcelos</given-names>
          </name>
          <xref ref-type="aff" rid="A1">1</xref>
          <email xlink:type="simple">nicools.eugenio@gmail.com</email>
        </contrib>
        <contrib contrib-type="author" xlink:type="simple" corresp="no">
          <name name-style="western">
            <surname>Hara</surname>
            <given-names>Marcos Ryotaro</given-names>
          </name>
          <xref ref-type="aff" rid="A2">2</xref>
        </contrib>
        <contrib contrib-type="author" xlink:type="simple" corresp="no">
          <name name-style="western">
            <surname>DaSilva</surname>
            <given-names>Marcio Bernardino</given-names>
          </name>
          <xref ref-type="aff" rid="A1">1</xref>
        </contrib>
      </contrib-group>
      <aff id="A1">
        <label>1</label>
        <addr-line content-type="verbatim">Universidade Federal da Paraíba, Centro de Ciências Exatas e da Natureza, Departamento de Sistemática e Ecologia, Programa de Pós-Graduação em Ciências Biológicas (Zoologia), João Pessoa, PB, Brazil; Nícolas E. de V. Saraiva [nicools.eugenio@gmail.com]; Marcio B. DaSilva [1940@uol.com.br]</addr-line>
        <institution>Universidade Federal da Paraíba</institution>
        <addr-line content-type="city">João Pessoa</addr-line>
        <country>Brazil</country>
      </aff>
      <aff id="A2">
        <label>2</label>
        <addr-line content-type="verbatim">Universidade de São Paulo, Escola de Artes, Ciências e Humanidades (EACH), São Paulo, SP, Brazil; Marcos R. Hara [marcosrh@usp.br]</addr-line>
        <institution>Universidade de São Paulo</institution>
        <addr-line content-type="city">São Paulo</addr-line>
        <country>Brazil</country>
      </aff>
      <author-notes>
        <fn fn-type="edited-by">
          <p>Academic Editor: Lorenzo Prendini</p>
        </fn>
        <fn fn-type="corresp">
          <p>Corresponding author: Nícolas Eugenio de Vasconcelos Saraiva (<ext-link xlink:type="simple" ext-link-type="uri" xlink:href="http://nicools.eugenio@gmail.com">nicools.eugenio@gmail.com</ext-link><email xlink:type="simple">)</email></p>
        </fn>
      </author-notes>
      <pub-date pub-type="collection">
        <year>2021</year>
      </pub-date>
      <pub-date pub-type="epub">
        <day>08</day>
        <month>10</month>
        <year>2021</year>
      </pub-date>
      <volume>79</volume>
      <fpage>485</fpage>
      <lpage>507</lpage>
      <uri content-type="arpha" xlink:href="http://openbiodiv.net/12D8C5F9-E3F1-5CBC-A235-F81E56FA0BC8">12D8C5F9-E3F1-5CBC-A235-F81E56FA0BC8</uri>
      <uri content-type="zoobank" xlink:href="http://zoobank.org/3C3B731E-89B4-4D1B-9E03-47BED83F8530">3C3B731E-89B4-4D1B-9E03-47BED83F8530</uri>
      <history>
        <date date-type="received">
          <day>23</day>
          <month>03</month>
          <year>2021</year>
        </date>
        <date date-type="accepted">
          <day>18</day>
          <month>07</month>
          <year>2021</year>
        </date>
      </history>
      <permissions>
        <copyright-statement>Nícolas Eugenio de Vasconcelos Saraiva, Marcos Ryotaro Hara, Marcio Bernardino DaSilva</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">http://zoobank.org/3C3B731E-89B4-4D1B-9E03-47BED83F8530</self-uri>
      <abstract>
        <p>
          <bold>Abstract</bold>
        </p>
        <p><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="order">Opiliones</tp:taxon-name-part></tp:taxon-name> are highly diverse in the Neotropics. Because of biological constraints, most harvestmen communities are associated with humid forests, exhibiting a high species diversity and endemism in these habitats. Drier formations, such as the Caatinga biome in northeastern Brazil, are less diverse and still considered under-sampled for the order. This study represents an effort to examine the aforementioned diversity by describing a new <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="family">Gonyleptidae</tp:taxon-name-part></tp:taxon-name> genus, <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">Sertaneja</tp:taxon-name-part></tp:taxon-name></italic><bold>gen. nov.</bold>, comprising two new species from Ceará state, <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">Sertaneja</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="bicuspidata">bicuspidata</tp:taxon-name-part></tp:taxon-name></italic><bold>sp. nov.</bold> and <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">Sertaneja</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="crassitibialis">crassitibialis</tp:taxon-name-part></tp:taxon-name></italic><bold>sp. nov.</bold>, and one new species from Rio Grande do Norte state, <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">Sertaneja</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="falcata">falcata</tp:taxon-name-part></tp:taxon-name></italic><bold>sp. nov.</bold> A morphological cladistic analysis consisting of 20 terminals and 72 characters was performed to evaluate monophyly of the new genus and relate it to other <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="family">Gonyleptidae</tp:taxon-name-part></tp:taxon-name>. The analysis resulted in a single most parsimonious tree, corroborating <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">Sertaneja</tp:taxon-name-part></tp:taxon-name></italic><bold>gen. nov.</bold> monophyly and relatedness to <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Gyndoides">Gyndoides</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="springmanni">springmanni</tp:taxon-name-part></tp:taxon-name></italic> Soares &amp; Soares, 1947, which in turn is the sister group to the DRMN clade. Taking into account the morphological traits and phylogenetic placement of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">Sertaneja</tp:taxon-name-part></tp:taxon-name></italic><bold>gen. nov.</bold>, we chose to place the new genus in <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily">Pachylinae</tp:taxon-name-part></tp:taxon-name> despite its polyphyletic status, given that the <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">Sertaneja</tp:taxon-name-part></tp:taxon-name></italic><bold>gen. nov.</bold> clade is closely related to one of the Brazilian <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily">Pachylinae</tp:taxon-name-part></tp:taxon-name> lineage. A resolution to the <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily">Pachylinae</tp:taxon-name-part></tp:taxon-name> conundrum is needed to further explain the subfamily intricacies. Future research requires a larger scope, but currently, based on the new genus monophyly, support, and relatedness, we formally propose its creation and hope to shed light on the possible evolutionary scenarios for the subfamily.</p>
      </abstract>
      <kwd-group>
        <label>Keywords</label>
        <kwd>
          <tp:taxon-name>
            <tp:taxon-name-part taxon-name-part-type="class">Arachnida</tp:taxon-name-part>
          </tp:taxon-name>
        </kwd>
        <kwd>
          <tp:taxon-name>
            <tp:taxon-name-part taxon-name-part-type="infraorder">Grassatores</tp:taxon-name-part>
          </tp:taxon-name>
        </kwd>
        <kwd>Neotropics</kwd>
        <kwd>phylogeny</kwd>
        <kwd>upland forest</kwd>
      </kwd-group>
      <funding-group>
        <award-group>
          <funding-source>
            <named-content content-type="funder_name">Conselho Nacional de Desenvolvimento Científico e Tecnológico</named-content>
            <named-content content-type="funder_identifier">501100003593</named-content>
            <named-content content-type="funder_doi">http://doi.org/10.13039/501100003593</named-content>
          </funding-source>
        </award-group>
      </funding-group>
    </article-meta>
  </front>
  <body>
    <sec sec-type="1. Introduction" id="SECID0ECBAC">
      <title>1. Introduction</title>
      <p>The high species diversity in the Neotropics is well documented for many taxa, and harvestmen are no exception, with many studies describing their abundance and diversity in Neotropical rainforests (<xref ref-type="bibr" rid="B70">Pinto-da-Rocha and Bonaldo 2006</xref>; <xref ref-type="bibr" rid="B76">Proud et al. 2012</xref>; <xref ref-type="bibr" rid="B63">Nogueira et al. 2019</xref>). Considering this diversity, great taxonomic efforts in the Neotropics have consistently been expended, which trace back to the 1940s, with major efforts by two main researchers, Cândido Firmino Melo Leitão and Carl Friedrich Roewer. These researchers together described over 3000 harvestmen species, prominently from the Neotropics (<xref ref-type="bibr" rid="B89">Tourinho and Kury 2015</xref>). Currently, the description rate continues to be substantial, with many new species being cataloged and with numerous group revisions occurring (<xref ref-type="bibr" rid="B16">DaSilva and Gnaspini 2010</xref>; <xref ref-type="bibr" rid="B17">DaSilva and Pinto-da-Rocha 2010</xref>; <xref ref-type="bibr" rid="B31">Hara and Pinto-da-Rocha 2010</xref>; <xref ref-type="bibr" rid="B59">Mendes 2011</xref>; <xref ref-type="bibr" rid="B72">Pinto-da-Rocha and Bragagnolo 2013</xref>; <xref ref-type="bibr" rid="B90">Villarreal et al. 2019</xref>; <xref ref-type="bibr" rid="B14">Carvalho and Kury 2021</xref>; <xref ref-type="bibr" rid="B65">Pessoa-Silva et al. 2021</xref>). These high diversity rates are associated with particular traits of the order, such as a high degree of endemism, restricted distribution, dependence on humid habitats, and low resistance to desiccation, which makes populations much more prone to diversification events over time (<xref ref-type="bibr" rid="B18">DaSilva et al. 2015</xref>; <xref ref-type="bibr" rid="B20">Derkarabetian et al. 2021</xref>).</p>
      <p>Dry forests and open vegetation biomes (e.g., Caatinga and Cerrado) are less diverse compared to humid forests (<xref ref-type="bibr" rid="B63">Nogueira et al. 2019</xref>), but they still represent a frontier that remains to be explored for <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="order">Opiliones</tp:taxon-name-part></tp:taxon-name>. The Caatinga biome, located in northeastern Brazil, has a semiarid climate and is composed of dry forests and shrublands. Some efforts to study the aforementioned diversity of harvestmen have come as punctual descriptions (<xref ref-type="bibr" rid="B40">Kury 2008</xref>; <xref ref-type="bibr" rid="B74">Pinto-da-Rocha and Carvalho 2009</xref>), checklists (<xref ref-type="bibr" rid="B8">Azevedo et al. 2016</xref>), abundance and diversity studies (<xref ref-type="bibr" rid="B21">DeSouza et al. 2017</xref>), and biogeographical research (<xref ref-type="bibr" rid="B19">DaSilva et al. 2016</xref>), which has gradually helped unravel the actual diversity. The Caatinga biome is composed of a complex set of relictual humid forest formations that represent a relevant source of diversity for many taxa (<xref ref-type="bibr" rid="B48">Locatelli and Machado 2001</xref>; <xref ref-type="bibr" rid="B4">Albano and Girão 2008</xref>; <xref ref-type="bibr" rid="B83">Santos et al. 2011</xref>), but it is yet to be fully explored for <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="order">Opiliones</tp:taxon-name-part></tp:taxon-name> (<xref ref-type="bibr" rid="B41">Kury 2009</xref>). These formations, the Brejos de Altitude, are directly associated with the occurrence of high plateaus over 500 m in altitude, with precipitation exceeding 1200 mm/year, and were created mainly by the processes of expansion and retraction of different forest bulks, imposed by the glacial and interglacial events of the Pleistocene era (<xref ref-type="bibr" rid="B88">Tabarelli and Santos 2004</xref>; <xref ref-type="bibr" rid="B15">Cavalcante 2005</xref>; <xref ref-type="bibr" rid="B84">Silveira et al. 2019</xref>). Such heterogeneity provides potential for unexplored taxa of <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="order">Opiliones</tp:taxon-name-part></tp:taxon-name>, due to the altitudinal forest characteristics.</p>
      <p>One of the most under-sampled and enigmatic harvestmen groups in the Caatinga region is the <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily">Pachylinae</tp:taxon-name-part></tp:taxon-name>, the largest subfamily in <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="family">Gonyleptidae</tp:taxon-name-part></tp:taxon-name>, with slightly more than 300 registered species (Kury et al. 2001). This subfamily is not a monophyletic group (<xref ref-type="bibr" rid="B73">Pinto-da-Rocha et al. 2014</xref>; <xref ref-type="bibr" rid="B13">Carvalho and Kury 2018</xref>; <xref ref-type="bibr" rid="B7">Ázara et al. 2020</xref>; <xref ref-type="bibr" rid="B9">Benavides et al. 2021</xref>), and it includes several <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="family">Gonyleptidae</tp:taxon-name-part></tp:taxon-name> genera with symplesiomorphic characters and uncertain relationships. According to the <xref ref-type="bibr" rid="B39">Kury (2003)</xref> catalog, some <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily">Pachylinae</tp:taxon-name-part></tp:taxon-name> representatives are most likely to occur in the Caatinga domain. For instance, <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Discocyrtulus">Discocyrtulus</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="marginalis">marginalis</tp:taxon-name-part></tp:taxon-name></italic> Roewer, 1929 and <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Paradiscocyrtus">Paradiscocyrtus</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="cerayanus">cerayanus</tp:taxon-name-part></tp:taxon-name></italic> Roewer, 1929, are both described to the Ceará state where the Caatinga formation is considerable and are only known from their original descriptions, currently lacking official confirmation. This lack of information regarding this subfamily in the Caatinga leads to an underestimation of its true diversity. This can be confirmed by the most recent inventory effort of harvestmen in the Caatinga developed by <xref ref-type="bibr" rid="B21">DeSouza et al. (2017)</xref> based on the literature, depositories, and new collection data from the Semiarid Biodiversity project (<xref ref-type="bibr" rid="B11">Bravo 2017</xref>). Despite the sampling deficit for the region, the study was able to document a total of 10 species for the subfamily, five of which were previously unknown.</p>
      <p>The suspicion of <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily">Pachylinae</tp:taxon-name-part></tp:taxon-name> polyphyly could be traced back at least 20 years (<xref ref-type="bibr" rid="B68">Pinto-da-Rocha 2002</xref>), and is fueled by its comprehensive diagnosis, based on the lack of exclusive diagnostic features and four scute areas (<xref ref-type="bibr" rid="B73">Pinto-da-Rocha et al. 2014</xref>). Because of such poor taxonomic characterization, monophyly of the group is frequently not recovered, both by morphological and molecular data (<xref ref-type="bibr" rid="B68">Pinto-da-Rocha 2002</xref>; <xref ref-type="bibr" rid="B32">Hara et al. 2012</xref>; <xref ref-type="bibr" rid="B73">Pinto-da-Rocha et al. 2014</xref>; <xref ref-type="bibr" rid="B13">Carvalho and Kury 2018</xref>). The reason for this situation is not exclusive to <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily">Pachylinae</tp:taxon-name-part></tp:taxon-name>, but <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="order">Opiliones</tp:taxon-name-part></tp:taxon-name> as a whole because of the so called Roewerian system, named by <xref ref-type="bibr" rid="B33">Henriksen (1932)</xref> and explained many times in the past (for instance, <xref ref-type="bibr" rid="B67">Pinto-da-Rocha 1997</xref>, <xref ref-type="bibr" rid="B68">2002</xref>; <xref ref-type="bibr" rid="B16">DaSilva and Gnaspini 2010</xref>; and <xref ref-type="bibr" rid="B31">Hara and Pinto-da-Rocha 2010</xref>). Simply put, Roewer subjectively chose certain set of characters to circumscribe families (e.g. type of tarsal claws and armature on anterior margin of carapace), subfamilies (e.g. number of scute areas and type of ocularium and its placement on carapace) and so on. Thus, it overlooked intraspecific variation and resulted in many monotypic groups, as well as groups of phylogenetically unrelated species (see <xref ref-type="bibr" rid="B36">Kury 1992</xref> for instance). The Soares couple (<xref ref-type="bibr" rid="B85">Soares and Soares 1954</xref>) revised all genera of <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily">Pachylinae</tp:taxon-name-part></tp:taxon-name> in their catalogue, but still under strong influence of the Roewerian system. Since their catalogue, no one has attempted to make a comprehensive revision of <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily">Pachylinae</tp:taxon-name-part></tp:taxon-name>. Nevertheless, Ringuelet and Acosta made noteworthy contributions, albeit limited, by revising Argentinean (<xref ref-type="bibr" rid="B77">Ringuelet 1959</xref>; <xref ref-type="bibr" rid="B1">Acosta 1999</xref>) and Peruvian genera (<xref ref-type="bibr" rid="B2">Acosta 2001</xref>), but most of the subfamily remained untouched. Current efforts have attempted to resolve this issue by revising key taxa and using morphological and/or molecular data, which has resulted in the circumscription of the <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily">Pachylinae</tp:taxon-name-part></tp:taxon-name><abbrev xlink:title="sensu stricto" id="ABBRID0ENKAC">s.s</abbrev>. to only four southern South American genera, the erection of the new subfamilies to accommodate some Brazillian <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily">Pachylinae</tp:taxon-name-part></tp:taxon-name> genera, such as <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily">Roeweriinae</tp:taxon-name-part></tp:taxon-name> and <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily">Neopachylinae</tp:taxon-name-part></tp:taxon-name>, and recognition of the megadiverse genus <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Discocyrtus">Discocyrtus</tp:taxon-name-part></tp:taxon-name></italic> Holmberg, 1878 <abbrev xlink:title="sensu stricto" id="ABBRID0EHLAC">s.s</abbrev>. lineage. However, a multitude of other genera still need to go through similar revisionary treatment (<xref ref-type="bibr" rid="B73">Pinto-da-Rocha et al. 2014</xref>; <xref ref-type="bibr" rid="B43">Kury and Carvalho 2016</xref>; <xref ref-type="bibr" rid="B13">Carvalho and Kury 2018</xref>; <xref ref-type="bibr" rid="B14">Carvalho and Kury 2021</xref>).</p>
      <p>In the present paper, we describe a new <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily">Pachylinae</tp:taxon-name-part></tp:taxon-name> genus for the northern Caatinga region from Ceará and Rio Grande do Norte states, comprising three new species, based on external morphological characters. We also provide a phylogeny with representatives of some of the main <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily">Pachylinae</tp:taxon-name-part></tp:taxon-name> lineages, aiming to shed light on the intricate history of the Caatinga’s harvestmen diversity, which has been barely explored.</p>
    </sec>
    <sec sec-type="methods" id="SECID0EHMAC">
      <title>2. Methods</title>
      <sec sec-type="2.1. Taxonomy" id="SECID0ELMAC">
        <title>2.1. Taxonomy</title>
        <p>Description of the external morphology, topological terms of appendages, mensuration, meristics, genital preparation, and examination mainly follows <xref ref-type="bibr" rid="B3">Acosta et al. (2007)</xref> with minor modifications, such as those by <xref ref-type="bibr" rid="B32">Hara et al. (2012)</xref>, namely, the posterior margin of the dorsal scute, carapace, and spine definitions. Dorsal scute shape terminology, penial macrosetae nomenclature, and ozopore morphology follow <xref ref-type="bibr" rid="B44">Kury and Medrano (2016)</xref>, Kury and Villarreal M. (2015), and <xref ref-type="bibr" rid="B29">Hara and Gnaspini (2003)</xref>, respectively. Description of colors were based on specimens in 70% ethanol preservation, and follows the notation and numeration of the 267 Color Centroids of the NBS/ISCC Color System, as described by Kury and Orrico (2006).</p>
        <p>External morphology examination was conducted using a stereomicroscope Leica M205C. Penial examination and illustrations were performed using a Zeiss Primo Star binocular microscope fixed with a photo camera and the software ZEN 2 Lite Blue Edition (Zeiss, Germany). Illustration of the external morphology and penis were made in the vector graphics editor Inkscape v. 0.92 (<ext-link xlink:type="simple" ext-link-type="uri" xlink:href="https://inkscape.org">https://inkscape.org</ext-link>), based on a focus-stacked image taken using the Leica stereo microscope associated with the software Leica Application Suite v. 4.2 (Leica Microsystems, Germany). Scanning electron micrographs were obtained using Shimadzu’s SSX-550-SUPERSCAN from the Laboratório de Ensaios de Materiais of the Centro de Tecnologias do Gás e Energias Renováveis, Rio Grande do Norte, Brazil. The material was prepared following the methodology of <xref ref-type="bibr" rid="B68">Pinto-da-Rocha (2002)</xref>.</p>
        <p>The generic characters are not repeated in the species descriptions. Specific descriptions are based only on the male holotype. Females and other described specimens (variation) are stated in separate sections of the description and are solely based on characters that differ from the holotype. Setiferous tubercles (i = small, I = large) of the pedipalp, are described from basal to apical order. All measurements are in millimeters.</p>
        <p>Every specimen described here is deposited at the <named-content xlink:type="simple" content-type="institution" xlink:href="http://grbio.org/institution/departamento-de-sistematica-e-ecologia">Coleção de Miriápodes e Aracnídeos da Universidade Federal da Paraíba, João Pessoa, Brazil</named-content> (<named-content content-type="dwc:institutional_code">UFPB</named-content>); <named-content xlink:type="simple" content-type="institution" xlink:href="http://grbio.org/institution/museu-de-zoologia-da-universidade-de-sao-paulo">Museu de Zoologia da Universidade de São Paulo, São Paulo, Brazil</named-content> (<named-content content-type="dwc:institutional_code">MZUSP</named-content>); and <named-content xlink:type="simple" content-type="institution" xlink:href="http://grbio.org/institution/museu-nacionaluniversidade-federal-de-rio-de-janeiro">Museu Nacional do Rio de Janeiro, Rio de Janeiro, Brazil</named-content> (<named-content content-type="dwc:institutional_code">MNRJ</named-content>).</p>
      </sec>
      <sec sec-type="2.2. Taxon sampling" id="SECID0E5NAC">
        <title>2.2. Taxon sampling</title>
        <p>All specimens used in the phylogenetic analysis came from loans from Coleção de Aracnídeos e Miriápodes da Universidade Federal da Paraíba (<named-content content-type="dwc:institutional_code">UFPB</named-content>), Museu de Zoologia da Universidade de São Paulo (<named-content content-type="dwc:institutional_code">MZUSP</named-content>), and Museu Nacional do Rio de Janeiro (<named-content content-type="dwc:institutional_code">MNRJ</named-content>). Considering that the main goal of this study was to evaluate monophyly of the new genus and its phylogenetic placement, the terminals were chosen based on <xref ref-type="bibr" rid="B73">Pinto-da-Rocha et al. (2014)</xref> and <xref ref-type="bibr" rid="B13">Carvalho and Kury (2018)</xref>, focusing on insights of subfamilial relationships, using only the most relevant set of taxa without an unnecessary load for larger analysis. For this purpose, our ingroup was composed by the three new species of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">Sertaneja</tp:taxon-name-part></tp:taxon-name></italic> gen. nov., and the outgroup included 17 species representing four <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="superfamily">Gonyleptoidea</tp:taxon-name-part></tp:taxon-name> families and seven <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="family">Gonyleptidae</tp:taxon-name-part></tp:taxon-name> subfamilies, totaling 20 terminals. A list of outgroup information is shown in Table <xref ref-type="table" rid="T1">1</xref>.</p>
        <table-wrap id="T1" position="float" orientation="portrait">
          <label>Table 1.</label>
          <caption>
            <p>List of the species and their respective voucher information, used as outgroup taxa in the cladistic analysis. — <bold><italic>Abbreviations</italic></bold>: <abbrev xlink:title="sensu stricto" id="ABBRID0E3PAC">s.s.</abbrev> = sensu stricto; <abbrev xlink:title="sensu lato" id="ABBRID0EBAAE">s.l.</abbrev> = sensu lato.</p>
          </caption>
          <table id="TID0E5BBI" rules="all">
            <tbody>
              <tr>
                <td rowspan="1" colspan="1">
                  <bold>Family</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>Subfamily</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>Species</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>Locality</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>Depository</bold>
                </td>
              </tr>
              <tr>
                <td rowspan="1" colspan="1">
                  <tp:taxon-name>
                    <tp:taxon-name-part taxon-name-part-type="family">Stygnidae</tp:taxon-name-part>
                  </tp:taxon-name>
                </td>
                <td rowspan="1" colspan="1">
                  <tp:taxon-name>
                    <tp:taxon-name-part taxon-name-part-type="subfamily">Stygninae</tp:taxon-name-part>
                  </tp:taxon-name>
                </td>
                <td rowspan="1" colspan="1"><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Pickeliana">Pickeliana</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="pickeli">pickeli</tp:taxon-name-part></tp:taxon-name></italic> Mello-Leitão, 1932</td>
                <td rowspan="1" colspan="1">Brazil, São Vicente Férrer – PE</td>
                <td rowspan="1" colspan="1"><named-content content-type="dwc:institutional_code">UFPB</named-content> OP-789</td>
              </tr>
              <tr>
                <td rowspan="1" colspan="1">
                  <tp:taxon-name>
                    <tp:taxon-name-part taxon-name-part-type="family">Manaosbiidae</tp:taxon-name-part>
                  </tp:taxon-name>
                </td>
                <td rowspan="1" colspan="1">
                  <tp:taxon-name>
                    <tp:taxon-name-part taxon-name-part-type="subfamily">Manaosbiinae</tp:taxon-name-part>
                  </tp:taxon-name>
                </td>
                <td rowspan="1" colspan="1"><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Saramacia">Saramacia</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="lucasae">lucasae</tp:taxon-name-part></tp:taxon-name></italic> (Jim and Soares, 1991)</td>
                <td rowspan="1" colspan="1">Brazil, Porto Velho – RO, Abunã</td>
                <td rowspan="1" colspan="1"><named-content content-type="dwc:institutional_code">MZUSP</named-content> 58150</td>
              </tr>
              <tr>
                <td rowspan="1" colspan="1">
                  <tp:taxon-name>
                    <tp:taxon-name-part taxon-name-part-type="family">Cranaidae</tp:taxon-name-part>
                  </tp:taxon-name>
                </td>
                <td rowspan="1" colspan="1">
                  <tp:taxon-name>
                    <tp:taxon-name-part taxon-name-part-type="subfamily">Phareicranainae</tp:taxon-name-part>
                  </tp:taxon-name>
                </td>
                <td rowspan="1" colspan="1"><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Phareicranaus">Phareicranaus</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="manaura">manaura</tp:taxon-name-part></tp:taxon-name></italic> (Pinto-da-Rocha, 1994)</td>
                <td rowspan="1" colspan="1">Brazil, Manaus – AM, Fazenda UFAM</td>
                <td rowspan="1" colspan="1"><named-content content-type="dwc:institutional_code">MZUSP</named-content> 49326</td>
              </tr>
              <tr>
                <td rowspan="1" colspan="1">
                  <tp:taxon-name>
                    <tp:taxon-name-part taxon-name-part-type="family">Gonyleptidae</tp:taxon-name-part>
                  </tp:taxon-name>
                </td>
                <td rowspan="1" colspan="1">
                  <tp:taxon-name>
                    <tp:taxon-name-part taxon-name-part-type="subfamily">Heteropachylinae</tp:taxon-name-part>
                  </tp:taxon-name>
                </td>
                <td rowspan="1" colspan="1"><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Pseudopucrolia">Pseudopucrolia</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="discrepans">discrepans</tp:taxon-name-part></tp:taxon-name></italic> (Roewer, 1943)</td>
                <td rowspan="1" colspan="1">Brazil, Caaporã – PB</td>
                <td rowspan="1" colspan="1"><named-content content-type="dwc:institutional_code">UFPB</named-content> OP-788</td>
              </tr>
              <tr>
                <td rowspan="1" colspan="1">
                  <tp:taxon-name>
                    <tp:taxon-name-part taxon-name-part-type="family">Gonyleptidae</tp:taxon-name-part>
                  </tp:taxon-name>
                </td>
                <td rowspan="1" colspan="1">
                  <tp:taxon-name>
                    <tp:taxon-name-part taxon-name-part-type="subfamily">Goniosomatinae</tp:taxon-name-part>
                  </tp:taxon-name>
                </td>
                <td rowspan="1" colspan="1"><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Heteromitobates">Heteromitobates</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="inscriptus">inscriptus</tp:taxon-name-part></tp:taxon-name></italic> (Mello-Leitão, 1922)</td>
                <td rowspan="1" colspan="1">Brazil, Caraguatatuba – SP, base do Morro S. Antônio</td>
                <td rowspan="1" colspan="1"><named-content content-type="dwc:institutional_code">UFPB</named-content> OP-182</td>
              </tr>
              <tr>
                <td rowspan="1" colspan="1">
                  <tp:taxon-name>
                    <tp:taxon-name-part taxon-name-part-type="family">Gonyleptidae</tp:taxon-name-part>
                  </tp:taxon-name>
                </td>
                <td rowspan="1" colspan="1">
                  <tp:taxon-name>
                    <tp:taxon-name-part taxon-name-part-type="subfamily">Gonyleptinae</tp:taxon-name-part>
                  </tp:taxon-name>
                </td>
                <td rowspan="1" colspan="1"><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Gonyleptes">Gonyleptes</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="horridus">horridus</tp:taxon-name-part></tp:taxon-name></italic> Kirby, 1818</td>
                <td rowspan="1" colspan="1">Brazil, Guapimirim – RJ</td>
                <td rowspan="1" colspan="1"><named-content content-type="dwc:institutional_code">MZUSP</named-content> 903</td>
              </tr>
              <tr>
                <td rowspan="1" colspan="1">
                  <tp:taxon-name>
                    <tp:taxon-name-part taxon-name-part-type="family">Gonyleptidae</tp:taxon-name-part>
                  </tp:taxon-name>
                </td>
                <td rowspan="1" colspan="1">
                  <tp:taxon-name>
                    <tp:taxon-name-part taxon-name-part-type="subfamily">Gonyleptinae</tp:taxon-name-part>
                  </tp:taxon-name>
                </td>
                <td rowspan="1" colspan="1"><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Parapachyloides">Parapachyloides</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="uncinatus">uncinatus</tp:taxon-name-part></tp:taxon-name></italic> (Sørensen, 1879)</td>
                <td rowspan="1" colspan="1">Paraguay, San Pedro, Liberacion</td>
                <td rowspan="1" colspan="1"><named-content content-type="dwc:institutional_code">MNRJ</named-content> 8469</td>
              </tr>
              <tr>
                <td rowspan="1" colspan="1">
                  <tp:taxon-name>
                    <tp:taxon-name-part taxon-name-part-type="family">Gonyleptidae</tp:taxon-name-part>
                  </tp:taxon-name>
                </td>
                <td rowspan="1" colspan="1"><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily">Pachylinae</tp:taxon-name-part></tp:taxon-name><abbrev xlink:title="sensu stricto" id="ABBRID0E4LAE">s.s</abbrev>.</td>
                <td rowspan="1" colspan="1"><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Pachylus">Pachylus</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="chilensis">chilensis</tp:taxon-name-part></tp:taxon-name></italic> (Gray, 1833)</td>
                <td rowspan="1" colspan="1">Chile, Parque Nacional La Camapana</td>
                <td rowspan="1" colspan="1"><named-content content-type="dwc:institutional_code">MZUSP</named-content> 36797</td>
              </tr>
              <tr>
                <td rowspan="1" colspan="1">
                  <tp:taxon-name>
                    <tp:taxon-name-part taxon-name-part-type="family">Gonyleptidae</tp:taxon-name-part>
                  </tp:taxon-name>
                </td>
                <td rowspan="1" colspan="1"><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily">Pachylinae</tp:taxon-name-part></tp:taxon-name><abbrev xlink:title="sensu stricto" id="ABBRID0EPNAE">s.s</abbrev>.</td>
                <td rowspan="1" colspan="1"><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Acanthopachylus">Acanthopachylus</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="aculeatus">aculeatus</tp:taxon-name-part></tp:taxon-name></italic> (Kirby, 1819)</td>
                <td rowspan="1" colspan="1">Brazil, Porto Alegre – RS, Ponta Grossa</td>
                <td rowspan="1" colspan="1"><named-content content-type="dwc:institutional_code">MZUSP</named-content> 13830</td>
              </tr>
              <tr>
                <td rowspan="1" colspan="1">
                  <tp:taxon-name>
                    <tp:taxon-name-part taxon-name-part-type="family">Gonyleptidae</tp:taxon-name-part>
                  </tp:taxon-name>
                </td>
                <td rowspan="1" colspan="1"><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily">Pachylinae</tp:taxon-name-part></tp:taxon-name><abbrev xlink:title="sensu stricto" id="ABBRID0EBPAE">s.s</abbrev>.</td>
                <td rowspan="1" colspan="1"><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Acanthoprocta">Acanthoprocta</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="pustulata">pustulata</tp:taxon-name-part></tp:taxon-name></italic> Loman, 1899</td>
                <td rowspan="1" colspan="1">Chile, Araucania, Parque Nacional Nahuelbuta</td>
                <td rowspan="1" colspan="1"><named-content content-type="dwc:institutional_code">MZUSP</named-content> 36807</td>
              </tr>
              <tr>
                <td rowspan="1" colspan="1">
                  <tp:taxon-name>
                    <tp:taxon-name-part taxon-name-part-type="family">Gonyleptidae</tp:taxon-name-part>
                  </tp:taxon-name>
                </td>
                <td rowspan="1" colspan="1">
                  <tp:taxon-name>
                    <tp:taxon-name-part taxon-name-part-type="genus" reg="Mitobatinae">Mitobatinae</tp:taxon-name-part>
                  </tp:taxon-name>
                </td>
                <td rowspan="1" colspan="1"><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Longiperna">Longiperna</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="kuryi">kuryi</tp:taxon-name-part></tp:taxon-name></italic> Pinto-da-Rocha and Bragagnolo, 2010</td>
                <td rowspan="1" colspan="1">Brazil, Bertioga – SP, trilha descendo rio Itapanhaú</td>
                <td rowspan="1" colspan="1"><named-content content-type="dwc:institutional_code">UFPB</named-content> OP-42</td>
              </tr>
              <tr>
                <td rowspan="1" colspan="1">
                  <tp:taxon-name>
                    <tp:taxon-name-part taxon-name-part-type="family">Gonyleptidae</tp:taxon-name-part>
                  </tp:taxon-name>
                </td>
                <td rowspan="1" colspan="1">
                  <tp:taxon-name>
                    <tp:taxon-name-part taxon-name-part-type="subfamily">Roeweriinae</tp:taxon-name-part>
                  </tp:taxon-name>
                </td>
                <td rowspan="1" colspan="1"><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Roeweria">Roeweria</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="bittencourti">bittencourti</tp:taxon-name-part></tp:taxon-name></italic> Mello-Leitão, 1923</td>
                <td rowspan="1" colspan="1">Brazil, Ilhota – SC, Parque Botânico Morro do Báu</td>
                <td rowspan="1" colspan="1"><named-content content-type="dwc:institutional_code">MZUSP</named-content> 18659</td>
              </tr>
              <tr>
                <td rowspan="1" colspan="1">
                  <tp:taxon-name>
                    <tp:taxon-name-part taxon-name-part-type="family">Gonyleptidae</tp:taxon-name-part>
                  </tp:taxon-name>
                </td>
                <td rowspan="1" colspan="1">
                  <tp:taxon-name>
                    <tp:taxon-name-part taxon-name-part-type="subfamily">Roeweriinae</tp:taxon-name-part>
                  </tp:taxon-name>
                </td>
                <td rowspan="1" colspan="1"><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Roeweria">Roeweria</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="virescens">virescens</tp:taxon-name-part></tp:taxon-name></italic> (Mello-Leitão, 1940)</td>
                <td rowspan="1" colspan="1">Brazil, São Miguel Arcanjo – SP, Parque da Onça Parda</td>
                <td rowspan="1" colspan="1"><named-content content-type="dwc:institutional_code">MZUSP</named-content> 46930</td>
              </tr>
              <tr>
                <td rowspan="1" colspan="1">
                  <tp:taxon-name>
                    <tp:taxon-name-part taxon-name-part-type="family">Gonyleptidae</tp:taxon-name-part>
                  </tp:taxon-name>
                </td>
                <td rowspan="1" colspan="1">
                  <tp:taxon-name>
                    <tp:taxon-name-part taxon-name-part-type="subfamily">Neopachylinae</tp:taxon-name-part>
                  </tp:taxon-name>
                </td>
                <td rowspan="1" colspan="1"><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Pachylobos">Pachylobos</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="longicornis">longicornis</tp:taxon-name-part></tp:taxon-name></italic> (Mello-Leitão, 1922)</td>
                <td rowspan="1" colspan="1">Brazil, Cubatão – SP, COPEBRAS, trilha Grande Fenda 1</td>
                <td rowspan="1" colspan="1"><named-content content-type="dwc:institutional_code">MZUSP</named-content> 31726</td>
              </tr>
              <tr>
                <td rowspan="1" colspan="1">
                  <tp:taxon-name>
                    <tp:taxon-name-part taxon-name-part-type="family">Gonyleptidae</tp:taxon-name-part>
                  </tp:taxon-name>
                </td>
                <td rowspan="1" colspan="1"><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily">Pachylinae</tp:taxon-name-part></tp:taxon-name><abbrev xlink:title="sensu lato" id="ABBRID0EMWAE">s.l</abbrev>.</td>
                <td rowspan="1" colspan="1"><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Eusarcus">Eusarcus</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="nigrimaculatus">nigrimaculatus</tp:taxon-name-part></tp:taxon-name></italic> Mello-Leitão, 1924</td>
                <td rowspan="1" colspan="1">Brazil, Rio de Janeiro – RJ, Floresta da Tijuca</td>
                <td rowspan="1" colspan="1"><named-content content-type="dwc:institutional_code">UFPB</named-content> OP-46</td>
              </tr>
              <tr>
                <td rowspan="1" colspan="1">
                  <tp:taxon-name>
                    <tp:taxon-name-part taxon-name-part-type="family">Gonyleptidae</tp:taxon-name-part>
                  </tp:taxon-name>
                </td>
                <td rowspan="1" colspan="1"><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily">Pachylinae</tp:taxon-name-part></tp:taxon-name><abbrev xlink:title="sensu lato" id="ABBRID0E5XAE">s.l</abbrev>.</td>
                <td rowspan="1" colspan="1"><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Discocyrtus">Discocyrtus</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="fenax">fenax</tp:taxon-name-part></tp:taxon-name></italic> Kury, Pinto-da-Rocha and Carvalho, 2018</td>
                <td rowspan="1" colspan="1">Brazil, Blumenau – SC, Parque Natural Municipal Nascentes do Garcia</td>
                <td rowspan="1" colspan="1"><named-content content-type="dwc:institutional_code">MZUSP</named-content> 30664</td>
              </tr>
              <tr>
                <td rowspan="1" colspan="1">
                  <tp:taxon-name>
                    <tp:taxon-name-part taxon-name-part-type="family">Gonyleptidae</tp:taxon-name-part>
                  </tp:taxon-name>
                </td>
                <td rowspan="1" colspan="1"><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily">Pachylinae</tp:taxon-name-part></tp:taxon-name><abbrev xlink:title="sensu lato" id="ABBRID0EQZAE">s.l</abbrev>.</td>
                <td rowspan="1" colspan="1"><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Gyndoides">Gyndoides</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="springmanni">springmanni</tp:taxon-name-part></tp:taxon-name></italic> Soares and Soares, 1947</td>
                <td rowspan="1" colspan="1">Brazil, Florianópolis – SC, Ilha do Francês</td>
                <td rowspan="1" colspan="1"><named-content content-type="dwc:institutional_code">MZUSP</named-content> 1943</td>
              </tr>
            </tbody>
          </table>
        </table-wrap>
      </sec>
      <sec sec-type="2.3. Character sampling" id="SECID0EP1AE">
        <title>2.3. Character sampling</title>
        <p>The analysis included a total of 72 morphological characters, including five related to the ocularium, 17 to the dorsal scute, three to free tergites, one to chelicerae, one to pedipalps, 31 to leg IV, and 14 to the penis. Characters were mainly based on <xref ref-type="bibr" rid="B28">Hara (2016)</xref> and <xref ref-type="bibr" rid="B13">Carvalho and Kury (2018)</xref>, with adjustments and new characters created according to our ingroup. The codification considered both discrete and multistate characters. In total, 30 multistate characters were proposed, of which 19 were treated as ordered when a clinal variation of the state’s transformation series was identifiable. The character matrix was edited using the software Mesquite v. 3.61 (<xref ref-type="bibr" rid="B51">Maddison and Maddison 2019</xref>) and exported to the respective parsimony analysis programs. Inapplicable state entries were coded as “–”, whereas uncertain ones were coded as “?”.</p>
      </sec>
      <sec sec-type="2.4. Parsimony analysis" id="SECID0EB2AE">
        <title>2.4. Parsimony analysis</title>
        <p>The phylogenetic parsimony analysis was performed using TNT v. 1.5 (<xref ref-type="bibr" rid="B25">Goloboff and Catalano 2016</xref>). Heuristic searches were conducted with characters under implied weighting following <xref ref-type="bibr" rid="B60">Mirande (2009)</xref> TNT search script parameters. These parameters select 11 <italic>K</italic> values based on average character fits distributed in 11 regular intervals between 50% and 90% of the fit of a perfectly hierarchical one, i.e., 1.0. Then for each <italic>K</italic> value, the most parsimonious trees and their consensuses were generated, and as a criterion for choosing the most stable trees, a similarity matrix with the values of the tree’s distortion coefficient (<xref ref-type="bibr" rid="B24">Farris 1989</xref>) and SPR distance (<xref ref-type="bibr" rid="B27">Goloboff et al. 2008</xref>) was elaborated. Taxon+ notation was utilized when referring to a given taxon plus its sister group, as proposed by <xref ref-type="bibr" rid="B5">Amorim (1982)</xref>. We also employed the notation [X(y)], where X is the character number and y is the character state.</p>
        <p>Visualization, character evolution analysis, and optimization were performed using the software Winclada v. 1.00.08 (<xref ref-type="bibr" rid="B62">Nixon 2002</xref>). Relative Bremer support (<xref ref-type="bibr" rid="B26">Goloboff and Farris 2001</xref>) was calculated using TNT, also under implied weighting, retaining suboptimal trees with up to ten extra steps and relative fit difference of 1. All character discussions are based on ACCTRAN optimization.</p>
      </sec>
      <sec sec-type="2.5. Abbreviations" id="SECID0EJ3AE">
        <title>2.5. Abbreviations</title>
        <p>Morphology: <bold><abbrev xlink:title="dorsal scute" id="ABBRID0EQ3AE">DS</abbrev></bold> dorsal scute; <bold><abbrev xlink:title="dorsal scute length" id="ABBRID0EV3AE">DSL</abbrev></bold> dorsal scute length; <bold><abbrev xlink:title="dorsal scute maximum width" id="ABBRID0E13AE">DSW</abbrev></bold> dorsal scute maximum width; <bold><abbrev xlink:title="leg I" id="ABBRID0E63AE">LI</abbrev></bold> leg I; <bold><abbrev xlink:title="leg II" id="ABBRID0EE4AE">LII</abbrev></bold> leg II; <bold><abbrev xlink:title="leg III" id="ABBRID0EJ4AE">LIII</abbrev></bold> leg III; <bold><abbrev xlink:title="leg IV" id="ABBRID0EO4AE">LIV</abbrev></bold> leg IV; <bold><abbrev xlink:title="ventral plate" id="ABBRID0ET4AE">VP</abbrev></bold> ventral plate; <bold><abbrev xlink:title="group A macrosetae" id="ABBRID0EY4AE">MS A</abbrev></bold> group A macrosetae; <bold><abbrev xlink:title="group B macrosetae" id="ABBRID0E44AE">MS B</abbrev></bold> group B macrosetae; <bold><abbrev xlink:title="group C macrosetae" id="ABBRID0EC5AE">MS C</abbrev></bold> group C macrosetae; <bold><abbrev xlink:title="group D macrosetae" id="ABBRID0EH5AE">MS D</abbrev></bold> group D macrosetae; <bold><abbrev xlink:title="group E macrosetae" id="ABBRID0EM5AE">MS E</abbrev></bold> group E macrosetae.</p>
        <p>Repositories (all in Brazil): <bold><named-content content-type="dwc:institutional_code">MZUSP</named-content></bold> Museu de Zoologia, Universidade de São Paulo, São Paulo; <bold><named-content content-type="dwc:institutional_code">UFPB</named-content></bold> Coleção de Aracnídeos e Miriápodes, Universidade Federal da Paraíba, João Pessoa. <bold><named-content content-type="dwc:institutional_code">MNRJ</named-content></bold> Museu Nacional, Universidade Federal do Rio de Janeiro, Rio de Janeiro.</p>
        <p>Others: <bold><abbrev xlink:title="scanning electron microscopy" id="ABBRID0EH6AE">SEM</abbrev></bold> scanning electron microscopy.</p>
      </sec>
    </sec>
    <sec sec-type="3. Results" id="SECID0EL6AE">
      <title>3. Results</title>
      <sec sec-type="3.1. Character list" id="SECID0EP6AE">
        <title>3.1. Character list</title>
        <p>Character and states used in the cladistic analysis of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">Sertaneja</tp:taxon-name-part></tp:taxon-name></italic> gen. nov. Taxon and character states matrix is included in the Supplementary Material File 1.</p>
        <p><bold>1</bold> Ocularium type: <bold>(0)</bold> divided (<xref ref-type="bibr" rid="B67">Pinto-da-Rocha 1997</xref>: fig. 349); <bold>(1)</bold> undivided (Figs <xref ref-type="fig" rid="F3">3A, G</xref>, <xref ref-type="fig" rid="F6">6A, G</xref>, <xref ref-type="fig" rid="F9">9A, G</xref>).</p>
        <p><bold>2</bold> Undivided ocularium width in dorsal view: <bold>(0)</bold> width at least 2 × the length (<xref ref-type="bibr" rid="B66">Pinto-da-Rocha 1994</xref>: fig. 1a); <bold>(1)</bold> width ca. the same as length (Figs <xref ref-type="fig" rid="F3">3A</xref>, <xref ref-type="fig" rid="F6">6A</xref>, <xref ref-type="fig" rid="F9">9A</xref>).</p>
        <p><bold>3</bold> Ocularium dorsal armature: <bold>(0)</bold> paramedian pair (Figs <xref ref-type="fig" rid="F3">3G</xref>, <xref ref-type="fig" rid="F9">9G</xref>); <bold>(1)</bold> central and single (Fig. <xref ref-type="fig" rid="F6">6G</xref>).</p>
        <p><bold>4</bold> Ocularium dorsal pair armature length: <bold>(0)</bold> at least the ocularium height (Figs <xref ref-type="fig" rid="F3">3G</xref>, <xref ref-type="fig" rid="F6">6G</xref>, <xref ref-type="fig" rid="F9">9G</xref>); <bold>(1)</bold> up to eye diameter (<xref ref-type="bibr" rid="B31">Hara and Pinto-da-Rocha 2010</xref>: fig. 26b).</p>
        <p><bold>5</bold> Ocularium height in relation to eye: <bold>(0)</bold> low, ca. 1 × the eye diameter; <bold>(1)</bold> medium, up to 1.5 × the eye diameter; <bold>(2)</bold> high, at least 2 × the eye diameter (Figs <xref ref-type="fig" rid="F3">3C</xref>, <xref ref-type="fig" rid="F6">6C</xref>, <xref ref-type="fig" rid="F9">9C</xref>). — Treated as ordered.</p>
        <p><bold>6</bold> Number of pairs of ozopores openings: <bold>(0)</bold> one; <bold>(1)</bold> two.</p>
        <p><bold>7</bold> Type of <abbrev xlink:title="dorsal scute" id="ABBRID0E2DAG">DS</abbrev> γ: <bold>(0)</bold> γR (<xref ref-type="bibr" rid="B44">Kury and Medrano 2016</xref>: fig. 1m–o); <bold>(1)</bold> γP (<xref ref-type="bibr" rid="B44">Kury and Medrano 2016</xref>: fig. 1t–v); <bold>(2)</bold> γT (<xref ref-type="bibr" rid="B44">Kury and Medrano 2016</xref>: fig. 1w, x).</p>
        <p><bold>8</bold><abbrev xlink:title="dorsal scute" id="ABBRID0EVEAG">DS</abbrev> anterior margin: <bold>(0)</bold> smooth; <bold>(1)</bold> bearing a pair or row of distinct projections.</p>
        <p><bold>9</bold> Type of <abbrev xlink:title="dorsal scute" id="ABBRID0EBFAG">DS</abbrev> anterior margin armature: <bold>(0)</bold> paralateral high spines (<xref ref-type="bibr" rid="B66">Pinto-da-Rocha 1994</xref>: fig. 1a); <bold>(1)</bold> row of distinct tubercles throughout the margin; <bold>(2)</bold> pair of paramedian tubercles (<xref ref-type="bibr" rid="B80">Roewer 1929</xref>: fig. 526).</p>
        <p><bold>10</bold><abbrev xlink:title="dorsal scute" id="ABBRID0EXFAG">DS</abbrev> lateral margin ornamentation: <bold>(0)</bold> with external row of distinct tubercles; <bold>(1)</bold> without external row of distinct tubercles.</p>
        <p><bold>11</bold> Size of tubercles in the external row of the <abbrev xlink:title="dorsal scute" id="ABBRID0EDGAG">DS</abbrev> lateral margin: <bold>(0)</bold> equally sized; <bold>(1)</bold> slightly increasing in size posteriorly throughout the row (Fig. <xref ref-type="fig" rid="F6">6C</xref>); <bold>(2)</bold> with sudden enlargement of tubercles on the posterior distal third (<xref ref-type="bibr" rid="B10">Bragagnolo and Pinto-da-Rocha 2009</xref>: fig. 1b).</p>
        <p><bold>12</bold><abbrev xlink:title="dorsal scute" id="ABBRID0EZGAG">DS</abbrev> posterior margin integumentary ornamentation: <bold>(0)</bold> with row of equally sized tubercles throughout the entire margin; <bold>(1)</bold> with single median apophysis (<xref ref-type="bibr" rid="B52">Maury 1991</xref>: fig. 1); <bold>(2)</bold> with paramedian pair of distinct projections.</p>
        <p><bold>13</bold><abbrev xlink:title="dorsal scute" id="ABBRID0ELHAG">DS</abbrev> number of areas: <bold>(0)</bold> three; <bold>(1)</bold> four.</p>
        <p><bold>14</bold> Scute areas general tuberculation aspect: <bold>(0)</bold> symmetrical with proportional height and length; <bold>(1)</bold> flat and spread.</p>
        <p><bold>15</bold> Scute area I, armature: <bold>(0)</bold> with paramedian pair of distinct projections; <bold>(1)</bold> without paramedian pair of distinct projections.</p>
        <p><bold>16</bold> Scute area I, distinct paramedian projection type: <bold>(0)</bold> conical spines (<xref ref-type="bibr" rid="B37">Kury 1997</xref>: fig. 1e); <bold>(1)</bold> round tubercles.</p>
        <p><bold>17</bold> Scute area I, paramedian tubercles position: <bold>(0)</bold> placed approximately in the center of each half of scute area I; <bold>(1)</bold> placed close to the median longitudinal groove (Fig. <xref ref-type="fig" rid="F3">3A</xref>).</p>
        <p><bold>18</bold> Scute area II, armature: <bold>(0)</bold> with paramedian pair of distinct projections (Fig. <xref ref-type="fig" rid="F3">3A</xref>); <bold>(1)</bold> without paramedian pair of distinct projections.</p>
        <p><bold>19</bold> Scute area III, armature: <bold>(0)</bold> with paramedian pair of distinct projections; <bold>(1)</bold> without paramedian pair of distinct projections.</p>
        <p><bold>20</bold> Scute area III, type of paramedian pair of distinct projections: <bold>(0)</bold> pair of straight, high spines (<xref ref-type="bibr" rid="B67">Pinto-da-Rocha 1997</xref>: fig. 350); <bold>(1)</bold> pair of straight, high tubercles (<xref ref-type="bibr" rid="B10">Bragagnolo and Pinto-da-Rocha 2009</xref>: fig. 1b); <bold>(2)</bold> pair of spines curved posteriorly (Figs <xref ref-type="fig" rid="F3">3A, C</xref>, <xref ref-type="fig" rid="F6">6A, C</xref>); <bold>(3)</bold> pair of low, rounded tubercles (Fig. <xref ref-type="fig" rid="F9">9A, C</xref>).</p>
        <p><bold>21</bold> Median longitudinal division on scute area IV: <bold>(0)</bold> absent; <bold>(1)</bold> present.</p>
        <p><bold>22</bold> Scute area IV, armature: <bold>(0)</bold> without paramedian pair of distinct projections; <bold>(1)</bold> with paramedian pair of distinct projections (Fig. <xref ref-type="fig" rid="F3">3A, C</xref>).</p>
        <p><bold>23</bold> Free tergite I, type of integumentary ornamentation: <bold>(0)</bold> with row of equally sized tubercles; <bold>(1)</bold> with single, median apophysis (<xref ref-type="bibr" rid="B78">Roewer 1923</xref>: fig. 526); <bold>(2)</bold> with a pair of distinct paramedian projections (<xref ref-type="bibr" rid="B37">Kury 1997</xref>: fig. 1g).</p>
        <p><bold>24</bold> Free tergite II, paramedian pair of projection: <bold>(0)</bold> absent; <bold>(1)</bold> present.</p>
        <p><bold>25</bold> Free tergite III, paramedian pair of projection: <bold>(0)</bold> absent; <bold>(1)</bold> present.</p>
        <p><bold>26</bold> Chelicerae, segment I posterior face: <bold>(0)</bold> with projections; <bold>(1)</bold> without projections.</p>
        <p><bold>27</bold> Pedipalp femur, mesal apical seta: <bold>(0)</bold> absent; <bold>(1)</bold> present (Figs <xref ref-type="fig" rid="F3">3F</xref>, <xref ref-type="fig" rid="F6">6F</xref>, <xref ref-type="fig" rid="F9">9F</xref>).</p>
        <p><bold>28</bold> Male coxae IV and coxae I–III width ratio in situ, in dorsal view: <bold>(0)</bold> coxae IV as wide as coxae I–III; <bold>(1)</bold> coxae IV up to 2 × wider than coxae I–III (Figs <xref ref-type="fig" rid="F3">3A</xref>, <xref ref-type="fig" rid="F6">6A</xref>, <xref ref-type="fig" rid="F9">9A</xref>); <bold>(2)</bold> coxae IV more than 2 × wider than coxae I–III (<xref ref-type="bibr" rid="B71">Pinto-da-Rocha and Bragagnolo 2010</xref>: fig. 5). — Treated as ordered.</p>
        <p><bold>29</bold> Male coxa IV length compared to posterior margin of the stigmatic sternite in situ, ventral view: <bold>(0)</bold> not surpassing it (<xref ref-type="bibr" rid="B32">Hara et al. 2012</xref>: fig. 2b); <bold>(1)</bold> surpassing it (<xref ref-type="bibr" rid="B46">Kury et al. 2018</xref>: fig. 10b).</p>
        <p><bold>30</bold> Male coxa IV dorso-lateral face, integumentary ornamentation: <bold>(0)</bold> present (Figs <xref ref-type="fig" rid="F3">3A</xref>, <xref ref-type="fig" rid="F6">6A</xref>, <xref ref-type="fig" rid="F9">9A</xref>); <bold>(1)</bold> absent.</p>
        <p><bold>31</bold> Male coxa IV, integumentary ornamentation density: <bold>(0)</bold> low, ≤ 4 tubercles; <bold>(1)</bold> medium, &gt; four, ≤ 13 tubercles; <bold>(2)</bold> high, &gt; 13 (Figs <xref ref-type="fig" rid="F3">3A</xref>, <xref ref-type="fig" rid="F9">9A</xref>). — Treated as ordered.</p>
        <p><bold>32</bold> Male coxa IV, prodorsal apical apophysis, type: <bold>(0)</bold> slender spine (<xref ref-type="bibr" rid="B66">Pinto-da-Rocha 1994</xref>: fig. 1a); <bold>(1)</bold> robust projection (Figs <xref ref-type="fig" rid="F3">3D</xref>, <xref ref-type="fig" rid="F6">6D</xref>, <xref ref-type="fig" rid="F9">9D</xref>).</p>
        <p><bold>33</bold> Male coxa IV, prodorsal apical apophysis, length: <bold>(0)</bold> very small, similar to the eye diameter (<xref ref-type="bibr" rid="B67">Pinto-da-Rocha 1997</xref>: fig. 349); <bold>(1)</bold> small, ca. 1/4 of the <abbrev xlink:title="dorsal scute" id="ABBRID0EVQAG">DS</abbrev> posterior margin width (<xref ref-type="bibr" rid="B59">Mendes 2011</xref>: fig. 7a); <bold>(2)</bold> medium, ca. 1/3 of the <abbrev xlink:title="dorsal scute" id="ABBRID0E6QAG">DS</abbrev> posterior margin width (Fig. <xref ref-type="fig" rid="F9">9A</xref>); <bold>(3)</bold> long, &gt; 1/2 of the <abbrev xlink:title="dorsal scute" id="ABBRID0EJRAG">DS</abbrev> posterior margin width (Fig. <xref ref-type="fig" rid="F6">6A</xref>). — Treated as ordered.</p>
        <p><bold>34</bold> Male coxa IV, prodorsal apical apophysis, insertion angle in relation to body medial axis: <bold>(0)</bold> almost transversal (<xref ref-type="bibr" rid="B16">DaSilva and Gnaspini 2010</xref>: fig. 79); <bold>(1)</bold> oblique (Fig. <xref ref-type="fig" rid="F9">9A</xref>); <bold>(2)</bold> sub-parallel (<xref ref-type="bibr" rid="B52">Maury 1991</xref>: fig. 1). — Treated as ordered.</p>
        <p><bold>35</bold> Male coxa IV, retro-lateral projection: <bold>(0)</bold> absent; <bold>(1)</bold> tubercle like, height comparable to width; <bold>(2)</bold> robust, much higher than wider (Fig. <xref ref-type="fig" rid="F9">9D</xref>). — Treated as ordered.</p>
        <p><bold>36</bold> Male coxa IV, retro-lateral robust projection, number of branches: <bold>(0)</bold> only one (Fig. <xref ref-type="fig" rid="F9">9D</xref>); <bold>(1)</bold> two, bifid (<xref ref-type="bibr" rid="B71">Pinto-da-Rocha and Bragagnolo 2010</xref>: fig. 5).</p>
        <p><bold>37</bold> Male trochanter IV, shape in dorsal view: <bold>(0)</bold> as long as wide (<xref ref-type="bibr" rid="B16">DaSilva and Gnaspini 2010</xref>: fig. 79); <bold>(1)</bold> longer than wide (Fig. <xref ref-type="fig" rid="F10">10</xref>).</p>
        <p><bold>38</bold> Male trochanter IV, prolateral central apophysis: <bold>(0)</bold> absent (<xref ref-type="bibr" rid="B59">Mendes 2011</xref>: fig. 8a–d); <bold>(1)</bold> present (Fig. <xref ref-type="fig" rid="F10">10A</xref>).</p>
        <p><bold>39</bold> Male trochanter IV, proapical projection: <bold>(0)</bold> absent; <bold>(1)</bold> tubercle (Fig. <xref ref-type="fig" rid="F10">10B, C</xref>); <bold>(2)</bold> apophysis (Fig. <xref ref-type="fig" rid="F4">4A, B</xref>). — Treated as ordered.</p>
        <p><bold>40</bold> Male trochanter IV, proapical apophysis, size: <bold>(0)</bold> short, ≤1/2 the trochanter length (<xref ref-type="bibr" rid="B59">Mendes 2011</xref>: fig. 8a–d); <bold>(1)</bold> long, &gt; 1/2 the trochanter length (Fig. <xref ref-type="fig" rid="F4">4A, B</xref>).</p>
        <p><bold>41</bold> Male trochanter IV, retro-lateral central conical apophysis: <bold>(0)</bold> absent; <bold>(1)</bold> present (Fig. <xref ref-type="fig" rid="F10">10A</xref>).</p>
        <p><bold>42</bold> Male trochanter IV, retro-apical projection: <bold>(0)</bold> absent (<xref ref-type="bibr" rid="B31">Hara and Pinto-da-Rocha 2010</xref>: fig. 26e, f); <bold>(1)</bold> tubercle; <bold>(2)</bold> apophysis (Figs <xref ref-type="fig" rid="F4">4A</xref>, <xref ref-type="fig" rid="F7">7A</xref>, <xref ref-type="fig" rid="F10">10A</xref>). — Treated as ordered.</p>
        <p><bold>43</bold> Male femur IV and <abbrev xlink:title="dorsal scute" id="ABBRID0ERWAG">DS</abbrev> length comparison: <bold>(0)</bold> less or equal to <abbrev xlink:title="dorsal scute" id="ABBRID0EXWAG">DS</abbrev>; <bold>(1)</bold> slightly longer than <abbrev xlink:title="dorsal scute" id="ABBRID0E4WAG">DS</abbrev>; <bold>(2)</bold> at least 2 × longer than <abbrev xlink:title="dorsal scute" id="ABBRID0EDXAG">DS</abbrev>. — Treated as ordered.</p>
        <p><bold>44</bold> Male femur IV, lateral curvature in relation to trochanter IV main axis: <bold>(0)</bold> straight, ca. straight angle; <bold>(1)</bold> slightly arched, ca. obtuse angle; <bold>(2)</bold> very arched, ca. acute angle. — Treated as ordered.</p>
        <p><bold>45</bold> Male femur IV, retro-basal projection: <bold>(0)</bold> absent; <bold>(1)</bold> present.</p>
        <p><bold>46</bold> Male femur IV, retro-basal projection, type: <bold>(0)</bold> conical tubercle, slightly larger than the ones covering the podomere surface; <bold>(1)</bold> large apophysis (Ázara &amp; Ferreira 2018: fig. 28c).</p>
        <p><bold>47</bold> Male femur IV, centro-dorsal projection: <bold>(0)</bold> absent; <bold>(1)</bold> present.</p>
        <p><bold>48</bold> Male femur IV, centro-dorsal projection, curvature: <bold>(0)</bold> straight; <bold>(1)</bold> curved retrolaterally.</p>
        <p><bold>49</bold> Male femur IV, medio-apical dorsal projection: <bold>(0)</bold> absent; <bold>(1)</bold> present.</p>
        <p><bold>50</bold> Male femur IV, prodorsal apical distinct projection: <bold>(0)</bold> absent; <bold>(1)</bold> present.</p>
        <p><bold>51</bold> Male femur IV, prodorsal apical distinct projection, shape: <bold>(0)</bold> slender spine with tapered apex (<xref ref-type="bibr" rid="B16">DaSilva and Gnaspini 2010</xref>: fig. 81); <bold>(1)</bold> spine with rounded apex (Figs <xref ref-type="fig" rid="F7">7B</xref>, <xref ref-type="fig" rid="F10">10B</xref>).</p>
        <p><bold>52</bold> Male femur IV, retro-dorsal apical distinct projection: <bold>(0)</bold> absent; <bold>(1)</bold> present.</p>
        <p><bold>53</bold> Male femur IV, ventro-apical distinct projections, type: <bold>(0)</bold> tubercles; <bold>(1)</bold> spines (Figs <xref ref-type="fig" rid="F4">4C</xref>, <xref ref-type="fig" rid="F7">7C</xref>, <xref ref-type="fig" rid="F10">10C</xref>); <bold>(2)</bold> apophyses. — Treated as ordered.</p>
        <p><bold>54</bold> Male patella IV, dorsal face ornamentation: <bold>(0)</bold> a pair of paralateral apical spines (<xref ref-type="bibr" rid="B30">Hara and Pinto-da-Rocha 2008</xref>: fig. 4); <bold>(1)</bold> rounded tubercles (<xref ref-type="bibr" rid="B10">Bragagnolo and Pinto-da-Rocha 2009</xref>: fig. 3a, b); <bold>(2)</bold> with high spines (Fig. <xref ref-type="fig" rid="F4">4B, D</xref>).</p>
        <p><bold>55</bold> Male patella IV, ventral face ornamentation: <bold>(0)</bold> granule-like projections (<xref ref-type="bibr" rid="B71">Pinto-da-Rocha and Bragagnolo 2010</xref>: fig. 13); <bold>(1)</bold> rounded tubercles (<xref ref-type="bibr" rid="B10">Bragagnolo and Pinto-da-Rocha 2009</xref>: fig. 3c); <bold>(2)</bold> with spines (Figs <xref ref-type="fig" rid="F4">4B</xref>, <xref ref-type="fig" rid="F10">10B</xref>); <bold>(3)</bold> with distinct retro-lateral apophysis.</p>
        <p><bold>56</bold> Male tibia IV, retro-ventral row, type of integumentary ornamentation: <bold>(0)</bold> similar sized tubercles; <bold>(1)</bold> tubercles that increase in size posteriorly (Figs <xref ref-type="fig" rid="F7">7D</xref>, <xref ref-type="fig" rid="F10">10B, D</xref>); <bold>(2)</bold> similar sized spines.</p>
        <p><bold>57</bold> Male tibia IV, ventro-apical armature: <bold>(0)</bold> tubercles; <bold>(1)</bold> spines; <bold>(2)</bold> apophyses. — Treated as ordered.</p>
        <p><bold>58</bold> Male tarsal process on legs III–IV: <bold>(0)</bold> vestigial, setae-like (<xref ref-type="bibr" rid="B67">Pinto-da-Rocha 1997</xref>: fig. 593); <bold>(1)</bold> &lt; 1/2 claw length; <bold>(2)</bold> almost claw length (<xref ref-type="bibr" rid="B37">Kury 1997</xref>: figs 27, 28).</p>
        <p><bold>59</bold> Penis glans ventral process: <bold>(0)</bold> absent (Figs <xref ref-type="fig" rid="F5">5</xref>, <xref ref-type="fig" rid="F8">8</xref>, <xref ref-type="fig" rid="F11">11</xref>); <bold>(1)</bold> present (<xref ref-type="bibr" rid="B69">Pinto-da-Rocha et al. 2012</xref>: fig. 7). — Treated as ordered.</p>
        <p><bold>60</bold> Penis glans, ventral process, stem: <bold>(0)</bold> absent (<xref ref-type="bibr" rid="B42">Kury and Villarreal 2015</xref>: fig. 13a–c); <bold>(1)</bold> present, slightly shorter than stylus (<xref ref-type="bibr" rid="B69">Pinto-da-Rocha et al. 2012</xref>: fig. 7); <bold>(2)</bold> present, ≥ than stylus (<xref ref-type="bibr" rid="B71">Pinto-da-Rocha and Bragagnolo 2010</xref>: figs 28–30). — Treated as ordered.</p>
        <p><bold>61</bold> Ventral process, apex shape: <bold>(0)</bold> as a triangle shaped tongue with fringes (<xref ref-type="bibr" rid="B42">Kury and Villarreal 2015</xref>: fig. 13a–c); <bold>(1)</bold> as a small fan (<xref ref-type="bibr" rid="B71">Pinto-da-Rocha and Bragagnolo 2010</xref>: figs 28–30); <bold>(2)</bold> as a wide flabellum (<xref ref-type="bibr" rid="B69">Pinto-da-Rocha et al. 2012</xref>: fig. 7). — Treated as ordered.</p>
        <p><bold>62</bold> Dorsal process of glans: <bold>(0)</bold> present (<xref ref-type="bibr" rid="B71">Pinto-da-Rocha and Bragagnolo 2010</xref>: figs 28–30); <bold>(1)</bold> absent (Figs <xref ref-type="fig" rid="F5">5B</xref>, <xref ref-type="fig" rid="F8">8B</xref>, <xref ref-type="fig" rid="F11">11B</xref>).</p>
        <p><bold>63</bold> Penis <abbrev xlink:title="ventral plate" id="ABBRID0ETABG">VP</abbrev>, apical margin, shape: <bold>(0)</bold> straight or roughly straight (Figs <xref ref-type="fig" rid="F5">5</xref>, <xref ref-type="fig" rid="F8">8</xref>, <xref ref-type="fig" rid="F11">11</xref>); <bold>(1)</bold> with shallow cleft (<xref ref-type="bibr" rid="B16">DaSilva and Gnaspini 2010</xref>: fig. 164); <bold>(2)</bold> with deep cleft (<xref ref-type="bibr" rid="B69">Pinto-da-Rocha et al. 2012</xref>: fig. 7a, b). — Treated as ordered.</p>
        <p><bold>64</bold> Penis <abbrev xlink:title="ventral plate" id="ABBRID0EVBBG">VP</abbrev>, basal lobes in dorsal view, shape: <bold>(0)</bold> indistinct from <abbrev xlink:title="ventral plate" id="ABBRID0E2BBG">VP</abbrev> outline; <bold>(1)</bold> laterally projected, as long or slightly longer than distal part of <abbrev xlink:title="ventral plate" id="ABBRID0EBCBG">VP</abbrev> (<xref ref-type="bibr" rid="B71">Pinto-da-Rocha and Bragagnolo 2010</xref>: fig. 28); <bold>(2)</bold> laterally projected, much longer than distal part of <abbrev xlink:title="ventral plate" id="ABBRID0ELCBG">VP</abbrev> (<xref ref-type="bibr" rid="B10">Bragagnolo and Pinto-da-Rocha 2009</xref>: fig. 6a). — Treated as ordered.</p>
        <p><bold>65</bold> Stylus apex, trichomes: <bold>(0)</bold> absent; <bold>(1)</bold> present.</p>
        <p><bold>66</bold> Stylus apex, trichomes, density: <bold>(0)</bold> low, few sparse (Figs <xref ref-type="fig" rid="F5">5B</xref>, <xref ref-type="fig" rid="F8">8B</xref>, <xref ref-type="fig" rid="F11">11B</xref>); <bold>(1)</bold> high (<xref ref-type="bibr" rid="B46">Kury et al. 2018</xref>: fig. 11d).</p>
        <p><bold>67</bold> Stylus apex, winglet like projections: <bold>(0)</bold> without those projections; <bold>(1)</bold> with a dorsal, single projection (Figs <xref ref-type="fig" rid="F5">5</xref>, <xref ref-type="fig" rid="F8">8</xref>, <xref ref-type="fig" rid="F11">11</xref>); <bold>(2)</bold> with paralateral projections (<xref ref-type="bibr" rid="B10">Bragagnolo and Pinto-da-Rocha 2009</xref>: fig. 6a–c).</p>
        <p><bold>68</bold> Penis <abbrev xlink:title="ventral plate" id="ABBRID0EREBG">VP</abbrev>, <abbrev xlink:title="group A macrosetae" id="ABBRID0EVEBG">MS A</abbrev> arrangement: <bold>(0)</bold> single row (<xref ref-type="bibr" rid="B69">Pinto-da-Rocha et al. 2012</xref>: fig. 7c); <bold>(1)</bold> clustered (Figs <xref ref-type="fig" rid="F5">5B</xref>, <xref ref-type="fig" rid="F8">8B</xref>, <xref ref-type="fig" rid="F11">11B</xref>).</p>
        <p><bold>69</bold> Penis <abbrev xlink:title="ventral plate" id="ABBRID0ERFBG">VP</abbrev>, <abbrev xlink:title="group C macrosetae" id="ABBRID0EVFBG">MS C</abbrev> shape: <bold>(0)</bold> robust, not twisted (Figs <xref ref-type="fig" rid="F5">5</xref>, <xref ref-type="fig" rid="F11">11</xref>); <bold>(1)</bold> slender and twisted (<xref ref-type="bibr" rid="B71">Pinto-da-Rocha and Bragagnolo 2010</xref>: figs 28, 30).</p>
        <p><bold>70</bold> Penis <abbrev xlink:title="ventral plate" id="ABBRID0ENGBG">VP</abbrev>, <abbrev xlink:title="group C macrosetae" id="ABBRID0ERGBG">MS C</abbrev> arrangement: <bold>(0)</bold> clustered and equally spaced (Figs <xref ref-type="fig" rid="F8">8A</xref>, <xref ref-type="fig" rid="F11">11A</xref>); <bold>(1)</bold> subequally spaced, distance between setae increasing basally; <bold>(2)</bold> apical setae clustered, most basal one far apart from the others (<xref ref-type="bibr" rid="B10">Bragagnolo and Pinto-da-Rocha 2009</xref>: fig. 6a). — Treated as ordered.</p>
        <p><bold>71</bold> Penis <abbrev xlink:title="ventral plate" id="ABBRID0ELHBG">VP</abbrev>, <abbrev xlink:title="group D macrosetae" id="ABBRID0EPHBG">MS D</abbrev> quantity: <bold>(0)</bold> one pair; <bold>(1)</bold> two pairs.</p>
        <p><bold>72</bold> Penis, podium position relative to MS insertion points: <bold>(0)</bold> placed basally, not reaching <abbrev xlink:title="group A macrosetae" id="ABBRID0E4HBG">MS A</abbrev>/B (<xref ref-type="bibr" rid="B37">Kury 1997</xref>: figs 12, 13); <bold>(1)</bold> reaching middle of <abbrev xlink:title="group A macrosetae" id="ABBRID0EHIBG">MS A</abbrev> set; <bold>(2)</bold> reaching top of most apical <abbrev xlink:title="group A macrosetae" id="ABBRID0ENIBG">MS A</abbrev> pair (<xref ref-type="bibr" rid="B69">Pinto-da-Rocha et al. 2012</xref>: fig. 7a, c); <bold>(3)</bold> reaching <abbrev xlink:title="group D macrosetae" id="ABBRID0EXIBG">MS D</abbrev> (<xref ref-type="bibr" rid="B42">Kury and Villarreal 2015</xref>: fig. 13a, b) — Treated as ordered.</p>
      </sec>
      <sec sec-type="3.2. Cladistic analysis" id="SECID0E6IBG">
        <title>3.2. Cladistic analysis</title>
        <p>The implied weighting analysis retrieved a single most parsimonious tree for each fit interval, but the most stable trees (L = 240; CI = 0.43; RI = 0.63), according to the SPR distance and distortion coefficient similarity matrices, were found from the fifth to the eleventh intervals at <italic>K</italic> values of 2.496, 3, 3.659, 4.558, 5.857, 7.898 and 11.571, respectively (Table <xref ref-type="table" rid="T2">2</xref>). The tree presented in Figure <xref ref-type="fig" rid="F1">1</xref> is the single topology retrieved in this range.</p>
        <table-wrap id="T2" position="float" orientation="portrait">
          <label>Table 2.</label>
          <caption>
            <p>Summary of the results from the <xref ref-type="bibr" rid="B60">Mirande (2009)</xref> script search. DC (distortion coefficient) and SPR distance columns indicates the mean values of each fit interval (kx) in relation to the others; intervals with higher mean values are highlighted in bold and represent the most stable topology.</p>
          </caption>
          <table id="TID0EARBI" rules="all">
            <tbody>
              <tr>
                <td rowspan="1" colspan="1"/>
                <td rowspan="1" colspan="1">
                  <bold>
                    <italic>K</italic>
                  </bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>Steps</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>Nº of trees</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>Fit</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>DC</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>SPR</bold>
                </td>
              </tr>
              <tr>
                <td rowspan="1" colspan="1">k1</td>
                <td rowspan="1" colspan="1">1.286</td>
                <td rowspan="1" colspan="1">244</td>
                <td rowspan="1" colspan="1">1</td>
                <td rowspan="1" colspan="1">36.005</td>
                <td rowspan="1" colspan="1">0.871427</td>
                <td rowspan="1" colspan="1">0.80586</td>
              </tr>
              <tr>
                <td rowspan="1" colspan="1">k2</td>
                <td rowspan="1" colspan="1">1.509</td>
                <td rowspan="1" colspan="1">242</td>
                <td rowspan="1" colspan="1">1</td>
                <td rowspan="1" colspan="1">33.800</td>
                <td rowspan="1" colspan="1">0.963156</td>
                <td rowspan="1" colspan="1">0.93531</td>
              </tr>
              <tr>
                <td rowspan="1" colspan="1">k3</td>
                <td rowspan="1" colspan="1">1.776</td>
                <td rowspan="1" colspan="1">242</td>
                <td rowspan="1" colspan="1">1</td>
                <td rowspan="1" colspan="1">31.523</td>
                <td rowspan="1" colspan="1">0.963156</td>
                <td rowspan="1" colspan="1">0.93531</td>
              </tr>
              <tr>
                <td rowspan="1" colspan="1">k4</td>
                <td rowspan="1" colspan="1">2.098</td>
                <td rowspan="1" colspan="1">242</td>
                <td rowspan="1" colspan="1">1</td>
                <td rowspan="1" colspan="1">29.174</td>
                <td rowspan="1" colspan="1">0.963156</td>
                <td rowspan="1" colspan="1">0.93531</td>
              </tr>
              <tr>
                <td rowspan="1" colspan="1">
                  <bold>k5</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>2.496</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>240</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>1</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>26.737</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>0.980001</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>0.96471</bold>
                </td>
              </tr>
              <tr>
                <td rowspan="1" colspan="1">
                  <bold>k6</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>3.000</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>240</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>1</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>24.192</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>0.980001</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>0.96471</bold>
                </td>
              </tr>
              <tr>
                <td rowspan="1" colspan="1">
                  <bold>k7</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>3.659</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>240</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>1</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>21.537</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>0.980001</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>0.96471</bold>
                </td>
              </tr>
              <tr>
                <td rowspan="1" colspan="1">
                  <bold>k8</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>4.558</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>240</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>1</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>18.757</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>0.980001</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>0.96471</bold>
                </td>
              </tr>
              <tr>
                <td rowspan="1" colspan="1">
                  <bold>k9</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>5.857</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>240</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>1</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>15.830</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>0.980001</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>0.96471</bold>
                </td>
              </tr>
              <tr>
                <td rowspan="1" colspan="1">
                  <bold>k10</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>7.898</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>240</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>1</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>12.732</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>0.980001</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>0.96471</bold>
                </td>
              </tr>
              <tr>
                <td rowspan="1" colspan="1">
                  <bold>k11</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>11.571</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>240</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>1</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>9.432</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>0.980001</bold>
                </td>
                <td rowspan="1" colspan="1">
                  <bold>0.96471</bold>
                </td>
              </tr>
            </tbody>
          </table>
        </table-wrap>
        <p>All three new species were recovered as a monophyletic group closely related to <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Gyndoides">G.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="springmanni">springmanni</tp:taxon-name-part></tp:taxon-name></italic>. The clade <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Gyndoides">G.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="springmanni">springmanni</tp:taxon-name-part></tp:taxon-name></italic>+ is supported by three exclusive synapomorphies: (i) scute area I with a pair of slightly prominent tubercles placed near the median groove [17(1)]; (ii) scute area III bearing a pair of paramedian spines curved posteriorly [20(2)]; and (iii) scute area IV with a pair of paramedian tubercles slightly more prominent than the surrounding ones [22(1)]. Despite the new genus being sister taxa to <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Gyndoides">G.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="springmanni">springmanni</tp:taxon-name-part></tp:taxon-name></italic>, the former’s penial structure differs considerably, being characterized by a rectangular <abbrev xlink:title="ventral plate" id="ABBRID0ETYBG">VP</abbrev>, particular macrosetae disposition, stylus morphology, and the absence of a ventral process of the glans. The <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Gyndoides">G.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="springmanni">springmanni</tp:taxon-name-part></tp:taxon-name></italic>+ clade, in turn, is a sister group to representatives that could be related to that which <xref ref-type="bibr" rid="B13">Carvalho and Kury (2018)</xref> defined as DRMN (Fig. <xref ref-type="fig" rid="F2">2</xref>).</p>
        <p>The new genus is supported by 10 synapomorphies of which two are exclusive: (i) external row of tubercles on the <abbrev xlink:title="dorsal scute" id="ABBRID0EMZBG">DS</abbrev> lateral margin slightly increasing in size posteriorly [11(1)], and (ii) <abbrev xlink:title="group A macrosetae" id="ABBRID0EQZBG">MS A</abbrev> in a clustered arrangement [68(1)] (Fig. <xref ref-type="fig" rid="F1">1</xref>). Moreover, the non-exclusive synapomorphies that commonly supported <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">Sertaneja</tp:taxon-name-part></tp:taxon-name></italic> gen. nov. are: (i) the presence of a retro-apical apophysis on male trochanter IV [42(2)], (ii) male tibia IV with a retro-ventral row of tubercles increasing in size posteriorly [56(1)], (iii) penis glans without ventral process [59(0)], (iv) basal lobes of the penis <abbrev xlink:title="ventral plate" id="ABBRID0E6ZBG">VP</abbrev> indistinct in the dorsal view [64(0)], (v) penis stylus apex with trichomes [65(1)], (vi) stylus apex with a distinct dorsal, single projection [67(1)], (vii) penis <abbrev xlink:title="ventral plate" id="ABBRID0ED1BG">VP</abbrev> with two pairs of <abbrev xlink:title="group D macrosetae" id="ABBRID0EH1BG">MS D</abbrev> [71(1)], (viii) and penis podium placed very basally, not reaching MSA/B group[72(0)].</p>
        <fig id="F1" position="float" orientation="portrait">
          <object-id content-type="doi">10.3897/asp.79.e66321.figure1</object-id>
          <object-id content-type="arpha">B1A43BF8-B7EE-51AD-A438-C18EA745935F</object-id>
          <label>Figure 1.</label>
          <caption>
            <p>Most parsimonious and stable tree topology retrieved under implied weighting trough <xref ref-type="bibr" rid="B60">Mirande (2009)</xref> search script, representing the <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">Sertaneja</tp:taxon-name-part></tp:taxon-name></italic> gen. nov. new species relationship among some representatives of the <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="family">Gonyleptidae</tp:taxon-name-part></tp:taxon-name> family (L = 240; CI = 0.43; RI = 0.63). The dark circles on stems represent unique synapomorphies, the white ones homoplasies. Each circle is labeled by its character number (above) and character state (below). The highlighted character numbers in red are unambiguous. Numbers below the branches represent relative Bremer support, calculated for <italic>K</italic> = 11.571 under implied weighting. The characters are optimized in ACCTRAN.</p>
          </caption>
          <graphic xlink:href="arthropod-systematics-79-485-g001.jpg" position="float" orientation="portrait" xlink:type="simple" id="oo_596974.jpg">
            <uri content-type="original_file">https://binary.pensoft.net/fig/596974</uri>
          </graphic>
        </fig>
        <fig id="F2" position="float" orientation="portrait">
          <object-id content-type="doi">10.3897/asp.79.e66321.figure2</object-id>
          <object-id content-type="arpha">112BAF23-A720-5CC5-8F56-76D95A3CC251</object-id>
          <label>Figure 2.</label>
          <caption>
            <p>Most parsimonious and stable tree topology retrieved under implied weighting (see Fig. <xref ref-type="fig" rid="F1">1</xref>), highlighting the main groups. — <bold><italic>Abbreviations</italic></bold>: PACss (red) = <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily">Pachylinae</tp:taxon-name-part></tp:taxon-name><abbrev xlink:title="sensu stricto" id="ABBRID0E52BG">s.s</abbrev>.; DRMN (magenta) = monophyletic group first defined by <xref ref-type="bibr" rid="B13">Carvalho and Kury (2018)</xref>.</p>
          </caption>
          <graphic xlink:href="arthropod-systematics-79-485-g002.jpg" position="float" orientation="portrait" xlink:type="simple" id="oo_596975.jpg">
            <uri content-type="original_file">https://binary.pensoft.net/fig/596975</uri>
          </graphic>
        </fig>
      </sec>
      <sec sec-type="3.3. Taxonomy" id="SECID0EL3BG">
        <title>3.3. Taxonomy</title>
        <p><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="family">Gonyleptidae</tp:taxon-name-part></tp:taxon-name> Sundevall, 1833</p>
        <p><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily">Pachylinae</tp:taxon-name-part></tp:taxon-name> Sørensen, 1884</p>
        <tp:taxon-treatment>
          <tp:treatment-meta>
            <kwd-group>
              <label>Taxon classification</label>
              <kwd>
                <named-content content-type="kingdom" xlink:type="simple">Animalia</named-content>
              </kwd>
              <kwd>
                <named-content content-type="order" xlink:type="simple">Opiliones</named-content>
              </kwd>
              <kwd>
                <named-content content-type="family" xlink:type="simple">Gonyleptidae</named-content>
              </kwd>
            </kwd-group>
          </tp:treatment-meta>
          <tp:nomenclature>
            <label>3.3.1.</label>
            <tp:taxon-name><object-id content-type="arpha">4B631D34-6BA5-5325-8989-5C907484FFED</object-id>
              <tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">Sertaneja</tp:taxon-name-part>
              <object-id content-type="zoobank" xlink:type="simple">http://zoobank.org/E8C17C0C-3C72-48A2-B38F-3CEC73078D51</object-id>
            </tp:taxon-name>
            <tp:taxon-status>gen. nov.</tp:taxon-status>
            <xref ref-type="fig" rid="F3">Figs 3</xref>
            <xref ref-type="fig" rid="F4">, 4</xref>
            <xref ref-type="fig" rid="F5">, 5</xref>
            <xref ref-type="fig" rid="F6">, 6</xref>
            <xref ref-type="fig" rid="F7">, 7</xref>
            <xref ref-type="fig" rid="F8">, 8</xref>
            <xref ref-type="fig" rid="F9">, 9</xref>
            <xref ref-type="fig" rid="F10">, 10</xref>
            <xref ref-type="fig" rid="F11">, 11</xref>
          </tp:nomenclature>
          <tp:treatment-sec sec-type="diagnosis" id="SECID0EG6BG">
            <title>Diagnosis.</title>
            <p><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">Sertaneja</tp:taxon-name-part></tp:taxon-name></italic> gen. nov. resembles <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Gyndoides">Gyndoides</tp:taxon-name-part></tp:taxon-name></italic> because of the ocularium armature (despite being variable in <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">Sertaneja</tp:taxon-name-part></tp:taxon-name></italic>), four scute areas, a pair of paramedian spines on scute area II (except <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">S.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="falcata">falcata</tp:taxon-name-part></tp:taxon-name> sp. nov.) and unarmed free tergites. S<italic>ertaneja</italic> gen. nov. differs from G<italic>yndoides</italic> Mello-Leitão, 1927a by: (i) the lateral margin of <abbrev xlink:title="dorsal scute" id="ABBRID0EQAAI">DS</abbrev> with an external row of tubercles slightly increasing in size posteriorly, (ii) presence of the mesal apical seta on the pedipalp femur (Figs <xref ref-type="fig" rid="F3">3F</xref>, <xref ref-type="fig" rid="F6">6F</xref>, <xref ref-type="fig" rid="F9">9F</xref>), (iii) male trochanter IV retro-apical projection as a straight apophysis instead of a tubercle (Figs <xref ref-type="fig" rid="F3">3D</xref>, <xref ref-type="fig" rid="F6">6D</xref>, <xref ref-type="fig" rid="F9">9D</xref>), (iv) the absence of a retro-basal apophysis on male femur IV, (v) male femur IV bearing a prodorsal apical distinguished apophysis, (vi) male tibia IV ventral face armed, (vii) glans without ventral process (Figs <xref ref-type="fig" rid="F5">5</xref>, <xref ref-type="fig" rid="F8">8</xref>, <xref ref-type="fig" rid="F11">11</xref>), (viii) stylus apex bearing distinct projections (Figs <xref ref-type="fig" rid="F5">5</xref>, <xref ref-type="fig" rid="F8">8</xref>, <xref ref-type="fig" rid="F11">11</xref>), (ix) <abbrev xlink:title="ventral plate" id="ABBRID0EECAI">VP</abbrev> of penis without prominent ventral lobes (Figs <xref ref-type="fig" rid="F5">5</xref>, <xref ref-type="fig" rid="F8">8</xref>, <xref ref-type="fig" rid="F11">11</xref>), and, (x) 4 pairs of <abbrev xlink:title="group A macrosetae" id="ABBRID0EUCAI">MS A</abbrev> clustered instead of lined up in a row (Figs <xref ref-type="fig" rid="F5">5</xref>, <xref ref-type="fig" rid="F8">8</xref>, <xref ref-type="fig" rid="F11">11</xref>). It differs from other <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily">Pachylinae</tp:taxon-name-part></tp:taxon-name> genera by the combination of the sub-rectangular <abbrev xlink:title="ventral plate" id="ABBRID0EJDAI">VP</abbrev>, 2 paralateral pairs of <abbrev xlink:title="group D macrosetae" id="ABBRID0ENDAI">MS D</abbrev>, glans stylus bearing a dorso-apical longitudinal projection and lack of ventral process of the glans.</p>
            <fig id="F3" position="float" orientation="portrait">
              <object-id content-type="doi">10.3897/asp.79.e66321.figure3</object-id>
              <object-id content-type="arpha">BC0C0E98-666E-5A5F-9315-5B6CF0291925</object-id>
              <label>Figure 3.</label>
              <caption>
                <p><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">Sertaneja</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="bicuspidata">bicuspidata</tp:taxon-name-part></tp:taxon-name></italic> sp. nov. (<bold>A</bold>, <bold>C</bold>–<bold>G</bold>) Male holotype (<named-content content-type="dwc:institutional_code">UFPB</named-content> OP-163), <bold>A</bold>: habitus, dorsal view; <bold>C</bold>: same, right lateral view; <bold>D</bold>: right coxa and trochanter IV in dorsal view; <bold>E</bold>: right pedipalp lateral view; <bold>F</bold>: same, mesal view; <bold>G</bold>: ocularium frontal view. (<bold>B</bold>) Female paratype (<named-content content-type="dwc:institutional_code">UFPB</named-content> OP-726) habitus, dorsal view. Scale bars: 1 mm.</p>
              </caption>
              <graphic xlink:href="arthropod-systematics-79-485-g003.jpg" position="float" orientation="portrait" xlink:type="simple" id="oo_596976.jpg">
                <uri content-type="original_file">https://binary.pensoft.net/fig/596976</uri>
              </graphic>
            </fig>
          </tp:treatment-sec>
          <tp:treatment-sec sec-type="description" id="SECID0EHFAI">
            <title>Description.</title>
            <p><abbrev xlink:title="dorsal scute" id="ABBRID0ENFAI">DS</abbrev> gamma (γ) to alpha (α) shaped (Figs <xref ref-type="fig" rid="F3">3A, B</xref>, <xref ref-type="fig" rid="F6">6A, B</xref>, <xref ref-type="fig" rid="F9">9A, B</xref>). Ocularium height at least two to up to three times the size the eye diameter, with posterior face tuberculate, and slightly close to the anterior margin of <abbrev xlink:title="dorsal scute" id="ABBRID0E4FAI">DS</abbrev>, in lateral view (Figs <xref ref-type="fig" rid="F3">3C</xref>, <xref ref-type="fig" rid="F6">6C</xref>, <xref ref-type="fig" rid="F9">9C</xref>); bearing a pair of divergent large spines (Figs <xref ref-type="fig" rid="F3">3G</xref>, <xref ref-type="fig" rid="F9">9G</xref>), or a single central robust one (Fig. <xref ref-type="fig" rid="F6">6G</xref>). Four scute areas; scute areas I, II and IV with one to two pairs of slightly enlarged paramedian tubercles; scute area III with a pair of distinct paramedian elevations, ranging from acuminated tubercles (Fig. <xref ref-type="fig" rid="F9">9A, C</xref>) to large posteriorly curved spines (Figs <xref ref-type="fig" rid="F3">3A, C</xref>, <xref ref-type="fig" rid="F6">6A, C</xref>). Chelicerae segment I posterior face covered with acuminated tubercles. Pedipalp femora with a mesal sub-apical setiferous tubercle. Coxa IV well developed, bearing dense and high tuberculation, with robust prodorsal apical apophysis. Trochanter III with a retro-ventral apical conical tubercle. Trochanter IV with a straight retro-apical conical apophysis (Figs <xref ref-type="fig" rid="F4">4A, C, D</xref>, <xref ref-type="fig" rid="F7">7A, C, D</xref>, <xref ref-type="fig" rid="F10">10A, C, D</xref>), and a short probasal apophysis. Penis <abbrev xlink:title="ventral plate" id="ABBRID0ERHAI">VP</abbrev> sub-rectangular (Figs <xref ref-type="fig" rid="F5">5A</xref>, <xref ref-type="fig" rid="F8">8A</xref>, <xref ref-type="fig" rid="F11">11A</xref>); glans without dorsal or ventral processes (Figs <xref ref-type="fig" rid="F5">5B</xref>, <xref ref-type="fig" rid="F8">8B</xref>, <xref ref-type="fig" rid="F11">11B</xref>), stylus with a dorso-apical projection slightly curved posteriorly, ventral face with sub-apical transversal row of trichome-like projections. <abbrev xlink:title="group A macrosetae" id="ABBRID0ENIAI">MS A</abbrev> group generally composed of four to five pairs of paralateral setae, at instances showing asymmetry between the sides (Fig. <xref ref-type="fig" rid="F8">8A</xref>). <abbrev xlink:title="group C macrosetae" id="ABBRID0EVIAI">MS C</abbrev> composed by three (Figs <xref ref-type="fig" rid="F5">5</xref>, <xref ref-type="fig" rid="F8">8</xref>) or five pairs of setae (Fig. <xref ref-type="fig" rid="F12">12</xref>) inserted laterally on the apical third of the <abbrev xlink:title="ventral plate" id="ABBRID0EFJAI">VP</abbrev>. <abbrev xlink:title="group D macrosetae" id="ABBRID0EJJAI">MS D</abbrev> as two pairs of paralateral setae, inserted more dorsally on the <abbrev xlink:title="ventral plate" id="ABBRID0ENJAI">VP</abbrev>, between de <abbrev xlink:title="group A macrosetae" id="ABBRID0ERJAI">MS A</abbrev> and C sets. <abbrev xlink:title="group E macrosetae" id="ABBRID0EVJAI">MS E</abbrev> as a pair of paralateral small setae, inserted ventrally near the <abbrev xlink:title="group C macrosetae" id="ABBRID0EZJAI">MS C</abbrev> and D groups. Ventral surface of <abbrev xlink:title="ventral plate" id="ABBRID0E4JAI">VP</abbrev> sparsely covered by microsetae.</p>
          </tp:treatment-sec>
          <tp:treatment-sec sec-type="Included species" id="SECID0EBKAI">
            <title>Included species.</title>
            <p><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">S.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="bicupidata">bicupidata</tp:taxon-name-part></tp:taxon-name></italic> sp. nov., <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">S.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="crassitibialis">crassitibialis</tp:taxon-name-part></tp:taxon-name></italic> sp. nov., and <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">S.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="falcata">falcata</tp:taxon-name-part></tp:taxon-name></italic> sp. nov.</p>
          </tp:treatment-sec>
          <tp:treatment-sec sec-type="type species" id="SECID0EILAI">
            <title>Type species.</title>
            <p><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">S.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="bicuspidata">bicuspidata</tp:taxon-name-part></tp:taxon-name></italic> sp. nov.</p>
          </tp:treatment-sec>
          <tp:treatment-sec sec-type="etymology" id="SECID0EZLAI">
            <title>Etymology.</title>
            <p>‘<tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">Sertaneja</tp:taxon-name-part></tp:taxon-name>’ is a Brazilian adjective (fem.) that refers to a woman who lives in the Sertão regions in rural communities often in harsh survival conditions. Sertão is the largest sub-region of Brazilian Northeast characterized by dry climates and Caatinga vegetation.</p>
          </tp:treatment-sec>
        </tp:taxon-treatment>
        <sec sec-type="3.3.2. Key to species of Sertaneja gen. nov" id="SECID0EFMAI">
          <title>3.3.2. Key to species of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">Sertaneja</tp:taxon-name-part></tp:taxon-name></italic> gen. nov.</title>
          <table-wrap content-type="key" position="anchor" orientation="portrait">
            <table id="TID0EXNAE" rules="all">
              <tbody>
                <tr>
                  <td rowspan="1" colspan="1">
                    <bold>1</bold>
                  </td>
                  <td rowspan="1" colspan="1">Ocularium with a single robust apical spine (Fig. <xref ref-type="fig" rid="F6">6G</xref>); trochanter IV square-shaped (Fig. <xref ref-type="fig" rid="F6">6D</xref>); tibia IV swollen in males (Fig. <xref ref-type="fig" rid="F7">7</xref>); most penis macrosetae spatulate, with basal <abbrev xlink:title="group D macrosetae" id="ABBRID0EQNAI">MS D</abbrev> closer to <abbrev xlink:title="group A macrosetae" id="ABBRID0EUNAI">MS A</abbrev> set, and <abbrev xlink:title="group B macrosetae" id="ABBRID0EYNAI">MS B</abbrev> inserted basally near the podium (Fig. <xref ref-type="fig" rid="F8">8</xref>).</td>
                  <td rowspan="1" colspan="1">
                    <bold><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">S.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="crassitibialis">crassitibialis</tp:taxon-name-part></tp:taxon-name></italic> sp. nov.</bold>
                  </td>
                </tr>
                <tr>
                  <td rowspan="1" colspan="1">
                    <bold>1’</bold>
                  </td>
                  <td rowspan="1" colspan="1">Ocularium with a pair of apical spines (Figs <xref ref-type="fig" rid="F3">3G</xref>, <xref ref-type="fig" rid="F9">9G</xref>); trochanter IV elongated (Figs <xref ref-type="fig" rid="F3">3D</xref>, <xref ref-type="fig" rid="F9">9D</xref>); legs IV bearing strong armature (Figs <xref ref-type="fig" rid="F4">4</xref>, <xref ref-type="fig" rid="F10">10</xref>); tibia IV not swollen in males (Figs <xref ref-type="fig" rid="F4">4</xref>, <xref ref-type="fig" rid="F10">10</xref>); penis macrosetae conical, basal <abbrev xlink:title="group D macrosetae" id="ABBRID0E3PAI">MS D</abbrev> pair closer to <abbrev xlink:title="group C macrosetae" id="ABBRID0EAQAI">MS C</abbrev>, <abbrev xlink:title="group B macrosetae" id="ABBRID0EEQAI">MS B</abbrev> adjacent to <abbrev xlink:title="group A macrosetae" id="ABBRID0EIQAI">MS A</abbrev> set (Figs <xref ref-type="fig" rid="F5">5</xref>, <xref ref-type="fig" rid="F11">11</xref>).</td>
                  <td rowspan="1" colspan="1">
                    <bold>2</bold>
                  </td>
                </tr>
                <tr>
                  <td rowspan="1" colspan="1">
                    <bold>2</bold>
                  </td>
                  <td rowspan="1" colspan="1">Body surface densely tuberculate (Fig. <xref ref-type="fig" rid="F3">3A</xref>); scute area III with a paramedian pair of spines (Figs <xref ref-type="fig" rid="F3">3A, C</xref>); coxa IV with a bifid prodorsal apical apophysis, and a conical retro-apical apophysis (Fig. <xref ref-type="fig" rid="F3">3A, D</xref>); trochanter IV with much developed retro- and proapical apophyses (Fig. <xref ref-type="fig" rid="F4">4</xref>); penis with three pairs of <abbrev xlink:title="group C macrosetae" id="ABBRID0EVRAI">MS C</abbrev> (Fig. <xref ref-type="fig" rid="F5">5</xref>).</td>
                  <td rowspan="1" colspan="1">
                    <bold><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">S.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="bicuspidata">bicuspidata</tp:taxon-name-part></tp:taxon-name></italic> sp. nov.</bold>
                  </td>
                </tr>
                <tr>
                  <td rowspan="1" colspan="1"><bold>2</bold>’</td>
                  <td rowspan="1" colspan="1">Body surface sparsely tuberculate (Fig. <xref ref-type="fig" rid="F9">9A</xref>); scute area III with a paramedian pair of rounded tubercles (Fig. <xref ref-type="fig" rid="F9">9A, C</xref>); coxa IV with a simple prodorsal apical apophysis, and a developed, internally curved retro-apical apophysis (Fig. <xref ref-type="fig" rid="F9">9A, D</xref>); trochanter IV retro-apical apophysis small, proapical one absent (Fig. <xref ref-type="fig" rid="F10">10</xref>); penis with five pairs of <abbrev xlink:title="group C macrosetae" id="ABBRID0EKTAI">MS C</abbrev> (Fig. <xref ref-type="fig" rid="F11">11</xref>).</td>
                  <td rowspan="1" colspan="1">
                    <bold><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">S.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="falcata">falcata</tp:taxon-name-part></tp:taxon-name></italic> sp. nov.</bold>
                  </td>
                </tr>
              </tbody>
            </table>
          </table-wrap>
        </sec>
        <tp:taxon-treatment>
          <tp:treatment-meta>
            <kwd-group>
              <label>Taxon classification</label>
              <kwd>
                <named-content content-type="kingdom" xlink:type="simple">Animalia</named-content>
              </kwd>
              <kwd>
                <named-content content-type="order" xlink:type="simple">Opiliones</named-content>
              </kwd>
              <kwd>
                <named-content content-type="family" xlink:type="simple">Gonyleptidae</named-content>
              </kwd>
            </kwd-group>
          </tp:treatment-meta>
          <tp:nomenclature>
            <label>3.3.3.</label>
            <tp:taxon-name><object-id content-type="arpha">16745D71-82FB-52BB-A0D0-F111980E6995</object-id>
              <tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">Sertaneja</tp:taxon-name-part>
              <tp:taxon-name-part taxon-name-part-type="species" reg="bicuspidata">bicuspidata</tp:taxon-name-part>
              <object-id content-type="zoobank" xlink:type="simple">http://zoobank.org/4C09C7B0-0FF4-4ED4-9BCD-78FC1E8B9A31</object-id>
            </tp:taxon-name>
            <tp:taxon-status>sp. nov.</tp:taxon-status>
            <xref ref-type="fig" rid="F3">Figs 3</xref>
            <xref ref-type="fig" rid="F4">, 4</xref>
            <xref ref-type="fig" rid="F5">, 5</xref>
            <xref ref-type="fig" rid="F12">, 12B</xref>
            <xref ref-type="fig" rid="F13">, 13</xref>
          </tp:nomenclature>
          <tp:treatment-sec sec-type="type locality" id="SECID0EBWAI">
            <title>Type locality.</title>
            <p>BRAZIL, Ceará: Ubajara, Parque Nacional de Ubajara.</p>
          </tp:treatment-sec>
          <tp:treatment-sec sec-type="type material" id="SECID0EGWAI">
            <title>Type material.</title>
            <p><bold>Holotype.</bold> BRAZIL. Ceará: Ubajara PARNA de Ubajara, Rio Gameleira, elev. 840 m, 27.i.2014, DaSilva M.B. Saraiva N.E.V. and Sampaio C., ♂ (<named-content content-type="dwc:institutional_code">UFPB</named-content> OP-163) [dissected]. <bold>Paratypes.</bold> BRAZIL. Ceará: Quixadá, Serra do Estevão, estrada para Dom Maurício, elev. 482 m, 18.iv.2014, DaSilva M.B. and Saraiva N.E.V., 1 ♂ (<named-content content-type="dwc:institutional_code">UFPB</named-content> OP-724) [dissected]; Quixadá, Serra do Urucu, Santuário de Nossa Senhora Imaculada Rainha do Sertão, elev. 344 m, 19.iv.2014, DaSilva M.B. and Saraiva N.E.V., 1 ♂ 2 imm (<named-content content-type="dwc:institutional_code">MZUSP</named-content> 76645) [male genitalia used for <abbrev xlink:title="scanning electron microscopy" id="ABBRID0E6WAI">SEM</abbrev>], 1 ♂ (<named-content content-type="dwc:institutional_code">MNRJ</named-content> 60616) [dissected]; Quixadá, Jardim dos Monólitos, inselbergs do Açude Euclides, elev. 180–200 m, 20.iv.2014, DaSilva M.B. and Saraiva N.E.V., 1 ♀ (<named-content content-type="dwc:institutional_code">UFPB</named-content> OP-726) [female description].</p>
          </tp:treatment-sec>
          <tp:treatment-sec sec-type="diagnosis" id="SECID0ENXAI">
            <title>Diagnosis.</title>
            <p>This species can be distinguished from the other species of the genus by the denser tuberculation of the body surface (Fig. <xref ref-type="fig" rid="F3">3A</xref>); scute area III paramedian pair of spines enlarged and slightly more robust when compared to <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">S.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="crassitibialis">crassitibialis</tp:taxon-name-part></tp:taxon-name></italic> sp. nov. (Fig. <xref ref-type="fig" rid="F3">3A, C</xref>); coxa IV with uniquely shaped bifid prodorsal apical apophysis and conical retro-apical apophysis (Fig. <xref ref-type="fig" rid="F3">3A, D</xref>); trochanter IV with the largest retro-apical apophysis among the genus, and a large proapical apophysis curved dorsally (Figs <xref ref-type="fig" rid="F3">3D</xref>, <xref ref-type="fig" rid="F4">4</xref>); femur IV with a retro-lateral row of large conical apophyses (Fig. <xref ref-type="fig" rid="F4">4A, D</xref>). It most resembles <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">S.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="falcata">falcata</tp:taxon-name-part></tp:taxon-name></italic> sp. nov. by the male femur IV dorsal row with equally sized high tubercles; penis glans’ stylus straight and with a rounded dorso-apical projection; <abbrev xlink:title="ventral plate" id="ABBRID0EBZAI">VP</abbrev> macrosetae conical, <abbrev xlink:title="group A macrosetae" id="ABBRID0EFZAI">MS A</abbrev> and <abbrev xlink:title="group B macrosetae" id="ABBRID0EJZAI">MS B</abbrev> sets adjacent, and <abbrev xlink:title="group D macrosetae" id="ABBRID0ENZAI">MS D</abbrev> pairs closer to each other and to <abbrev xlink:title="group C macrosetae" id="ABBRID0ERZAI">MS C</abbrev> set (Fig. <xref ref-type="fig" rid="F5">5</xref>).</p>
            <fig id="F4" position="float" orientation="portrait">
              <object-id content-type="doi">10.3897/asp.79.e66321.figure4</object-id>
              <object-id content-type="arpha">ED022836-60BA-5C9B-9D6E-0A4492FB86F6</object-id>
              <label>Figure 4.</label>
              <caption>
                <p><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">Sertaneja</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="bicuspidata">bicuspidata</tp:taxon-name-part></tp:taxon-name></italic> sp. nov. Male holotype (<named-content content-type="dwc:institutional_code">UFPB</named-content> OP-163) right trochanter–tibia IV. <bold>A</bold>: dorsal view; <bold>B</bold>: prolateral view; <bold>C</bold>: ventral view; <bold>D</bold>: retro-lateral view. — <bold><italic>Abbreviations</italic></bold>: Pro = prolateral; Ret = retro-lateral. Scale bars: 1 mm.</p>
              </caption>
              <graphic xlink:href="arthropod-systematics-79-485-g004.jpg" position="float" orientation="portrait" xlink:type="simple" id="oo_596977.jpg">
                <uri content-type="original_file">https://binary.pensoft.net/fig/596977</uri>
              </graphic>
            </fig>
            <fig id="F5" position="float" orientation="portrait">
              <object-id content-type="doi">10.3897/asp.79.e66321.figure5</object-id>
              <object-id content-type="arpha">5BA4035E-484F-5333-B362-2246B646CAB9</object-id>
              <label>Figure 5.</label>
              <caption>
                <p><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">Sertaneja</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="bicuspidata">bicuspidata</tp:taxon-name-part></tp:taxon-name></italic> sp. nov. (UPFB OP-725), apical portion of penis. <bold>A</bold>: dorsal view; <bold>B</bold>: right lateral view.</p>
              </caption>
              <graphic xlink:href="arthropod-systematics-79-485-g005.jpg" position="float" orientation="portrait" xlink:type="simple" id="oo_596978.jpg">
                <uri content-type="original_file">https://binary.pensoft.net/fig/596978</uri>
              </graphic>
            </fig>
          </tp:treatment-sec>
          <tp:treatment-sec sec-type="description" id="SECID0E42AI">
            <title>Description.</title>
            <p><bold>Holotype MALE</bold> (<named-content content-type="dwc:institutional_code">UFPB</named-content> OP-163; Figs <xref ref-type="fig" rid="F3">3</xref>–<xref ref-type="fig" rid="F4">4</xref>): <bold>Measurements</bold>: <abbrev xlink:title="dorsal scute length" id="ABBRID0EU3AI">DSL</abbrev>: 4.86; <abbrev xlink:title="dorsal scute maximum width" id="ABBRID0EY3AI">DSW</abbrev>: 4.97; <abbrev xlink:title="leg I" id="ABBRID0E33AI">LI</abbrev>: 9.13; <abbrev xlink:title="leg II" id="ABBRID0EA4AI">LII</abbrev>: 17.62; <abbrev xlink:title="leg III" id="ABBRID0EE4AI">LIII</abbrev>: 10.78 (broken metatarsus); <abbrev xlink:title="leg IV" id="ABBRID0EI4AI">LIV</abbrev>: 15.48. <bold>Dorsum</bold> (Fig. <xref ref-type="fig" rid="F3">3A, C, G</xref>): <abbrev xlink:title="dorsal scute" id="ABBRID0ES4AI">DS</abbrev> anterior margin with a pair of small tubercles on each side. Prosoma covered with distinctive large tubercles concentrated on the middle of posterior half. Ocularium tuberculate, with a pair of spines slightly longer than the ocularium height, and a pair of large tubercles just behind (Fig. <xref ref-type="fig" rid="F3">3C</xref>). Two pairs of ozopores of similar size, anterior one placed more laterally, and posterior one more rounded and slightly dislocated dorsally; lateral channel well developed followed by distinguished tuberculate oblong sensorial pegs. Scute areas I–IV densely tuberculate, tubercles increasing in size medially. Scute area III paramedian pair of spines recurved, slightly reaching scute area IV. Lateral margin of <abbrev xlink:title="dorsal scute" id="ABBRID0E14AI">DS</abbrev> with an external row of tubercles increasing in size towards scute area II, becoming slightly acuminated (Fig. <xref ref-type="fig" rid="F3">3C</xref>). Posterior margin of <abbrev xlink:title="dorsal scute" id="ABBRID0EC5AI">DS</abbrev> and free tergites I–III each with a transversal row of tubercles. Free tergite I with tubercles increasing in size medially. Anal operculum tuberculate. <bold>Venter</bold>: Coxa I with three longitudinal rows of tubercles increasing in size apically, median row largest; coxae II–III with slightly enlarged apical tubercles; coxa IV tuberculate. <bold>Chelicerae</bold>: Segment I with a transversal row of five tubercles on the posterior face of bulla. Fixed and movable fingers with five and four teeth; respectively. <bold>Pedipalps</bold> (Fig. <xref ref-type="fig" rid="F3">3E, F</xref>): Trochanter inflated dorsally, ventral face with a pair of setiferous tubercles, mesal largest (Fig. <xref ref-type="fig" rid="F3">3E</xref>). Femur with a dorsal median row of five tubercles, ventral face with a basal large setiferous tubercle (Fig. <xref ref-type="fig" rid="F3">3E, F</xref>); an external lateral row of five tubercles. Tibial setation: mesal and lateral IiIi/Iii. Tarsal setation: mesal IIi, lateral IiIi. <bold>Legs</bold> (Figs <xref ref-type="fig" rid="F3">3D</xref>, <xref ref-type="fig" rid="F4">4</xref>): Coxae I–IV each with one prodorsal and one retro-dorsal apophysis; coxa II with a trifid retro-lateral apophysis. Coxa IV bearing a robust, bifid, prodorsal apical apophysis, almost square-shaped, the large branch pointing backwards and the smaller one almost transversal, obliquely angled (Fig. <xref ref-type="fig" rid="F3">3D</xref>); and a conical retro-lateral apophysis, comparable in size and shape with the small, transversal branch of the prolateral one (Fig. <xref ref-type="fig" rid="F3">3D</xref>). Trochanter IV apically swollen in dorsal view, prolateral surface with a short, blunt, conical, basal apophysis, and a large, apical apophysis, perpendicular in lateral view, dorsally curved along its entire length, bearing a basal small acute straight apophysis pointing posteriorly (Fig. <xref ref-type="fig" rid="F4">4B</xref>); retro-lateral face with a basal short conical apophysis (ca. same size as the coxa IV retro-lateral apophysis), a sub-apical small, straight, transversal conical apophysis, and a long, straight apical apophysis 2/3 the length as the podomere (Fig. <xref ref-type="fig" rid="F4">4</xref>). Femur III slightly curved in dorsal view, with a paralateral pair of dorso-apical tubercles (retro-dorsal largest); ventral surface with two rows of tubercles increasing in size apically from their apical half, prolateral ones larger. Femur IV slightly curved inwards and upwards; dorsal surface with a median row of five enlarged, blunt, conical tubercles placed between the sub-basal and sub-apical regions of the podomere (Fig. <xref ref-type="fig" rid="F4">4B</xref>); dorso-apical surface with two paralateral large spines; prolateral row of low rounded tubercles; retro-lateral row of seven high apophyses roughly decreasing in size apically, the large basal ones approximately the same size as the trochanter IV retro-apical apophysis (Fig. <xref ref-type="fig" rid="F4">4A</xref>); two ventral rows of tubercles, proventral row with seven enlarged, blunt, conical tubercles on the basal half, retro-ventral row of small rounded tubercles (Fig. <xref ref-type="fig" rid="F4">4C</xref>); ventro-apical surface with a pair of paralateral enlarged acuminated tubercles, ca. three times the size of the immediately following tubercles (prolateral largest). Patella IV covered with conical tubercles that increase in size apically, ventral face with two rows of tubercles increasing in size apically, retro-lateral ones larger. Tibia IV covered by conical tubercles, ventral row of tubercles slightly increasing in size apically (Fig. <xref ref-type="fig" rid="F4">4B, D</xref>). Tarsal counts: 6, 10, 6, 6. <bold>Penis</bold> (<named-content content-type="dwc:institutional_code">UFPB</named-content> OP-725; Fig. <xref ref-type="fig" rid="F5">5</xref>): Glans stylus cylindrical. <abbrev xlink:title="ventral plate" id="ABBRID0ENABI">VP</abbrev> apex convex with a slight median concavity, lateral margins slightly concave presenting a subtle constriction on its medial portion. <abbrev xlink:title="ventral plate" id="ABBRID0ERABI">VP</abbrev> bearing three paralateral pairs of <abbrev xlink:title="group A macrosetae" id="ABBRID0EVABI">MS A</abbrev> in a tight cluster in lateral view (Fig. <xref ref-type="fig" rid="F5">5B</xref>); one pair of <abbrev xlink:title="group B macrosetae" id="ABBRID0E4ABI">MS B</abbrev> of same size as <abbrev xlink:title="group A macrosetae" id="ABBRID0EBBBI">MS A</abbrev>, placed more basally and adjacent to the <abbrev xlink:title="group A macrosetae" id="ABBRID0EFBBI">MS A</abbrev> cluster; three pairs of <abbrev xlink:title="group C macrosetae" id="ABBRID0EJBBI">MS C</abbrev>, the apical spine slightly smaller; <abbrev xlink:title="group D macrosetae" id="ABBRID0ENBBI">MS D</abbrev> set closer to <abbrev xlink:title="group C macrosetae" id="ABBRID0ERBBI">MS C</abbrev> group, setae close to each other; and two pairs of reduced, sub-apical, ventro-lateral <abbrev xlink:title="group E macrosetae" id="ABBRID0EVBBI">MS E</abbrev> positioned between the <abbrev xlink:title="group C macrosetae" id="ABBRID0EZBBI">MS C</abbrev> setae (not visible in the <abbrev xlink:title="scanning electron microscopy" id="ABBRID0E4BBI">SEM</abbrev> photograph, but confirmed in the other dissected males). <bold>Coloration</bold>: <abbrev xlink:title="dorsal scute" id="ABBRID0EDCBI">DS</abbrev>, tergites I–III, chelicerae, pedipalps coxae, coxae I–IV, and leg IV general coloration strong yellowish brown (74). <abbrev xlink:title="dorsal scute" id="ABBRID0EHCBI">DS</abbrev> with posterior and lateral margins bearing a moderate yellowish brown (77) outline; scute areas, prosoma and ocularium with moderate yellowish brown (77) granulation. Pedipalps trochanter–tibia, and legs I–III dark yellow (88).</p>
            <p><bold>FEMALE</bold> (<named-content content-type="dwc:institutional_code">UFPB</named-content> OP-726; Fig. <xref ref-type="fig" rid="F3">3B</xref>): <bold>Measurements</bold>: <abbrev xlink:title="dorsal scute length" id="ABBRID0E1CBI">DSL</abbrev>: 4.34; <abbrev xlink:title="dorsal scute maximum width" id="ABBRID0E5CBI">DSW</abbrev>: 4.20; <abbrev xlink:title="leg I" id="ABBRID0ECDBI">LI</abbrev>: 8.32; <abbrev xlink:title="leg II" id="ABBRID0EGDBI">LII</abbrev>: 15.48; <abbrev xlink:title="leg III" id="ABBRID0EKDBI">LIII</abbrev>: 10.77; <abbrev xlink:title="leg IV" id="ABBRID0EODBI">LIV</abbrev>: 14.27. <bold>Dorsum</bold>: <abbrev xlink:title="dorsal scute" id="ABBRID0EUDBI">DS</abbrev> gamma (γ), but coda section is slightly longer. Ocularium spines length as tall as the ocularium. Scute area III central armature shorter than male and more acuminated. Scute area IV with median pair of tubercles more conspicuous than male. Posterior margin of <abbrev xlink:title="dorsal scute" id="ABBRID0EYDBI">DS</abbrev> and free tergites I–III each with leaner tubercles on the sides. <bold>Legs</bold>: Coxa IV narrower and shorter than in male, with a short, conical, proapical apophysis obliquely inserted; retro-apical apophysis reduced. Trochanter III retro-apical projection smaller than in male. Trochanter IV shorter than in male, apical half swollen, bearing a terminal tubercle, with unarmed prolateral face; retro-lateral face with short basal apophysis, and blunt apical apophysis smaller than in male. Femur III ventral row and ventro-apical tubercles smaller than in male. Femur IV dorso-medial row with small and slender projections on basal 4/5; a retro-lateral, a proventral and a retro-ventral rows of small conical tubercles; dorso-apical and ventro-apical paralateral projections reduced. Tibia III proventral and retro-ventral rows of small granule-like tubercles. Patella–tibia IV dorsal face covered by conical blunt tubercles. Tarsal count: 6, 9–10, 6, 6.</p>
          </tp:treatment-sec>
          <tp:treatment-sec sec-type="variation" id="SECID0E5DBI">
            <title>Variation.</title>
            <p><bold>Males</bold> (n = 4): <bold>Measurements</bold>: <abbrev xlink:title="dorsal scute length" id="ABBRID0EIEBI">DSL</abbrev>: 4.33–4.86; <abbrev xlink:title="dorsal scute maximum width" id="ABBRID0EMEBI">DSW</abbrev>: 4.47–4.97; <abbrev xlink:title="leg I" id="ABBRID0EQEBI">LI</abbrev>: 8.52–9.13; <abbrev xlink:title="leg II" id="ABBRID0EUEBI">LII</abbrev>: 15.60–17.62; <abbrev xlink:title="leg III" id="ABBRID0EYEBI">LIII</abbrev>: 10.78–12.30; <abbrev xlink:title="leg IV" id="ABBRID0E3EBI">LIV</abbrev>: 14.25–15.83. <bold>Dorsum</bold>: Ocularium spines as tall as, or slightly taller than the ocularium. Scute area III paramedian pair of spines medium to large, length reaching backwards up to halfway of scute area IV. <bold>Pedipalps</bold>: Pedipalpal setation: tibial mesal IiIi, lateral IiIi/i-Ii; tarsal mesal IIi/IIii, lateral IiIi/Iii. <bold>Legs</bold>: Minor males, compared to major males as the holotype, with less developed armature on scute area III and weaker armature of legs: coxa IV narrower and shorter, prodorsal apical and retro-apical apophyses smaller and slender (on major males prodorsal apical apophysis shorter projection can be acuminate); trochanter III retro-lateral projection reduced; trochanter IV all apophyses smaller; femur III prolateral and ventral rows of tubercles less developed, with smaller proapical tubercles; femur IV pro- and ventro-apical tubercles smaller; tibia IV proventral and retro-ventral rows reduced. Tarsal count: 6, 9–10, 6, 6.</p>
          </tp:treatment-sec>
          <tp:treatment-sec sec-type="etymology" id="SECID0EGFBI">
            <title>Etymology.</title>
            <p>‘Bicuspidata’ is a Latin adjective (adj. perf. part., nom. fem.) that refers to the diagnostic bifid apophysis of male coxa IV in this species.</p>
          </tp:treatment-sec>
          <tp:treatment-sec sec-type="distribution" id="SECID0ELFBI">
            <title>Distribution (Fig. <xref ref-type="fig" rid="F13">13</xref>).</title>
            <p>Caatinga shrublands and dry forests of northern interior Ceará and Brejos de Altitude humid montane forests of Ibiapaba mountains.</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" xlink:type="simple">Animalia</named-content>
              </kwd>
              <kwd>
                <named-content content-type="order" xlink:type="simple">Opiliones</named-content>
              </kwd>
              <kwd>
                <named-content content-type="family" xlink:type="simple">Gonyleptidae</named-content>
              </kwd>
            </kwd-group>
          </tp:treatment-meta>
          <tp:nomenclature>
            <label>3.3.4.</label>
            <tp:taxon-name><object-id content-type="arpha">4A856BC3-DDED-52B3-AA40-7B7662A38AAC</object-id>
              <tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">Sertaneja</tp:taxon-name-part>
              <tp:taxon-name-part taxon-name-part-type="species" reg="crassitibialis">crassitibialis</tp:taxon-name-part>
              <object-id content-type="zoobank" xlink:type="simple">http://zoobank.org/EA58E870-AE35-4802-AB14-665CE6ACDB39</object-id>
            </tp:taxon-name>
            <tp:taxon-status>sp. nov.</tp:taxon-status>
            <xref ref-type="fig" rid="F6">Figs 6</xref>
            <xref ref-type="fig" rid="F7">, 7</xref>
            <xref ref-type="fig" rid="F8">, 8</xref>
            <xref ref-type="fig" rid="F12">, 12A</xref>
            <xref ref-type="fig" rid="F13">, 13</xref>
          </tp:nomenclature>
          <tp:treatment-sec sec-type="type locality" id="SECID0ESHBI">
            <title>Type locality.</title>
            <p>BRAZIL, Ceará: Quixadá, Serra do Urucu, Santuário Nossa Senhora Imaculada Rainha do Sertão.</p>
          </tp:treatment-sec>
          <tp:treatment-sec sec-type="type material" id="SECID0EXHBI">
            <title>Type material.</title>
            <p><bold>Holotype.</bold> BRAZIL. Ceará: Quixadá, Serra do Urucu, Santuário Nossa Senhora Imaculada Rainha do Sertão, elev. 344 m, 19.iv.2014, DaSilva M.B. and Saraiva N.E.V., ♂ (<named-content content-type="dwc:institutional_code">UFPB</named-content> OP-487). <bold>Paratypes.</bold> BRAZIL. Ceará: Ubajara, PARNA de Ubajara, Brejo de Altitude, 700 m, 27.i.2014, DaSilva M.B., Saraiva N.E.V. and Sampaio C., 1 ♂ (<named-content content-type="dwc:institutional_code">MNRJ</named-content> 60614) [genitalia used for <abbrev xlink:title="scanning electron microscopy" id="ABBRID0ELIBI">SEM</abbrev>]; Ubajara, PARNA de Ubajara, Rio Gameleira, 840 m, 27.i.2014, DaSilva M.B.; Saraiva N.E.V. and Sampaio C., 2 ♀ (<named-content content-type="dwc:institutional_code">UFPB</named-content> OP-480), 1 ♀ (<named-content content-type="dwc:institutional_code">UFPB</named-content> OP-727) [female description]; Ubajara, PARNA de Ubajara, Gr. Morcego Branco, Gr. Ubajara, Trilha Portão Planalto, 22.x.2011, DeSouza A.M., Araujo E.S., Carvalho L., 1 ♀ (<named-content content-type="dwc:institutional_code">MNRJ</named-content> 60615); Ubajara, PARNA de Ubajara, Trilha da Samambaia, 30.iv.2018, Silvino A.C.S. and Saraiva N.E.V., 1 ♂ 1 ♀ 1 imm. (<named-content content-type="dwc:institutional_code">MZUSP</named-content> 76646) [male dissected].</p>
          </tp:treatment-sec>
          <tp:treatment-sec sec-type="diagnosis" id="SECID0EDJBI">
            <title>Diagnosis.</title>
            <p>Differs from the other species by the lower density of tubercles and armature (Fig. <xref ref-type="fig" rid="F6">6A</xref>); ocularium is the tallest in the genus and bears a robust, single spine (Fig. <xref ref-type="fig" rid="F6">6C</xref>); lateral margin of <abbrev xlink:title="dorsal scute" id="ABBRID0ERJBI">DS</abbrev> with a large acuminate tubercle on the external row, placed close to scute area III (Fig. <xref ref-type="fig" rid="F6">6C</xref>); scute area III paramedian pair of spines slender when compared to <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">S.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="bicuspidata">bicuspidata</tp:taxon-name-part></tp:taxon-name></italic> sp. nov. (Fig. <xref ref-type="fig" rid="F6">6C</xref>); coxa IV with an unbranched, robust prodorsal apical apophysis, missing a retro-apical apophysis (Fig. <xref ref-type="fig" rid="F6">6D</xref>); trochanter IV short, square-shaped with a robust, blunt central apophysis (Figs <xref ref-type="fig" rid="F6">6D</xref>, <xref ref-type="fig" rid="F7">7</xref>); femur IV less armed; tibia IV sexually dimorphic, swollen in males (Fig. <xref ref-type="fig" rid="F7">7</xref>); penis glans’ stylus with an angular dorso-apical projection (Fig. <xref ref-type="fig" rid="F8">8B</xref>); <abbrev xlink:title="ventral plate" id="ABBRID0E3KBI">VP</abbrev> macrosetae spatulated, except for the basal <abbrev xlink:title="group D macrosetae" id="ABBRID0EALBI">MS D</abbrev> pair and <abbrev xlink:title="group E macrosetae" id="ABBRID0EELBI">MS E</abbrev>; <abbrev xlink:title="group B macrosetae" id="ABBRID0EILBI">MS B</abbrev> inserted very basally; and <abbrev xlink:title="group D macrosetae" id="ABBRID0EMLBI">MS D</abbrev> pairs much apart from each other (Fig. <xref ref-type="fig" rid="F8">8</xref>).</p>
            <fig id="F6" position="float" orientation="portrait">
              <object-id content-type="doi">10.3897/asp.79.e66321.figure6</object-id>
              <object-id content-type="arpha">A8CFD010-B702-5E48-8BAE-74BEFCE0576D</object-id>
              <label>Figure 6.</label>
              <caption>
                <p><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">Sertaneja</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="crassitibialis">crassitibialis</tp:taxon-name-part></tp:taxon-name></italic> sp. nov. (<bold>A</bold>, <bold>C</bold>–<bold>G</bold>) Male holotype (<named-content content-type="dwc:institutional_code">UFPB</named-content> OP-487), <bold>A</bold>: habitus, dorsal view; <bold>C</bold>: same, right lateral view; <bold>D</bold>: right coxa and trochanter IV in dorsal view; <bold>E</bold>: right pedipalp in lateral view; <bold>F</bold>: same, mesal view; <bold>G</bold>: ocularium frontal view. (<bold>B</bold>) Female paratype (<named-content content-type="dwc:institutional_code">UFPB</named-content> OP-727) habitus, dorsal view. Scale bars: 1 mm.</p>
              </caption>
              <graphic xlink:href="arthropod-systematics-79-485-g006.jpg" position="float" orientation="portrait" xlink:type="simple" id="oo_596979.jpg">
                <uri content-type="original_file">https://binary.pensoft.net/fig/596979</uri>
              </graphic>
            </fig>
            <fig id="F7" position="float" orientation="portrait">
              <object-id content-type="doi">10.3897/asp.79.e66321.figure7</object-id>
              <object-id content-type="arpha">6E2BAA78-990D-55A8-94B4-E33533197769</object-id>
              <label>Figure 7.</label>
              <caption>
                <p><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">Sertaneja</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="crassitibialis">crassitibialis</tp:taxon-name-part></tp:taxon-name></italic> sp. nov. Male holotype (<named-content content-type="dwc:institutional_code">UFPB</named-content> OP-487) right trochanter–tibia IV. <bold>A</bold>: dorsal view; <bold>B</bold>: prolateral view; <bold>C</bold>: ventral view; <bold>D</bold>: retro-lateral view. Scale bars: 1 mm.</p>
              </caption>
              <graphic xlink:href="arthropod-systematics-79-485-g007.jpg" position="float" orientation="portrait" xlink:type="simple" id="oo_596980.jpg">
                <uri content-type="original_file">https://binary.pensoft.net/fig/596980</uri>
              </graphic>
            </fig>
            <fig id="F8" position="float" orientation="portrait">
              <object-id content-type="doi">10.3897/asp.79.e66321.figure8</object-id>
              <object-id content-type="arpha">EC787192-5ED2-5652-8B8C-9CBCBC888B4F</object-id>
              <label>Figure 8.</label>
              <caption>
                <p><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">Sertaneja</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="crassitibialis">crassitibialis</tp:taxon-name-part></tp:taxon-name></italic> sp. nov. (<named-content content-type="dwc:institutional_code">UFPB</named-content> OP-171), apical portion of penis. <bold>A</bold>: dorsal view; <bold>B</bold>: right lateral view.</p>
              </caption>
              <graphic xlink:href="arthropod-systematics-79-485-g008.jpg" position="float" orientation="portrait" xlink:type="simple" id="oo_596981.jpg">
                <uri content-type="original_file">https://binary.pensoft.net/fig/596981</uri>
              </graphic>
            </fig>
          </tp:treatment-sec>
          <tp:treatment-sec sec-type="description" id="SECID0EQPBI">
            <title>Description.</title>
            <p><bold>Holotype MALE</bold> (<named-content content-type="dwc:institutional_code">UFPB</named-content> OP-487; Figs <xref ref-type="fig" rid="F6">6</xref>, <xref ref-type="fig" rid="F7">7</xref>): <bold>Measurements</bold>: <abbrev xlink:title="dorsal scute length" id="ABBRID0EHQBI">DSL</abbrev>: 4.91; <abbrev xlink:title="dorsal scute maximum width" id="ABBRID0ELQBI">DSW</abbrev>: 4.67; <abbrev xlink:title="leg I" id="ABBRID0EPQBI">LI</abbrev>: 9.35; <abbrev xlink:title="leg II" id="ABBRID0ETQBI">LII</abbrev>: 16.17; <abbrev xlink:title="leg III" id="ABBRID0EXQBI">LIII</abbrev>: 12.44; <abbrev xlink:title="leg IV" id="ABBRID0E2QBI">LIV</abbrev>: 16.14. <bold>Dorsum</bold> (Fig. <xref ref-type="fig" rid="F6">6A, C, G</xref>): Prosoma sparsely covered by small granule-like tubercles. Ocularium twice as tall as the eye diameter, with a robust, conical spine projected anteriorly, slightly larger than the ocularium (Fig. <xref ref-type="fig" rid="F6">6G</xref>). Two pair of ozopores placed on the lateral surface, both slit shaped; lateral channel well developed, conspicuous and with small sensorial pegs. Scute area II, III and IV with a central transversal row of tubercles (Fig. <xref ref-type="fig" rid="F6">6A</xref>). Scute area III paramedian pair of spines slightly curved posteriorly in all its extension, barely reaching scute area IV (Fig. <xref ref-type="fig" rid="F6">6A</xref>). Lateral margin of <abbrev xlink:title="dorsal scute" id="ABBRID0ERRBI">DS</abbrev> with an external row of tubercles increasing in size posteriorly, becoming acuminated, largest one placed near scute area III (Fig. <xref ref-type="fig" rid="F6">6C</xref>). Posterior margin of <abbrev xlink:title="dorsal scute" id="ABBRID0EZRBI">DS</abbrev> and free tergites I–III each with a row of similar sized round tubercles. Anal operculum tuberculate. <bold>Venter</bold>: Coxae I–IV with low tubercles; coxa I with median row of enlarged tubercles. Coxa IV covered by granule-like tubercles. <bold>Chelicerae</bold>: Segment I with the posterior portion of the bulla bearing a transversal row of four tubercles. Fixed and movable fingers each with five and five to six teeth, respectively. <bold>Pedipalps</bold> (Fig. <xref ref-type="fig" rid="F6">6E, F</xref>): Trochanter inflated dorsally; ventral face with two setiferous tubercles, mesal tubercle largest. Femur with a dorsal median row of six tubercles (Fig. <xref ref-type="fig" rid="F6">6E</xref>); ventral surface with a large basal setiferous tubercle and a retro-lateral row of three tubercles on apical half. Tibial setation: mesal and lateral IiIi. Tarsal setation: mesal IIi, lateral IiIi. <bold>Legs</bold> (Figs <xref ref-type="fig" rid="F6">6D</xref>, <xref ref-type="fig" rid="F7">7</xref>): Coxae I–III each with one prodorsal and 1 retro-dorsal apophysis; coxa II retro-dorsal apophysis trifid and fused in the apex with coxa III prodorsal one. Coxa IV large, tuberculate, bearing a robust, unbranched prodorsal apical apophysis, this almost transversally inserted, slightly curved downwards and posteriorly (Fig. <xref ref-type="fig" rid="F6">6A, C, D</xref>). Trochanter IV with a robust, slightly bifid, blunt central apophysis, a prodorsal sub-apical enlarged tubercle, and an acuminated, straight retro-apical apophysis (Figs <xref ref-type="fig" rid="F6">6D</xref>, <xref ref-type="fig" rid="F7">7</xref>). Femur III with an enlarged retro-apical dorsal spine; ventral face with a pro- and retro-lateral rows of tubercles increasing in size apically on apical half. Tibia III sub-apical surface slightly swollen, with retro-ventral sub-apical row of enlarged tubercles. Femur IV slightly curved inwards and upwards; dorsal surface covered by small tubercles, with a pair of paralateral apical spines slightly curved upwards (prolateral spine largest) (Fig. <xref ref-type="fig" rid="F7">7A</xref>); lateral rows of tubercles slightly increasing in size apically, retro-lateral row largest; with pro and retro-ventral rows that increase in size apically, proventral row largest and with tubercles more close to each other (Fig. <xref ref-type="fig" rid="F7">7C</xref>); apically with a pair of paralateral spines, prolateral largest (Fig. <xref ref-type="fig" rid="F7">7C</xref>). Patella IV tuberculate, with a slightly swollen retro-dorsal apical spine (Fig. <xref ref-type="fig" rid="F7">7A</xref>). Tibia IV swollen at apical 3/4 of its length, with a proventral and retro-ventral row of enlarged sub-apical tubercles, and a pair of paralateral ventro-apical spines (Fig. <xref ref-type="fig" rid="F7">7B, C, D</xref>). Tarsal counts: 6, 8, 6, 6. <bold>Penis</bold> (<named-content content-type="dwc:institutional_code">UFPB</named-content> OP-171; Fig. <xref ref-type="fig" rid="F8">8</xref>): <abbrev xlink:title="ventral plate" id="ABBRID0EAUBI">VP</abbrev> apex slightly concave, lateral margin sub-straight. Proximal portion of <abbrev xlink:title="ventral plate" id="ABBRID0EEUBI">VP</abbrev> with four pairs <abbrev xlink:title="group A macrosetae" id="ABBRID0EIUBI">MS A</abbrev> and one pair <abbrev xlink:title="group B macrosetae" id="ABBRID0EMUBI">MS B</abbrev> placed far from A4 and placed more basally. <abbrev xlink:title="group C macrosetae" id="ABBRID0EQUBI">MS C</abbrev> set apically curved and showing asymmetry between left (3) and right (2) sides (Fig. <xref ref-type="fig" rid="F8">8A</xref>). <abbrev xlink:title="group D macrosetae" id="ABBRID0EYUBI">MS D</abbrev> apical pair flattened and acuminate, basal spine conical and blunt; and two pairs of <abbrev xlink:title="group E macrosetae" id="ABBRID0E3UBI">MS E</abbrev> placed more ventrally and close to <abbrev xlink:title="group C macrosetae" id="ABBRID0EAVBI">MS C</abbrev> and <abbrev xlink:title="group D macrosetae" id="ABBRID0EEVBI">MS D</abbrev> (Fig. <xref ref-type="fig" rid="F8">8B</xref>). <bold>Coloration</bold>: <abbrev xlink:title="dorsal scute" id="ABBRID0EOVBI">DS</abbrev> predominantly dark grayish yellowish brown (81) with scute areas limits, area III paramedian spines, and specks on prosoma dark orange yellow (72). Chelicerae, pedipalps, coxae I–III, and legs I–III dark yellow (88). Leg IV dark grayish yellowish brown (81).</p>
            <p><bold>FEMALE</bold> (<named-content content-type="dwc:institutional_code">UFPB</named-content> OP-727; Fig. <xref ref-type="fig" rid="F6">6B</xref>): <bold>Measurements</bold>: <abbrev xlink:title="dorsal scute length" id="ABBRID0EBWBI">DSL</abbrev>: 4.70; <abbrev xlink:title="dorsal scute maximum width" id="ABBRID0EFWBI">DSW</abbrev>: 4.26; <abbrev xlink:title="leg I" id="ABBRID0EJWBI">LI</abbrev>: 8.88; <abbrev xlink:title="leg II" id="ABBRID0ENWBI">LII</abbrev>: 15.36; <abbrev xlink:title="leg III" id="ABBRID0ERWBI">LIII</abbrev>: 11.19; <abbrev xlink:title="leg IV" id="ABBRID0EVWBI">LIV</abbrev>: 14.81. <bold>Dorsum</bold>: Overall less developed armature and tubercles. <abbrev xlink:title="dorsal scute" id="ABBRID0E2WBI">DS</abbrev> alpha (α), coda slightly longer. Ocularium spine slender. Scute area III central armature small. Lateral margin of <abbrev xlink:title="dorsal scute" id="ABBRID0E6WBI">DS</abbrev> with external row of smaller tubercles than in male. <bold>Legs</bold>: Coxa IV narrower and shorter than in male, with an obliquely inserted, slender, conical, prodorsal apical apophysis, slightly curved downwards. Trochanter III retro-apical apophysis reduced. Trochanter IV narrower than in male, prolateral face unarmed, retro-lateral face as in males but with smaller apical apophysis. Femur III with ventral rows of small tubercles. Femur IV less armed, ventral rows of tubercles slightly increasing in size apically, dorso- and ventro-apical pair of spines small. Patella IV prodorsal apical projection reduced. Tibiae III–IV unarmed, not inflated. Tarsal counts: 6, 7, 6, 6.</p>
          </tp:treatment-sec>
          <tp:treatment-sec sec-type="variation" id="SECID0EFXBI">
            <title>Variation.</title>
            <p><bold>Males</bold> (n = 3): <bold>Measurements</bold>: <abbrev xlink:title="dorsal scute length" id="ABBRID0EPXBI">DSL</abbrev>: 4.91–4.99; <abbrev xlink:title="dorsal scute maximum width" id="ABBRID0ETXBI">DSW</abbrev>: 4.67–4.90; <abbrev xlink:title="leg I" id="ABBRID0EXXBI">LI</abbrev>: 8.98–10.08; <abbrev xlink:title="leg II" id="ABBRID0E2XBI">LII</abbrev>: 15.31–16.17; <abbrev xlink:title="leg III" id="ABBRID0E6XBI">LIII</abbrev>: 11.58–12.44; <abbrev xlink:title="leg IV" id="ABBRID0EDYBI">LIV</abbrev>: 16.14–16.34. <bold>Dorsum</bold>: Ocularium spine more, or less acute. <abbrev xlink:title="dorsal scute" id="ABBRID0EJYBI">DS</abbrev> lateral margin external row of rounded to acuminate tubercles, becoming almost spine-like. Scute area II with tubercles placed near the lateral margins. <bold>Legs</bold>: Tibia IV retro-ventral apical spine single or bifid. Tarsal counts: 6, 8–9, 6, 6. <bold>Females</bold> (n = 5): <bold>Measurements</bold>: <abbrev xlink:title="dorsal scute length" id="ABBRID0ETYBI">DSL</abbrev>: 4.61–4.75; <abbrev xlink:title="dorsal scute maximum width" id="ABBRID0EXYBI">DSW</abbrev>: 4.20–4.55; <abbrev xlink:title="leg I" id="ABBRID0E2YBI">LI</abbrev>: 8.56–9.45; <abbrev xlink:title="leg II" id="ABBRID0E6YBI">LII</abbrev>: 13.93–15.97; <abbrev xlink:title="leg III" id="ABBRID0EDZBI">LIII</abbrev>: 10.25–11.28; <abbrev xlink:title="leg IV" id="ABBRID0EHZBI">LIV</abbrev>: 14.80–15.52. <bold>Pedipalps</bold>: Pedipalp tibial setation: mesal IiIi/IIi, lateral IiIi; tarsal setation: mesal IIi, lateral IiIi/Iiii. <bold>Legs</bold>: Femur IV proventral row of tubercles slightly enlarged or not. Patella IV with or without prodorsal apical projection. Tarsal counts: 5–6, 8–9, 6, 6.</p>
          </tp:treatment-sec>
          <tp:treatment-sec sec-type="etymology" id="SECID0EPZBI">
            <title>Etymology.</title>
            <p>‘Crassi-’ is a Greek adjective, meaning thick, and ‘tibia’ is the Latin noun meaning the podomere; combined to ‘crassitibia’ (nom. sing. fem.) in reference to the diagnostic male tibia IV of the species.</p>
          </tp:treatment-sec>
          <tp:treatment-sec sec-type="distribution" id="SECID0EUZBI">
            <title>Distribution (Fig. <xref ref-type="fig" rid="F13">13</xref>).</title>
            <p>Brejos de Altitude humid montane forests of Ibiapaba mountains and Caatinga shrublands and dry forests of northern interior Ceará.</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" xlink:type="simple">Animalia</named-content>
              </kwd>
              <kwd>
                <named-content content-type="order" xlink:type="simple">Opiliones</named-content>
              </kwd>
              <kwd>
                <named-content content-type="family" xlink:type="simple">Gonyleptidae</named-content>
              </kwd>
            </kwd-group>
          </tp:treatment-meta>
          <tp:nomenclature>
            <label>3.3.5.</label>
            <tp:taxon-name><object-id content-type="arpha">3590AB43-E999-5608-9841-5D2E3131545B</object-id>
              <tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">Sertaneja</tp:taxon-name-part>
              <tp:taxon-name-part taxon-name-part-type="species" reg="falcata">falcata</tp:taxon-name-part>
              <object-id content-type="zoobank" xlink:type="simple">http://zoobank.org/D2951940-FBC8-45DB-B91B-5B968A11B1B8</object-id>
            </tp:taxon-name>
            <tp:taxon-status>sp. nov.</tp:taxon-status>
            <xref ref-type="fig" rid="F9">Figs 9</xref>
            <xref ref-type="fig" rid="F10">, 10</xref>
            <xref ref-type="fig" rid="F11">, 11</xref>
            <xref ref-type="fig" rid="F12">, 12C–E</xref>
            <xref ref-type="fig" rid="F13">, 13</xref>
          </tp:nomenclature>
          <tp:treatment-sec sec-type="type locality" id="SECID0E22BI">
            <title>Type locality.</title>
            <p>BRAZIL, Rio Grande do Norte: Portalegre, Cachoeira do Pinga.</p>
          </tp:treatment-sec>
          <tp:treatment-sec sec-type="type material" id="SECID0EA3BI">
            <title>Type material.</title>
            <p><bold>Holotype.</bold> BRAZIL. Rio Grande do Norte: Portalegre, Cachoeira do Pinga, encosta da serra, elev. 431 m, 23–24.iv.2014, DaSilva M.B. and Saraiva N.E.V., ♂ (<named-content content-type="dwc:institutional_code">UFPB</named-content> OP-481). <bold>Paratypes.</bold> same as for holotype, 3 ♂ (<named-content content-type="dwc:institutional_code">UFPB</named-content> OP-482), 1 ♂ (<named-content content-type="dwc:institutional_code">UFPB</named-content> OP-728) [dissected], 2 ♀ (<named-content content-type="dwc:institutional_code">UFPB</named-content> OP-729) [female description], 1 ♂ (<named-content content-type="dwc:institutional_code">MZUSP</named-content> 76647), 1 ♂ (<named-content content-type="dwc:institutional_code">MNRJ</named-content> 60617).</p>
          </tp:treatment-sec>
          <tp:treatment-sec sec-type="diagnosis" id="SECID0EI4BI">
            <title>Diagnosis.</title>
            <p>Distinguished from other species by the presence of a pair of slightly enlarged paramedian tubercles on scute area III (Fig. <xref ref-type="fig" rid="F9">9A, C</xref>), instead of spines; coxa IV bearing a short, conical, straight prodorsal apical apophysis and a long, curved, sickle-like retro-apical apophysis (Fig. <xref ref-type="fig" rid="F9">9D</xref>); femur IV retro-lateral face with three central elongated apophysis (Fig. <xref ref-type="fig" rid="F10">10A, D</xref>); and contains five pairs of <abbrev xlink:title="group C macrosetae" id="ABBRID0E14BI">MS C</abbrev> (Fig. <xref ref-type="fig" rid="F11">11</xref>). Most similar to <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">S.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="bicuspidata">bicuspidata</tp:taxon-name-part></tp:taxon-name></italic> sp. nov. by the slightly elongated trochanter IV; penis glans’ stylus with a rounded dorso-apical projection; similar <abbrev xlink:title="group A macrosetae" id="ABBRID0EN5BI">MS A</abbrev> and <abbrev xlink:title="group B macrosetae" id="ABBRID0ER5BI">MS B</abbrev>; and <abbrev xlink:title="group D macrosetae" id="ABBRID0EV5BI">MS D</abbrev> pairs close <abbrev xlink:title="group C macrosetae" id="ABBRID0EZ5BI">MS C</abbrev> group.</p>
            <fig id="F9" position="float" orientation="portrait">
              <object-id content-type="doi">10.3897/asp.79.e66321.figure9</object-id>
              <object-id content-type="arpha">59DCCACC-4F29-5B94-8352-609AE09B98FB</object-id>
              <label>Figure 9.</label>
              <caption>
                <p><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">Sertaneja</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="falcata">falcata</tp:taxon-name-part></tp:taxon-name></italic> sp. nov. (<bold>A</bold>, <bold>C</bold>–<bold>G</bold>) Male holotype (<named-content content-type="dwc:institutional_code">UFPB</named-content> OP-481), <bold>A</bold>: habitus, dorsal view; <bold>C</bold>: same, right lateral view; <bold>D</bold>: right coxa and trochanter IV in dorsal view; <bold>E</bold>: right pedipalp in lateral view; <bold>F</bold>: same, mesal view; <bold>G</bold>: ocularium frontal view. (<bold>B</bold>) Female paratype (<named-content content-type="dwc:institutional_code">UFPB</named-content> OP-729) habitus, dorsal view. Scale bars: 1 mm.</p>
              </caption>
              <graphic xlink:href="arthropod-systematics-79-485-g009.jpg" position="float" orientation="portrait" xlink:type="simple" id="oo_596982.jpg">
                <uri content-type="original_file">https://binary.pensoft.net/fig/596982</uri>
              </graphic>
            </fig>
            <fig id="F10" position="float" orientation="portrait">
              <object-id content-type="doi">10.3897/asp.79.e66321.figure10</object-id>
              <object-id content-type="arpha">53DFB069-E8F2-5828-A7B2-C61CDFD45DF7</object-id>
              <label>Figure 10.</label>
              <caption>
                <p><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">Sertaneja</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="falcata">falcata</tp:taxon-name-part></tp:taxon-name></italic> sp. nov. Male holotype (<named-content content-type="dwc:institutional_code">UFPB</named-content> OP-481) right trochanter–tibia IV. <bold>A</bold>: dorsal view; <bold>B</bold>: prolateral view; <bold>C</bold>: ventral view; <bold>D</bold>: retro-lateral view. Scale bars: 1 mm.</p>
              </caption>
              <graphic xlink:href="arthropod-systematics-79-485-g010.jpg" position="float" orientation="portrait" xlink:type="simple" id="oo_596983.jpg">
                <uri content-type="original_file">https://binary.pensoft.net/fig/596983</uri>
              </graphic>
            </fig>
            <fig id="F11" position="float" orientation="portrait">
              <object-id content-type="doi">10.3897/asp.79.e66321.figure11</object-id>
              <object-id content-type="arpha">9A43A8A0-7233-50E9-B2E4-F371A6B1F9EC</object-id>
              <label>Figure 11.</label>
              <caption>
                <p><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">Sertaneja</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="falcata">falcata</tp:taxon-name-part></tp:taxon-name></italic> sp. nov. (<named-content content-type="dwc:institutional_code">UFPB</named-content> OP-728), apical portion of penis. <bold>A</bold>: dorsal view; <bold>B</bold>: right lateral view.</p>
              </caption>
              <graphic xlink:href="arthropod-systematics-79-485-g011.jpg" position="float" orientation="portrait" xlink:type="simple" id="oo_596984.jpg">
                <uri content-type="original_file">https://binary.pensoft.net/fig/596984</uri>
              </graphic>
            </fig>
          </tp:treatment-sec>
          <tp:treatment-sec sec-type="description" id="SECID0EZCCI">
            <title>Description.</title>
            <p><bold>Holotype MALE</bold> (<named-content content-type="dwc:institutional_code">UFPB</named-content> OP-481; Figs <xref ref-type="fig" rid="F9">9</xref>, <xref ref-type="fig" rid="F10">10</xref>): <bold>Measurements</bold>: <abbrev xlink:title="dorsal scute length" id="ABBRID0EQDCI">DSL</abbrev>: 4.43; <abbrev xlink:title="dorsal scute maximum width" id="ABBRID0EUDCI">DSW</abbrev>: 4.87; <abbrev xlink:title="leg I" id="ABBRID0EYDCI">LI</abbrev>: 8.91; <abbrev xlink:title="leg II" id="ABBRID0E3DCI">LII</abbrev>: 19.48; <abbrev xlink:title="leg III" id="ABBRID0EAECI">LIII</abbrev>: 12.24; <abbrev xlink:title="leg IV" id="ABBRID0EEECI">LIV</abbrev>: 16.53. <bold>Dorsum</bold> (Fig. <xref ref-type="fig" rid="F9">9A, C, G</xref>): Prosoma with few tubercles. Front margin bearing a single small median tubercle. Ocularium twice as tall as the eye diameter, with a pair of divergent spines slightly projected anteriorly (Fig. <xref ref-type="fig" rid="F9">9C, G</xref>). Two pairs of ozopores of similar size, anterior one placed laterally, and posterior one rounded and more dorsal; lateral channel developed and followed by oblong sensorial pegs that increase in size posteriorly. Scute area I with tubercles placed in a row along the longitudinal groove and scute groove II, with a pair of slightly enlarged paramedian tubercles (Fig. <xref ref-type="fig" rid="F9">9A</xref>). Scute areas II–IV each with a transversal central row of enlarged tubercles increasing in size towards the middle, paramedian pair larger than the others. Scute areas III–IV with more conical tubercles compared to those on other areas. Lateral margin of <abbrev xlink:title="dorsal scute" id="ABBRID0EWECI">DS</abbrev> with an external row of low, rounded tubercles slightly increasing in size posteriorly. Posterior margin of <abbrev xlink:title="dorsal scute" id="ABBRID0E1ECI">DS</abbrev> and free tergites I–III each with a row of conical tubercles. Anal operculum tuberculate. <bold>Venter</bold>: Coxa I tuberculate, median row of large ones, apical face with two prolateral and two retro-lateral tubercles. Coxae II–III with small tubercles, pro- and retro-apical tubercles reduced. Coxa IV tuberculate. <bold>Chelicerae</bold>: Segment I with ectodorsal row of three tubercles on posterior face of bulla. Fixed and movable fingers with five and three teeth, respectively. <bold>Pedipalps</bold> (Fig. <xref ref-type="fig" rid="F9">9E, F</xref>): Trochanter inflated dorsally, ventral face with two setiferous tubercles, mesal largest. Femur with a basal setiferous tubercle, an external lateral row of 2–3 smaller setiferous tubercles on the middle 1/3 (Fig. <xref ref-type="fig" rid="F9">9E</xref>), and a mesal apical seta. Tibial setation: mesal IiIi, lateral IiIii. Tarsal setation: mesal IIi, lateral IiIi/Iii. <bold>Legs</bold> (Figs <xref ref-type="fig" rid="F9">9D</xref>, <xref ref-type="fig" rid="F10">10</xref>): Coxae I–III each with one prodorsal and one retro-dorsal apophysis; coxa II retro-dorsal apophysis trifid and fused at the apex with coxa III prodorsal apophysis. Coxa IV large, covered by more acuminate tubercles than those of the rest of the body (Fig. <xref ref-type="fig" rid="F9">9A</xref>); with an obliquely inserted, conical prodorsal apical apophysis that is slightly curved downwards (Fig. <xref ref-type="fig" rid="F9">9C, D</xref>); and a sickle-shaped retro-apical apophysis, twice the size of proapical apophysis, curved out and downwards (Figs <xref ref-type="fig" rid="F9">9D</xref>, <xref ref-type="fig" rid="F10">10D</xref>). Trochanter III with a reduced retro-apical projection. Trochanter IV long, with pro- and a retro-lateral central blunt apophyses, the prolateral one slightly acuminated (Fig. <xref ref-type="fig" rid="F10">10A</xref>); apical portion with a long, conical retro-apical apophysis and a small proapical round tubercle (Fig. <xref ref-type="fig" rid="F10">10</xref>). Femur III slightly curved retrolaterally in dorsal view, with a slightly acuminated retro-apical dorsal tubercle; ventral surface with two rows of tubercles increasing in size subapically, prolateral row larger. Femur IV slightly curved inwards at the base, medio-dorsal row of tubercles twice the height of those covering the podomere, almost on the entire femur (except the sub-apical surface), basal and sub-apical tubercles more conspicuous (Fig. <xref ref-type="fig" rid="F10">10A, B, D</xref>); a pair of long, curved dorso-apical paralateral spines, retro-lateral spine largest and strongly curved upwards (Fig. <xref ref-type="fig" rid="F10">10A, D</xref>); retro-lateral face with three long, conical, central apophyses (Fig. <xref ref-type="fig" rid="F10">10A, D</xref>); ventral surface with a prolateral row of large tubercles alternating with small ones on apical half, and a retro-lateral row with round tubercles (Fig. <xref ref-type="fig" rid="F10">10B, C</xref>); ventro-apical portion with two paralateral large straight spiniform apophyses, proapical largest (Fig. <xref ref-type="fig" rid="F10">10C</xref>). Patella IV tuberculate, ventral surface covered by enlarged, acuminated tubercles, with a large proapical spine (twice the size of the surrounding ones) (Fig. <xref ref-type="fig" rid="F10">10B</xref>). Tibia IV with two ventral rows of tubercles increasing in size apically, pointing posteriorly (Fig. <xref ref-type="fig" rid="F10">10B, D</xref>). Metatarsus I slightly swollen. Tarsal counts: 6, 9, 6, 6. <bold>Penis</bold> (<named-content content-type="dwc:institutional_code">UFPB</named-content> OP-728; Fig. <xref ref-type="fig" rid="F11">11</xref>): <abbrev xlink:title="ventral plate" id="ABBRID0EVHCI">VP</abbrev> apex and lateral margins slightly concave. <abbrev xlink:title="group A macrosetae" id="ABBRID0EZHCI">MS A</abbrev> set showing asymmetry between right (4) and left (3) sides (Fig. <xref ref-type="fig" rid="F10">10A, B</xref>); <abbrev xlink:title="group B macrosetae" id="ABBRID0EBICI">MS B</abbrev> almost undistinguishable from <abbrev xlink:title="group A macrosetae" id="ABBRID0EFICI">MS A</abbrev> but inserted more basally. Five pairs of conical, curved <abbrev xlink:title="group C macrosetae" id="ABBRID0EJICI">MS C</abbrev>, decreasing in size apically; two pairs of <abbrev xlink:title="group D macrosetae" id="ABBRID0ENICI">MS D</abbrev> close to MS C5, but slightly smaller and placed more dorsally; two pairs of small <abbrev xlink:title="group E macrosetae" id="ABBRID0ERICI">MS E</abbrev>, ventral to the <abbrev xlink:title="group C macrosetae" id="ABBRID0EVICI">MS C</abbrev> set (Fig. <xref ref-type="fig" rid="F10">10B</xref>). <bold>Coloration</bold>: General coloration predominantly moderate yellow (87). <abbrev xlink:title="dorsal scute" id="ABBRID0E6ICI">DS</abbrev> scute areas, prosoma and margins, free tergites I–III moderate olive brown (95) granulation.</p>
            <p><bold>FEMALE</bold> (<named-content content-type="dwc:institutional_code">UFPB</named-content> OP-729; Figs <xref ref-type="fig" rid="F6">6B</xref>, <xref ref-type="fig" rid="F12">12D</xref>) <bold>Measurements</bold>: <abbrev xlink:title="dorsal scute length" id="ABBRID0EWJCI">DSL</abbrev>: 4.13; <abbrev xlink:title="dorsal scute maximum width" id="ABBRID0E1JCI">DSW</abbrev>: 4.32; <abbrev xlink:title="leg I" id="ABBRID0E5JCI">LI</abbrev>: 8.83; <abbrev xlink:title="leg II" id="ABBRID0ECKCI">LII</abbrev>: 16.57; <abbrev xlink:title="leg III" id="ABBRID0EGKCI">LIII</abbrev>: 10.93; <abbrev xlink:title="leg IV" id="ABBRID0EKKCI">LIV</abbrev>: 14.40. <bold>Dorsum</bold>: Less armed compared to male. <abbrev xlink:title="dorsal scute" id="ABBRID0EQKCI">DS</abbrev> narrower. Lateral margin of <abbrev xlink:title="dorsal scute" id="ABBRID0EUKCI">DS</abbrev> with an external row of tubercles, posterior tubercles slightly larger than in male. <bold>Pedipalps</bold>: Pedipalp tibial setation: lateral IiIi. <bold>Legs</bold>: Coxa IV narrower and shorter than in male, with a small prolateral apophysis, and a conical, straight retro-apical apophysis of same size. Trochanter IV narrower and shorter than in male, the prolateral basal apophysis as a large, blunt tubercle, and a small retro-lateral apophysis. Femur III lacking a proventral row of enlarged tubercles, reduced retro-dorsal apical tubercle. Femur IV unarmed, covered by small conical tubercles that slightly increase in size apically, with a pair of small dorso-apical spines of similar size. Patella–tibia IV unarmed. Tarsal counts: 6, 9–10, 6, 6.</p>
          </tp:treatment-sec>
          <tp:treatment-sec sec-type="variation" id="SECID0E3KCI">
            <title>Variation.</title>
            <p><bold>Males</bold> (n = 6): <bold>Measurements</bold>: <abbrev xlink:title="dorsal scute length" id="ABBRID0EGLCI">DSL</abbrev> 4.43–4.66; <abbrev xlink:title="dorsal scute maximum width" id="ABBRID0EKLCI">DSW</abbrev> 4.84–5.06; <abbrev xlink:title="leg I" id="ABBRID0EOLCI">LI</abbrev> 8.91–10.21; <abbrev xlink:title="leg II" id="ABBRID0ESLCI">LII</abbrev> 17.52–19.48; <abbrev xlink:title="leg III" id="ABBRID0EWLCI">LIII</abbrev> 12.24–13.08; <abbrev xlink:title="leg IV" id="ABBRID0E1LCI">LIV</abbrev> 16.19–17.51. <bold>Dorsum</bold>: Front margin with or without tubercles. Ocularium with parallel or diverging spines, inclination of these ranging from near-horizontal to vertical. <bold>Pedipalps</bold>: Femur external lateral row with 2–3 sub-apical tubercles. <bold>Legs</bold>: Femur IV dorso-apical spines with similar size to retro-lateral largest and strongly curved upwards; retro-lateral central conical apophyses sometimes with an additional apophysis of half the height of the remaining apophyses in the middle; apical half of proventral row bearing small tubercles alternated with large ones. Tarsal counts: 6, 10–12, 6, 4–6. <bold>Females</bold> (n = 2): <bold>Measurements</bold>: <abbrev xlink:title="dorsal scute length" id="ABBRID0EIMCI">DSL</abbrev> 4.13–4.27; <abbrev xlink:title="dorsal scute maximum width" id="ABBRID0EMMCI">DSW</abbrev> 4.32–4.46; <abbrev xlink:title="leg I" id="ABBRID0EQMCI">LI</abbrev> 8.83–8.84; <abbrev xlink:title="leg II" id="ABBRID0EUMCI">LII</abbrev> 16.16–16.57; <abbrev xlink:title="leg III" id="ABBRID0EYMCI">LIII</abbrev> 10.93–11.62; <abbrev xlink:title="leg IV" id="ABBRID0E3MCI">LIV</abbrev> 10.09. <bold>Pedipalps</bold>: Pedipalp tibial setation: mesal IiIi, lateral IiIi. Tarsal setation: mesal IIi, lateral IiIi/IiIii. <bold>Legs</bold>: Tarsal counts: 6, 9–10, 6, 6.</p>
          </tp:treatment-sec>
          <tp:treatment-sec sec-type="etymology" id="SECID0EENCI">
            <title>Etymology.</title>
            <p>‘Falcata’ is a Latin adjective (adj. nom. fem.) that means sickle-shaped and refers to the diagnostic retro-apical apophysis of male coxa IV of the species.</p>
          </tp:treatment-sec>
          <tp:treatment-sec sec-type="distribution" id="SECID0EJNCI">
            <title>Distribution (Fig. <xref ref-type="fig" rid="F13">13</xref>).</title>
            <p>Known only from type locality. Caatinga dry forest of tableland slopes of interior Rio Grande do Norte.</p>
            <fig id="F12" position="float" orientation="portrait">
              <object-id content-type="doi">10.3897/asp.79.e66321.figure12</object-id>
              <object-id content-type="arpha">21723C16-6707-5309-853B-DD25BCA566C3</object-id>
              <label>Figure 12.</label>
              <caption>
                <p>Photographs of live <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">Sertaneja</tp:taxon-name-part></tp:taxon-name></italic> gen. nov. <bold>A</bold>: Female of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">S.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="crassitibialis">crassitibialis</tp:taxon-name-part></tp:taxon-name></italic> sp. nov. (courtesy of Leonardo Sousa Carvalho); <bold>B</bold>: Male of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">S.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="bicuspidata">bicuspidata</tp:taxon-name-part></tp:taxon-name></italic> sp. nov.; <bold>C</bold>, <bold>E</bold>: Male of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">S.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="falcata">falcata</tp:taxon-name-part></tp:taxon-name></italic> sp. nov.; <bold>D</bold>: Female of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">S.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="falcata">falcata</tp:taxon-name-part></tp:taxon-name></italic> sp. nov.</p>
              </caption>
              <graphic xlink:href="arthropod-systematics-79-485-g012.jpg" position="float" orientation="portrait" xlink:type="simple" id="oo_596985.jpg">
                <uri content-type="original_file">https://binary.pensoft.net/fig/596985</uri>
              </graphic>
            </fig>
            <fig id="F13" position="float" orientation="portrait">
              <object-id content-type="doi">10.3897/asp.79.e66321.figure13</object-id>
              <object-id content-type="arpha">384EAA42-C6E6-549F-9C08-9582CBAAD722</object-id>
              <label>Figure 13.</label>
              <caption>
                <p>Geographic distribution of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">Sertaneja</tp:taxon-name-part></tp:taxon-name></italic> gen. nov. and biomes. <bold>A</bold>: northeastern Brazil detail; <bold>B</bold>: distribution compared to <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily">Pachylinae</tp:taxon-name-part></tp:taxon-name> groups.</p>
              </caption>
              <graphic xlink:href="arthropod-systematics-79-485-g013.jpg" position="float" orientation="portrait" xlink:type="simple" id="oo_596986.jpg">
                <uri content-type="original_file">https://binary.pensoft.net/fig/596986</uri>
              </graphic>
            </fig>
          </tp:treatment-sec>
        </tp:taxon-treatment>
      </sec>
    </sec>
    <sec sec-type="4. Discussion" id="SECID0E1QCI">
      <title>4. Discussion</title>
      <p>These three new species represent a great discovery for Brazilian semiarid diversity and <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="family">Gonyleptidae</tp:taxon-name-part></tp:taxon-name> phylogeny. Taxonomically, we could assign the three new species to <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Gyndoides">Gyndoides</tp:taxon-name-part></tp:taxon-name></italic> based on their apparent morphological similarity. However, the undivided scute area IV and male genitalia homogeneity of the three new species differed considerably from that of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Gyndoides">Gyndoides</tp:taxon-name-part></tp:taxon-name></italic> by the (i) lack of a glans ventral process; (ii) mostly rectangular and long ventral plate; and (iii) amount and placement of the MS. Additionally, the three new species inhabit northeastern Brazil in the Ceará and Rio Grande do Norte states, approximately 2,700 km from where <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Gyndoides">Gyndoides</tp:taxon-name-part></tp:taxon-name></italic> species are found (Fig. <xref ref-type="fig" rid="F13">13</xref>). Therefore, as a result of the distinct penis morphology, its phylogenetic placement, and the disjunct distribution, we decided to propose <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">Sertaneja</tp:taxon-name-part></tp:taxon-name></italic> gen. nov. as a new genus. As mentioned above, the penis morphology of the new genus is quite homogeneous, despite the heterogeneous external body features.</p>
      <p>From a historical perspective (namely, the Roewerian system) and intuitively, based solely on the overall morphology (except for the penile one) it would be plausible to propose three different genera based on such external variation. But as thoroughly discussed (<xref ref-type="bibr" rid="B35">Kury 1990</xref>), this classification system relied on a small set of external variable characters (i.e., tarsal counts, ocularium armature, scute area III armature) to define different supraspecific groups, resulting in many artificial units. There are many cases demonstrating those issues, such as in <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Eusarcus">Eusarcus</tp:taxon-name-part></tp:taxon-name></italic> Perty, 1833 (<xref ref-type="bibr" rid="B31">Hara and Pinto-da-Rocha 2010</xref>). In that case, there were four <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily">Pachylinae</tp:taxon-name-part></tp:taxon-name> genera bearing a central spine in scute area III (<italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Metagraphinotus">Metagraphinotus</tp:taxon-name-part></tp:taxon-name></italic> Mello-Leitão, 1927a, <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Pareusarcus">Pareusarcus</tp:taxon-name-part></tp:taxon-name></italic> Roewer, 1929 and <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Antetriceras">Antetriceras</tp:taxon-name-part></tp:taxon-name></italic> Roewer, 1949, besides <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Eusarcus">Eusarcus</tp:taxon-name-part></tp:taxon-name></italic> itself) before the revision. Those could be distinguished by the different combination of states of the ocularium armature, number of tarsal counts, armature on both scute area IV and femur pedipalp. After the revision that also performed a cladistic analysis, all those characters did not corroborate those genera, and they were synonymized with <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Eusarcus">Eusarcus</tp:taxon-name-part></tp:taxon-name></italic>, which has a typical penile pattern. Another example would be <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sadocus">Sadocus</tp:taxon-name-part></tp:taxon-name></italic> Sørensen, 1886, recently revised by <xref ref-type="bibr" rid="B65">Pessoa-Silva et al. (2021)</xref> where <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Carampangue">Carampangue</tp:taxon-name-part></tp:taxon-name></italic> Mello-Leitão, 1937 and <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sadocus">Sadocus</tp:taxon-name-part></tp:taxon-name></italic> differed from each other mainly by the number of scute areas, the former bearing three, while the latter had four. <xref ref-type="bibr" rid="B39">Kury (2003)</xref> noted their similarity, and propose their synonymization, that proved to be right later on. As can be seen from such examples, current taxonomical studies with the order always take the Roewerian characters and morphological variations into account, including a greater number of phylogenetic evidence in the form of characters, especially those from the penile structure, which are considered one of the main foundations of the harvestmen taxonomy (<xref ref-type="bibr" rid="B50">Macías-Ordóñez et al. 2010</xref>).</p>
      <p><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Gyndoides">Gyndoides</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="springmanni">springmanni</tp:taxon-name-part></tp:taxon-name></italic>+ is the sister group to the clade that is equivalent to DRMN in the analyses (Figs <xref ref-type="fig" rid="F1">1</xref>, <xref ref-type="fig" rid="F2">2</xref>). <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Gyndoides">Gyndoides</tp:taxon-name-part></tp:taxon-name></italic> is a genus that currently comprises two species, <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Gyndoides">G.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="springmanni">springmanni</tp:taxon-name-part></tp:taxon-name></italic> and <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Gyndoides">G.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="elaphus">elaphus</tp:taxon-name-part></tp:taxon-name></italic> Mello-Leitão, 1927a, both recorded from the Santa Catarina state in southern Brazil. Previously, <xref ref-type="bibr" rid="B69">Pinto-da-Rocha et al. (2012)</xref> based on the overall morphology of the body, suggested a close relationship between <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Gyndoides">Gyndoides</tp:taxon-name-part></tp:taxon-name></italic>, <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Discocyrtus">Discocyrtus</tp:taxon-name-part></tp:taxon-name></italic>, <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Gyndesops">Gyndesops</tp:taxon-name-part></tp:taxon-name></italic> Roewer, 1943, and <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Paraluederwaldtia">Paraluederwaldtia</tp:taxon-name-part></tp:taxon-name></italic> Mello-Leitão, 1927b, even suggesting the synonymy of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Gyndoides">Gyndoides</tp:taxon-name-part></tp:taxon-name></italic> and the latter two under <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Discocyrtus">Discocyrtus</tp:taxon-name-part></tp:taxon-name></italic>. However, <xref ref-type="bibr" rid="B73">Pinto-da-Rocha et al. (2014)</xref> and <xref ref-type="bibr" rid="B13">Carvalho and Kury (2018)</xref> proposed a close relationship between <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Discocyrtus">Discocyrtus</tp:taxon-name-part></tp:taxon-name></italic> and <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Mitobatinae">Mitobatinae</tp:taxon-name-part></tp:taxon-name></italic>. In the present analysis, we could not retrieve this sister-group relationship, but we found evidence that <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Gyndoides">Gyndoides</tp:taxon-name-part></tp:taxon-name></italic> is not closely related to <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Discocyrtus">Discocyrtus</tp:taxon-name-part></tp:taxon-name></italic> as once suggested.</p>
      <p>As a side note, we justify why we did not assign the three new species to other genera deemed close to <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Gyndoides">Gyndoides</tp:taxon-name-part></tp:taxon-name></italic> according to <xref ref-type="bibr" rid="B69">Pinto-da-Rocha et al. (2012)</xref>. The monotypic <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Gyndesops">Gyndesops</tp:taxon-name-part></tp:taxon-name></italic> penis (<xref ref-type="bibr" rid="B69">Pinto-da-Rocha et al. 2012</xref>: fig. 17) closely resembles that of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Gyndoides">Gyndoides</tp:taxon-name-part></tp:taxon-name></italic>, the leg II tarsal counts are unusually high (12–13) while <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">Sertaneja</tp:taxon-name-part></tp:taxon-name></italic> gen. nov. has up to 10 tarsal segments, and femur IV is straight and unarmed, in addition to inhabiting Santa Catarina, a southern state in Brazil. <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Paraluederwaldtia">Paraluederwaldtia</tp:taxon-name-part></tp:taxon-name></italic> comprises two species, both with a divided scute area IV: <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Paraluederwaldtia">P.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="bituberculata">bituberculata</tp:taxon-name-part></tp:taxon-name></italic> (Mello-Leitão, 1922) from Rio de Janeiro is only known from the female holotype, hampering further comparisons, and <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Paraluederwaldtia">P.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="caramaschii">caramaschii</tp:taxon-name-part></tp:taxon-name></italic> Soares and Soares, 1979 from Amazonas and Pará, northern Brazilian states, have unknown penis morphology.</p>
      <p>In the present analyses, <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily">Pachylinae</tp:taxon-name-part></tp:taxon-name><abbrev xlink:title="sensu stricto" id="ABBRID0EN2CI">s.s</abbrev>., represented by <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Acanthoprocta">A.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="pustulata">pustulata</tp:taxon-name-part></tp:taxon-name></italic>+, was also retrieved, and is supported by 17 synapomorphies with relative Bremer support of 52 (Figs <xref ref-type="fig" rid="F1">1</xref>, <xref ref-type="fig" rid="F2">2</xref>). The remainder of <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily">Pachylinae</tp:taxon-name-part></tp:taxon-name> included in this analysis, the <abbrev xlink:title="sensu lato" id="ABBRID0EJ3CI">s.l</abbrev>. classification compose the clade <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Eusarcus">E.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="nigrimaculatus">nigrimaculatus</tp:taxon-name-part></tp:taxon-name></italic>+ (relative Bremer support 15) in conjunction with DRMN (Figs <xref ref-type="fig" rid="F1">1</xref>, <xref ref-type="fig" rid="F2">2</xref>). The DRMN clade, here represented by members of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Discocyrtus">Discocyrtus</tp:taxon-name-part></tp:taxon-name></italic>, <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Pachylobos">Pachylobos</tp:taxon-name-part></tp:taxon-name></italic>, <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Longiperna">Longiperna</tp:taxon-name-part></tp:taxon-name></italic>, and <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Roeweria">Roeweria</tp:taxon-name-part></tp:taxon-name></italic> was recovered as a monophyletic group (relative Bremer support 45), even though the internal generic relationships were not consistent with the most recent proposition (<xref ref-type="bibr" rid="B14">Carvalho and Kury 2021</xref>: fig. 7). This is not an issue, considering that DRMN internal relationships are not settled (<xref ref-type="bibr" rid="B13">Carvalho and Kury 2018</xref>; <xref ref-type="bibr" rid="B14">Carvalho and Kury 2021</xref>). Therefore, despite this divergence, our results corroborated the DRMN group in general.</p>
      <p>Our goal was not to present a <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily">Pachylinae</tp:taxon-name-part></tp:taxon-name><abbrev xlink:title="sensu lato" id="ABBRID0EP5CI">s.l</abbrev>. phylogeny, which would certainly be a large, exhaustive, and meticulous task. Currently, the subfamily <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily">Pachylinae</tp:taxon-name-part></tp:taxon-name> is one of the greatest challenges in <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="family">Gonyleptidae</tp:taxon-name-part></tp:taxon-name> systematics because it is species-rich, polyphyletic (<xref ref-type="bibr" rid="B68">Pinto-da-Rocha 2002</xref>; <xref ref-type="bibr" rid="B32">Hara et al. 2012</xref>; <xref ref-type="bibr" rid="B73">Pinto-da-Rocha et al. 2014</xref>), and with ill-circumscribed genera. The polyphyly issue of <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily">Pachylinae</tp:taxon-name-part></tp:taxon-name> has been gradually addressed by different approaches, such as using molecular data as in <xref ref-type="bibr" rid="B73">Pinto-da-Rocha et al. (2014)</xref> and <xref ref-type="bibr" rid="B9">Benavides et al. (2021)</xref>, which pointed out major clades that were further corroborated by morphological data, resulting in the proposal of new groups, such as <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily">Roeweriinae</tp:taxon-name-part></tp:taxon-name>, <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily">Neopachylinae</tp:taxon-name-part></tp:taxon-name>, DRMN group, and <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily">Pachylinae</tp:taxon-name-part></tp:taxon-name><abbrev xlink:title="sensu stricto" id="ABBRID0EFADI">s.s</abbrev>. Many other ongoing revisions (<xref ref-type="bibr" rid="B28">Hara 2016</xref>; <xref ref-type="bibr" rid="B13">Carvalho and Kury 2018</xref>; <xref ref-type="bibr" rid="B45">Kury et al. 2020</xref>) should further aid the proposal of monophyletic units, as well as their relationships within <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="family">Gonyleptidae</tp:taxon-name-part></tp:taxon-name>. We are confident regarding the proposal of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">Sertaneja</tp:taxon-name-part></tp:taxon-name></italic> gen. nov., based on its monophyletic status, which was supported by many unambiguous synapomorphies, as well as its sister-relationship to <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Gyndoides">G.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="springmanni">springmanni</tp:taxon-name-part></tp:taxon-name></italic> that is equally well corroborated. We should have our hypothesis tested using more taxa and characters in a more comprehensive phylogeny, including those genera putatively close to <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Gyndoides">Gyndoides</tp:taxon-name-part></tp:taxon-name></italic> (<xref ref-type="bibr" rid="B69">Pinto-da-Rocha et al. 2012</xref>).</p>
      <p>The semiarid region of northeastern Brazil contains 29 <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="suborder">Laniatores</tp:taxon-name-part></tp:taxon-name> species north of the São Francisco River, which is considered a major geographical barrier in the region (<xref ref-type="bibr" rid="B12">Carnaval et al. 2009</xref>; <xref ref-type="bibr" rid="B61">Nascimento et al. 2013</xref>). Most (17 spp.) are restricted to humid forests, mainly the Brejos de Altitude, whereas others can live in drier vegetation, such as the Caatinga shrublands and dry forests (<xref ref-type="bibr" rid="B21">DeSouza et al. 2017</xref>). <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">Sertaneja</tp:taxon-name-part></tp:taxon-name></italic> gen. nov. matches the latter pattern, as all three species have been recorded from dry vegetation. <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">Sertaneja</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="bicuspidata">bicuspidata</tp:taxon-name-part></tp:taxon-name></italic> sp. nov. and <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">S.</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="crassitibialis">crassitibialis</tp:taxon-name-part></tp:taxon-name></italic> sp. nov. are sympatric with records in the shrublands and dry forests of low mountain slopes of Quixadá, and in the humid altitudinal forests of Ubajara. <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">Sertaneja</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="falcata">falcata</tp:taxon-name-part></tp:taxon-name></italic> sp. nov. is only known from the slopes of a dry forest remnant plateau in the southwestern Rio Grande do Norte state. Other species that share the same pattern of occurrence and are commonly found in drier locations include the cosmetids <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Cynorta">Cynorta</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="unciscripta">unciscripta</tp:taxon-name-part></tp:taxon-name></italic> Roewer, 1927, <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Eupoecilaema">Eupoecilaema</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="megaypsilon">megaypsilon</tp:taxon-name-part></tp:taxon-name></italic> Piza, 1938, <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Gryne">Gryne</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="perlata">perlata</tp:taxon-name-part></tp:taxon-name></italic> Mello-Leitão, 1936, <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Gryne">Gryne</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="pluriarcuata">pluriarcuata</tp:taxon-name-part></tp:taxon-name></italic> Mello-Leitão, 1936, and the stygnid <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Stygnus">Stygnus</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species" reg="polyacanthus">polyacanthus</tp:taxon-name-part></tp:taxon-name></italic> (Mello-Leitão, 1923) (<xref ref-type="bibr" rid="B21">DeSouza et al. 2017</xref>). Figure <xref ref-type="fig" rid="F13">13</xref> here, page width</p>
      <p>The high diversity and endemicity rates of the harvestmen in the northeastern region of coastal Atlantic Forest, when compared to interior drier formations, are generally associated to intrinsic physiological traits, such as the group propensity for rapid dehydration, as well as behavior attributes (<xref ref-type="bibr" rid="B49">Machado and Macias-Ordonez 2007</xref>), like philopatry and low vagility. As a result, most neotropical harvestmen species, such as gonyleptids, exhibit narrow and endemic ranges (<xref ref-type="bibr" rid="B18">DaSilva et al. 2015</xref>), resulting in historically-driven distribution patterns (<xref ref-type="bibr" rid="B63">Nogueira et al. 2019</xref>). Similar range and distributional patterns are also observed in harvestmen groups outside of the neotropics (<xref ref-type="bibr" rid="B23">Emata and Hedin 2016</xref>; <xref ref-type="bibr" rid="B20">Derkarabetian et al. 2021</xref>; Giribet et al. 2021). Although <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="order">Opiliones</tp:taxon-name-part></tp:taxon-name> occurrence in arid formations is not something unheard of for some <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="suborder">Laniatores</tp:taxon-name-part></tp:taxon-name> families—e.g., representatives of <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="family">Cosmetidae</tp:taxon-name-part></tp:taxon-name>, <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="family">Stygnidae</tp:taxon-name-part></tp:taxon-name>, <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="family">Phalangodidae</tp:taxon-name-part></tp:taxon-name> (e.g., <xref ref-type="bibr" rid="B22">DiDomenico and Hedin 2016</xref>, infer <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sitalcina">Sitalcina</tp:taxon-name-part></tp:taxon-name> species diversification in North America deserts)—this new genus is one of the few records for <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="family">Gonyleptidae</tp:taxon-name-part></tp:taxon-name>. Nevertheless, Neotropical drier ecosystems, just as the Caatinga vegetation, should harbor a diversity of harvestmen yet to be discovered, like the new genus described here.</p>
    </sec>
    <sec sec-type="5. Conclusion" id="SECID0EPHDI">
      <title>5. Conclusion</title>
      <p><italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus" reg="Sertaneja">Sertaneja</tp:taxon-name-part></tp:taxon-name></italic> gen. nov. is the first <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="family">Gonyleptidae</tp:taxon-name-part></tp:taxon-name> recorded from semiarid vegetation, except for some cavernicolous species from Bahia, and was an unexpected find because harvestmen are often associated with humid environments. Through the cladistic analysis, we were able to evaluate the monophyly of the new genus and its proximity to some key, recently revised, <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily">Pachylinae</tp:taxon-name-part></tp:taxon-name><abbrev xlink:title="sensu lato" id="ABBRID0EGIDI">s.l</abbrev>. groups.</p>
      <p>These new findings help shed light on the potential diversity of the order in northeastern Brazil, which currently is the leading country in the number of registered harvestmen species, with slightly more than 1000 according to <xref ref-type="bibr" rid="B38">Kury (2002</xref>+). However, little is known about the Caatinga opilionofauna in the semiarid and humid forest enclaves. Nevertheless, we hope to have moved forward in <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily">Pachylinae</tp:taxon-name-part></tp:taxon-name> systematics, and expect to find more unknown harvestmen in Caatinga semiarid vegetation as more comprehensive collection projects are conducted in this vast and complex ecosystem in the near future.</p>
    </sec>
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    <ack>
      <title>6. Acknowledgments</title>
      <p>The authors would like to thank Dr. Ricardo Pinto da Rocha (<named-content content-type="dwc:institutional_code">MZUSP</named-content>) and Dr. Adriano Brilhante Kury (<named-content content-type="dwc:institutional_code">MNRJ</named-content>) for the loaning of the specimens used in the study. Dr. Adriano Brilhante Kury (<named-content content-type="dwc:institutional_code">MNRJ</named-content>) is also thanked for the valuable comments and suggestions in the manuscript. The PPBio semiarid project for the opportunity and funding to collect the described specimens. The OmniPaper Project for the huge database of readily available taxonomic publications for the order <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="order">Opiliones</tp:taxon-name-part></tp:taxon-name>. For the financial support, MBD and MRH thanks the Fundação de Amparo à Pesquisa do Estado de São Paulo – FAPESP (Process 2013/50297-0), the National Science Foundation (NSF/DOB 1343578) and NASA. MRH thanks the Fundação de Amparo à Pesquisa do Estado de São Paulo – FAPESP (Process 2018/07193-2). MBS thanks the Conselho Nacional de Desenvolvimento Científico e Tecnológico (Edital MCT/CNPq nº 35/2012 – PPBio/Geoma – Redes de Pesquisa, Monitoramento e Modelagem em Biodiversidade e Ecossistemas. Parte I – PPBio) and the Programa de Pesquisas em Biodiversidade do Semiárido (PPBio – Nº: 558317/2009-0 and 457471/2012-3). NEVS thanks Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) for the master fellowship.</p>
    </ack>
    <ref-list>
      <title>7. References</title>
      <ref id="B1">
        <mixed-citation xlink:type="simple"><person-group><name name-style="western"><surname>Acosta</surname><given-names>LE</given-names></name></person-group> (<year>1999</year>) <article-title>The identity of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus">Pachyloides</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species">tucumanus</tp:taxon-name-part></tp:taxon-name></italic> n. comb. (ex <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus">Bosqia</tp:taxon-name-part></tp:taxon-name></italic>), with a proposal of generic synonymy and the new name <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus">Pachyloides</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species">yungarum</tp:taxon-name-part></tp:taxon-name></italic> (<tp:taxon-name><tp:taxon-name-part taxon-name-part-type="order">Opiliones</tp:taxon-name-part></tp:taxon-name>, <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="family">Gonyleptidae</tp:taxon-name-part></tp:taxon-name>, <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily">Pachylinae</tp:taxon-name-part></tp:taxon-name>).</article-title><source>The Journal of Arachnology</source><volume>27</volume>(<issue>2</issue>): <fpage>458</fpage>–<lpage>464</lpage>.</mixed-citation>
      </ref>
      <ref id="B2">
        <mixed-citation xlink:type="simple"><person-group><name name-style="western"><surname>Acosta</surname><given-names>LE</given-names></name></person-group> (<year>2001</year>) <article-title>The identity of <italic><tp:taxon-name><tp:taxon-name-part taxon-name-part-type="genus">Acrographinotus</tp:taxon-name-part> <tp:taxon-name-part taxon-name-part-type="species">erectispina</tp:taxon-name-part></tp:taxon-name></italic>, with a review of the generic diagnosis, and the description of a new species (<tp:taxon-name><tp:taxon-name-part taxon-name-part-type="order">Opiliones</tp:taxon-name-part></tp:taxon-name>, <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="family">Gonyleptidae</tp:taxon-name-part></tp:taxon-name>, <tp:taxon-name><tp:taxon-name-part taxon-name-part-type="subfamily">Pachylinae</tp:taxon-name-part></tp:taxon-name>).</article-title><source>Bulletin of the British Arachnological Society</source><volume>12</volume>(<issue>2</issue>): <fpage>58</fpage>–<lpage>66</lpage>.</mixed-citation>
      </ref>
      <ref id="B3">
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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.79.e66321.suppl1</object-id>
        <object-id content-type="arpha">2D846B32-3926-5BAD-AFD2-1B2EE44D9D42</object-id>
        <label>Supplementary material 1</label>
        <caption>
          <p>Character matrix</p>
        </caption>
        <statement content-type="dataType">
          <label>Data type</label>
          <p><bold/>: .pdf</p>
        </statement>
        <statement content-type="notes">
          <label>Explanation note</label>
          <p><bold/>: Character matrix.</p>
        </statement>
        <media xlink:href="arthropod-systematics-79-485-s001.pdf" mimetype="application" mime-subtype="pdf" position="float" orientation="portrait" xlink:type="simple" id="oo_596987.pdf">
          <uri content-type="original_file">https://binary.pensoft.net/file/596987</uri>
        </media>
        <permissions>
          <license xlink:type="simple">
            <license-p>This dataset is made available under the Open Database License (http://opendatacommons.org/licenses/odbl/1.0). 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">Saraiva et al. (2021)</attrib>
      </supplementary-material>
    </sec>
  </back>
</article>
