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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">EG201903</article-id>
<article-id pub-id-type="doi">10.3989/egeol.43417.514</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Articles</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Evoluci&#x00F3;n paleoambiental de una turbera finiholocena en el sector suroccidental del Parque Nacional de Do&#x00F1;ana (S.O. Espa&#x00F1;a)</article-title>
<trans-title-group xml:lang="en">
<trans-title>Palaeoenviromental evolution of a Late Holocene peat bog in the southwestern sector of the Do&#x00F1;ana National Park (SW Spain)</trans-title>
</trans-title-group>
<alt-title alt-title-type="running-head">Evoluci&#x00F3;n paleoambiental de una turbera finiholocena en el sector suroccidental del Parque Nacional de Do&#x00F1;ana (S.O. Espa&#x00F1;a)</alt-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Abad</surname>
<given-names>M.</given-names>
</name>
<xref ref-type="aff" rid="aff0001">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Mu&#x00F1;oz</surname>
<given-names>A.F.</given-names>
</name>
<xref ref-type="aff" rid="aff0002">2</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Gonz&#x00E1;lez-Regalado</surname>
<given-names>M.L.</given-names>
</name>
<xref ref-type="aff" rid="aff0003">3</xref>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Ruiz</surname>
<given-names>F.</given-names>
</name>
<xref ref-type="aff" rid="aff0003">3</xref>
<xref ref-type="aff" rid="aff0004">4</xref>
<xref ref-type="aff" rid="aff0007">7</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Rodr&#x00ED;guez-Vidal</surname>
<given-names>J.</given-names>
</name>
<xref ref-type="aff" rid="aff0003">3</xref>
<xref ref-type="aff" rid="aff0007">7</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>C&#x00E1;ceres</surname>
<given-names>L.M.</given-names>
</name>
<xref ref-type="aff" rid="aff0003">3</xref>
<xref ref-type="aff" rid="aff0007">7</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Carretero</surname>
<given-names>M.I.</given-names>
</name>
<xref ref-type="aff" rid="aff0005">5</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Monge</surname>
<given-names>G.</given-names>
</name>
<xref ref-type="aff" rid="aff0005">5</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Pozo</surname>
<given-names>M.</given-names>
</name>
<xref ref-type="aff" rid="aff0006">6</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Prudencio</surname>
<given-names>M.I.</given-names>
</name>
<xref ref-type="aff" rid="aff0004">4</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Dias</surname>
<given-names>M.I.</given-names>
</name>
<xref ref-type="aff" rid="aff0004">4</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Marques</surname>
<given-names>R.</given-names>
</name>
<xref ref-type="aff" rid="aff0004">4</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Izquierdo</surname>
<given-names>T.</given-names>
</name>
<xref ref-type="aff" rid="aff0001">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Tosquella</surname>
<given-names>J.</given-names>
</name>
<xref ref-type="aff" rid="aff0003">3</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Romero</surname>
<given-names>V.</given-names>
</name>
<xref ref-type="aff" rid="aff0003">3</xref>
</contrib>
</contrib-group>
<aff id="aff0001"><label>1</label>Universidad de Atacama. Avda. Copayapu 485, Copiap&#x00F3;, Chile. ORCID ID: <ext-link ext-link-type="uri" xlink:href="http://orcid.org/0000-0003-1930-2650">http://orcid.org/0000-0003-1930-2650</ext-link></aff>
<aff id="aff0002"><label>2</label>Departamento de Ciencias Integradas, Universidad de Huelva, Avda. Tres de Marzo, s/n, 21071-Huelva, Espa&#x00F1;a. ORCID ID: <ext-link ext-link-type="uri" xlink:href="http://orcid.org/0000-0002-1647-357X">http://orcid.org/0000-0002-1647-357X</ext-link></aff>
<aff id="aff0003"><label>3</label>Departamento de Ciencias de la Tierra., Universidad de Huelva, Avda. Tres de Marzo, s/n, 21071-Huelva, Espa&#x00F1;a. Email: <email xlink:href="ruizmu@dgyp.uhu.es">ruizmu@dgyp.uhu.es</email>, ORCID ID: <ext-link ext-link-type="uri" xlink:href="http://orcid.org/0000-0002-2626-9142">http://orcid.org/0000-0002-2626-9142</ext-link>, ORCID ID: <ext-link ext-link-type="uri" xlink:href="http://orcid.org/0000-0002-7110-3133">http://orcid.org/0000-0002-7110-3133</ext-link>; ORCID ID: <ext-link ext-link-type="uri" xlink:href="http://orcid.org/0000-0002-9475-3307">http://orcid.org/0000-0002-9475-3307</ext-link>, ORCID ID: <ext-link ext-link-type="uri" xlink:href="https://orcid.org/0000-0002-1381-2476">https://orcid.org/0000-0002-1381-2476</ext-link>, ORCID ID: <ext-link ext-link-type="uri" xlink:href="http://orcid.org/0000-0001-7951-0561">http://orcid.org/0000-0001-7951-0561</ext-link>, ORCID ID: <ext-link ext-link-type="uri" xlink:href="https://orcid.org/0000-0002-6879-0243">https://orcid.org/0000-0002-6879-0243</ext-link></aff>
<aff id="aff0004"><label>4</label>C2TN, Instituto Superior T&#x00E9;cnico, Universidad de Lisboa, 2695-066-Bobadela, Portugal. ORCID ID: <ext-link ext-link-type="uri" xlink:href="https://orcid.org/0000-0003-2311-1806">https://orcid.org/0000-0003-2311-1806</ext-link>, ORCID ID: <ext-link ext-link-type="uri" xlink:href="http://orcid.org/0000-0002-7033-0502">http://orcid.org/0000-0002-7033-0502</ext-link>, <ext-link ext-link-type="uri" xlink:href="https://orcid.org/0000-0001-6239-5456">https://orcid.org/0000-0001-6239-5456</ext-link></aff>
<aff id="aff0005"><label>5</label>Departamento de Cristalograf&#x00ED;a, Mineralog&#x00ED;a y Qu&#x00ED;mica Agr&#x00ED;cola, Universidad de Sevilla, C/ Profesor Garc&#x00ED;a Gonz&#x00E1;lez, 1, 41012-Sevilla, Espa&#x00F1;a. ORCID ID: <ext-link ext-link-type="uri" xlink:href="https://orcid.org/0000-0002-7277-0851">https://orcid.org/0000-0002-7277-0851</ext-link>. ORCID ID: <ext-link ext-link-type="uri" xlink:href="https://orcid.org/0000-0002-3171-3439">https://orcid.org/0000-0002-3171-3439</ext-link></aff>
<aff id="aff0006"><label>6</label>Departamento de Geolog&#x00ED;a y Geoqu&#x00ED;mica, Universidad Aut&#x00F3;noma de Madrid, 28049-Madrid, Espa&#x00F1;a. ORCID ID: <ext-link ext-link-type="uri" xlink:href="http://orcid.org/0000-0002-6706-440X">http://orcid.org/0000-0002-6706-440X</ext-link></aff>
<aff id="aff0007"><label>7</label>Centro de Investigaci&#x00F3;n en Patrimonio Hist&#x00F3;rico, Cultural y Natural (CIPHCN), Universidad de Huelva, Facultad de Humanidades, Avda. Tres de Marzo s/n, 21071-Huelva, Espa&#x00F1;a</aff>
<pub-date pub-type="epub">
<day>30</day>
<month>06</month>
<year>2019</year>
</pub-date>
<pub-date pub-type="collection">
<year>2019</year>
</pub-date>
<volume>75</volume>
<issue>1</issue>
<elocation-id>10.3989/egeol.43417.514</elocation-id>
<history>
<date date-type="received">
<day>13</day>
<month>11</month>
<year>2018</year>
</date>
<date date-type="accepted">
<day>12</day>
<month>02</month>
<year>2019</year>
</date>
<date date-type="Publicado on-line">
<day>29</day>
<month>03</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>RESUMEN</title>
<p>El an&#x00E1;lisis multidisciplinar de un perfil descubierto por las tormentas invernales en el litoral del Parque Nacional de Do&#x00F1;ana ha permitido reconstruir la evoluci&#x00F3;n de su sector occidental durante el Holoceno superior. Se han definido 3 fases que reflejan el paso desde una marisma de aguas salobres (FA-1) a una laguna de aguas dulces transformada en turbera (FA-2), para finalizar con el dep&#x00F3;sito de cordones dunares (FA-3).</p>
</abstract>
<trans-abstract xml:lang="en">
<title>ABSTRACT</title>
<p>The multidisciplinary analysis of a profile discovered by the winter storms on the coast of the Do&#x00F1;ana National Park has allowed us to reconstruct the evolution of its western sector during the Late Holocene. Three phases have been defined, which reflect the transition from a brackish water marsh (FA-1) to a freshwater lagoon transformed into peat bog (FA-2), to end with the deposit of dune systems (FA-3).</p>
</trans-abstract>
<kwd-group xml:lang="es">
<title>Palabras clave</title>
<kwd>Facies sedimentarias</kwd>
<kwd>evoluci&#x00F3;n paleogeogr&#x00E1;fica</kwd>
<kwd>Holoceno superior</kwd>
<kwd>Do&#x00F1;ana</kwd>
<kwd>S.O. Espa&#x00F1;a</kwd>
</kwd-group>
<kwd-group xml:lang="en">
<title>Keywords</title>
<kwd>Sedimentary facies</kwd>
<kwd>palaeogeographical evolution</kwd>
<kwd>Late Holocene</kwd>
<kwd>Do&#x00F1;ana</kwd>
<kwd>S.W. Spain</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<sec id="sec1" sec-type="intro">
<title>Introducci&#x00F3;n</title>
<p>En los &#x00FA;ltimos a&#x00F1;os, han proliferado los estudios sobre el registro holoceno de medios costeros, con especial atenci&#x00F3;n a la incidencia de los cambios clim&#x00E1;ticos y las fluctuaciones del nivel del mar sobre ellos (Cohen <italic>et al</italic>., <xref ref-type="bibr" rid="cit0022">2016</xref>; Fanget <italic>et al</italic>., <xref ref-type="bibr" rid="cit0025">2016</xref>; Araujo <italic>et al</italic>., <xref ref-type="bibr" rid="cit0008">2017</xref>; Chase &#x0026; Quick, <xref ref-type="bibr" rid="cit0021">2018</xref>). Sus resultados suelen basarse en el an&#x00E1;lisis pluridisciplinar de testigos continuos o secciones superficiales, que a menudo incluye la identificaci&#x00F3;n de diatomeas o polen para poder deducir su evoluci&#x00F3;n paleogeogr&#x00E1;fica y ambiental (Anderson, <xref ref-type="bibr" rid="cit0005">2000</xref>; Leventer <italic>et al</italic>., <xref ref-type="bibr" rid="cit0039">2010</xref>; Prieto <italic>et al</italic>., <xref ref-type="bibr" rid="cit0055">2017</xref>; Bl&#x00E1;zquez <italic>et al</italic>., <xref ref-type="bibr" rid="cit0012">2017</xref>; Quick <italic>et al</italic>., <xref ref-type="bibr" rid="cit0057">2018</xref>).</p>
<p>Otras investigaciones se han centrado en los eventos de alta energ&#x00ED;a (tormentas, tsunamis). Algunas de ellas inciden en sus periodicidades y duraci&#x00F3;n (Castele <italic>et al</italic>., <xref ref-type="bibr" rid="cit0019">2018</xref>; Pouzet <italic>et al</italic>., <xref ref-type="bibr" rid="cit0054">2018</xref>) en tanto que otras se centran en las evidencias geol&#x00F3;gicas asociadas (Ruiz <italic>et al</italic>., <xref ref-type="bibr" rid="cit0067">2013</xref>; Rubin <italic>et al</italic>., <xref ref-type="bibr" rid="cit0062">2017</xref>; Putra, <xref ref-type="bibr" rid="cit0056">2018</xref>) o en la producci&#x00F3;n de mapas de riesgos de las posibles zonas inundables (Aniel-Quiroga <italic>et al</italic>., <xref ref-type="bibr" rid="cit0006">2017</xref>; Arias <italic>et al</italic>., <xref ref-type="bibr" rid="cit0009">2017</xref>; Aguirre-Ayerbe <italic>et al</italic>., <xref ref-type="bibr" rid="cit0001">2018</xref>).</p>
<p>En el suroeste de la Pen&#x00ED;nsula Ib&#x00E9;rica se han intensificado estos estudios en las &#x00FA;ltimas d&#x00E9;cadas. Sus temas principales han sido la identificaci&#x00F3;n de las fases de progradaci&#x00F3;n y erosi&#x00F3;n costeras (p.e. Zazo <italic>et al</italic>., <xref ref-type="bibr" rid="cit0080">1994</xref>; Dabrio <italic>et al.</italic>, <xref ref-type="bibr" rid="cit0023">1999</xref>, <xref ref-type="bibr" rid="cit0024">2000</xref>), la evoluci&#x00F3;n paleoambiental y paleogeogr&#x00E1;fica de sus estuarios y parajes naturales (p.e. Borrego <italic>et al</italic>., <xref ref-type="bibr" rid="cit0016">1999</xref>; Ruiz <italic>et al</italic>., <xref ref-type="bibr" rid="cit0063">2004</xref>, <xref ref-type="bibr" rid="cit0064">2005a</xref>; Borja, <xref ref-type="bibr" rid="cit0014">2013</xref>) o el registro geol&#x00F3;gico de tsunamis y tormentas (p.e. Alonso <italic>et al</italic>., <xref ref-type="bibr" rid="cit0003">2004</xref>; Lario <italic>et al</italic>., <xref ref-type="bibr" rid="cit0037">2010</xref>; Rodr&#x00ED;guez Vidal <italic>et al</italic>., <xref ref-type="bibr" rid="cit0060">2011a</xref>,<xref ref-type="bibr" rid="cit0061">b</xref>; Ruiz <italic>et al</italic>., <xref ref-type="bibr" rid="cit0066">2008</xref>, <xref ref-type="bibr" rid="cit0067">2013</xref>). Algunos de ellos se han centrado en el an&#x00E1;lisis evolutivo holoceno de distintas turberas que jalonan su litoral (p.e. Men&#x00E9;ndez Amor &#x0026; Florsch&#x00FC;tz, <xref ref-type="bibr" rid="cit0047">1963</xref>; Stevenson, <xref ref-type="bibr" rid="cit0073">1985b</xref>).</p>
<p>En este trabajo, se efect&#x00FA;a un an&#x00E1;lisis granulom&#x00E9;trico, estratigr&#x00E1;fico, mineral&#x00F3;gico y paleontol&#x00F3;gico de un perfil costero situado en el sector occidental del Parque Nacional de Do&#x00F1;ana. Este estudio multidisciplinar permite efectuar una reconstrucci&#x00F3;n paleoambiental de esta zona durante el Holoceno superior.</p>
</sec>
<sec id="sec2">
<title>El Parque Nacional de Do&#x00F1;ana</title>
<sec id="sec2.1">
<title>Caracterizaci&#x00F3;n geomorfol&#x00F3;gica b&#x00E1;sica</title>
<p>El Parque Nacional de Do&#x00F1;ana (S.O. de Espa&#x00F1;a) se encuentra en la orilla occidental del estuario del r&#x00ED;o Guadalquivir, con una extensi&#x00F3;n de 54.251 ha. Constituye uno de los mayores humedales de Europa y se compone principalmente de marismas fluvio-mareales con una modesta topograf&#x00ED;a (&#x003C; 2-3 m). Estas marismas est&#x00E1;n drenadas por dos cauces principales (r&#x00ED;o Guadiamar y arroyo Madre de las Marismas) y numerosos canales finalizadores, con sus m&#x00E1;rgenes actuales ocupados por levees arcillosos y cheniers.</p>
<p>Las zonas internas del Parque est&#x00E1;n protegidas por dos flechas arenosas (Do&#x00F1;ana-La Algaida) que incluyen sistemas activos de dunas dispuestos en alineaciones estrechas (&#x003C;100 m), alargadas (1-2 km) y con alturas m&#x00E1;ximas que rondan los 30 m. En la zona interna de la flecha de Do&#x00F1;ana se observan crestas arenosas y cheniers con una direcci&#x00F3;n NE-SW dispuestos sobre las marismas y enraizadas en la propia flecha. En esta zona tambi&#x00E9;n se disponen un conjunto de lagunas costeras, con unas propiedades hidrol&#x00F3;gicas, geoqu&#x00ED;micas, mineral&#x00F3;gicas y edafol&#x00F3;gicas especiales (Recio <italic>et al.</italic>, <xref ref-type="bibr" rid="cit0058">2009</xref>). Muchas de ellas son semipermanentes, de escasa profundidad (&#x003C; 3 m), presentan bajas conductividades (&#x003C; 10 mS/cm excepto en &#x00E9;pocas de sequ&#x00ED;a) un pH levemente &#x00E1;cido a muy alcalino (5-11) y se localizan en suelos e&#x00F3;licos muy permeables (Vanney &#x0026; Menanteau, <xref ref-type="bibr" rid="cit0078">1985</xref>; Toja <italic>et al.</italic>, <xref ref-type="bibr" rid="cit0075">1991</xref>).</p>
</sec>
<sec id="sec2.2">
<title>Registro geol&#x00F3;gico holoceno</title>
<p>El registro del sector meridional del Parque Nacional de Do&#x00F1;ana ha sido analizado recientemente con mayor profundidad en base a numerosos sondeos realizados por el Instituto Geol&#x00F3;gico y Minero de Espa&#x00F1;a (Salvany &#x0026; Custodio, <xref ref-type="bibr" rid="cit0069">1995</xref>; Salvany <italic>et al</italic>., <xref ref-type="bibr" rid="cit0070">2010</xref>). De forma sint&#x00E9;tica, estos sondeos han puesto de manifiesto la presencia de un sustrato ne&#x00F3;geno compuesto por la Formaci&#x00F3;n Arenas de Huelva (Civis <italic>et al</italic>., <xref ref-type="bibr" rid="cit0020">1987</xref>) y la Formaci&#x00F3;n Arenas de Bonares (Mayoral &#x0026; Pend&#x00F3;n, <xref ref-type="bibr" rid="cit0045">1986-7</xref>), sobre las que se disponen un manto aluvial (Formaci&#x00F3;n Arenas y Gravas de Almonte; Salvany <italic>et al</italic>., <xref ref-type="bibr" rid="cit0070">2010</xref>), unidades aluviales, arenas e&#x00F3;licas (Formaci&#x00F3;n Arenas de El Abalario; Salvany <italic>et al</italic>., <xref ref-type="bibr" rid="cit0070">2010</xref>) y, localmente, flechas litorales.</p>
<p>En el sur peninsular, las barreras arenosas han evolucionado mediante una alternancia de fases de progradaci&#x00F3;n con otras de erosi&#x00F3;n o no dep&#x00F3;sito, condicionadas por variaciones clim&#x00E1;ticas (Zazo et al., <xref ref-type="bibr" rid="cit0082">2008</xref>). En este sentido, Zazo <italic>et al.</italic> (<xref ref-type="bibr" rid="cit0080">1994</xref>) han reconocido cuatro etapas de progradaci&#x00F3;n (H<sub>1</sub>: 6500-4400 cal. yr BP; H<sub>2</sub>: 4200-2550 cal. yr BP; H<sub>3</sub>: 2300-800 cal. yr. BP; H<sub>4</sub>: 500 cal. yr BP hasta la actualidad), de las cu&#x00E1;les las dos &#x00FA;ltimas est&#x00E1;n representadas en la flecha de Do&#x00F1;ana.</p>
</sec>
<sec id="sec2.3">
<title>Hidrodin&#x00E1;mica</title>
<p>Los principales procesos hidrodin&#x00E1;micos est&#x00E1;n controlados por el r&#x00E9;gimen fluvial, los aportes mareales, el oleaje dominante procedente del suroeste y las corrientes de deriva litoral, de sentido W-E. El r&#x00ED;o Guadalquivir tiene un r&#x00E9;gimen muy irregular, con una media anual de 185 m<sup>3</sup>/s y un m&#x00E1;ximo algo superior a los 1.000 m<sup>3</sup>/s (Vanney, <xref ref-type="bibr" rid="cit0077">1970</xref>; Menanteau, <xref ref-type="bibr" rid="cit0046">1979</xref>). El r&#x00E9;gimen mareal es mesomareal y semidiurno, con un rango medio mareal de 3,6 m (Borrego <italic>et al</italic>., <xref ref-type="bibr" rid="cit0015">1993</xref>).</p>
</sec>
<sec id="sec2.4">
<title>Eventos de alta energ&#x00ED;a: pasado y presente</title>
<p>La costa suratl&#x00E1;ntica de la Pen&#x00ED;nsula Ib&#x00E9;rica es un &#x00E1;rea de baja probabilidad tsunamig&#x00E9;nica (Campos, <xref ref-type="bibr" rid="cit0018">1991</xref>; Reicherter, <xref ref-type="bibr" rid="cit0059">2001</xref>), con 16 tsunamis registrados entre el 218 a.C. y 1900 (Galbis, <xref ref-type="bibr" rid="cit0029">1932</xref>). El registro geol&#x00F3;gico en las zonas costeras y cuencas oce&#x00E1;nicas pr&#x00F3;ximas ha sido objeto de numerosos trabajos en las &#x00FA;ltimas dos d&#x00E9;cadas, que han permitido conocer las formaciones sedimentarias derivadas de su acci&#x00F3;n erosiva-deposicional (p.e. Luque <italic>et al</italic>., <xref ref-type="bibr" rid="cit0041">2001</xref>, <xref ref-type="bibr" rid="cit0042">2002</xref>; Scheffers &#x0026; Kelletat, <xref ref-type="bibr" rid="cit0071">2005</xref>; Guti&#x00E9;rrez-M&#x00E1;s <italic>et al</italic>., <xref ref-type="bibr" rid="cit0034">2009</xref>; Rodr&#x00ED;guez Vidal <italic>et al</italic>., <xref ref-type="bibr" rid="cit0060">2011a</xref>,<xref ref-type="bibr" rid="cit0061">b</xref>; Guti&#x00E9;rrez-M&#x00E1;s &#x0026; M&#x00E1;s, <xref ref-type="bibr" rid="cit0033">2013</xref>; Ruiz <italic>et al</italic>., <xref ref-type="bibr" rid="cit0067">2013</xref>; Font <italic>et al</italic>., <xref ref-type="bibr" rid="cit0028">2013</xref>; Alonso <italic>et al</italic>., <xref ref-type="bibr" rid="cit0004">2015</xref>) y ampliar este registro hasta hace unos 7.000 a&#x00F1;os (Gr&#x00E0;cia <italic>et al</italic>., <xref ref-type="bibr" rid="cit0031">2010</xref>; Lario <italic>et al</italic>., <xref ref-type="bibr" rid="cit0038">2011</xref>).</p>
<p>Este litoral est&#x00E1; sujeto tambi&#x00E9;n a la acci&#x00F3;n de fuertes temporales invernales. Periodos prolongados de tormentas coinciden con fases negativas de la NAO (North Atlantic Oscillation) y la AO (Artic Oscillation) (Anfuso <italic>et al</italic>., <xref ref-type="bibr" rid="cit0007">2016</xref>). En el litoral de Do&#x00F1;ana, el estudio de series temporales de tormentas invernales ha permitido definir dos ciclos de periodicidad de estos eventos energ&#x00E9;ticos (2-3 y 6-7 a&#x00F1;os), con nueve grandes periodos de tormentas entre 1960 y 1999 (Ruiz <italic>et al.</italic>, <xref ref-type="bibr" rid="cit0065">2005b</xref>).</p>
</sec>
</sec>
<sec id="sec3" sec-type="methods">
<title>Metodolog&#x00ED;a</title>
<sec id="sec3.1">
<title>Trabajo de campo</title>
<p>Las tormentas invernales de 2010 ocasionaron la erosi&#x00F3;n de la playa del sector suroccidental del Parque Nacional de Do&#x00F1;ana (<xref ref-type="fig" rid="f0001">Fig. 1, A</xref>), pr&#x00F3;ximo a la localidad de Matalasca&#x00F1;as (Huelva, S.O. de Espa&#x00F1;a). Esta erosi&#x00F3;n provoc&#x00F3; la aparici&#x00F3;n de un sustrato arcilloso-turboso a lo largo de m&#x00E1;s de un centenar de metros, situado en el l&#x00ED;mite de la pleamar.</p>
<fig id="f0001">
<label>Figura 1</label>
<caption>
<p>A. Situaci&#x00F3;n geogr&#x00E1;fica del perfil estudiado. B. Corte geol&#x00F3;gico del perfil. C. Columna litoestratigr&#x00E1;fica con las facies diferenciadas. D. Vista general del perfil. E. Corte sint&#x00E9;tico con las tres facies distinguidas.</p>
</caption>
<graphic xlink:href="EG201903-87-g001.tif" xmlns:xlink="http://www.w3.org/1999/xlink"/>
</fig>
<p>En una primera fase, se determinaron las distintas facies presentes en un perfil perpendicular a la costa (<xref ref-type="fig" rid="f0001">Fig. 1, B-D</xref>). A continuaci&#x00F3;n se extrajo1 kg de muestra en cada uno de los cuatro niveles (<xref ref-type="fig" rid="f0001">Fig. 1, C</xref>: DN-1 a DN-4) representativos de las dos facies m&#x00E1;s extendidas en el perfil para su an&#x00E1;lisis textural, mineral&#x00F3;gico, micropaleontol&#x00F3;gico y cronoestratigr&#x00E1;fico.</p>
</sec>
<sec id="sec3.2">
<title>An&#x00E1;lisis granulom&#x00E9;trico</title>
<p>El an&#x00E1;lisis granulom&#x00E9;trico de la fracci&#x00F3;n mayor de 100 &#x03BC;m se realiz&#x00F3; mediante tamizado en h&#x00FA;medo. Previamente las muestras se dispersaron en agua mediante agitaci&#x00F3;n durante dos horas, empleando hexametafosfato s&#x00F3;dico como agente dispersante. La distribuci&#x00F3;n granulom&#x00E9;trica de la fracci&#x00F3;n menor de 100 &#x03BC;m se determin&#x00F3; mediante fotosedimentaci&#x00F3;n, utilizando un equipo (MicromeriticsR SediGraph 5100 ET).</p>
</sec>
<sec id="sec3.3">
<title>An&#x00E1;lisis mineral&#x00F3;gico</title>
<p>Se analizaron cuatro muestras de los distintos niveles diferenciados mediante difracci&#x00F3;n de rayos X para obtener la mineralog&#x00ED;a total. El equipamiento usado fue un difract&#x00F3;metro Philips PW 1130/90, con radiaci&#x00F3;n K&#x03B1; de Cu y un filtro de Ni a 20 mA y 40 kv. La fracci&#x00F3;n menor de 2 &#x03BC;m fue separada por un m&#x00E9;todo est&#x00E1;ndar de sedimentaci&#x00F3;n (Barahona, <xref ref-type="bibr" rid="cit0011">1974</xref>).</p>
</sec>
<sec id="sec3.4">
<title>An&#x00E1;lisis macropaleontol&#x00F3;gico</title>
<sec id="s3d1">
<title>Bivalvos</title>
<p>Se realiz&#x00F3; un estudio morfom&#x00E9;trico de <italic>Barnea candida</italic> (L.), el &#x00FA;nico bivalvo hallado en el perfil, para deducir la edad de los ejemplares presentes. Adem&#x00E1;s, se estudi&#x00F3; la distribuci&#x00F3;n y densidad de sus perforaciones (<italic>Gastrochaenolites</italic> isp.), de acuerdo con la metodolog&#x00ED;a de Pinn <italic>et al</italic>. (<xref ref-type="bibr" rid="cit0052">2005</xref>).</p>
</sec>
<sec id="s3d2">
<title>Estructuras macrosc&#x00F3;picas vegetales</title>
<p>Se analizaron 3 fragmentos de 5 g de turba (DN-4) recogidos en distintas zonas del afloramiento. En la lupa binocular se disgreg&#x00F3; cada porci&#x00F3;n, con la observaci&#x00F3;n y clasificaci&#x00F3;n de las estructuras macrosc&#x00F3;picas presentes.</p>
</sec>
</sec>
<sec id="sec3.5">
<title>An&#x00E1;lisis micropaleontol&#x00F3;gico</title>
<sec id="s3e1">
<title>Polen</title>
<p>A continuaci&#x00F3;n se efectu&#x00F3; el an&#x00E1;lisis micropaleontol&#x00F3;gico de los cuatro niveles muestreados, con la determinaci&#x00F3;n de la abundancia y diversidad de polen mediante una c&#x00E1;mara de Neubauer. Para cada nivel (DN-1 a DN-4) se extrajeron 4 muestras (16 en total), que fueron disueltas en agua y homogeneizadas para proceder al contaje de la cantidad de granos de polen y de diatomeas (enteras o fracciones conspicuas) contenidas en 4 c&#x00E1;maras de 1 mm<sup>2</sup> de superficie (0,1 mm<sup>3</sup>). Se procedi&#x00F3; al contaje de polen para obtener su concentraci&#x00F3;n media total en cada nivel.</p>
<p>Para cuantificar el contenido pol&#x00ED;nico, se extrajeron tantas muestras de 10 mm<sup>3</sup> como fueron necesarias para obtener, al menos, 250 granos. Estas muestras se analizaron mediante un microscopio &#x00F3;ptico a 1000 aumentos. Los granos de polen fueron identificados a partir de los datos de Vald&#x00E9;s <italic>et al</italic>. (<xref ref-type="bibr" rid="cit0076">1987</xref>).</p>
</sec>
<sec id="s3e2">
<title>Diatomeas</title>
<p>El procedimiento fue similar para las diatomeas. La mayor&#x00ED;a de las diatomeas de gran tama&#x00F1;o (p.e. <italic>Nitzschia</italic>, <italic>Ulnaria</italic>) presentaron un alto grado de fragmentaci&#x00F3;n en todas las muestras, as&#x00ED; como los individuos de todas las especies en los niveles DN-1 y DN-2. Este grupo fue identificado a nivel gen&#x00E9;rico a partir de Kelly <italic>et al.</italic> (<xref ref-type="bibr" rid="cit0035">2005</xref>), y utilizando diversas monograf&#x00ED;as para la determinaci&#x00F3;n espec&#x00ED;fica, unificando la nomenclatura de acuerdo con Guiry &#x0026; Guiry (<xref ref-type="bibr" rid="cit0032">2010</xref>).</p>
</sec>
<sec id="s3e3">
<title>Ostr&#x00E1;codos y foramin&#x00ED;feros</title>
<p>Se extrajeron 10 g de cada nivel muestreado, que fueron disueltos en agua con adici&#x00F3;n de Calg&#x00F3;n y per&#x00F3;xido de hidr&#x00F3;geno. Esta soluci&#x00F3;n fue tamizada a continuaci&#x00F3;n (125 &#x03BC;m). El residuo obtenido fue secado en estufa a una temperatura constante de 60&#x00BA; C y analizado mediante lupa binocular de hasta 80 aumentos. No se han observado ejemplares de ambos grupos en ninguna de las muestras analizadas.</p>
</sec>
</sec>
<sec id="sec3.6">
<title>Dataciones</title>
<p>Se realizaron dos dataciones en el Centro Nacional de Aceleradores de Sevilla. La primera muestra procedi&#x00F3; del tramo superior de turba y fue calibrada por el programa IntCal09. El resultado final correspondi&#x00F3; a edades calibradas (cal.) con un rango de 2 sigmas. La segunda muestra fue un ejemplar completo de <italic>Barnea candida</italic> extra&#x00ED;do de una perforaci&#x00F3;n (<italic>Gastrochaenolites</italic> isp.) realizada en la parte superior del nivel turboso, que no pudo ser calibrada debido a ser excesivamente reciente y quedar fuera del rango de calibraci&#x00F3;n (ver apartado siguiente).</p>
</sec>
</sec>
<sec id="sec4" sec-type="results">
<title>Resultados</title>
<sec id="sec4.1">
<title>Facies sedimentarias</title>
<p>Los an&#x00E1;lisis de campo, granulom&#x00E9;trico y mineral&#x00F3;gico han permitido diferenciar tres facies en el perfil estudiado (<xref ref-type="fig" rid="f0001">Fig. 1, C</xref>).</p>
<p>Facies 1 (FA-1: limo arcilloso). Los 15 cm inferiores de este perfil est&#x00E1;n constituidos por limos arcillosos gris&#x00E1;ceos masivos (<xref ref-type="fig" rid="f0001">Fig. 1, E</xref>), con porcentajes crecientes de arcilla y ligeramente descendentes de arena hacia techo (<xref ref-type="table" rid="t0001">Tab. 1</xref>). Los filosilicatos son los minerales dominantes (<xref ref-type="table" rid="t0001">Tab. 1</xref>: 55-58%), con proporciones significativas de cuarzo (23-25%) y, en menor medida, plagioclasa (7-9%) y pirita (6-8%). Dentro de los filosilicatos, esmectita (44-47%) e illita (40-48%) presentan similares porcentajes, en tanto que la caolinita aumenta hacia techo (hasta un 13%).</p>
<table-wrap id="t0001">
<label>Tabla 1</label>
<caption>
<p>An&#x00E1;lisis granulom&#x00E9;trico y mineral&#x00F3;gico de los niveles muestreados (en %).</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left">MUESTRAS</th>
<th align="center">DN-1</th>
<th align="center">DN-2</th>
<th align="center">DN-3</th>
<th align="center">DN-4</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" colspan="5"><bold>GRANULOMETR&#x00CD;A</bold></td>
</tr>
<tr>
<td align="left">Arena</td>
<td align="center">8.09</td>
<td align="center">6.55</td>
<td align="center">12.92</td>
<td align="center">13.19</td>
</tr>
<tr>
<td align="left">Limo</td>
<td align="center">80.29</td>
<td align="center">75.23</td>
<td align="center">71.66</td>
<td align="center">74.35</td>
</tr>
<tr>
<td align="left">Arcilla</td>
<td align="center">11.62</td>
<td align="center">18.22</td>
<td align="center">15.41</td>
<td align="center">12.46</td>
</tr>
<tr>
<td align="left" colspan="5"><bold>MINERALOG&#x00CD;A TOTAL</bold></td>
</tr>
<tr>
<td align="left">Filosilicatos</td>
<td align="center">58</td>
<td align="center">55</td>
<td align="center">60</td>
<td align="center">55</td>
</tr>
<tr>
<td align="left">Cuarzo</td>
<td align="center">25</td>
<td align="center">23</td>
<td align="center">22</td>
<td align="center">36</td>
</tr>
<tr>
<td align="left">Plagioclasa</td>
<td align="center">7</td>
<td align="center">9</td>
<td align="center">4</td>
<td align="center">2</td>
</tr>
<tr>
<td align="left">Halita</td>
<td align="center">2</td>
<td align="center">3</td>
<td align="center">6</td>
<td align="center">6</td>
</tr>
<tr>
<td align="left">Pirita</td>
<td align="center">6</td>
<td align="center">8</td>
<td align="center">8</td>
<td align="center"/>
</tr>
<tr>
<td align="left">Yeso</td>
<td align="center">2</td>
<td align="center">2</td>
<td align="center">Identificado</td>
<td align="center">1</td>
</tr>
<tr>
<td align="left">Otros</td>
<td align="center"/>
<td align="center">Silvina, jarosita</td>
<td align="center">Silvina, jarosita</td>
<td align="center"/>
</tr>
<tr>
<td align="left" colspan="5"><bold>FILOSILICATOS</bold></td>
</tr>
<tr>
<td align="left">Esmectita</td>
<td align="center">44</td>
<td align="center">47</td>
<td align="center">35</td>
<td align="center">Illita e interestratificados irregulares</td>
</tr>
<tr>
<td align="left">Illita</td>
<td align="center">48</td>
<td align="center">40</td>
<td align="center">52</td>
<td align="center"/>
</tr>
<tr>
<td align="left">Caolinita</td>
<td align="center">8</td>
<td align="center">13</td>
<td align="center">13</td>
<td align="center"/>
</tr>
</tbody>
</table>
</table-wrap>
<p>A techo, esta facies presenta un gran n&#x00FA;mero de perforaciones circulares en secci&#x00F3;n ecuatorial y c&#x00F3;nicas en secci&#x00F3;n transversal (<xref ref-type="fig" rid="f0001">Fig. 1, E</xref>; <xref ref-type="fig" rid="f0004">Fig. 4, N</xref>: <italic>Gastrochaenolites</italic> isp.), ocupadas por numerosos ejemplares del bivalvo <italic>Barnea candida</italic> en posici&#x00F3;n natural. La longitud de estos ejemplares var&#x00ED;a entre 15 y m&#x00E1;s de 40 mm, con una mayor&#x00ED;a de perforaciones ocupadas por individuos con menos de 25 mm de longitud.</p>
<p>Facies 2 (FA-2: turba). Esta facies est&#x00E1; caracterizada por la presencia de numerosos restos vegetales dentro de una matriz limosa-arcillosa negra (<xref ref-type="table" rid="t0001">Tab. 1</xref>), con un aumento importante de los porcentajes de arena (hasta un 13,2%) en relaci&#x00F3;n a FA-1. La mineralog&#x00ED;a total est&#x00E1; dominada por los filosilicatos (55-60%), si bien el contenido en cuarzo aumenta hacia techo (22-36%). La pirita solo se ha identificado en la base (<xref ref-type="table" rid="t0001">Tab. 1</xref>: 8%), en tanto que los contenidos en halita son relativamente constantes (~6%) en esta facies. Dentro de los filosilicatos, la principal diferencia mineral&#x00F3;gica con FA-1 es el predominio de illita (52%) sobre esmectita (35%) en su base, as&#x00ED; como la presencia de illita e interestratificados irregulares hacia techo.</p>
<p>Se han identificado cuatro tipos de estructuras macrosc&#x00F3;picas vegetales en FA-2. La mayor&#x00ED;a (12) corresponden a utr&#x00ED;culos y c&#x00E1;psulas de ciper&#x00E1;ceas del g&#x00E9;nero <italic>Carex</italic>, que por su tama&#x00F1;o posiblemente pertenezcan a <italic>C. pseudocyperus</italic> L. Tambi&#x00E9;n han aparecido tres aquenios de <italic>Eleocharis palustris</italic> (L.) Roem. &#x0026; Schult., dos esporangios de helechos con anillo de dehiscencia y dos semillas que por su morfolog&#x00ED;a y anatom&#x00ED;a podr&#x00ED;an corresponder a alguna especie de la familia Poeaceae (subfamilia Panicoideae).</p>
<p>Facies 3 (FA-3: arena media y fina). Presenta una base erosiva dispuesta sobre FA-2. Est&#x00E1; constituida por arenas finas a medias amarillentas, bien clasificadas, ricas en cuarzo y feldespatos y con escaso contenido limo-arcilloso. Presenta una continuidad lateral con los cordones dunares situados hacia el norte del perfil estudiado (<xref ref-type="fig" rid="f0001">Fig. 1, D</xref>).</p>
</sec>
<sec id="sec4.2">
<title>Polen</title>
<p>Se han determinado un total de 33 tipos pol&#x00ED;nicos en los cuatro niveles analizados, con un porcentaje de granos no identificables comprendido entre el 4,69% y el 7,6% (<xref ref-type="table" rid="t0002">Tab. 2</xref>). Los principales taxones se detallan en la <xref ref-type="fig" rid="f0002">Fig. 2</xref>. Este registro pol&#x00ED;nico permite diferenciar dos grupos de muestras, coincidentes con las facies delimitadas:</p>
<table-wrap id="t0002">
<label>Tabla 2</label>
<caption>
<p>An&#x00E1;lisis pol&#x00ED;nico: distribuci&#x00F3;n y abundancia de los taxones determinados (en %).</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left">ESPECIES/MUESTRAS</th>
<th align="center">DN-1</th>
<th align="center">DN-2</th>
<th align="center">DN-3</th>
<th align="center">DN-4</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left"><bold>Vegetaci&#x00F3;n acu&#x00E1;tica</bold></td>
<td align="center"><bold>7.61</bold></td>
<td align="center"><bold>17.58</bold></td>
<td align="center"><bold>40.8</bold></td>
<td align="center"><bold>36.46</bold></td>
</tr>
<tr>
<td align="left">Typha sp.</td>
<td align="center">0.99</td>
<td align="center">10.94</td>
<td align="center">30</td>
<td align="center">27.08</td>
</tr>
<tr>
<td align="left">Cyperaceae</td>
<td align="center">6.62</td>
<td align="center">5.86</td>
<td align="center">6.4</td>
<td align="center">6.25</td>
</tr>
<tr>
<td align="left">Sparganium sp.</td>
<td align="center"/>
<td align="center">0.78</td>
<td align="center">3.2</td>
<td align="center">3.13</td>
</tr>
<tr>
<td align="left">Ranunculus sp.</td>
<td align="center"/>
<td align="center"/>
<td align="center">1.2</td>
<td align="center"/>
</tr>
<tr>
<td align="left"><bold>Vegetaci&#x00F3;n higr&#x00F3;fila</bold></td>
<td align="center"><bold>5.63</bold></td>
<td align="center"><bold>1.95</bold></td>
<td align="center"><bold>5.2</bold></td>
<td align="center"><bold>11.46</bold></td>
</tr>
<tr>
<td align="left">Salix sp.</td>
<td align="center">1.32</td>
<td align="center">0.78</td>
<td align="center">1.2</td>
<td align="center">4.95</td>
</tr>
<tr>
<td align="left"><italic>Fraxinus-Phillyrea</italic></td>
<td align="center">1.32</td>
<td align="center"/>
<td align="center">1.2</td>
<td align="center">1.56</td>
</tr>
<tr>
<td align="left">Erica sp.</td>
<td align="center">2.65</td>
<td align="center">1.17</td>
<td align="center">2</td>
<td align="center">4.43</td>
</tr>
<tr>
<td align="left">Myrtus communis L.</td>
<td align="center"/>
<td align="center"/>
<td align="center"/>
<td align="center">0.26</td>
</tr>
<tr>
<td align="left">Hypericum sp.</td>
<td align="center"/>
<td align="center"/>
<td align="center">0.8</td>
<td align="center">0.26</td>
</tr>
<tr>
<td align="left">Potentilla sp.</td>
<td align="center">0.33</td>
<td align="center"/>
<td align="center"/>
<td align="center"/>
</tr>
<tr>
<td align="left"><bold>Marismas y Estepas</bold></td>
<td align="center"><bold>46.03</bold></td>
<td align="center"><bold>53.52</bold></td>
<td align="center"><bold>9.2</bold></td>
<td align="center"><bold>5.99</bold></td>
</tr>
<tr>
<td align="left">Familia Chenopodiaceae</td>
<td align="center">43.05</td>
<td align="center">36.33</td>
<td align="center">8.8</td>
<td align="center">5.47</td>
</tr>
<tr>
<td align="left">Artemisia sp.</td>
<td align="center">2.98</td>
<td align="center">16.41</td>
<td align="center">0.4</td>
<td align="center">0.52</td>
</tr>
<tr>
<td align="left">Ephedra sp.</td>
<td align="center"/>
<td align="center">0.78</td>
<td align="center"/>
<td align="center"/>
</tr>
<tr>
<td align="left"><bold>Vegetaci&#x00F3;n le&#x00F1;osa climat&#x00F3;fila</bold></td>
<td align="center"><bold>26.49</bold></td>
<td align="center"><bold>7.03</bold></td>
<td align="center"><bold>20.8</bold></td>
<td align="center"><bold>13.02</bold></td>
</tr>
<tr>
<td align="left">Quercus sp.</td>
<td align="center">4.64</td>
<td align="center">1.56</td>
<td align="center">5.2</td>
<td align="center">5.99</td>
</tr>
<tr>
<td align="left">Pinus sp.</td>
<td align="center">9.27</td>
<td align="center">1.95</td>
<td align="center">4.4</td>
<td align="center">3.65</td>
</tr>
<tr>
<td align="left">Olea europaea L.</td>
<td align="center">7.95</td>
<td align="center">1.95</td>
<td align="center">5.6</td>
<td align="center">2.34</td>
</tr>
<tr>
<td align="left">Juniperus sp.</td>
<td align="center">1.66</td>
<td align="center">1.56</td>
<td align="center">4.8</td>
<td align="center">0.78</td>
</tr>
<tr>
<td align="left">Pistacia sp.</td>
<td align="center">2.65</td>
<td align="center"/>
<td align="center">0.4</td>
<td align="center">0.26</td>
</tr>
<tr>
<td align="left">Chamaerops humilis L.</td>
<td align="center">0.33</td>
<td align="center"/>
<td align="center">0.4</td>
<td align="center"/>
</tr>
<tr>
<td align="left"><bold>Otras</bold></td>
<td align="center"><bold>8.27</bold></td>
<td align="center"><bold>15.23</bold></td>
<td align="center"><bold>16.4</bold></td>
<td align="center"><bold>25.52</bold></td>
</tr>
<tr>
<td align="left">Familia Poaceae</td>
<td align="center">4.3</td>
<td align="center">8.2</td>
<td align="center">12</td>
<td align="center">13.54</td>
</tr>
<tr>
<td align="left">Rumex sp.</td>
<td align="center">0.99</td>
<td align="center">0.78</td>
<td align="center">0.8</td>
<td align="center">1.3</td>
</tr>
<tr>
<td align="left">Familia Lamiaceae</td>
<td align="center">0.33</td>
<td align="center"/>
<td align="center">0.8</td>
<td align="center">2.86</td>
</tr>
<tr>
<td align="left">Plantago sp.</td>
<td align="center">0.99</td>
<td align="center"/>
<td align="center">0.4</td>
<td align="center"/>
</tr>
<tr>
<td align="left">Urtica membranacea Poir.</td>
<td align="center">0.66</td>
<td align="center">0.78</td>
<td align="center">0.8</td>
<td align="center">0.52</td>
</tr>
<tr>
<td align="left">Familia Apiaceae</td>
<td align="center">0.66</td>
<td align="center">0.78</td>
<td align="center"/>
<td align="center">0.52</td>
</tr>
<tr>
<td align="left">Familia Inuleae</td>
<td align="center"/>
<td align="center">3.13</td>
<td align="center"/>
<td align="center">6.25</td>
</tr>
<tr>
<td align="left">Familia Liguliflorae</td>
<td align="center">0.33</td>
<td align="center">0.39</td>
<td align="center"/>
<td align="center">0.26</td>
</tr>
<tr>
<td align="left">Familia Anthemideae</td>
<td align="center"/>
<td align="center">0.39</td>
<td align="center"/>
<td align="center"/>
</tr>
<tr>
<td align="left">Familia Fabaceae</td>
<td align="center"/>
<td align="center"/>
<td align="center">1.2</td>
<td align="center"/>
</tr>
<tr>
<td align="left">Familia Liliaceae</td>
<td align="center"/>
<td align="center"/>
<td align="center">0.4</td>
<td align="center"/>
</tr>
<tr>
<td align="left">Echium sp.</td>
<td align="center"/>
<td align="center"/>
<td align="center"/>
<td align="center">0.26</td>
</tr>
<tr>
<td align="left">Cistus sp.</td>
<td align="center"/>
<td align="center">0.39</td>
<td align="center"/>
<td align="center"/>
</tr>
<tr>
<td align="left">Corylus sp.</td>
<td align="center"/>
<td align="center">0.39</td>
<td align="center"/>
<td align="center"/>
</tr>
<tr>
<td align="left"><bold>Indeterminadas</bold></td>
<td align="center"><bold>5.96</bold></td>
<td align="center"><bold>4.69</bold></td>
<td align="center"><bold>7.6</bold></td>
<td align="center"><bold>7.55</bold></td>
</tr>
<tr>
<td align="left"><bold>N&#x00FA;mero medio de granos/mm<sup>3</sup></bold></td>
<td align="center"><bold>50</bold></td>
<td align="center"><bold>80</bold></td>
<td align="center"><bold>700</bold></td>
<td align="center"><bold>1400</bold></td>
</tr>
<tr>
<td align="left"><bold>FACIES</bold></td>
<td align="center" colspan="2"><bold>1</bold></td>
<td align="center" colspan="2"><bold>2</bold></td>
</tr>
</tbody>
</table>
</table-wrap>
<fig id="f0002">
<label>Figura 2</label>
<caption>
<p>An&#x00E1;lisis pol&#x00ED;nico: principales taxones determinados.</p>
</caption>
<graphic xlink:href="EG201903-87-g002.tif" xmlns:xlink="http://www.w3.org/1999/xlink"/>
</fig>
<p>Facies 1 (muestras DN-1 y DN-2). En el tramo basal de esta facies, el contenido pol&#x00ED;nico es escaso (50 granos/mm<sup>3</sup>). Predomina la familia Chenopodiaceae (43%), con <italic>Pinus</italic> sp. (&#x003E;9%), <italic>Olea europea</italic> L. (~8%) y granos de polen de la familia Cyperaceae (6,6%) como principales elementos secundarios de la asociaci&#x00F3;n pol&#x00ED;nica. A techo de esta facies, disminuye levemente el polen de quenopodi&#x00E1;ceas (36,3%), en tanto que se incrementa el procedente de <italic>Artemisia</italic> (16,4%), de la vegetaci&#x00F3;n acu&#x00E1;tica (17.6%; <italic>Typha</italic>: ~11%) y de la familia Poaceae (8,2%).</p>
<p>Facies 2 (muestras DIN-3 y DIN-4). El espectro pol&#x00ED;nico es bastante similar en las dos muestras analizadas. Est&#x00E1; dominado por granos de polen procedentes de la vegetaci&#x00F3;n acu&#x00E1;tica (36,4-40,8%), entre la que destaca por su abundancia <italic>Typha</italic> sp. (27-30%) y la familia Cyperaceae (6,2-6,4%). Tambi&#x00E9;n se observa un aumento de las gram&#x00ED;neas (familia Poaceae: 12-13,5%) en relaci&#x00F3;n a FA-1, as&#x00ED; como porcentajes bajos pero relativamente constantes de quenopodi&#x00E1;ceas (5,5-8,8%), <italic>Quercus</italic> sp. (5,2-6%), <italic>Pinus</italic> sp. (3,6-4,4%) y <italic>Olea europea</italic> L. (2,3-5,6%).</p>
</sec>
<sec id="sec4.3">
<title>Diatomeas</title>
<sec id="s4c1">
<title>Autoecolog&#x00ED;a</title>
<p>Los principales par&#x00E1;metros autoecol&#x00F3;gicos de las especies m&#x00E1;s abundantes se detallan en la <xref ref-type="table" rid="t0003">Tab. 3</xref>. La mayor&#x00ED;a de los taxones tienen un h&#x00E1;bitat bent&#x00F3;nico o planct&#x00F3;nico-bent&#x00F3;nico. <italic>Limnicola hungarica</italic> (Grunow) Round &#x0026; Basson es el &#x00FA;nico tax&#x00F3;n espec&#x00ED;ficamente ep&#x00ED;fito, si bien <italic>Diploneis bombus</italic> Ehrenb. puede compartir este h&#x00E1;bitat.</p>
<table-wrap id="t0003">
<label>Tabla 3</label>
<caption>
<p>Autoecolog&#x00ED;a de las especies determinadas de diatomeas. Los datos han sido extra&#x00ED;dos de Buczk&#x00F3; (<xref ref-type="bibr" rid="cit0017">2007</xref>), Piskova et al. (<xref ref-type="bibr" rid="cit0053">2009</xref>), Guiry &#x0026; Guiry (<xref ref-type="bibr" rid="cit0032">2010</xref>), Novelo (<xref ref-type="bibr" rid="cit0050">2012</xref>), Perissinotto et al. (<xref ref-type="bibr" rid="cit0051">2013</xref>), L&#x00F3;pez-Fuerte et al. (<xref ref-type="bibr" rid="cit0040">2015</xref>), Tavera et al. (<xref ref-type="bibr" rid="cit0074">2018</xref>) y Niyatbekov &#x0026; Barinova (<xref ref-type="bibr" rid="cit0049">2018</xref>).</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left">ESPECIES</th>
<th align="left">H&#x00C1;BITAT</th>
<th align="left">TEMPERATURA</th>
<th align="left">OXIGENACI&#x00D3;N E HIDRODIN&#x00C1;MICA</th>
<th align="left">pH</th>
<th align="left">SALINIDAD</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left"><italic>Cocconeis placentula var. euglypta</italic> (Ehrenb.) Grunow</td>
<td align="left">Planct&#x00F3;nico-Bent&#x00F3;nico</td>
<td align="left">Templada</td>
<td align="left">Aguas estancadas</td>
<td align="left">Alcal&#x00F3;fila</td>
<td align="left">Indiferente</td>
</tr>
<tr>
<td align="left"><italic>Cyclotella meneghiniana</italic> K&#x00FC;tz.</td>
<td align="left">Planct&#x00F3;nico-Bent&#x00F3;nico</td>
<td align="left">Templada</td>
<td align="left">Aguas estancadas</td>
<td align="left">Alcal&#x00F3;fila</td>
<td align="left">Hal&#x00F3;fila</td>
</tr>
<tr>
<td align="left"><italic>Cymbella affinis</italic> K&#x00FC;tz.</td>
<td align="left">Bent&#x00F3;nica</td>
<td align="left">Templada</td>
<td align="left">Aguas estancadas-fluyentes</td>
<td align="left">Alcal&#x00F3;fila</td>
<td align="left">Indiferente</td>
</tr>
<tr>
<td align="left"><italic>Diploneis bombus</italic> Ehrenb.</td>
<td align="left">Bent&#x00F3;nica-Ep&#x00ED;fita</td>
<td align="left">Templada-Fr&#x00ED;a</td>
<td align="left">Aguas fluyentes: medios marinos y estuarinos</td>
<td align="left">-</td>
<td align="left">Mesohal&#x00F3;fila</td>
</tr>
<tr>
<td align="left"><italic>Epithemia turgida</italic> (Ehrenb.) K&#x00FC;tz.</td>
<td align="left">Bent&#x00F3;nica</td>
<td align="left">Templada</td>
<td align="left">Aguas estancada</td>
<td align="left">Alcal&#x00F3;fila</td>
<td align="left">Indiferente</td>
</tr>
<tr>
<td align="left"><italic>Eunotia bilunaris</italic> (Ehrenb.) Schars.</td>
<td align="left">Bent&#x00F3;nica</td>
<td align="left">Templada</td>
<td align="left">Aguas estancadas-fluyentes</td>
<td align="left">Acid&#x00F3;fila</td>
<td align="left">Indiferente</td>
</tr>
<tr>
<td align="left"><italic>Lemnicola hungarica</italic> (Grunow) Round &#x0026; Basson</td>
<td align="left">Ep&#x00ED;fita</td>
<td align="left">Templada</td>
<td align="left">Aguas estancadas-fluyentes</td>
<td align="left">Alcal&#x00F3;fila</td>
<td align="left">Indiferente</td>
</tr>
<tr>
<td align="left"><italic>Melosira varians</italic> C. Agardh</td>
<td align="left">Planct&#x00F3;nico-Bent&#x00F3;nico</td>
<td align="left">Templada</td>
<td align="left">Aguas estancadas-fluyentes</td>
<td align="left">Alcal&#x00F3;fila</td>
<td align="left">Indiferente</td>
</tr>
<tr>
<td align="left"><italic>Navicula radiosa</italic> K&#x00FC;tz.</td>
<td align="left">Bent&#x00F3;nica</td>
<td align="left">Templada</td>
<td align="left">Aguas estancadas-fluyentes</td>
<td align="left">Indiferente</td>
<td align="left">Indiferente</td>
</tr>
<tr>
<td align="left"><italic>Pseudostaurosira brevistriata</italic> (Grunow) D.M.Williams &#x0026; Round</td>
<td align="left">Planct&#x00F3;nico-Bent&#x00F3;nico</td>
<td align="left">Templada</td>
<td align="left">Aguas estancadas-fluyentes</td>
<td align="left">Alcal&#x00F3;fila</td>
<td align="left">Indiferente</td>
</tr>
<tr>
<td align="left"><italic>Rhopalodia gibba</italic> (Ehrenb.) O.M&#x00FC;ll.</td>
<td align="left">Bent&#x00F3;nica</td>
<td align="left">Templada</td>
<td align="left">Aguas estancadas-fluyentes</td>
<td align="left">Alcal&#x00F3;fila</td>
<td align="left">Indiferente</td>
</tr>
<tr>
<td align="left"><italic>Rhopalodia gibberula</italic> (Ehrenb.) O.M&#x00FC;ll.</td>
<td align="left">Bent&#x00F3;nica</td>
<td align="left">Templada</td>
<td align="left">Aguas fluyentes</td>
<td align="left">Alcal&#x00F3;fila</td>
<td align="left">Mesohal&#x00F3;fila</td>
</tr>
<tr>
<td align="left"><italic>Staurosira construens</italic> Ehrenb.</td>
<td align="left">Planct&#x00F3;nico-Bent&#x00F3;nico</td>
<td align="left">Templada</td>
<td align="left">Aguas estancadas-fluyentes</td>
<td align="left">Alcal&#x00F3;fila</td>
<td align="left">Indiferente</td>
</tr>
<tr>
<td align="left"><italic>Ulnaria capitata</italic> (Ehrenb.) Comp&#x00E8;re</td>
<td align="left">Planct&#x00F3;nico-Bent&#x00F3;nico</td>
<td align="left">Templada</td>
<td align="left">Aguas estancadas-fluyentes</td>
<td align="left">Alcal&#x00F3;fila</td>
<td align="left">Indiferente</td>
</tr>
</tbody>
</table>
</table-wrap>
<p>La mayor&#x00ED;a de las especies determinadas pueden vivir tanto en aguas estancadas como fluyentes de climas templados, con un pH alcalino y una salinidad variable. Solo se ha determinado una especie t&#x00ED;pica de medios marinos o estuarinos (<italic>D. bombus</italic> Ehrenb.) y un tax&#x00F3;n acid&#x00F3;filo (<italic>Eunotia bilunaris</italic> (Ehrenb.) Schars.) (<xref ref-type="fig" rid="f0003">Fig. 3</xref>).</p>
<fig id="f0003">
<label>Figura 3</label>
<caption>
<p>Diatomeas: principales taxones determinados.</p>
</caption>
<graphic xlink:href="EG201903-87-g003.tif" xmlns:xlink="http://www.w3.org/1999/xlink"/>
</fig>
</sec>
<sec id="s4c2">
<title>Distribuci&#x00F3;n</title>
<p>El registro de diatomeas presenta notables diferencias entre las muestras analizadas, incluso dentro de la misma facies sedimentaria (<xref ref-type="table" rid="t0004">Tab. 4</xref>).</p>
<table-wrap id="t0004">
<label>Tabla 4</label>
<caption>
<p>Diatomeas: distribuci&#x00F3;n y abundancia de los taxones determinados (en %).</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left">ESPECIES/MUESTRAS</th>
<th align="center">DN-1</th>
<th align="center">DN-2</th>
<th align="center">DN-3</th>
<th align="center">DN-4</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left"><italic>Cocconeis placentula</italic> var. <italic>euglypta</italic> (Ehrenb.) Grunow</td>
<td align="center">28.87</td>
<td align="center"/>
<td align="center"/>
<td align="center"/>
</tr>
<tr>
<td align="left"><italic>Cyclotella meneghiniana</italic> K&#x00FC;tz.</td>
<td align="center"/>
<td align="center">7.19</td>
<td align="center">3.72</td>
<td align="center"/>
</tr>
<tr>
<td align="left"><italic>Cymbella affinis</italic> K&#x00FC;tz.</td>
<td align="center"/>
<td align="center">0.65</td>
<td align="center"/>
<td align="center"/>
</tr>
<tr>
<td align="left"><italic>Diploneis bombus</italic> Ehrenb.</td>
<td align="center">3.09</td>
<td align="center"/>
<td align="center">0.37</td>
<td align="center"/>
</tr>
<tr>
<td align="left"><italic>Diploneis</italic> sp.</td>
<td align="center"/>
<td align="center">0.65</td>
<td align="center">1.12</td>
<td align="center"/>
</tr>
<tr>
<td align="left"><italic>Epithemia turgida</italic> (Ehrenb.) K&#x00FC;tz.</td>
<td align="center">3.09</td>
<td align="center">2.61</td>
<td align="center">3.72</td>
<td align="center"/>
</tr>
<tr>
<td align="left"><italic>Eunotia bilunaris</italic> (Ehrenb.) Schars.</td>
<td align="center">1.03</td>
<td align="center">0.33</td>
<td align="center">0.37</td>
<td align="center"/>
</tr>
<tr>
<td align="left"><italic>Lemnicola hungarica</italic> (Grunow) Round &#x0026; Basson</td>
<td align="center"/>
<td align="center">0.65</td>
<td align="center"/>
<td align="center"/>
</tr>
<tr>
<td align="left"><italic>Melosira varians</italic> C.Agardh</td>
<td align="center"/>
<td align="center">1.96</td>
<td align="center">0.74</td>
<td align="center"/>
</tr>
<tr>
<td align="left"><italic>Navicula radiosa</italic> K&#x00FC;tz.</td>
<td align="center"/>
<td align="center">3.92</td>
<td align="center"/>
<td align="center">Fragmentos</td>
</tr>
<tr>
<td align="left"><italic>Nitzschia</italic> sp.</td>
<td align="center">1.03</td>
<td align="center">0.65</td>
<td align="center">1.12</td>
<td align="center"/>
</tr>
<tr>
<td align="left"><italic>Pinnularia</italic> sp.</td>
<td align="center">3.09</td>
<td align="center"/>
<td align="center">1.86</td>
<td align="center"/>
</tr>
<tr>
<td align="left"><italic>Pseudostaurosira brevistriata</italic> (Grunow) D.M.Williams &#x0026; Round</td>
<td align="center">1.03</td>
<td align="center">39.54</td>
<td align="center">17.84</td>
<td align="center"/>
</tr>
<tr>
<td align="left"><italic>Rhopalodia gibba</italic> (Ehrenb.) O.M&#x00FC;ll.</td>
<td align="center">3.09</td>
<td align="center">5.88</td>
<td align="center">2.97</td>
<td align="center"/>
</tr>
<tr>
<td align="left"><italic>Rhopalodia gibberula</italic> (Ehrenb.) O.M&#x00FC;ll.</td>
<td align="center">3.09</td>
<td align="center">4.58</td>
<td align="center">8.55</td>
<td align="center"/>
</tr>
<tr>
<td align="left"><italic>Staurosira construens</italic> Ehrenb.</td>
<td align="center">1.03</td>
<td align="center">14.71</td>
<td align="center">11.9</td>
<td align="center"/>
</tr>
<tr>
<td align="left"><italic>Ulnaria capitata</italic> (Ehrenb.) Comp&#x00E8;re</td>
<td align="center">44.33</td>
<td align="center">14.38</td>
<td align="center">39.03</td>
<td align="center"/>
</tr>
<tr>
<td align="left">Indeterminadas</td>
<td align="center">7.22</td>
<td align="center">2.29</td>
<td align="center">6.69</td>
<td align="center"/>
</tr>
<tr>
<td align="left"><bold>N&#x00FA;mero medio de individuos/mm<sup>3</sup>
</bold></td>
<td align="center"><bold>500</bold></td>
<td align="center"><bold>1,10,000</bold></td>
<td align="center"><bold>35,000</bold></td>
<td align="center"/>
</tr>
<tr>
<td align="left"><bold>FACIES</bold></td>
<td align="left" colspan="2"><bold>1</bold></td>
<td align="left" colspan="2"><bold>2</bold></td>
</tr>
</tbody>
</table>
</table-wrap>
<p>Facies 1. Su tramo basal se caracteriza por la escasez de este grupo (500 individuos/mm<sup>3</sup>). Est&#x00E1; dominado por <italic>Ulnaria capitata</italic> (Ehrenb.) Comp&#x00E8;re (44,3%) y <italic>Cocconeis placentula</italic> var. <italic>euglypta</italic> (Ehrenb.) Grunow (28,9%). A techo, aumenta de forma notable la concentraci&#x00F3;n de diatomeas (110.000 individuos/mm<sup>3</sup>), con una disminuci&#x00F3;n acusada de la primera especie (14,4%) y la desaparici&#x00F3;n de la segunda. Ambas son reemplazadas por <italic>Pseudostaurosira brevistriata</italic> (Grunow) D.M.Williams &#x0026; Round (39,5%), <italic>Staurosira construens</italic> Ehrenb. (14,7%) y <italic>Cyclotella meneghiniana</italic> K&#x00FC;tz (7,2%), en tanto que aumenta levemente sus porcentajes el g&#x00E9;nero <italic>Rophalodia</italic> (de 6,2% a 10,4%).</p>
<p>Facies 2. Su base presenta una disminuci&#x00F3;n de este grupo (35.000 individuos/mm<sup>3</sup>). Destaca el repunte de <italic>U. capitata</italic> (39%), la disminuci&#x00F3;n de <italic>P. brevistriata</italic> (17,8%) y los porcentajes significativos de <italic>S. construens</italic> (11,9%) y <italic>Rhopalodia gibberula</italic> (Ehrenb.) O. M&#x00FC;ll. (8,5%). Finalmente, no se han encontrado diatomeas en la parte superior de esta facies (DN-4).</p>
</sec>
</sec>
<sec id="sec4.4">
<title>Edades</title>
<p>El rango de edad calibrada del nivel turboso superior (DN-4), muy pr&#x00F3;ximo al contacto erosivo con FA-3, se sit&#x00FA;a entre 390-200 a&#x00F1;os a.C. (2340-2150 cal. yr BP), en tanto que la edad del ejemplar de <italic>Barnea candida</italic> es actual-subactual (edad convencional no calibrada: -667 &#x00B1; 34 a&#x00F1;os BP).</p>
</sec>
</sec>
<sec id="sec5" sec-type="discussion">
<title>Discusi&#x00F3;n: evoluci&#x00F3;n paleoambiental</title>
<p>El an&#x00E1;lisis pluridisciplinar de las distintas facies observadas en el perfil estudiado permite efectuar una aproximaci&#x00F3;n a la evoluci&#x00F3;n paleogeogr&#x00E1;fica de este sector durante el Holoceno superior. Pueden diferenciarse cinco fases (<xref ref-type="fig" rid="f0004">Fig. 4</xref>):</p>
<fig id="f0004">
<label>Figura 4</label>
<caption>
<p>Evoluci&#x00F3;n paleoambiental del perfil estudiado.</p>
</caption>
<graphic xlink:href="EG201903-87-g004.tif" xmlns:xlink="http://www.w3.org/1999/xlink"/>
</fig>
<p><bold>Fase 1 (</bold><xref ref-type="fig" rid="f0004"><bold>Fig. 4, A-B-C</bold></xref><bold>)</bold>. Este sector estar&#x00ED;a ocupado por un sustrato limoso-arcilloso (Facies 1: DN-1) sobre el que se desarrollar&#x00ED;a ampliamente la familia Chenopodiaceae, t&#x00ED;pica de marismas con aportes de aguas saladas. Este car&#x00E1;cter salobre tambi&#x00E9;n est&#x00E1; sustentado por la abundancia de la diatomea <italic>Cocconeis placentula</italic> var. <italic>euglypta</italic> (<xref ref-type="fig" rid="f0003">Fig. 3</xref>), t&#x00ED;pica de estos medios (Sabater, <xref ref-type="bibr" rid="cit0068">2000</xref>). La presencia de pirita implicar&#x00ED;a la existencia de condiciones reductoras en el fondo de estas marismas, como consecuencia de la diag&#x00E9;nesis de sedimentos ricos en materia org&#x00E1;nica procedente de la degradaci&#x00F3;n de esta vegetaci&#x00F3;n circundante (Gonz&#x00E1;lez <italic>et al</italic>., <xref ref-type="bibr" rid="cit0030">2008</xref>). Adem&#x00E1;s, su presencia avalar&#x00ED;a el car&#x00E1;cter alcalino de las aguas deducido a partir de las asociaciones de diatomeas (<xref ref-type="table" rid="t0003">Tab. 3</xref>), dado que las bacterias responsables de la reducci&#x00F3;n del sulfato, una reacci&#x00F3;n implicada en su origen, no operan en condiciones &#x00E1;cidas (Fern&#x00E1;ndez, <xref ref-type="bibr" rid="cit0026">1999</xref>). Por otro lado, los bajos niveles de polen podr&#x00ED;an ser explicados por la baja producci&#x00F3;n pol&#x00ED;nica de las comunidades de marisma (Fern&#x00E1;ndez-Illescas <italic>et al</italic>., <xref ref-type="bibr" rid="cit0027">2010</xref>) y por la peor conservaci&#x00F3;n del polen en estos medios (Stevenson, <xref ref-type="bibr" rid="cit0072">1985a</xref>).</p>
<p>La vegetaci&#x00F3;n del entorno estar&#x00ED;a constituida por olivos (<italic>Olea europea</italic>), encinas (<italic>Quercus</italic>) y pinos (<italic>Pinus</italic>), que ocupa actualmente una parte significativa del Parque Nacional de Do&#x00F1;ana, donde los bosques de la asociaci&#x00F3;n <italic>Oleo sylvestris</italic>-<italic>Quercetum suberis</italic> constituir&#x00ED;an su cl&#x00ED;max. La abundancia de polen de <italic>Pinus</italic> sp. confirmar&#x00ED;a el car&#x00E1;cter de acompa&#x00F1;ante habitual de esta especie en estos bosques, o al menos constatar&#x00ED;a la existencia de pinares en los trenes de dunas m&#x00F3;viles cercanos a la zona (Allier, <xref ref-type="bibr" rid="cit0002">1977</xref>).</p>
<p><bold>Fase 2 (</bold><xref ref-type="fig" rid="f0004"><bold>Fig. 4, D-E-F</bold></xref><bold>)</bold>. Se produce un tr&#x00E1;nsito a una laguna somera de aguas dulces (Facies 1: DN-2), con desarrollo de hel&#x00F3;fitos (<italic>Typha</italic>, <italic>Sparganium</italic>) en las zonas m&#x00E1;s profundas. Este aislamiento tambi&#x00E9;n queda reflejado en las asociaciones de diatomeas, con la desaparici&#x00F3;n de especies t&#x00ED;picas de medios salobres (<italic>C. placentula</italic> var. <italic>euglypta</italic>, <italic>Diploneis bombus</italic>) y la aparici&#x00F3;n de taxones propios de aguas estancadas (<xref ref-type="fig" rid="f0003">Fig. 3</xref>: <italic>Cyclotella meneghiniana</italic>) (Niyatbekov &#x0026; Barinova, <xref ref-type="bibr" rid="cit0049">2018</xref>).</p>
<p>Este aislamiento relativo tambi&#x00E9;n se detecta en el sedimento del fondo. Se produce una disminuci&#x00F3;n del tama&#x00F1;o medio de grano, con una disminuci&#x00F3;n del porcentaje en arena, probablemente por la interrupci&#x00F3;n de las conexiones hidrodin&#x00E1;micas con otros medios costeros (<xref ref-type="table" rid="t0001">Tab. 1</xref>). Adem&#x00E1;s, aumenta levemente el contenido en pirita (<xref ref-type="table" rid="t0002">Tab. 2</xref>: del 6% al 8%) y domina la esmectita sobre la illita dentro de los filosilicatos.</p>
<p>En esta fase, tiene su m&#x00E1;xima abundancia la asociaci&#x00F3;n Chenopodiaceae-<italic>Ephedra</italic>-<italic>Artemisia</italic> (<xref ref-type="table" rid="t0002">Tab. 2</xref>)<italic>.</italic> Esta conjunci&#x00F3;n indicar&#x00ED;a un enfriamiento clim&#x00E1;tico, ya que constituir&#x00ED;an una vegetaci&#x00F3;n esteparia (Men&#x00E9;ndez Amor &#x0026; Florsch&#x00FC;tz, <xref ref-type="bibr" rid="cit0047">1963</xref>; Men&#x00E9;ndez <italic>et al.</italic>, <xref ref-type="bibr" rid="cit0048">2012</xref>). Este periodo podr&#x00ED;a coincidir, de acuerdo con la dataci&#x00F3;n de FA-3, con un evento fr&#x00ED;o que tuvo lugar hacia los siglos VII-VIII a.C. (2.7 ky cal. BP; Bond <italic>et al</italic>., <xref ref-type="bibr" rid="cit0013">1997</xref>).</p>
<p><bold>Fase 3 (</bold><xref ref-type="fig" rid="f0004"><bold>Fig. 4, G-H-I</bold></xref><bold>).</bold> El espectro pol&#x00ED;nico y los elementos macrosc&#x00F3;picos de FA-2 (DN-3 y DN-4) apuntan a la existencia de lagunas permanentes de agua dulce, donde prosperar&#x00ED;an las comunidades de hel&#x00F3;fitos, con abundancia de eneas (<italic>Typha</italic>) y probablemente de carrizo (<italic>Phragmites australis</italic>). Los bosques pr&#x00F3;ximos estar&#x00ED;an constituidos por fresnedas (<italic>Fraxinus</italic>, <italic>Salix</italic>), entre otros. Esta reconstrucci&#x00F3;n es similar a la efectuada por Stevenson (<xref ref-type="bibr" rid="cit0073">1985b</xref>) en la cercana Laguna de las Madres, con formaci&#x00F3;n de turberas por ausencia de drenaje debido al cierre de la conexi&#x00F3;n marina por el avance de frentes dunares, si bien el cierre de esta laguna es anterior a la aqu&#x00ED; descrita (4200 a&#x00F1;os BP; Zazo <italic>et al</italic>., <xref ref-type="bibr" rid="cit0081">1996</xref>) . Este avance se constata en la granulometr&#x00ED;a, con un incremento sustancial (<xref ref-type="table" rid="t0001">Tab. 1</xref>: hasta el 13,2%) del contenido en arenas.</p>
<p>El proceso de turbificaci&#x00F3;n tambi&#x00E9;n se aprecia en la mineralog&#x00ED;a, con desaparici&#x00F3;n de la pirita y la presencia de illita e interestratificados irregulares a techo de FA-2 (<xref ref-type="table" rid="t0001">Tab. 1</xref>), que tendr&#x00ED;an un origen diagen&#x00E9;tico (Ar&#x00F3;stegui <italic>et al</italic>., <xref ref-type="bibr" rid="cit0010">1993</xref>). Es tambi&#x00E9;n patente en las diatomeas, donde solo se aprecian fragmentos indiferenciados cerca de la transici&#x00F3;n a FA-3 (<xref ref-type="table" rid="t0003">Tab. 3</xref>). La progresiva desecaci&#x00F3;n de la laguna y el incremento de los procesos e&#x00F3;licos ser&#x00ED;an factores desfavorables para el desarrollo de este grupo (Witkowski <italic>et al</italic>., <xref ref-type="bibr" rid="cit0079">2009</xref>).</p>
<p>La ausencia de ostr&#x00E1;codos y foramin&#x00ED;feros podr&#x00ED;a deberse a la presencia de condiciones &#x00E1;cidas temporales en la superficie del sedimento, como consecuencia de los altos niveles de materia org&#x00E1;nica, lo que impedir&#x00ED;a la preservaci&#x00F3;n de caparazones y valvas de estos grupos (Laprida <italic>et al.,</italic> <xref ref-type="bibr" rid="cit0036">2014</xref>).</p>
<p><bold>Fase 4 (</bold><xref ref-type="fig" rid="f0004"><bold>Fig. 4, J-K-L</bold></xref><bold>)</bold>. La evoluci&#x00F3;n de la turbera finaliza hacia el siglo III a.C., con la implantaci&#x00F3;n posterior de sistemas de dunas (FA-3) sobre los espacios lagunares previos, de acuerdo con la dataci&#x00F3;n obtenida a techo de FA-2 (390-200 a.C.). La edad de este brusco cambio coincide con el final del siglo III a.C., un periodo caracterizado por un tsunami hist&#x00F3;rico (218 a.C.) y la inundaci&#x00F3;n de C&#x00E1;diz (210 a.C.), ambos eventos incluidos dentro del cat&#x00E1;logo de tsunamis en las costas espa&#x00F1;olas (Campos, <xref ref-type="bibr" rid="cit0018">1991</xref>). La progradaci&#x00F3;n posterior de los sistemas dunares circundantes coincidir&#x00ED;a con el inicio de la fase regional H<sub>3</sub> de Zazo <italic>et al</italic>. (<xref ref-type="bibr" rid="cit0080">1994</xref>), que se extender&#x00ED;a aproximadamente desde el siglo III a.C. hasta el siglo XII d.C.</p>
<p>
<bold>Fase 5 (</bold><xref ref-type="fig" rid="f0004"><bold>Fig. 4, M-N-O</bold></xref><bold>)</bold>. La edad de los ejemplares de <italic>B. candida</italic> y su aparici&#x00F3;n como consecuencia de tormentas invernales sugieren que la colonizaci&#x00F3;n de FA-1 por este bivalvo vino precedida de un evento erosivo que expuso las arcillas inferiores, ya ligeramente litificadas, y el perfil estudiado en los &#x00FA;ltimos siglos. Esta zona es erosionada de forma peri&#x00F3;dica por grandes tormentas invernales, con un ciclo largo de 6-7 a&#x00F1;os que precede a un ciclo corto posterior de 2-3, de acuerdo con los an&#x00E1;lisis estad&#x00ED;sticos efectuados entre 1960 y 1996 (Ruiz <italic>et al</italic>., <xref ref-type="bibr" rid="cit0065">2005b</xref>). Este sector de la playa habr&#x00ED;a permanecido invadido por el mar durante, al menos, 4 a&#x00F1;os, de acuerdo con la longitud y densidad de los ejemplares de <italic>B</italic>. <italic>candida</italic> (Pinn <italic>et al</italic>., <xref ref-type="bibr" rid="cit0052">2005</xref>).</p>
</sec>
<sec id="sec6" sec-type="conclusions">
<title>Conclusiones</title>
<p>El an&#x00E1;lisis multidisciplinar (textura, mineralog&#x00ED;a, paleontolog&#x00ED;a, dataciones) de un perfil situado en el sector occidental del Parque Nacional de Do&#x00F1;ana permite perfilar su evoluci&#x00F3;n durante el Holoceno superior. Este estudio delimita las caracter&#x00ED;sticas geol&#x00F3;gicas de los diferentes paleoambientes deducidos: a) marisma salobre, con abundancia de quenopodi&#x00E1;ceas sobre un sustrato arcilloso y un entorno dominado por olivos, encinas y pinos; b) laguna somera de aguas dulces, relativamente aislada, con hel&#x00F3;fitos en las zonas profundas y quenopodi&#x00E1;ceas en las m&#x00E1;s someras, sometidas a un clima fr&#x00ED;o; y c) sistemas dunares, caracterizados por su alto contenido de arenas cuarc&#x00ED;feras. Su an&#x00E1;lisis cronoestratigr&#x00E1;fico permite distinguir cinco fases, que abarcan desde una marisma salobre inicial (&#x003E;2700 a&#x00F1;os BP) hasta una colonizaci&#x00F3;n reciente por bivalvos lit&#x00F3;fagos.</p>
</sec>
</body>
<back>
<ack>
<title>AGRADECIMIENTOS</title>
<p>Este trabajo ha sido financiado por los Grupos de Investigaci&#x00F3;n RNM-238 (Paleontolog&#x00ED;a y Ecolog&#x00ED;a Aplicadas), RNM-293 (Geomorfolog&#x00ED;a Ambiental y Recursos H&#x00ED;dricos), RNM-349 (Mineralog&#x00ED;a y Geoqu&#x00ED;mica Ambiental y de la Salud) y RNM-358 (Marismas y Playas) de la Junta de Andaluc&#x00ED;a, as&#x00ED; como por el Plan Propio de Investigaci&#x00F3;n de la Universidad de Huelva. Es una contribuci&#x00F3;n al Centro de Investigaci&#x00F3;n en Patrimonio Hist&#x00F3;rico, Cultural y Natural (CIPHCN) de la Universidad de Huelva.</p>
</ack>
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