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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">EGEOL</journal-id>
<journal-title-group>
<journal-title>Estudios Geol&#x00F3;gicos</journal-title>
<abbrev-journal-title>Estud. Geol.</abbrev-journal-title>
</journal-title-group>
<issn pub-type="epub">0367-0449</issn>
<publisher>
<publisher-name>Consejo Superior de Investigaciones Cientificas</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="publisher-id">EG201909</article-id>
<article-id pub-id-type="doi">10.3989/egeol.43586.549</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Articles</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Palaeontological analyses across the Ediacaran-Cambrian boundary, Upper Corumb&#x00E1; Group, Brazil</article-title>
<trans-title-group xml:lang="es">
<trans-title>An&#x00E1;lisis paleontol&#x00F3;gicos a trav&#x00E9;s l&#x00ED;mite Ediac&#x00E1;rico-C&#x00E1;mbrico, Grupo Alto Corumb&#x00E1;, Brasil</trans-title>
</trans-title-group>
<alt-title alt-title-type="running-head">Palaeontological analyses across the Ediacaran-Cambrian boundary, Upper Corumb&#x00E1; Group, Brazil</alt-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Ad&#x00F4;rno</surname>
<given-names>R.R.</given-names>
</name>
<xref ref-type="aff" rid="aff0001">1</xref>
<xref ref-type="aff" rid="aff0002">2</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Walde</surname>
<given-names>D.H.G.</given-names>
</name>
<xref ref-type="aff" rid="aff0001">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Do Carmo</surname>
<given-names>D.A.</given-names>
</name>
<xref ref-type="aff" rid="aff0001">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Denezine</surname>
<given-names>M.</given-names>
</name>
<xref ref-type="aff" rid="aff0001">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Cortijo</surname>
<given-names>I.</given-names>
</name>
<xref ref-type="aff" rid="aff0007">7</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Sanchez</surname>
<given-names>E.A.M.</given-names>
</name>
<xref ref-type="aff" rid="aff0003">3</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Tobias</surname>
<given-names>T.C.</given-names>
</name>
<xref ref-type="aff" rid="aff0001">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Fazio</surname>
<given-names>G.</given-names>
</name>
<xref ref-type="aff" rid="aff0001">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Warren</surname>
<given-names> L.V.</given-names>
</name>
<xref ref-type="aff" rid="aff0005">5</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Erdtmann</surname>
<given-names> B.D.</given-names>
</name>
<xref ref-type="aff" rid="aff0006">6</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Cai</surname>
<given-names>Y.</given-names>
</name>
<xref ref-type="aff" rid="aff0008">8</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Giorgioni</surname>
<given-names>M.</given-names>
</name>
<xref ref-type="aff" rid="aff0001">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Ramos</surname>
<given-names>M.E.A.F.</given-names>
</name>
<xref ref-type="aff" rid="aff0001">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Baptista</surname>
<given-names>M.C.</given-names>
</name>
<xref ref-type="aff" rid="aff0001">1</xref>
<xref ref-type="aff" rid="aff0002">2</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Guimar&#x00E3;es</surname>
<given-names>E.M.</given-names>
</name>
<xref ref-type="aff" rid="aff0001">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Figueiredo</surname>
<given-names>M.F.</given-names>
</name>
<xref ref-type="aff" rid="aff0004">4</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Germs</surname>
<given-names>G.J.</given-names>
</name>
<xref ref-type="aff" rid="aff0009">9</xref>
</contrib>
</contrib-group>
<aff id="aff0001">
<label>1</label>University of Bras&#x00ED;lia, Institute of Geosciences, Campus Darcy Ribeiro, 70.910-900 Bras&#x00ED;lia DF, Brazil. Email: <email xlink:href="rodrigo.adorno@cprm.gov.br">rodrigo.adorno@cprm.gov.br</email>; ORCID ID: <ext-link ext-link-type="uri" xlink:href="https://orcid.org/0000-0003-1781-0694">https://orcid.org/0000-0003-1781-0694</ext-link>, <ext-link ext-link-type="uri" xlink:href="http://orcid.org/0000-0001-5324-5480">http://orcid.org/0000-0001-5324-5480</ext-link>, <ext-link ext-link-type="uri" xlink:href="http://orcid.org/0000-0002-1613-7242">http://orcid.org/0000-0002-1613-7242</ext-link>, <ext-link ext-link-type="uri" xlink:href="http://orcid.org/0000-0003-4629-0907">http://orcid.org/0000-0003-4629-0907</ext-link>, <ext-link ext-link-type="uri" xlink:href="http://orcid.org/0000-0001-6290-1910">http://orcid.org/0000-0001-6290-1910</ext-link>, <ext-link ext-link-type="uri" xlink:href="http://orcid.org/0000-0003-3325-5096">http://orcid.org/0000-0003-3325-5096</ext-link>, <ext-link ext-link-type="uri" xlink:href="http://orcid.org/0000-0003-0565-3150">http://orcid.org/0000-0003-0565-3150</ext-link> , <ext-link ext-link-type="uri" xlink:href="http://orcid.org/0000-0002-1741-3210">http://orcid.org/0000-0002-1741-3210</ext-link>, <ext-link ext-link-type="uri" xlink:href="http://orcid.org/0000-0002-1178-5208">http://orcid.org/0000-0002-1178-5208</ext-link>, <ext-link ext-link-type="uri" xlink:href="http://orcid.org/0000-0002-2383-3254">http://orcid.org/0000-0002-2383-3254</ext-link>
</aff>
<aff id="aff0002">
<label>2</label>Geological Survey of Brazil - Center for Technological Development-CEDES, Setor Banc&#x00E1;rio Norte, 70040-904 Bras&#x00ED;lia, DF, Brazil</aff>
<aff id="aff0003">
<label>3</label>Centro de Estudos em Geoci&#x00EA;ncias, Instituto de Ci&#x00EA;ncia e Tecnologia, Universidade Federal dos Vales do Jequitinhonha e Mucuri, 39100-000 Diamantina, Brazil. ORCID ID: <ext-link ext-link-type="uri" xlink:href="https://orcid.org/0000-0002-1136-733X">https://orcid.org/0000-0002-1136-733X</ext-link>
</aff>
<aff id="aff0004">
<label>4</label>PETROBRAS-CENPES-PDGEO/BPA, Avenida Hor&#x00E1;cio Macedo, 950, 21.940-900 Rio de Janeiro, Brazil. ORCID ID: <ext-link ext-link-type="uri" xlink:href="http://orcid.org/0000-0002-7778-6190">http://orcid.org/0000-0002-7778-6190</ext-link>
</aff>
<aff id="aff0005">
<label>5</label>Departamento de Geologia Aplicada, Instituto de Geoci&#x00EA;ncias e Ci&#x00EA;ncias Exatas, Universidade Estadual Paulista, Avenida 24A, 1515, 13506-900 Rio Claro, Brazil. <ext-link ext-link-type="uri" xlink:href="http://orcid.org/0000-0002-2050-6514">http://orcid.org/0000-0002-2050-6514</ext-link></aff>
<aff id="aff0006">
<label>6</label>Freie Universit&#x00E4;t Berlin (FUB). Kaiserswerther Street 16-18, 14195 Berlin. Germany. <ext-link ext-link-type="uri" xlink:href="http://orcid.org/0000-0002-2383-3254">http://orcid.org/0000-0002-2383-3254</ext-link></aff>
<aff id="aff0007">
<label>7</label>&#x00C1;rea de Paleontolog&#x00ED;a, Facultad de Ciencias, Universidad de Extremadura, Avenida de Elvas s/n, 06071 Badajoz, Spain. <ext-link ext-link-type="uri" xlink:href="http://orcid.org/0000-0002-6027-9002">http://orcid.org/0000-0002-6027-9002</ext-link></aff>
<aff id="aff0008">
<label>8</label>State Key Laboratory of Continental Dynamics, Department of Geology, Northwest University, 710069 Xian, China. <ext-link ext-link-type="uri" xlink:href="http://orcid.org/0000-0002-9867-8156">http://orcid.org/0000-0002-9867-8156</ext-link>
</aff>
<aff id="aff0009">
<label>9</label>Department of Geology, University of the Free State, Bloemfontein, South Africa. <ext-link ext-link-type="uri" xlink:href="http://orcid.org/0000-0003-3622-0788">http://orcid.org/0000-0003-3622-0788</ext-link>
</aff>
<pub-date pub-type="epub">
<day>31</day>
<month>12</month>
<year>2019</year>
</pub-date>
<pub-date pub-type="collection">
<year>2019</year>
</pub-date>
<volume>75</volume>
<issue>2</issue>
<elocation-id>10.3989/egeol.43586.549</elocation-id>
<history>
<date date-type="received">
<day>01</day>
<month>05</month>
<year>2019</year>
</date>
<date date-type="accepted">
<day>01</day>
<month>07</month>
<year>2019</year>
</date>
<date date-type="Publicado on-line">
<day>12</day>
<month>11</month>
<year>2019</year>
</date>
</history>
<permissions>
<copyright-statement>&#x00A9; 2019 CSIC</copyright-statement>
<copyright-year>2019</copyright-year>
<license license-type="open-access" xlink:href="https://creativecommons.org/licenses/by/4.0/">
<license-p>This is an open-access article distributed under the terms of the Creative Commons Attribution-Non 4.0 International License</license-p>
</license>
</permissions>
<abstract>
<title>ABSTRACT</title>
<p>This work presents the results of a palaeontological analysis focused on twenty-six species sampled in five sections of the Tamengo and Guaicurus formations, Corumb&#x00E1; and Lad&#x00E1;rio regions: Corcal and Laginha quarries, Porto Sobramil, Porto Figueiras and Ecoparque Cacimba. Besides, palaeoecological and palaeoenvironmental inferences are presented based on the occurrence of this fossil assemblage. <italic>Cloudina carinata</italic> Cortijo <italic>et al</italic>., 2010, previously documented in Spain and Siberia, presents an unprecedented occurrence in the American continent, in siltstones of the Tamengo Formation at Porto Figueiras section, Municipality of Corumb&#x00E1;, Mato Grosso do Sul State, Brazil. The biota of the Tamengo Formation is updated and composed of three biomineralizing metazoans, including poriferan spicules, putative sponge gemmule, and a sessile epibiontic prokaryotic colony. The present work also deals with the taxonomy and stratigraphic distribution of four ichnospecies and three vendotaenid species that integrate the updated benthic fauna for the upper portion of Corumb&#x00E1; Group. The species diversity of the Tamengo Formation was complemented by the occurrence of sixteen microfossil species that possibly represent a marine planktic assemblage. A dramatic change was identified in the palaeoenvironmental conditions of the Tamengo to Guaicurus formations, followed by a mass extinction event, possibly linked to the global Ediacaran-Cambrian mass extinction. In addition, organic-walled microfossils were prepared and analyzed from sections of three countries: nine species from the Nomtsas Formation, Namibia; four species from the Tagatiya Guazu Formation, Paraguay; and six species from the Dengying Formation, China. An international biostratigraphic essay consisting of six biozones is proposed for the uppermost Ediacaran and one biozone for the earliest Cambrian.</p>
</abstract>
<trans-abstract xml:lang="es">
<title>RESUMEN</title>
<p>Se presenta en este trabajo el an&#x00E1;lisis paleontol&#x00F3;gico de 26 especies f&#x00F3;siles muestradas en cinco cortes de las Formaciones de Tamengo y Guaicurus en las regines de Corumb&#x00E1; y Lad&#x00E1;rio: canteras de Corcal y Laginha, Porto Sobramil, Porto Figueiras y Ecoparque Cacimba. Adem&#x00E1;s, se a&#x00F1;aden varias interpretaciones paleoecol&#x00F3;gicas y ambientales, basadas en el registro f&#x00F3;sil. <italic>Cloudina carinata</italic> Cortijo <italic>et al</italic>., 2010, previamente citada en Espa&#x00F1;a y Siberia, aparece por primera vez en el continente Americano, concretamente en limolitas de la Formaci&#x00F3;n Tamengo en el corte de Porto Figueiras, Corumb&#x00E1;, Estado de Mato Grosso do Sul, Brasil. La biota de la Formaci&#x00F3;n Tamengo incluye tres metazoos mineralizados, que incluyen esp&#x00ED;culas de por&#x00ED;feros, posibles g&#x00E9;mulas de esponjas y una colonia s&#x00E9;sil de procaiotas epibent&#x00F3;nicos. Este trabajo se centra en la taxonom&#x00ED;a y distribuci&#x00F3;n estratigr&#x00E1;fica de cuatro icnoespecies y tres especies de vendot&#x00E9;nidos que forman la fauna bent&#x00F3;nica de la parte superior del Grupo de Corumb&#x00E1;. La biodiversidad de la Formaci&#x00F3;n Tamengo ha sido completada con el registro de 16 especies microf&#x00F3;siles que representan posiblemente una asociaci&#x00F3;n plant&#x00F3;nica marina. Se ha identificado un cambio dr&#x00E1;stico en las condiciones ambientales de las Formaciones Tamengo y Guaicurus, que culminan en un evento de extincin&#x00F3;n masiva posiblemente relacionado con la extincici&#x00F3;n en masa que marca el tr&#x00E1;nsito global Edi&#x00E1;carico-C&#x00E1;mbrico. Por otro lado, se han extra&#x00ED;do microf&#x00F3;siles de pared org&#x00E1;nica de varios afloramientos: nueve especies de la Formaci&#x00F3;n de Nomtsas (Namibia), cuatro de la Formaci&#x00F3;n Tagatiya Guazu (Paraguay) y seis de la Formaci&#x00F3;n Dengying (China). Se propone un marco bioestratigr&#x00E1;fico para el Ediac&#x00E1;rico terminal que incluye seis biozonas y una biozona para el C&#x00E1;mbrico basal.</p>
</trans-abstract>
<kwd-group xml:lang="en">
<title>Keywords</title>
<kwd>Ediacaran-Cambrian</kwd>
<kwd>Corumb&#x00E1; Group</kwd>
<kwd>Biostratigraphy</kwd>
<kwd>Micropaleontology</kwd>
</kwd-group>
<kwd-group xml:lang="es">
<title>Palabras clave</title>
<kwd>Ediac&#x00E1;rico-C&#x00E1;mbrico</kwd>
<kwd>Grupo de Corumb&#x00E1;</kwd>
<kwd>Bioestratigraf&#x00ED;a</kwd>
<kwd>Micropaleontolog&#x00ED;a</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<sec id="sec1" sec-type="intro">
<title>Introduction</title>
<p>The aim of this work is to present an analysis on the taxonomy and stratigraphic distribution of some selected species of the Tamengo and Guaicurus formations, Ediacaran-Cambrian boundary interval in Brazil, in order to propose a chronobiostratigraphic framework for the Ediacaran-Cambrian transition. In addition, palaeoecological and palaeoenvironmental inferences are presented as well as a lithostratigraphic update of the sections in Corumb&#x00E1; and Lad&#x00E1;rio regions, Mato Grosso do Sul State, Brazil. Considering the scarcity of micropalaeontological data from uppermost Ediacaran sections, samples from three additional localities were prepared and analyzed from the Nomtsas Formation (Namibia), the Tagatiya Guazu Formation (Paraguay) and the Dengying Formation (China). Finally, another objective of this work is to compare the results obtained from the palaeontological analysis of the Tamengo Formation with those already published from uppermost Ediacaran sections, especially in Paraguay, Uruguay, Argentina, Namibia, China, Russia, Canada, United States and Oman.</p>
</sec>
<sec id="sec2" sec-type="result">
<title>Results</title>
<p>Twenty-six species integrate the study fossil assemblage of the Tamengo and Guaicurus formations. They were clustered into six categories: biomineralizing metazoans, biomineralizing microfossils, vendotaenids, ichnofossils, organic-permineralized microfossils and organic-walled microfossils.</p>
<p>The studied fossil assemblage of the Tamengo Formation consists of twenty-three species, four of which represent benthic and sessile, biomineralizing epibionts: <italic>Cloudina lucianoi</italic> (Beurlen &#x0026; Sommer, <xref ref-type="bibr" rid="cit0004">1957</xref>), <italic>C. carinata</italic> Cortijo et al., <xref ref-type="bibr" rid="cit0005">2010</xref>, <italic>Corumbella werneri</italic> Hahn et al., <xref ref-type="bibr" rid="cit0011">1982</xref> and indeterminate sponge remains. Three ichnospecies represent activity of vagile organisms of benthic habit: <italic>Multina minima</italic> Uchman, <xref ref-type="bibr" rid="cit0023">2001</xref>, <italic>Gordia marina</italic> Emmons, <xref ref-type="bibr" rid="cit0008">1844</xref> and <italic>Pilichnus</italic> cf. <italic>P. dichotomus</italic> Uchman, <xref ref-type="bibr" rid="cit0022">1999</xref>. <italic>Multina minima</italic> points to an endobiot organism, while <italic>Gordia marina</italic> and <italic>Pilichnus</italic> cf. <italic>P. dichotomus</italic> represent epibiont vagile explorers on the water-sediment interface. Additionally, sixteen species probably derived from planktic organism, fifteen of which are small organic-walled sphaeromorph microfossils that possibly represent the marine plankton: <italic>Arctacellularia januarensis</italic> Denezine, <xref ref-type="bibr" rid="cit0006">2018</xref> <italic>nomem nudum, Leiosphaeridia ternata</italic> (Timofeev, <xref ref-type="bibr" rid="cit0020">1966</xref>)<italic>, L. crassa</italic> (Naumova, <xref ref-type="bibr" rid="cit0015">1949</xref>)<italic>, L. jacutica</italic> (Timofeev, <xref ref-type="bibr" rid="cit0020">1966</xref>)<italic>, L. minutissima</italic> (Naumova, <xref ref-type="bibr" rid="cit0015">1949</xref>)<italic>, L. tenuissima</italic> Eisenack, <xref ref-type="bibr" rid="cit0007">1958</xref>
<italic>, L. obsuleta</italic> (Naumova, <xref ref-type="bibr" rid="cit0015">1949</xref>)<italic>, Bavlinella faveolata</italic> Vidal, <xref ref-type="bibr" rid="cit0024">1976</xref>
<italic>, Bambuites erichsenii</italic> Sommer, <xref ref-type="bibr" rid="cit0019">1971</xref>, <italic>Synsphaeridium</italic> sp.<italic>, Jacutianema</italic> sp.<italic>, Lophosphaeridium</italic> sp.<italic>, Ostiama microcystis</italic> Hermann (in Timofeev et al., <xref ref-type="bibr" rid="cit0021">1976</xref>)<italic>, Navifusa</italic> sp., gen. et sp. 1 and one species of permineralized microfossils, <italic>Chuaria circularis</italic> Walcott, <xref ref-type="bibr" rid="cit0025">1899</xref>. The sessile epibiont prokaryotic-colony <italic>Vendotaenia antiqua</italic> was previously reported from the Cerradinho and Bocaina formations (Zaine, <xref ref-type="bibr" rid="cit0031">1991</xref>), and herein the occurrence is confirmed from the Tamengo Formation.</p>
<p>Four species represent the benthic fossil assemblage for Guaicurus Formation: <italic>Eoholynia corumbensis</italic> Gaucher et al., <xref ref-type="bibr" rid="cit0009">2005</xref>, <italic>Tawuia dalensis</italic> Hofmann (in Hofmann &#x0026; Aitken, <xref ref-type="bibr" rid="cit0012">1979</xref>), <italic>Multina minima</italic> and <italic>Didymaulichnus lyelli</italic> (Rouault, <xref ref-type="bibr" rid="cit0017">1850</xref>). From the total, three species have occurrences restricted to this formation: <italic>Eoholynia corumbensis</italic>, <italic>Tawuia dalensis</italic> Hofmann (in Hofmann &#x0026; Aitken, <xref ref-type="bibr" rid="cit0012">1979</xref>) and <italic>Didymaulichnus lyelli</italic>; only <italic>Multina minima</italic> also occurs in the Tamengo Formation. It is noticeable that the Tamengo Formation exhibits the greatest biodiversity.</p>
<p>The integration of the information regarding the taxonomy and stratigraphic distribution of the above-reported species was presented as a biostratigraphic essay composed of seven biozones, respectively named, from base to top: <italic>Cloudina</italic> Assemblage Superzone that is distributed in all 15 analyzed sections. There are three biozones inserted in this superzone distributed in sections of Brazil and Paraguay: <italic>Cloudina lucianoi/Corumbella werneri</italic> Interval Zone; <italic>Corumbella werneri</italic> Range Zone; and <italic>Corumbellla werneri/Cloudina lucianoi</italic> Interval Zone (Ad&#x00F4;rno et al., <xref ref-type="bibr" rid="cit0002">2016</xref>, <xref ref-type="bibr" rid="cit0003">2017</xref>). It was possible to propose two subzones: <italic>Bavlinella faveolata - Leiosphaeridia minutissima</italic> Assemblage Subzone inserted in the basal part of <italic>Corumbella werneri</italic> Range Zone and <italic>Vendotaenia antiqua-Cloudina lucianoi</italic> Concurrent-Range Subzone at the upper portion of the <italic>Corumbella werneri/Cloudina lucianoi</italic> Interval Zone. The first subzone spans across Brazil, Argentina, Uruguay, Namibia and China; the second across Brazil, Namibia, China and Siberia. Finally, <italic>Eoholynia corumbensis</italic> Range Zone was proposed for the base of the Guaicurus Formation at Laginha quarry, lowermost Cambrian. The geographic distribution of this biozone is restricted to Laginha quarry locality so far (<xref ref-type="fig" rid="f0001">Fig. 1</xref>).</p>
<fig id="f0001">
<label>Fig. 1</label>
<caption>
<p>Biostratigraphic proposal based on the stratigraphic distribution of the species from the Tamengo Formation; palaeontological informations from the selected sections out of Brazil (Zang &#x0026; Walter, <xref ref-type="bibr" rid="cit0032">1992</xref>; Hagadorn &#x0026; Waggoner, <xref ref-type="bibr" rid="cit0010">2000</xref>; Hofmann &#x0026; Mountjoy, <xref ref-type="bibr" rid="cit0013">2001</xref>; Amthor et al., 2003; Gaucher et al., <xref ref-type="bibr" rid="cit0009">2005</xref>; Kontorovich et al., <xref ref-type="bibr" rid="cit0014">2009</xref>; Warren et al., <xref ref-type="bibr" rid="cit0026">2011</xref>, 2012, <xref ref-type="bibr" rid="cit0027">2013</xref>, <xref ref-type="bibr" rid="cit0029">2017</xref>, <xref ref-type="bibr" rid="cit0030">2019</xref>; Smith et al., <xref ref-type="bibr" rid="cit0018">2017</xref>; Ad&#x00F4;rno <xref ref-type="bibr" rid="cit0001">2019</xref>); data from Corcal quarry after Parry et al. (<xref ref-type="bibr" rid="cit0016">2017</xref>).</p>
</caption>
<graphic xlink:href="EG201909-94-g001.tif" xmlns:xlink="http://www.w3.org/1999/xlink"/>
</fig>
</sec>
<sec id="sec3" sec-type="conclusions">
<title>Conclusions</title>
<p>Twenty-six species were studied from the Tamengo and Guaicurus formations, twenty-three of which represent benthic biomineralizing epibionts of sessile habit: <italic>Cloudina lucianoi</italic>, <italic>C. carinata</italic>, <italic>Corumbella werneri</italic> and an indeterminate species of porifera. <italic>Vendotaenia antiqua</italic> represents a sessile epibiont prokaryotic-colony. Three ichnospecies represent activity of vagile organisms: <italic>Multina minima</italic>, <italic>Gordia marina</italic> and <italic>Pilichnus</italic> cf. <italic>P. dichotomus</italic>. <italic>Multina minima</italic> represents endobiot organisms while <italic>Gordia marina</italic> and <italic>Pilichnus</italic> cf. <italic>P. dichotomus</italic> represent epibiont vagile explorers on the water-sediment interface. Additionally, sixteen species probably derived from planktic organisms, such as <italic>Arctacellularia januarensis nomem nudum, Leiosphaeridia ternata, L. crassa, L. jacutica, L. minutissima, L. tenuissima, L. obsuleta, Bavlinella faveolata, Bambuites erichsenii</italic> , <italic>Synsphaeridium</italic> sp.<italic>, Jacutianema</italic> sp.<italic>, Lophosphaeridium</italic> sp.<italic>, Ostiama microcystis, Navifusa</italic> sp., gen. 1 sp. 1 and one species of organic-permineralized microfossils, <italic>Chuaria circularis</italic>.</p>
<p>Four species represent a benthic fossil assemblage for the Guaicurus Formation: <italic>Eoholynia corumbensis</italic>, <italic>Tawuia dalensis</italic>, <italic>Multina minima</italic> and <italic>Didymaulichnus lyelli</italic>. From the total, three species have occurrences restricted to this formation, and only <italic>Multina minima</italic> shows occurrences in the Tamengo Formation.</p>
<p>Seven biozones were proposed, from bottom to top: <italic>Cloudina</italic> Assemblage Superzone that is distributed in all 15 analyzed sections in Brazil, Paraguay, Uruguay, Argentina, United States, Canada, Namibia, Oman, Russia and China. Inserted in this superzone, there are three biozones, distributed in sections of Brazil and Paraguay: <italic>Cloudina lucianoi/Corumbella werneri</italic> Interval Zone; <italic>Corumbella werneri</italic> Range Zone; <italic>Corumbellla werneri/Cloudina lucianoi</italic> Interval Zone. It was possible to propose two subzones: <italic>Bavlinella faveolata - Leiosphaeridia minutissima</italic> Assemblage Subzone inserted in the base of <italic>Corumbella werneri</italic> Range Zone and <italic>Vendotaenia antiqua-Cloudina lucianoi</italic> Concurrent-Range Subzone at the upper portion of the <italic>Corumbella werneri/Cloudina lucianoi</italic> Interval Zone. The first subzone spam across Brazil, Argentina, Uruguay, Namibia and China, the second across Brazil, Namibia, China and Siberia. Finally, <italic>Eoholynia corumbensis</italic> Range Zone was proposed at the base of Guaicurus Formation at Laginha quarry, lowermost Cambrian. The geographic distribution of this biozone is restricted to Laginha quarry locality so far.</p>
</sec>
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