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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Ecol. Evol.</journal-id>
<journal-title>Frontiers in Ecology and Evolution</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Ecol. Evol.</abbrev-journal-title>
<issn pub-type="epub">2296-701X</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3389/fevo.2023.1227020</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Ecology and Evolution</subject>
<subj-group>
<subject>Original Research</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>A multiproxy approach to reconstruct the Late Holocene environmental dynamics of the semiarid Andes of central Chile (29&#xb0;S)</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Martel-Cea</surname>
<given-names>Alejandra</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/830903"/>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Maldonado</surname>
<given-names>Antonio</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
<xref ref-type="author-notes" rid="fn001">
<sup>*</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/337502"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>de Porras</surname>
<given-names>Mar&#xed;a Eugenia</given-names>
</name>
<xref ref-type="aff" rid="aff4">
<sup>4</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/337481"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Mu&#xf1;oz</surname>
<given-names>Praxedes</given-names>
</name>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/518372"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Maidana</surname>
<given-names>Nora I.</given-names>
</name>
<xref ref-type="aff" rid="aff5">
<sup>5</sup>
</xref>
<xref ref-type="aff" rid="aff6">
<sup>6</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/2349548"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Massaferro</surname>
<given-names>Julieta</given-names>
</name>
<xref ref-type="aff" rid="aff7">
<sup>7</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/1656294"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Schittek</surname>
<given-names>Karsten</given-names>
</name>
<xref ref-type="aff" rid="aff8">
<sup>8</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/2321153"/>
</contrib>
</contrib-group>
<aff id="aff1">
<sup>1</sup>
<institution>Laboratorio de Paleoecolog&#xed;a y Paleoclimatolog&#xed;a, Centro de Estudios Avanzados en Zonas &#xc1;ridas (CEAZA)</institution>, <addr-line>La Serena</addr-line>, <country>Chile</country>
</aff>
<aff id="aff2">
<sup>2</sup>
<institution>Laboratorio de Palinolog&#xed;a y Reconstrucciones Ambientales, Instituto Ciencias de la Tierra, Universidad Austral de Chile</institution>, <addr-line>Valdivia</addr-line>, <country>Chile</country>
</aff>
<aff id="aff3">
<sup>3</sup>
<institution>Departamento de Biolog&#xed;a Marina, Universidad Cat&#xf3;lica del Norte</institution>, <addr-line>Coquimbo</addr-line>, <country>Chile</country>
</aff>
<aff id="aff4">
<sup>4</sup>
<institution>Instituto Argentino de Nivolog&#xed;a, Glaciolog&#xed;a y Ciencias Ambientales &#x2013; Consejo Nacional de Investigaciones Cient&#xed;ficas y T&#xe9;cnicas de Argentina (IANIGLA-CONICET)</institution>, <addr-line>Mendoza</addr-line>, <country>Argentina</country>
</aff>
<aff id="aff5">
<sup>5</sup>
<institution>Laboratorio de Diatomeas Continentales, Facultad de Ciencias Exactas y Naturales, Departamento de Biodiversidad y Biolog&#xed;a Experimental, Universidad de Buenos Aires</institution>, <addr-line>Buenos Aires</addr-line>, <country>Argentina</country>
</aff>
<aff id="aff6">
<sup>6</sup>
<institution>Laboratorio de Diatomeas Continentales, Consejo Nacional de Investigaciones Cient&#xed;ficas y T&#xe9;cnicas de Argentina (CONICET) &#x2013; Universidad de Buenos Aires, Instituto de Biodiversidad y Biolog&#xed;a Experimental y Aplicada (IBBEA)</institution>, <addr-line>Buenos Aires</addr-line>, <country>Argentina</country>
</aff>
<aff id="aff7">
<sup>7</sup>
<institution>Programa de Estudios Aplicados a la Biodiversidad del Parque Nacional Nahuel Huapi &#x2013; Consejo Nacional de Investigaciones Cient&#xed;ficas y T&#xe9;cnicas de Argentina (CENAC-CONICET)</institution>, <addr-line>Bariloche</addr-line>, <country>Argentina</country>
</aff>
<aff id="aff8">
<sup>8</sup>
<institution>Institute of Geography Education, University of Cologne</institution>, <addr-line>Cologne</addr-line>, <country>Germany</country>
</aff>
<author-notes>
<fn fn-type="edited-by">
<p>Edited by: Laura Parducci, Sapienza University of Rome, Italy</p>
</fn>
<fn fn-type="edited-by">
<p>Reviewed by: Keely Mills, The Lyell Centre, United Kingdom</p>
<p>Neal Michelutti, Queen&#x2019;s University, Canada</p>
<p>Thomas A. Minckley, University of Wyoming, United States</p>
</fn>
<fn fn-type="corresp" id="fn001">
<p>*Correspondence: Antonio Maldonado, <email xlink:href="mailto:antonio.maldonado@ceaza.cl">antonio.maldonado@ceaza.cl</email>
</p>
</fn>
</author-notes>
<pub-date pub-type="epub">
<day>08</day>
<month>12</month>
<year>2023</year>
</pub-date>
<pub-date pub-type="collection">
<year>2023</year>
</pub-date>
<volume>11</volume>
<elocation-id>1227020</elocation-id>
<history>
<date date-type="received">
<day>22</day>
<month>05</month>
<year>2023</year>
</date>
<date date-type="accepted">
<day>17</day>
<month>11</month>
<year>2023</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#xa9; 2023 Martel-Cea, Maldonado, de Porras, Mu&#xf1;oz, Maidana, Massaferro and Schittek</copyright-statement>
<copyright-year>2023</copyright-year>
<copyright-holder>Martel-Cea, Maldonado, de Porras, Mu&#xf1;oz, Maidana, Massaferro and Schittek</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/">
<p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</p>
</license>
</permissions>
<abstract>
<p>Mountain ecosystems located in the Andes cordillera of central Chile (29&#x2013;35&#xb0;S) have been strongly affected by the ongoing Mega Drought since 2010, impacting the snow cover, the surficial water resources (and thereby water storage), as well as the mountain biota and ecosystem services. Paleoenvironmental records in this part of the semiarid Andes are key to estimating the effects of past climate changes on local communities helping to forecast the ecological and biological responses under the aridification trend projected during the 21<sup>st</sup> century. Here we present a 2400-year multiproxy paleoenvironmental reconstruction based on pollen, diatoms, chironomids, sedimentological and geochemical data (XRF and ICP-MS data) of Laguna El Calvario (29&#xb0;S; 3994 m a.s.l), a small and shallow Andean lake. Four main hydrological phases were established based on changes in the lithogenic and geochemical results associated with allochthonous runoff input and the subsequent response of the biological proxies. Between 2400 and 1400 cal yrs BP, wetter than present conditions occurred based on the intense weathering of the lake basin and the dominance of upper Andean vegetation. A decrease in moisture along with sub-centennial discrete wet pulses and lake-level changes occurred until ~800 cal yrs BP followed long-term stable climate conditions between 1850 and 1950 AD as suggested by a drop in vegetation productivity and low lake levels. From 1950 AD to the present, a decline in moisture with a severe trend to drier conditions occurring in the last decades occurred as reflected by an upward vegetation belt displacement around Laguna El Calvario along with a turnover of diatom assemblages and high productivity in the water column.</p>
</abstract>
<kwd-group>
<kwd>semiarid Andes</kwd>
<kwd>climate change</kwd>
<kwd>multiproxy analysis</kwd>
<kwd>mountain ecosystems</kwd>
<kwd>lake sediments</kwd>
<kwd>Late Holocene</kwd>
</kwd-group>
<counts>
<fig-count count="6"/>
<table-count count="1"/>
<equation-count count="0"/>
<ref-count count="115"/>
<page-count count="15"/>
<word-count count="8518"/>
</counts>
<custom-meta-wrap>
<custom-meta>
<meta-name>section-in-acceptance</meta-name>
<meta-value>Paleoecology</meta-value>
</custom-meta>
</custom-meta-wrap>
</article-meta>
</front>
<body>
<sec id="s1" sec-type="intro">
<label>1</label>
<title>Introduction</title>
<p>Low water availability and uncontrolled changes in land use and cover are becoming the main stressors in semiarid western Andes (29&#xb0;&#x2013;34&#xb0;S) ecosystems under the ongoing scenario of climatic change. In this regard, the desertification process is critical in the northernmost area (especially in the Coquimbo region; 29&#xb0;&#x2013;32&#xb0;S) (<xref ref-type="bibr" rid="B18">Emanuelli et&#xa0;al., 2016</xref>; <xref ref-type="bibr" rid="B82">Pizarro-Tapia et&#xa0;al., 2021</xref>) given that it has negatively affected the biodiversity and the ecosystem services (e.g., socioeconomic activities). The Andes cordillera acts as a water reservoir of solid/liquid precipitation falling during a few rainy months and therefore, its role has taken key relevance under the decline of precipitation and rise of temperatures in the past decades (<xref ref-type="bibr" rid="B22">Falvey and Garreaud, 2009</xref>; <xref ref-type="bibr" rid="B83">Quintana and Aceituno, 2012</xref>; <xref ref-type="bibr" rid="B5">Barria et&#xa0;al., 2019</xref>; <xref ref-type="bibr" rid="B29">Garreaud et&#xa0;al., 2019</xref>). Given that those trends will be accentuated during the 21<sup>st</sup> century causing a reduction in the snow cover as well as in glacier extension and mass balance, the projected decrease in streamflow (water supply) to the lowlands is critical (<xref ref-type="bibr" rid="B103">Vicu&#xf1;a et&#xa0;al., 2011</xref>).</p>
<p>To have a deep comprehension of how climate-sensitive high mountain ecosystems in the semiarid Andes will respond to future climate change in the mid-to-long term scale, it is necessary to understand past environmental dynamics. Despite the scarce high-elevation paleoenvironmental records in the semiarid Andes, those published in the last decade have helped to infer hydrological changes associated with the latitudinal dynamics of the northern border of the Southern Westerly Winds (SWW) and its interaction with the Southeast Pacific Subtropical Anticyclone (SEPSA) (<xref ref-type="bibr" rid="B59">Martel-Cea et&#xa0;al., 2016</xref>; <xref ref-type="bibr" rid="B98">Tiner et&#xa0;al., 2018</xref>; <xref ref-type="bibr" rid="B64">Mayta and Maldonado, 2022</xref>). Pollen records from central Chile (33&#xb0;&#x2013;36&#xb0;S) suggested a high short-term variability during the Late Holocene attributed to an increased frequency of El Ni&#xf1;o Southern Oscillation (ENSO) events (<xref ref-type="bibr" rid="B45">Jenny et&#xa0;al., 2002a</xref>; <xref ref-type="bibr" rid="B55">Maldonado and Villagr&#xe1;n, 2006</xref>; <xref ref-type="bibr" rid="B25">Frugone-&#xc1;lvarez et&#xa0;al., 2020</xref>; <xref ref-type="bibr" rid="B76">Mu&#xf1;oz et&#xa0;al., 2020</xref>). The establishment of the modern semiarid conditions occurred around 600&#x2013;700 calibrated years before the present (hereafter cal yrs BP) in the semiarid Andes (<xref ref-type="bibr" rid="B59">Martel-Cea et&#xa0;al., 2016</xref>; <xref ref-type="bibr" rid="B64">Mayta and Maldonado, 2022</xref>).</p>
<p>This work therefore presents a new Late Holocene environmental reconstruction from a high-altitude lacustrine record in the semiarid Andes (29&#xb0;S) based on a multiproxy approach. Sedimentological and geochemical proxies such as organic/inorganic matter content and trace elements along with biological proxies such as pollen, diatoms, and chironomids were analyzed. Specifically, Laguna El Calvario was chosen because of its high sensitivity to changes in the snow cover (the main source of water input to the lake) which further allows for the reconstruction of long-term changes in the past 2400 years in hydrology and limnological conditions.</p>
</sec>
<sec id="s2">
<label>2</label>
<title>Study area</title>
<p>Laguna El Calvario (29&#xb0;34&#x2019;7.63&#x201d; S; 70&#xb0;21&#x2019;8.63&#x201d; W, 3994 m a.s.l., depth ca. 1 m, 0.8 ha area) is a small closed shallow lake located at the head of a west&#x2013;east oriented valley called Quebrada Matancilla in the semiarid Andes of central Chile (<xref ref-type="fig" rid="f1">
<bold>Figure&#xa0;1</bold>
</xref>). The lake is flanked by Pleistocene-Holocene glacier deposits. The surrounding hills and basal bedrock consist of K-rich intrusive plutonic rocks of the Permian period [Guanta plutonic complex Peg(t) and Peg(gd)] which are mainly composed of tonalite and granodiorite (<xref ref-type="bibr" rid="B78">Nasi et&#xa0;al., 1985</xref>; <xref ref-type="bibr" rid="B77">Murillo et&#xa0;al., 2017</xref>). Indeed, industrial mining activities for the exploitation of Cu, Au, and Fe have been developed during the last 100 years in the semiarid Andes of central Chile (<xref ref-type="bibr" rid="B89">SERPLAC, 1986</xref>) having important effects on high Andean ecosystems (e.g., on natural water reservoirs; <xref ref-type="bibr" rid="B81">Oyarz&#xfa;n et&#xa0;al., 2006</xref>).</p>
<fig id="f1" position="float">
<label>Figure&#xa0;1</label>
<caption>
<p>
<bold>(A)</bold> South America and central Chile map showing the location of Laguna El Calvario (LCA) and some of the sites mentioned in the text; <bold>(B)</bold> 3D image of the Laguna El Calvario valley (DEM ALOS PALSAR SRTM 12.5 m JAXTA); and <bold>(C)</bold> photograph of Laguna El Calvario from the west.</p>
</caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fevo-11-1227020-g001.tif"/>
</fig>
<p>The climate of the study area is cold semiarid with Mediterranean influence characterized by cold/wet winters and dry/warm summers. Annual precipitation reaches 130 mm (JJA: 60%) while the mean annual temperature is 3.8&#xb0;C (DJF: 7.7&#xb0;C; JJA: 0&#xb0;C) (CRU 1980&#x2013;2016). Winter precipitation originates from frontal systems associated with the northern border of the Southern Westerlies belt and is modulated by its interaction with the subtropical Anticyclone. While the frontal systems migrate in the NW-SE direction, they are intercepted by the Andes cordillera causing a strong rainfall gradient along the west side of the Andes (orographic enhancement) (<xref ref-type="bibr" rid="B21">Falvey and Garreaud, 2007</xref>). As the mean annual altitude of the 0&#xb0;C isotherm at 29&#xb0;S is located at ~4300 m a.s.l. (<xref ref-type="bibr" rid="B10">Carrasco et&#xa0;al., 2005</xref>; <xref ref-type="bibr" rid="B5">Barria et&#xa0;al., 2019</xref>), most of the precipitation around Laguna El Calvario falls as snow. During summertime, rainfall events are less frequent and correspond to convective storms coming from the eastern side of the Andes Cordillera accounting for less than 10% of the annual precipitation (<xref ref-type="bibr" rid="B30">Garreaud and Rutllant, 1997</xref>; <xref ref-type="bibr" rid="B102">Viale and Garreaud, 2014</xref>). However, summer storms bring fresh snow and cloud cover that reduce the albedo (and therefore sublimation), diminishing glacier melting in the semiarid Andes (<xref ref-type="bibr" rid="B1">Abermann et&#xa0;al., 2014</xref>). The climate interannual-to-quasidecadal variability in the area is strongly influenced by the El Ni&#xf1;o Southern Oscillation (ENSO; positive phase), which is responsible for higher-than-average amounts of winter precipitation (<xref ref-type="bibr" rid="B2">Aceituno, 1988</xref>; <xref ref-type="bibr" rid="B70">Montecinos and Aceituno, 2003</xref>; <xref ref-type="bibr" rid="B28">Garreaud, 2009</xref>; <xref ref-type="bibr" rid="B83">Quintana and Aceituno, 2012</xref>). The high correlation between the warm ENSO phase and above-average accumulation of snowpack, increased streamflow, and positive glacier mass balance have relieved the arid trend observed in the last decades in the subtropical semiarid Andes (<xref ref-type="bibr" rid="B60">Masiokas et&#xa0;al., 2006</xref>; <xref ref-type="bibr" rid="B31">Gascoin et&#xa0;al., 2011</xref>). On the other hand, the Southern Annular Mode (SAM) in its negative (positive) phase promotes higher(lower)-than-average precipitation in south-central Chile (<xref ref-type="bibr" rid="B83">Quintana and Aceituno, 2012</xref>).</p>
<p>The vegetation composition and distribution follow the steep gradient of the semiarid Andes (so-called vegetation belts) linked to the abrupt changes in temperature, precipitation, topography (such as slope orientation), and soil characteristics. Both species diversity and plant cover decline with elevation due to the extreme conditions in the high Andean environments (<xref ref-type="bibr" rid="B105">Villagr&#xe1;n et&#xa0;al., 1983</xref>; <xref ref-type="bibr" rid="B4">Arroyo et&#xa0;al., 1988</xref>; <xref ref-type="bibr" rid="B93">Squeo et&#xa0;al., 1993</xref>; <xref ref-type="bibr" rid="B51">L&#xf3;pez-Angulo et&#xa0;al., 2018</xref>). On the other hand, the length of the growing season also shortens with elevation and the maximum primary productivity is recorded from the late spring (Nov&#x2013;Dec) to late summer (March) (<xref ref-type="bibr" rid="B91">Squeo et&#xa0;al., 1994</xref>; <xref ref-type="bibr" rid="B87">Rudloff et&#xa0;al., 2021</xref>). Following the biogeographic data provided by <xref ref-type="bibr" rid="B53">Luebert and Pliscoff (2017)</xref> and the terminology of <xref ref-type="bibr" rid="B91">Squeo et&#xa0;al. (1994)</xref>, it is possible to differentiate three main vegetation belts:</p>
<p>Pre-Andean belt (&lt;2700m a.s.l.), characterized by major life forms such as shrubs, cacti, perennial and annual herbs. The most common species are <italic>Ephedra chilensis, Colliguaja odorifera</italic>, <italic>Adesmia confusa</italic>, <italic>A. microphylla, Haplopappus angustifolius, Cumulopuntia sphaerica.</italic> Tree species are restricted to azonal areas (meadows in ravines). This vegetation belt is strongly disturbed by anthropic activities and the vegetation cover reaches up to 40%.</p>
<p>Sub-Andean belt (2700&#x2013;3500 m a.s.l.), the major life forms are shrubs and perennial herbs such as <italic>Senecio proteus, Haplopappus baylahuen, Ephedra breana, Chuquiraga ulicina, Adesmia parviflora, A. hystrix. Atriplex imbricata, Chaetanthera limbate, Fabiana viscosa, F. imbricata, Viviania marifolia</italic>, and <italic>Cristaria andicola</italic>. Tree species may appear in meadows up to 2900 m. This belt also has a cover ca. 40%.</p>
<p>Andean belt (3500&#x2013;4450 masl) dominated by shrubs, perennial herbs, and cushion plants can be further divided into the lower and upper Andean belt. The lower Andean belt (up to 4250 m; cover ca. 27%) is characterized by <italic>Adesmia subterranea, A. echinus, A. aegiceras</italic>, <italic>Azorella madreporica, Stipa chrysophylla, S. frigida</italic>, <italic>Cistanthe picta, Chaetanthera minuta</italic>, and <italic>C. sphaeroidalis.</italic> The upper Andean belt (4250&#x2013;4450 m: cover ca. 0.7%) is mainly composed of perennial herbs and grasses and a few dwarf shrubs such as <italic>Chaetanthera sphaeroidalis</italic>, <italic>C. pulvinate, Stipa frigida, Adesmia subterranea, A. capitellata, Senecio pissisii</italic>, and <italic>S. socompae.</italic>
</p>
</sec>
<sec id="s3">
<label>3</label>
<title>Methodology</title>
<sec id="s3_1">
<label>3.1</label>
<title>Coring and sedimentological, chronological, and geochemical analyses</title>
<p>Four short cores of Laguna El Calvario (LCA) were retrieved in 2017 using a UWITEC<sup>&#xa9;</sup> gravity corer. All the cores were lithologically characterized through X-radiographs and visual descriptions. The LCA SHC-4 core was selected for performing the multiproxy analysis given it was the longest (33 cm long; <xref ref-type="supplementary-material" rid="SM1">
<bold>Figure&#xa0;1 Supplementary Material</bold>
</xref>). The sedimentological analysis included a loss on ignition, X<italic>-</italic>ray fluorescence analysis (XRF), and inductively coupled plasma mass spectrometry (ICP-MS). Loss-on ignition was assessed at a contiguous 1 cm interval to estimate organic, inorganic, and carbonate contents (<xref ref-type="bibr" rid="B39">Heiri et&#xa0;al., 2001</xref>). The chronology of the Laguna El Calvario record was established through <sup>210</sup>Pb and <sup>14</sup>C dating techniques. The <sup>210</sup>Pb activities (dpm g<sup>&#x2212;1</sup>) were estimated for the first 15 cm through its daughter radionuclide <sup>210</sup>Po which is in secular equilibrium (<xref ref-type="supplementary-material" rid="SM1">
<bold>Table&#xa0;1 Supplementary Material</bold>
</xref>). The chemical procedure included the acid digestion of sediment samples with the addition of <sup>209</sup>Po as a yield tracer and the deposition of the <sup>210</sup>Po onto ultrapure silver discs (<xref ref-type="bibr" rid="B23">Flynn, 1968</xref>). Activities were quantified in a Canberra Quad Alpha Spectrometer until a 1 &#x3c3; error was achieved. Additionally, five bulk sediment samples were analyzed for AMS radiocarbon dating in the Direct AMS laboratory, USA. Levels 0&#x2013;1 cm and 6&#x2013;7 cm were analyzed for the <sup>14</sup>C measurements in order to check any <sup>14</sup>C reservoir effect, a common issue in high Andean lakes. According to the <sup>210</sup>Pb model these levels correspond to the second half of the 20<sup>th</sup> century, &#x2212;60 and &#x2212;9 cal yrs BP, respectively. To estimate the reservoir effect in the Laguna El Calvario, the <sup>14</sup>C ages from levels 0&#x2013;1 cm and 6&#x2013;7 cm were averaged resulting in a reservoir age of 1041 <sup>14</sup>C yrs BP (950 cal yrs BP), which was subtracted from the remaining three older radiocarbon ages (<xref ref-type="table" rid="T1">
<bold>Table&#xa0;1</bold>
</xref>). Then, the radiocarbon ages were calibrated with the SHCal20 curve (<xref ref-type="bibr" rid="B42">Hogg et&#xa0;al., 2020</xref>) and the age-depth model was computed using Plum (<xref ref-type="bibr" rid="B500">Aquino-L&#xf3;pez et&#xa0;al., 2018</xref>) with the rPlum R package (<xref ref-type="bibr" rid="B7">Blaauw et&#xa0;al., 2020</xref>). rPlum is a recently developed Bayesian approach that permits computing integrated chronologies without pre-modeling the <sup>210</sup>Pb ages but combining other chronostratigraphic markers such as the <sup>14</sup>C ages.</p>
<table-wrap id="T1" position="float">
<label>Table&#xa0;1</label>
<caption>
<p>AMS radiocarbon dates of Laguna El Calvario record for the core LCA SHC4 core.</p>
</caption>
<table frame="hsides">
<thead>
<tr>
<th valign="middle" align="center">Laboratory ID</th>
<th valign="middle" align="center">Sample ID</th>
<th valign="middle" align="center">Depth (cm)</th>
<th valign="middle" align="center">Material</th>
<th valign="middle" align="center">
<sup>14</sup>C age</th>
<th valign="middle" align="center">Corrected cal. ages</th>
<th valign="middle" align="center">
<sup>210</sup>Pb ages (mid-point)</th>
</tr>
</thead>
<tbody>
<tr>
<td valign="bottom" align="left">D-AMS 021485</td>
<td valign="bottom" align="center">LCA SHC4 0&#x2013;1cm</td>
<td valign="bottom" align="center">0&#x2013;1</td>
<td valign="bottom" align="center">Bulk sediment</td>
<td valign="bottom" align="center">544 &#xb1; 28</td>
<td valign="bottom" align="center">&#x2013;</td>
<td valign="bottom" align="center">&#x2212;60</td>
</tr>
<tr>
<td valign="bottom" align="left">D-AMS 021486</td>
<td valign="bottom" align="center">LCA SHC4 6&#x2013;7cm</td>
<td valign="bottom" align="center">6&#x2013;7</td>
<td valign="bottom" align="center">Bulk sediment</td>
<td valign="bottom" align="center">1598 &#xb1; 21</td>
<td valign="bottom" align="center">&#x2013;</td>
<td valign="bottom" align="center">&#x2212;9</td>
</tr>
<tr>
<td valign="bottom" align="left">D-AMS 021487</td>
<td valign="bottom" align="center">LCA SHC4 18&#x2013;19cm</td>
<td valign="bottom" align="center">18&#x2013;19</td>
<td valign="bottom" align="center">Bulk sediment</td>
<td valign="bottom" align="center">2008 &#xb1; 31</td>
<td valign="bottom" align="center">937</td>
<td valign="bottom" align="center"/>
</tr>
<tr>
<td valign="bottom" align="left">D-AMS 021488</td>
<td valign="bottom" align="center">LCA SHC4 28&#x2013;29cm</td>
<td valign="bottom" align="center">28&#x2013;29</td>
<td valign="bottom" align="center">Bulk sediment</td>
<td valign="bottom" align="center">2549 &#xb1; 51</td>
<td valign="bottom" align="center">1478</td>
<td valign="bottom" align="center"/>
</tr>
<tr>
<td valign="bottom" align="left">D-AMS 021489</td>
<td valign="bottom" align="center">LCA SHC4 32&#x2013;32.5cm</td>
<td valign="bottom" align="center">32&#x2013;32.5</td>
<td valign="bottom" align="center">Bulk sediment</td>
<td valign="bottom" align="center">3765 &#xb1; 49</td>
<td valign="bottom" align="center">2694</td>
<td valign="bottom" align="center"/>
</tr>
</tbody>
</table>
</table-wrap>
<p>The XRF scanning was employed to measure the variability of geochemical elements on unprocessed sediments using an ITRAX core scanner (Cox Analytical Systems, <xref ref-type="bibr" rid="B15">Croudace et&#xa0;al., 2006</xref>) at the GEOPOLAR laboratory of the University of Bremen, Germany. Measures of the XRF series were established at each 2 mm interval and then a molybdenum tube at 40 kV and 10 mA was applied with an exposure time of 5 s for every measurement. The concentration of the different minerals was expressed in total counts (cnts) and elements over 100 cnts were selected. To support XRF data, continuous and discrete sediment samples were analyzed using an ICP-MS at UC-Davis facilities, from total digested sediment samples. The chemical procedure briefly consists of digesting ~250 mg of sediment with a mix of strong high-purity acids (HNO<sub>3</sub>, HCl, HCLO<sub>4</sub>, HF; Suprapure<sup>&#xae;</sup>Merck) in several steps until total dissolution, using screw-top PFA-Teflon&#x2122; vials and a hotplate Teflon&#x2122; PFA coating.</p>
</sec>
<sec id="s3_2">
<label>3.2</label>
<title>Inorganic proxies</title>
<p>Water content, organic matter, and grain size influence the scanning densities on XRF analysis (<xref ref-type="bibr" rid="B110">Zhang et&#xa0;al., 2020</xref>; <xref ref-type="bibr" rid="B69">Mondal et&#xa0;al., 2021</xref>), therefore ICP-MS was used to verify the trends of the measured elements included in this work. The elements Ti, K, Sr, and Rb can be associated with allochthonous detrital input into the lake (<xref ref-type="bibr" rid="B35">Guyard et&#xa0;al., 2007</xref>; <xref ref-type="bibr" rid="B17">Davies et&#xa0;al., 2015</xref>). The Ti/coh ratio was used as a proxy of clastic input (<xref ref-type="bibr" rid="B79">Ohlendorf et&#xa0;al., 2014</xref>; <xref ref-type="bibr" rid="B88">Schittek et&#xa0;al., 2016</xref>). The Zr/Ti ratio was used to infer the grain size given that Zr is highly abundant in the coarse silt fraction whereas Ti can be found in the clay to fine-silt fraction (<xref ref-type="bibr" rid="B80">Oldfield et&#xa0;al., 2003</xref>). Therefore, high Zr/Ti ratio values indicate increased coarse silt influx (<xref ref-type="bibr" rid="B90">Shala et&#xa0;al., 2014</xref>). The Si, P, Cd, U, and Cu elements were standardized by Titanium deposition.</p>
</sec>
<sec id="s3_3">
<label>3.3</label>
<title>Biological proxies</title>
<p>Pollen, diatom, and chironomid records were analyzed at 2 cm discrete intervals so each biological proxy record consisted of 17 samples. For the pollen analysis, 1 cm<sup>3</sup> of these sediment samples were processed following the standardized methods outlined by <xref ref-type="bibr" rid="B20">Faegri and Iversen (1989)</xref>, including KOH treatment, sieving, acids (HCl and HF for carbonate and silicate removal), and acetolysis. In levels with low pollen concentration, an additional 2 cm<sup>3</sup> of sediment was processed. For the estimation of pollen concentration (grains cm<sup>&#x2212;3</sup>), tablets of <italic>Lycopodium clavatum</italic> were added to each sediment sample (<xref ref-type="bibr" rid="B95">Stockmarr, 1971</xref>). The palynomorphs were determined at the most detailed taxonomic level under a microscope (400&#x2013;1000&#xd7;) aided by pollen taxonomic keys (<xref ref-type="bibr" rid="B41">Heusser, 1971</xref>; <xref ref-type="bibr" rid="B56">Markgraf and D'Antoni, 1978</xref>) and reference samples from the Laboratorio de Paleoecolog&#xed;a y Paleoclimatolog&#xed;a of the Centro de Estudios Avanzados en Zonas &#xc1;ridas (CEAZA). The basic pollen sum includes a minimum of 300 terrestrial pollen grains per sample while paludal, aquatic, and/or non-pollen taxa such as zygospores (Zygnemataceae) and microalgae were incorporated in a separate sum. Relative abundances were calculated for each taxon. Pollen accumulation rates (grains cm<sup>&#x2212;2</sup> yr<sup>&#x2212;1</sup>) were calculated employing the pollen concentration values and sedimentation rate derived from the age-depth model.</p>
<p>Two (2) grams of sediment were processed for diatom analysis following the methodology outlined by <xref ref-type="bibr" rid="B6">Battarbee (1986)</xref>. Each sample was dried, oxidized with H<sub>2</sub>O<sub>2,</sub> and heated for 2 minutes in a microwave. Finally, permanent preparations were mounted using Naphrax<sup>&#xae;</sup>. A minimum of 600 valves were counted to determine the relative abundances. For absolute abundances, the aliquot method (<xref ref-type="bibr" rid="B6">Battarbee, 1986</xref>) was used, following random transects. Results are expressed in valves per gram of dry sediment. The taxonomic literature on diatom determination included the monographic works of <xref ref-type="bibr" rid="B67">Metzeltin and Lange-Bertalot (1998)</xref>; <xref ref-type="bibr" rid="B68">Metzeltin and Lange-Bertalot (2007)</xref>, <xref ref-type="bibr" rid="B501">Rumrich et&#xa0;al. (2000)</xref>, and <xref ref-type="bibr" rid="B50">Lange-Bertalot et&#xa0;al. (2017)</xref>, among others.</p>
<p>Five (5) grams of wet sediment were processed for chironomid analysis. The sediment samples were deflocculated using 10% KOH solution at 50&#x2013;70&#xb0;C for 30 minutes and sieved through 100 and 200 um mesh sizes. Larval head capsules (HC) were hand-sorted from the residual sediment and mounted on permanent slides with Hidromatrix&#xae; mounting media. Taxonomic identification was performed under a Nikon Phase optic microscope at a magnification of 100&#x2013;1000&#xd7; with reference to available taxonomic literature (<xref ref-type="bibr" rid="B61">Massaferro and Brooks, 2002</xref>; <xref ref-type="bibr" rid="B62">Massaferro et&#xa0;al., 2013</xref>; <xref ref-type="bibr" rid="B14">Cranston, 2019</xref>).</p>
<p>Given the nature of each of the analyzed proxies in the Laguna El Calvario record, their sensitivity and response time to a given environmental/climatic change may differ from one to another. So we decided to analyze each of them separately and therefore integrate their signal in the discussion section taking into account the different spatial/temporal scales represented by each other.</p>
</sec>
</sec>
<sec id="s4" sec-type="results">
<label>4</label>
<title>Results</title>
<sec id="s4_1">
<label>4.1</label>
<title>Chronology, lithology, organic and inorganic content, XRF and ICP-MS analyses</title>
<p>The retrieved core of Laguna El Calvario spans the last 2400 cal yrs BP (<xref ref-type="fig" rid="f2">
<bold>Figure&#xa0;2</bold>
</xref>). The part of the age&#x2013;depth model based on the three radiocarbon dates is the most accurate possible concerning the given ages (<xref ref-type="table" rid="T1">
<bold>Table&#xa0;1</bold>
</xref>). The <sup>210</sup>Pb radioactive activities showed good exponential decay and the unsupported activities occurred in the first 15 cm reaching the age of 1833 AD (<xref ref-type="supplementary-material" rid="SM1">
<bold>Figure&#xa0;2</bold>
</xref>, <xref ref-type="supplementary-material" rid="SM1">
<bold>Table&#xa0;1 Supplementary Material</bold>
</xref>), determining a supported activity of 0.85 &#xb1; 0.17 dpm g<sup>&#x2212;1</sup>. The mean sedimentation rate ranges around 0.13 &#xb1; 0.01 cm year<sup>&#x2212;1</sup> in the first 5 cm.</p>
<fig id="f2" position="float">
<label>Figure&#xa0;2</label>
<caption>
<p>Bayesian age <italic>vs</italic> depth model constructed in rplum R package (<xref ref-type="bibr" rid="B7">Blaauw et&#xa0;al., 2020</xref>) based on the <sup>210</sup>Pb and radiocarbon ages of the LCA SH4 core. The weighted mean of the model is represented in the red dashed line where the black shadow shows the 95% confidence interval. Blue rectangles indicate the depth position and <sup>210</sup>Pb activities (dpm g<sup>&#x2212;1</sup>) (axis labels at the right) and <sup>14</sup>C samples correspond to the purple figures.</p>
</caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fevo-11-1227020-g002.tif"/>
</fig>
<p>The lithological description and organic content of the sedimentological record of Laguna El Calvario (LCA-SHC4; 33 cm) are summarized in <xref ref-type="fig" rid="f3">
<bold>Figure&#xa0;3</bold>
</xref>. Between 33 and 28 cm the sediment is composed of a porous dark brownish silty sand with gravel-sized clasts. The organic matter and carbonate contents are around 25% and 3%, respectively, while the inorganic density exhibits its highest values (0.21&#x2013;0.33 g cm<sup>&#x2212;3</sup>). The sediment composition shifts to clayey silt from 28 cm to the top of the core. Intercalated light&#x2013;dark brown and green laminated layers are present around 20&#x2013;28 cm and 2&#x2013;8 cm whereas a brown homogeneous layer is present between 20 and 8 cm. The content of organic matter and clasts fluctuates around 22&#x2013;42%, and 2.6&#x2013;3.9%, respectively. Inorganic density ranged between 0.1 and 0.2 g cm<sup>&#x2212;3</sup>.</p>
<fig id="f3" position="float">
<label>Figure&#xa0;3</label>
<caption>
<p>Lithology, water content and loss on ignition of the Laguna El Calvario record.</p>
</caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fevo-11-1227020-g003.tif"/>
</fig>
<p>Regarding the geochemical results, changes in XRF-Molybdenum Incoherent/Coherent ratio (inc/coh) follow the LOI organic matter (%) and water content (%) (<xref ref-type="fig" rid="f3">
<bold>Figure&#xa0;3</bold>
</xref>). The elements Ti, K and Sr show similar trends throughout the core according both, XRF and ICP-MS data (<xref ref-type="supplementary-material" rid="SM1">
<bold>Figure&#xa0;4</bold>
</xref>; <xref ref-type="supplementary-material" rid="SM1">
<bold>Tables&#xa0;2</bold>
</xref>, <xref ref-type="supplementary-material" rid="SM1">
<bold>3 Supplementary Material</bold>
</xref>), which validates the data obtained with XRF. Indeed, the strong coherence among these curves suggests the same origin of variability (<xref ref-type="supplementary-material" rid="SM1">
<bold>Table&#xa0;2 Supplementary Material</bold>
</xref>). The sparse plant cover in the surroundings and the hydrological changes associated with the precipitation regime dynamics can modulate the terrigenous input into the lake therefore, the Ti/coh ratio was applied as an indirect indicator of precipitation. Thus, high values of Ti/coh ratio along with Ti, K, and Sr in the ICP-MS were recorded between 32 and 28 cm (<xref ref-type="fig" rid="f4">
<bold>Figure&#xa0;4</bold>
</xref>). Between 28 and 20 cm, Ti/coh ratio shows highly variable values with maxima around 27 and 21 cm concomitant with the occurrence of a dark layer (<xref ref-type="fig" rid="f4">
<bold>Figure&#xa0;4</bold>
</xref>). Between 20 and 8 cm, these ratio values are more stable but show a rising trend. Ti, K, and Sr and the Ti/coh ratio values display a declining trend in the last 8 cm. Additionally, XRF data including Rb showed similar trends (<xref ref-type="fig" rid="f4">
<bold>Figure&#xa0;4</bold>
</xref>).</p>
<fig id="f4" position="float">
<label>Figure&#xa0;4</label>
<caption>
<p>XRF and MS-ICP data of trace elements of the Laguna El Calvario.</p>
</caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fevo-11-1227020-g004.tif"/>
</fig>
<p>The Zr/Ti ratio, a proxy of grain size changes, shows peak values and high variability that are concomitant with laminated sediments between 28 and 20 cm and then, in the last 8 cm (<xref ref-type="fig" rid="f4">
<bold>Figure&#xa0;4</bold>
</xref>). The silica data based on the XRF analysis were not included in the results due to the low counts. In this regard, the Si/Ti ratio in the ICP_MS analysis shows different trends of the detrital-related elements since increases are observed in the topmost 6 cm of the record (<xref ref-type="fig" rid="f4">
<bold>Figure&#xa0;4</bold>
</xref>). So, the variation of silica in the record could be attributed to intra-lake processes such as productivity. The P/Ti ratio from the ICP-MS data also shows the highest values in the topmost 6 cm supporting the silica interpretation. The ICP-MS Cd/Ti and U/Ti ratios were considered as proxies of sulfidic conditions and organic sedimentation given that the U content is normally well correlated with organic fluxes reaching the bottom of the lake. In fact, Cd/Ti and U/Ti ratios present their highest values in the topmost 8 cm. Finally, the ICP-MS Cu/Ti is considered an indicator of mining activity in the region, which displays the highest concentrations in the uppermost 6 cm.</p>
</sec>
<sec id="s4_2">
<label>4.2</label>
<title>Biological proxy analyses</title>
<p>The palynological record shows a high plant diversity with pollen taxa defining the three main vegetation belts in the western semiarid Andean region: Poaceae, <italic>Adesmia-</italic>type, and <italic>Nassauvia-</italic>type (high and lower Andean); <italic>Ephedra</italic> (sub-Andean), and Chenopodiaceae and arboreal taxa (pre-Andean) (<xref ref-type="fig" rid="f5">
<bold>Figure&#xa0;5A</bold>
</xref>).</p>
<fig id="f5" position="float">
<label>Figure&#xa0;5</label>
<caption>
<p>
<bold>(A)</bold> Pollen record; <bold>(B)</bold> Diatom record; <bold>(C)</bold> Chironomid record of the Laguna El Calvario. The grey shadows in the pollen and diatom records correspond to exaggeration at 3x.</p>
</caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fevo-11-1227020-g005.tif"/>
</fig>
<p>Between 32 and 22 cm (2400&#x2013;1000 cal yrs BP; <xref ref-type="fig" rid="f5">
<bold>Figure&#xa0;5A</bold>
</xref>), the pollen record is dominated by Poaceae (up to 22%), <italic>Chaethantera/Oriastrum</italic> (6&#x2013;17.3%), <italic>Senecio-</italic>type (6&#x2013;12%), <italic>Oxalis</italic> (3&#x2013;11%), <italic>Ephedra</italic> (&lt;10%), Chenopodiaceae (9&#x2013;14%) and <italic>Arenaria</italic> (4&#x2013;13%). The cold-tolerant pollen types such as <italic>Nassauvia</italic>-type (up to 3.6%), <italic>Adesmia-</italic>type (up to 6.2%), <italic>Laretia</italic>-type (up to 5%) reach their highest values at the top of the zone (1500&#x2013;1000 cal yrs BP) whereas Poaceae percentages gradually decline (8.5%). <italic>Arenaria values</italic> increase from 4 to 12% since 1300 cal yrs BP. Cyperaceae and <italic>Myriophyllum</italic>, paludal and aquatic taxa, display low frequencies (&lt;2%) while the non-pollen palynomorph <italic>Pediastrum</italic> presents maximum values of ~28 cm. Pollen accumulation rates (PAR) for local terrestrial taxa are relatively low ranging between 9 and 25 pollen grains cm<sup>&#x2212;2</sup> yr<sup>&#x2212;1</sup>.</p>
<p>Between 22 and 12 cm (1000&#x2013;75 cal yrs B; <xref ref-type="fig" rid="f5">
<bold>Figure&#xa0;5A</bold>
</xref>), the pollen assemblages are characterized by the slight recovery of Poaceae values up to 14.5% along with the decline of <italic>Chaethantera/Oriastrum</italic>, <italic>Nassauvia-</italic>type and <italic>Adesmia-</italic>type<italic>. Ephedra</italic> (up to 21.6%), Montiaceae (4&#x2013;17%) and Verbenaceae (2&#x2013;7%) values increase during this period. Cyperaceae percentages remain under 2% while <italic>Pediastrum</italic> values strongly decline to almost zero. <italic>Spirogyra</italic> spores display a mild increment and the <italic>Zygnema</italic> spores percentages increase at 16 cm (100 cal yrs BP). PAR values are the lowest for the whole record (total terrestrial pollen ca. 2 grains cm<sup>&#x2212;2</sup> yr<sup>&#x2212;1</sup>) increasing towards the end of this period (up to 40 grains cm<sup>&#x2212;2</sup> yr<sup>&#x2212;1</sup>).</p>
<p>Between 12 and 0 cm (75 cal yrs BP to present; <xref ref-type="fig" rid="f5">
<bold>Figure&#xa0;5A</bold>
</xref>), shrubs such as <italic>Ephedra</italic>, Chenopodiaceae, and <italic>Senecio-</italic>type percentages declined at the expenses of Poaceae (10&#x2013;37%) and herbs values such as <italic>Arenaria</italic> (12&#x2013;28%) and Montiaceae (13&#x2013;21.6%). Other taxa percentages such as Verbenaceae (5&#x2013;10%) and <italic>Plantago</italic> (1&#x2013;2.5%) increase during this period similar to Cyperaceae percentages that show an increment towards the top of the record (2.6&#x2013;12.8%). The non-pollen palynomorphs (NPPs), such as the algae <italic>Pediastrum</italic> and the <italic>Zygnema</italic> spores, values also show a significant increase whereas <italic>Spyrogyra</italic> spores are absent in this zone. PAR values are the highest for the whole sequence reaching up to 126 grains cm<sup>&#x2013;2</sup> yr<sup>&#x2013;1</sup>.</p>
<p>The diatom record of the Laguna El Calvario includes 15 taxa that have relative abundances over 5% (<xref ref-type="fig" rid="f5">
<bold>Figure&#xa0;5B</bold>
</xref>). Between 32 and 19 cm (2400&#x2013;700 cal yrs BP), diatom assemblages are characterized by a high frequency of <italic>Cymbella</italic> spp. (20&#x2013;42%), <italic>Halamphora veneta</italic> (15&#x2013;25%) and <italic>Gomphonema</italic> spp. (20&#x2013;50%). Associated taxa include <italic>Planothidium aff. biporomum</italic> (0&#x2013;5%), <italic>Pinnularia aff. brebissonii</italic> (1&#x2013;6%), <italic>Craticula pampeana</italic> (1&#x2013;11.6% at 25&#x2013;27 cm), <italic>Craticula halophila</italic> (0&#x2013;7%)<italic>, Caloneis silicuta</italic> (0&#x2013;3%) and <italic>Nitzchia</italic> spp. (0&#x2013;4%). Small fragilariods, including <italic>Pseudostaurosira pseudoconstruens</italic>, display a short-lived peak at the top of the period (ca. 1000 cal yrs BP). Diatoms abundance fluctuates between 60 and 130 &#xd7; 10<sup>7</sup> valves per gram of dry sediment (<xref ref-type="fig" rid="f5">
<bold>Figure&#xa0;5B</bold>
</xref>). Between 19 and 5 cm (700 cal yrs BP to 1970 AD), <italic>Gomphonema</italic> spp. (up to 45%) and the small fragilarioids (with more than 45% at the top of the period) dominate while <italic>Cymbella</italic> spp. and <italic>Halamphora veneta</italic> values decline. Other secondary taxa such as <italic>Fragilaria capucina</italic> var., <italic>Amphora copulata</italic>, <italic>Ulnaria ulna</italic>, and <italic>Encyonema silesiacum</italic> showed minor increments. The diatom record presents a major diatom assemblage change in the last 5 cm (1970 AD to present) when most of the taxa values decline at expenses of the small fragilarioids (82&#x2013;92%; <xref ref-type="fig" rid="f5">
<bold>Figure&#xa0;5B</bold>
</xref>). <italic>Ulnaria ulna</italic> exhibited a minor increase in the most surficial sample (5.6%).</p>
<p>The chironomid record is characterized by the presence of 3 morphotypes (<xref ref-type="fig" rid="f5">
<bold>Figure&#xa0;5C</bold>
</xref>). The dominant morphotype is <italic>Cricotopus</italic> sp1 with ca. 80% of the total relative abundance associated with <italic>Cricotopus</italic> sp 2 (ca.15%) and <italic>Parochlus</italic> &lt; 5%. From 32 to 14 cm (2400&#x2013;120 cal yrs BP), the chironomid assemblages are dominated by the morphotypes <italic>Cricotopus</italic> sp1 and <italic>Cricotopus</italic> sp2. The Head Capsules (HC) counts are highly variable ranging between 2 and 33 (<xref ref-type="fig" rid="f5">
<bold>Figure&#xa0;5C</bold>
</xref>). Between 14 and 0 cm (from 120 cal yrs BP to 2014 AD), the chironomid record shows a clear alternation of <italic>Cricotopus</italic> and <italic>Parochlus</italic> abundance whereas the HC counts ranged from 31 and 2. <italic>Cricotopus</italic> sp1 dominates the whole record except for a peak of <italic>Parochlus</italic> at 2 cm. <italic>Cricotopus</italic> sp 2 co-dominates the records but disappears in the topmost 2 cm (<xref ref-type="fig" rid="f5">
<bold>Figure&#xa0;5C</bold>
</xref>). Given the low counts of HC, we interpreted with caution the chironomid record which was supported with the other proxies.</p>
</sec>
</sec>
<sec id="s5" sec-type="discussion">
<label>5</label>
<title>Discussion</title>
<sec id="s5_1">
<label>5.1</label>
<title>Past environmental changes in Laguna El Calvario</title>
<p>The multiproxy analysis of Laguna El Calvario allows us to have a broad perspective of the past environmental changes during the last 2400 years in the western semiarid Andes (29&#xb0;S). Following the lithological and biological changes in the sedimentary record (<xref ref-type="fig" rid="f3">
<bold>Figures&#xa0;3</bold>
</xref>&#x2013;<xref ref-type="fig" rid="f5">
<bold>5</bold>
</xref>) four main phases can be distinguished.</p>
<sec id="s5_1_1">
<label>5.1.1</label>
<title>Phase 1: from 2400 to 1400 cal yr BP</title>
<p>Between 2400 and 1400 cal yrs BP the sedimentary record of Laguna El Calvario is characterized by the presence of sands with gravel-sized clasts (<xref ref-type="fig" rid="f2">
<bold>Figure&#xa0;2</bold>
</xref>) with high inorganic density and high values of Ti/coh ratio (particularly between 2400&#x2013;2000 cal yrs BP) as well other elements (<xref ref-type="fig" rid="f4">
<bold>Figures&#xa0;4</bold>
</xref>, <xref ref-type="fig" rid="f6">
<bold>6A, B</bold>
</xref>). These sedimentological and geochemical features suggest a relatively high-energy deposition together with intense allochthonous sediment input that might be associated with high precipitation by this time (<xref ref-type="bibr" rid="B37">Haberzettl et&#xa0;al., 2005</xref>; <xref ref-type="bibr" rid="B36">Haberzettl et&#xa0;al., 2007</xref>; <xref ref-type="bibr" rid="B88">Schittek et&#xa0;al., 2016</xref>). The latter may also indicate glacial activity or increased runoff of detrital material after glacial retreatment in the basin. A similar situation has been observed in the glacial sediments from an Andean lake in Per&#xfa;, where a high concentration of Sr was associated with erosion of granodiorite bedrock triggered by active glaciers (<xref ref-type="bibr" rid="B94">Stansell et&#xa0;al., 2013</xref>). More humid and colder than today conditions are reflected by the pollen record until 1400 cal yrs BP, supporting the latter. High Poaceae frequency and cold-tolerant taxa (<italic>Chaetanthera/Oriastrum</italic>, <italic>Nassauvia-</italic>type, <italic>Adesmia-</italic>type, <italic>Azorella-</italic>type, <italic>Laretia-</italic>type, <italic>Senecio-</italic>type, and Oxalis) percentages along with low pollen accumulation rates (PAR) before 1500 cal yrs BP (<xref ref-type="fig" rid="f5">
<bold>Figure&#xa0;5A</bold>
</xref>) reflect the upper Andean belt currently located 250 m above the Laguna El Calvario. However, the vegetation cover of the lower Andean belt that currently surrounds the lake catchment (4000 m a.s.l.; <xref ref-type="fig" rid="f1">
<bold>Figure&#xa0;1</bold>
</xref>) is low due to very low growth rates promoted by cold temperatures, even during the warmest months (<xref ref-type="bibr" rid="B87">Rudloff et&#xa0;al., 2021</xref>).</p>
<fig id="f6" position="float">
<label>Figure&#xa0;6</label>
<caption>
<p>
<bold>(A)</bold> Titanium/Molybdenum coherent ratio (XRF); <bold>(B)</bold> Sr (XRF); <bold>(C)</bold> Pollen; <bold>(D)</bold> Diatom and Phosphorus concentrations of the Laguna El Calvario; <bold>(E)</bold> Hydrological changes in the Andean lake Laguna El Negro Francisco (27&#xb0;S; 4125 m a.s.l., <xref ref-type="bibr" rid="B34">Grosjean et&#xa0;al., 1997</xref>); <bold>(F)</bold> Storm activity in the Andean lake Laguna Cerritos Blancos (30&#xb0;S, 3850 m a.s.l., <xref ref-type="bibr" rid="B98">Tiner et&#xa0;al., 2018</xref>); <bold>(G)</bold> Moisture changes in the Andean lake Laguna Chepical (32&#xb0;S, 3050 m a.s.l., <xref ref-type="bibr" rid="B59">Martel-Cea et&#xa0;al., 2016</xref>); <bold>(H)</bold> El Ni&#xf1;o activity inferred by Lithic influx in a sediment core located in the Peruvian offshore (<xref ref-type="bibr" rid="B85">Rein et&#xa0;al., 2005</xref>) and <bold>(I)</bold> Sand content in the Laguna El Junco, Gala&#x301;pagos archipelago, Ecuador (<xref ref-type="bibr" rid="B13">Conroy et&#xa0;al., 2008</xref>). Shadows bars correspond to the phases discussed in text.</p>
</caption>
<graphic mimetype="image" mime-subtype="tiff" xlink:href="fevo-11-1227020-g006.tif"/>
</fig>
<p>The diatom richness is characterized by the presence of the epiphytic diatoms <italic>Planothidium</italic> aff. <italic>biporomum</italic>, <italic>Cymbella</italic> spp. and <italic>Gomphonema</italic> spp. along with the benthic <italic>Halamphora veneta</italic> and <italic>Craticula</italic> spp. between 2400 to 1400 cal yrs BP. These assemblages reveal a shallow, vegetated, and saline-prone (particularly by the presence of <italic>Gomphonema </italic>spp. and <italic>Halamphora veneta)</italic> lacustrine environment (<xref ref-type="fig" rid="f5">
<bold>Figure&#xa0;5B</bold>
</xref>) (e.g., <xref ref-type="bibr" rid="B45">Jenny et&#xa0;al., 2002a</xref>; <xref ref-type="bibr" rid="B46">Jenny et&#xa0;al., 2002b</xref>; <xref ref-type="bibr" rid="B38">Hassan et&#xa0;al., 2013</xref>) but also the occurrence of oxygenated and shallow freshwater evidenced by the high frequency of the planktonic green algae <italic>Pediastrum</italic> sp. (<xref ref-type="fig" rid="f5">
<bold>Figure&#xa0;5A</bold>
</xref>) (<xref ref-type="bibr" rid="B44">Innes and Zong, 2021</xref>). The presence of the littoral cold-adapted <italic>Cricotopu</italic>s as the dominant taxa in this part of the chironomid record (<xref ref-type="fig" rid="f5">
<bold>Figure&#xa0;5C</bold>
</xref>) also supports the cold and shallow conditions (<xref ref-type="bibr" rid="B63">Matthews-Bird et&#xa0;al., 2016</xref>; <xref ref-type="bibr" rid="B73">Motta and Massaferro, 2019</xref>; <xref ref-type="bibr" rid="B58">Martel-Cea et&#xa0;al., 2021</xref>). Additionally, the lowest values of Phosphorus and diatom concentrations may evidence low primary productivity in the water column (<xref ref-type="fig" rid="f5"><bold>Figures 5B</bold></xref> and <xref ref-type="fig" rid="f6"><bold>6D</bold></xref>). Wet years before 1400 cal yrs BP may have increased the water input to the lake via snowmelt and/or upslope fluvio-glacial flow triggering the temporary rise of the lake level and promoting the increment of habitat opportunities for the aquatic biota (e.g., <xref ref-type="bibr" rid="B44">Innes and Zong, 2021</xref>).</p>
</sec>
<sec id="s5_1_2">
<label>5.1.2</label>
<title>Phase 2: from 1400 and 800 cal yr BP</title>
<p>After 1400 cal yrs BP, a shift from sand to laminated clayey silts characterized the sedimentary sequence until 800 cal yrs BP reflecting the onset of typical lacustrine-type sedimentation. The rise and fluctuation of the Zr/Ti ratio peaking around 1400&#x2013;1300 and 1000&#x2013;850 cal yrs BP (<xref ref-type="fig" rid="f4">
<bold>Figure&#xa0;4</bold>
</xref>) indicate an increased input of the coarser silt fraction to the lake (<xref ref-type="bibr" rid="B80">Oldfield et&#xa0;al., 2003</xref>). This might be associated with an increase in torrential rainfall, an upward displacement of the zero isotherm, or rapid melting of the snowpack as stated for the previous period. This is supported by the drop and variations of Ti/coh ratio values (<xref ref-type="fig" rid="f6">
<bold>Figure&#xa0;6A</bold>
</xref>) that imply a decrease of precipitation under a centennial-scale variability with moderate magnitude wet spells around 1200 and 1100 cal yrs BP. The pollen record shows the increment of cold-tolerant taxa (<italic>Chaethantera/Oriastrum, Adesmia-</italic>type, <italic>Azorella-</italic>type), <italic>Arenaria</italic> (<xref ref-type="fig" rid="f5">
<bold>Figure&#xa0;5A</bold>
</xref>), and a slight decline of Poaceae (<xref ref-type="fig" rid="f6">
<bold>Figure&#xa0;6C</bold>
</xref>) between 1400 and 800 cal yrs BP, suggesting the occurrence of cold conditions. The mild increment of PAR values (<xref ref-type="fig" rid="f5">
<bold>Figure&#xa0;5A</bold>
</xref>) can be related to an increase in temperature during the growing season (i.e., an amelioration of climatic conditions allowing the expansion of the plant cover; <xref ref-type="bibr" rid="B92">Squeo et&#xa0;al., 2006</xref>; <xref ref-type="bibr" rid="B87">Rudloff et&#xa0;al., 2021</xref>). <italic>Arenaria</italic> together with the persistence of <italic>Cricotopus</italic> spp. pointed out a decline in the lake level and/or expansion of the riparian/coastal zone (<xref ref-type="bibr" rid="B86">Riedemann et&#xa0;al., 2008</xref>; <xref ref-type="bibr" rid="B57">Markgraf et&#xa0;al., 2009</xref>; <xref ref-type="bibr" rid="B97">Teillier et&#xa0;al., 2011</xref>; <xref ref-type="bibr" rid="B59">Martel-Cea et&#xa0;al., 2016</xref>). This could be associated with a seasonal retraction of the lake that should have been constant over time in order to be recorded at sub-centennial time scales. The aquatic taxa also point out the decline of the lake level given the sustained drop of <italic>Pediastrum</italic> sp. (<xref ref-type="fig" rid="f5">
<bold>Figure&#xa0;5A</bold>
</xref>). In this context, <xref ref-type="bibr" rid="B90">Shala et&#xa0;al. (2014)</xref> recorded increased Zr/Ti ratio when silt deposits in the littoral zone were eroded after the decline of the water column in a Finnish glacial lake. Therefore, the Zr/Ti increase occurred around 1350 and ca. 900 cal yrs BP in the Laguna El Calvario record could be related to an increase of detrital material by erosion and/or transport. To sum up, increased or sustained precipitation associated with cold conditions under a more pronounced seasonality occurred between 1400 and 800 cal yrs BP, compared to the previous phase.</p>
</sec>
<sec id="s5_1_3">
<label>5.1.3</label>
<title>Phase 3: from 800 cal yrs BP to 1850 AD</title>
<p>A shift from laminated to homogenous clayey silt sediment, a decline of silt influxes (low Zr/Ti ratio, <xref ref-type="fig" rid="f4">
<bold>Figure&#xa0;4</bold>
</xref>), a mild increase and stabilization of Ti/coh (<xref ref-type="fig" rid="f6">
<bold>Figure&#xa0;6A</bold>
</xref>) and other detrital input indicators (Ti, K, Sr, Ca) trends may indicate stable climatic conditions regarding the previous phase. On the other hand, the pollen record shows a minor increase of Montiaceae and <italic>Arenaria</italic> along with the decline of cold-tolerant taxa (<italic>Chaethantera/Osriastrum, Nassauvia-</italic>type, and <italic>Adesmia-</italic>type) from the Andean belt associated with an expansion of shrubs from Sub-Andean (<italic>Ephedra</italic>, Verbenaceae) and the Pre-Andean belt pollen types (<italic>Baccharis</italic>) to a lesser extent (<xref ref-type="fig" rid="f5">
<bold>Figure&#xa0;5A</bold>
</xref>). This may imply an upward displacement of vegetation belts even PAR values decrease would still indicate very sparse vegetation. The increase of spores of <italic>Spirogyra</italic>, the absence of <italic>Pediastrum</italic> sp. (<xref ref-type="fig" rid="f5">
<bold>Figure&#xa0;5A</bold>
</xref>) along with the increase of the small fragilarioids between 800 and 250 cal yrs BP (<xref ref-type="fig" rid="f5">
<bold>Figure&#xa0;5B</bold>
</xref>) reveals the persistence of a shallow lake environment under dry conditions. Particularly, <italic>Spirogyra</italic> is common in standing water that experiences seasonal desiccation, regressive stage, and/or very shallow freshwater (<xref ref-type="bibr" rid="B43">Hoshaw and McCourt, 1988</xref>; <xref ref-type="bibr" rid="B65">Medeanic, 2006</xref>; <xref ref-type="bibr" rid="B100">van Geel et&#xa0;al., 2020</xref>). To sum up, the multiproxy record of Laguna El Calvario reflects a phase of increased aridity with an upward expansion of vegetation belts, low lake levels, and stable low precipitation between 800 cal yrs BP and 1850 AD.</p>
</sec>
<sec id="s5_1_4">
<label>5.1.4</label>
<title>Phase 4: from 1850 to 2014 AD</title>
<p>From 1850 AD to 1940 AD, the Ti/coh ratio and the allochthonous elements (Ti, K, Sr, Rb) present important peaks and then show a two-step decline during the last 50 years (<xref ref-type="fig" rid="f4">
<bold>Figures&#xa0;4</bold>
</xref>, <xref ref-type="fig" rid="f6">
<bold>6A, B</bold>
</xref>). In the first half of the 20<sup>th</sup> century, the PAR reached maximum values with pollen assemblages dominated by Poaceae, Montiaceae, Verbenaceae, and <italic>Arenaria</italic> (<xref ref-type="fig" rid="f4">
<bold>Figures&#xa0;4A</bold>
</xref>, <xref ref-type="fig" rid="f5">
<bold>5C</bold>
</xref>) which reflect the establishment of wetter conditions in the Laguna El Calvario basin regarding the previous phase. However, a vegetation turnover occurred in the early 2000s when lowland taxa such as Chenopodiaceae and <italic>Ephedra</italic> increased relative to Poaceae, Montiaceae, and <italic>Arenaria</italic>. This vegetation shift implies a transition from wetter than present to the current semiarid conditions that may be associated with a decrease in precipitation and a rise in temperature as recorded by instrumental records in the semiarid Andes of central Chile (<xref ref-type="bibr" rid="B72">Morales et&#xa0;al., 2020</xref>). The same trend has previously been recorded at a regional scale resulting in the glacier equilibrium line altitude, an upward shift of the zero-isotherm altitude (<xref ref-type="bibr" rid="B10">Carrasco et&#xa0;al., 2005</xref>; <xref ref-type="bibr" rid="B5">Barria et&#xa0;al., 2019</xref>), and reduction of the glacier-covered area (~35%) (<xref ref-type="bibr" rid="B40">Hess et&#xa0;al., 2020</xref>) that ultimately have directly affected the primary productivity and phenology of the Andean communities (<xref ref-type="bibr" rid="B87">Rudloff et&#xa0;al., 2021</xref>). The increment of the Zr/Ti ratio since 1940 AD (<xref ref-type="fig" rid="f4">
<bold>Figure&#xa0;4</bold>
</xref>) can be linked to the decline of the water level causing an increment of coarser silts in the sedimentary sequence accumulated in the catchment during the previous wetter decades. During the 20<sup>th</sup> century, the aquatic assemblages display the increment of <italic>Pediastrum</italic> sp. along with Cyperaceae and <italic>Zygnema</italic> (whose habitat preferences are associated with marsh environments, <xref ref-type="fig" rid="f5">
<bold>Figure&#xa0;5A</bold>
</xref>; <xref ref-type="bibr" rid="B44">Innes and Zong, 2021</xref>). On the other hand, the diatom assemblages display a complete dominance of the tychoplanktonic small fragilarioids and <italic>Ulnaria ulna</italic> (<xref ref-type="fig" rid="f5">
<bold>Figure&#xa0;5B</bold>
</xref>) whereas the chironomid record shows the establishment and increment of <italic>Parochlus</italic> sp., a cold-stenothermal (and an oxy-conformer) littoral taxon (<xref ref-type="fig" rid="f5">
<bold>Figure&#xa0;5C</bold>
</xref>). All the proxies together suggest a shift from a saline-prone to a cold freshwater lake probably associated with an increase of the rock glacier/snow melting along with an oxygenated (during springs) and oligo-mesotrophic water column possibly with the occurrence of ice cover during wintertime (<xref ref-type="bibr" rid="B52">Lotter and Bigler, 2000</xref>; <xref ref-type="bibr" rid="B3">Alvial et&#xa0;al., 2008</xref>; <xref ref-type="bibr" rid="B38">Hassan et&#xa0;al., 2013</xref>; <xref ref-type="bibr" rid="B59">Martel-Cea et&#xa0;al., 2016</xref>; <xref ref-type="bibr" rid="B58">Martel-Cea et&#xa0;al., 2021</xref>).</p>
<p>Recent human activity is also evident in the pollen record around Laguna El Calvario. A major increase of the palatable <italic>Plantago</italic> genera occurred around 1900&#x2013;1920 AD (<xref ref-type="fig" rid="f5">
<bold>Figure&#xa0;5A</bold>
</xref>) synchronous to the intense transhumant livestock farming (mainly goats) that began during the first part of the 20<sup>th</sup> century (<xref ref-type="bibr" rid="B11">Castillo, 2003</xref>). On the other hand, even with the persistence of <italic>Ephedra</italic> and Chenopodiaceae throughout the record, both taxa exhibit minima values around 1900&#x2013;1980 AD. <italic>Ephedra</italic> and Chenopodiaceae have been commonly and/or extensively used as fodder plants and/or fuel resources in the region (e.g. <xref ref-type="bibr" rid="B66">Meneses, 2017</xref>; <xref ref-type="bibr" rid="B75">Mu&#xf1;oz and Villase&#xf1;or, 2018</xref>) which may explain their low percentages in the pollen record during the 20<sup>th</sup> century.</p>
<p>High values of Ti/coh ratio, P/Ti and Si/Ti ratios (ICP-MS data), organic matter (<xref ref-type="fig" rid="f2">
<bold>Figures&#xa0;2</bold>
</xref>, <xref ref-type="fig" rid="f4">
<bold>4</bold>
</xref>), and diatom concentrations (<xref ref-type="fig" rid="f6">
<bold>Figure&#xa0;6D</bold>
</xref>) in the second half of the 20<sup>th</sup> century pinpoint an important increment of primary productivity. High rates of U accumulation (<xref ref-type="fig" rid="f4">
<bold>Figure&#xa0;4</bold>
</xref>) have been normally related to reducing conditions in marine and lacustrine environments which would be related to the reduction of the soluble phase of U(VI) to U(IV) in the vicinity of Fe(III) and SO<sub>4</sub> reduction (<xref ref-type="bibr" rid="B48">Klinkhammer and Palmer, 1991</xref>; <xref ref-type="bibr" rid="B24">Francois et&#xa0;al., 1993</xref>; <xref ref-type="bibr" rid="B111">Zheng et&#xa0;al., 2002</xref>; <xref ref-type="bibr" rid="B99">Tribovillard et&#xa0;al., 2006</xref>). This could explain the high concentration of U/Ti and Cd/Ti ratios, both increasing under reducing environmental conditions and in the presence of sulfides. These would have happened during periods characterized by high organic sedimentation rates which agrees with P/Ti ratio values and diatom concentration increase, reflecting the organic production in the column water or in the benthic zone. Notwithstanding, in some cases, the particulate U sedimentation overcomes the accumulation by diagenetic reactions (<xref ref-type="bibr" rid="B12">Chappaz et&#xa0;al., 2010</xref>). Instead, the Cu forms organic complexes with dissolved organic matter in superficial waters and is rapidly removed from natural waters (<xref ref-type="bibr" rid="B84">Rader et&#xa0;al., 2019</xref>). In sediments, it binds with clays, oxides, sulfides, and organic matter (<xref ref-type="bibr" rid="B8">Bryan et&#xa0;al., 2002</xref>; <xref ref-type="bibr" rid="B99">Tribovillard et&#xa0;al., 2006</xref>) increasing the concentrations of lake bottoms when anoxic conditions prevail (<xref ref-type="bibr" rid="B96">Sundelin and Eriksson, 2001</xref>). In this context, the increase of Cu (shown as Cu/Ti ratio; <xref ref-type="supplementary-material" rid="SM1">
<bold>Figure&#xa0;2 Supplementary Material</bold>
</xref>) would be caused by increased organic compounds in the water column derived from primary productivity within the lake and the basin. However, this coupled Cu-primary productivity increase was not observed earlier in the record. An alternative explanation could be that the metal increases could be caused by anthropogenic impact, due to in the last century mining activities, 50 km close to the lake, that has had an enormous influence on air pollution, as has been recorded both on the coast and in the Andes (<xref ref-type="bibr" rid="B106">von Gunten et&#xa0;al., 2009a</xref>; <xref ref-type="bibr" rid="B32">Gayo et&#xa0;al., 2022</xref>).</p>
</sec>
</sec>
<sec id="s5_2">
<label>5.2</label>
<title>Comparing the Laguna El Calvario record at the regional scale</title>
<p>In order to compare the long-term environmental changes of the Laguna El Calvario (LCA) record with other paleorecords of western South America, (1) the Ti/coh ratio was selected as a proxy of runoff-induced basin erosion (<xref ref-type="fig" rid="f6">
<bold>Figure&#xa0;6A</bold>
</xref>); (2) the high Andean grassland taxa Poaceae and lowland xerophytic <italic>Ephedra</italic> as a moisture availability proxy while <italic>Chaetanthera/Oriastrum</italic>, <italic>Adesmia</italic> type, <italic>Azorella</italic> type, <italic>Nassauvia</italic> type as a proxy of cold conditions (<xref ref-type="fig" rid="f6">
<bold>Figure&#xa0;6B</bold>
</xref>) and; (3) the P/Ti ratio (ICP-MS) and diatom concentration as a lake productivity proxies (<xref ref-type="fig" rid="f6">
<bold>Figure&#xa0;6C</bold>
</xref>).</p>
<p>The relative high persistence and dominance of humid taxa throughout the pollen record of the Laguna El Calvario are consistent with the establishment of a wet Late Holocene inferred by several paleorecords in central Chile (30&#x2013;35&#xb0;S). Increased winter precipitation has been recorded from 4000 cal yrs BP on in the subtropical Andes (<xref ref-type="bibr" rid="B101">Veit, 1996</xref>; <xref ref-type="bibr" rid="B34">Grosjean et&#xa0;al., 1997</xref>; <xref ref-type="bibr" rid="B19">Espizua, 2005</xref>; <xref ref-type="bibr" rid="B59">Martel-Cea et&#xa0;al., 2016</xref>; <xref ref-type="bibr" rid="B98">Tiner et&#xa0;al., 2018</xref>; <xref ref-type="bibr" rid="B25">Frugone-&#xc1;lvarez et&#xa0;al., 2020</xref>; <xref ref-type="bibr" rid="B64">Mayta and Maldonado, 2022</xref>), the lowlands (<xref ref-type="bibr" rid="B46">Jenny et&#xa0;al., 2002b</xref>; <xref ref-type="bibr" rid="B47">Jenny et&#xa0;al., 2003</xref>; <xref ref-type="bibr" rid="B104">Villa-Mart&#xed;nez et&#xa0;al., 2003</xref> and <xref ref-type="bibr" rid="B26">Frugone-&#xc1;lvarez et&#xa0;al., 2017</xref>) and the coastal areas (<xref ref-type="bibr" rid="B54">Maldonado and Villagr&#xe1;n, 2002</xref> and <xref ref-type="bibr" rid="B55">Maldonado and Villagr&#xe1;n, 2006</xref>). Intense glacial activity in El Encierro valley (29&#xb0;S; <xref ref-type="fig" rid="f1">
<bold>Figure&#xa0;1A</bold>
</xref>) located northwards of Laguna El Calvario was recorded before 2600 cal yrs BP (<xref ref-type="bibr" rid="B33">Grosjean et&#xa0;al., 1998</xref>; <xref ref-type="bibr" rid="B109">Zech et&#xa0;al., 2006</xref>). So after this period of glacial advance (3000&#x2013;2600 yrs cal BP; <xref ref-type="bibr" rid="B33">Grosjean et&#xa0;al., 1998</xref>), the Laguna El Calvario basin could have been formed when ice retreated around 2600 cal yrs BP. High lake levels in the Laguna El Negro Francisco in the Andes at 27&#xb0;S (4125 m a.s.l., <xref ref-type="fig" rid="f6"><bold>Figure 6D</bold></xref>) (<xref ref-type="bibr" rid="B34">Grosjean et al., 1997</xref>) and a smooth trend to wet conditions in small lakes at 30&#xb0;S (3900&#x2013;3800 m a.s.l.) (<xref ref-type="bibr" rid="B64">Mayta and Maldonado, 2022</xref>) were recorded after 2700 cal yr BP. This chronology is almost consistent with the high erosion around the lake basin (<xref ref-type="fig" rid="f6">
<bold>Figures&#xa0;6A, B</bold>
</xref>) and the downward distribution of the vegetation belts in Laguna El Calvario before 1500 cal yrs BP (<xref ref-type="fig" rid="f4">
<bold>Figures&#xa0;4</bold>
</xref>, <xref ref-type="fig" rid="f6">
<bold>6C</bold>
</xref>). On the other hand, grain size and geochemical analysis from two lakes located further south (Laguna El Cepo and Laguna Cerritos Blancos, 30&#xb0;S, 2900&#x2013;3800 m a.s.l.; <xref ref-type="fig" rid="f1">
<bold>Figure&#xa0;1A</bold>
</xref>) suggest an increment of storm frequency since 2200 cal yrs BP (<xref ref-type="fig" rid="f6">
<bold>Figure&#xa0;6F</bold>
</xref>) (<xref ref-type="bibr" rid="B98">Tiner et&#xa0;al., 2018</xref>) whereas the pollen assemblages of Laguna Quebrada Parada and Laguna Corralito (<xref ref-type="fig" rid="f1">
<bold>Figure&#xa0;1A</bold>
</xref>) pinpoint the establishment of wetter conditions from 1900 cal yrs BP (<xref ref-type="bibr" rid="B64">Mayta and Maldonado, 2022</xref>). Synchronous wet conditions inferred Laguna El Calvario record around 2400&#x2013;1600 cal yrs BP were recorded in Laguna Chepical (32&#xb0;S; <xref ref-type="fig" rid="f1">
<bold>Figures&#xa0;1B</bold>
</xref>, <xref ref-type="fig" rid="f6">
<bold>6G</bold>
</xref>) that shows wetter than present conditions between 2700&#x2013;1300 cal yrs BP (<xref ref-type="bibr" rid="B59">Martel-Cea et&#xa0;al., 2016</xref>). Coastal and lowland records reflect wetter conditions after 3000 cal yrs BP peaking after 1800 cal yrs BP that were associated with an equatorward position/migration of the northern border of the SWW (<xref ref-type="bibr" rid="B45">Jenny et&#xa0;al., 2002a</xref>; <xref ref-type="bibr" rid="B54">Maldonado and Villagr&#xe1;n, 2002</xref>; <xref ref-type="bibr" rid="B47">Jenny et&#xa0;al., 2003</xref>).</p>
<p>Between 1500 and 800 cal yrs BP, the Laguna El Calvario record reflects a high variability of precipitation at the centennial scale along with the persistence of cold conditions as recorded by the dominance of high-altitude pollen types. The other paleorecords from the Elqui valley (30&#xb0;S; <xref ref-type="fig" rid="f1">
<bold>Figure&#xa0;1A</bold>
</xref>) also show wetter conditions coupled with an increase in storm frequency (<xref ref-type="bibr" rid="B98">Tiner et&#xa0;al., 2018</xref>; <xref ref-type="bibr" rid="B64">Mayta and Maldonado, 2022</xref>). However, the Laguna Chepical record (33&#xb0;S) reflects a decrease of moisture by this time but an extended ice cover season (<xref ref-type="fig" rid="f5">
<bold>Figure&#xa0;5G</bold>
</xref>) (<xref ref-type="bibr" rid="B59">Martel-Cea et&#xa0;al., 2016</xref>). In the lowlands, the Laguna Aculeo (33&#xb0;S; <xref ref-type="fig" rid="f1">
<bold>Figure&#xa0;1A</bold>
</xref>) record pinpoints wet conditions between 2500&#x2013;700 cal yrs BP (<xref ref-type="bibr" rid="B104">Villa-Mart&#xed;nez et&#xa0;al., 2003</xref>) while Palo Colorado (32&#xb0;S; <xref ref-type="fig" rid="f1">
<bold>Figure&#xa0;1A</bold>
</xref>), a coastal record, displays a retraction of wet indicators around 700 cal yrs BP (<xref ref-type="bibr" rid="B55">Maldonado and Villagr&#xe1;n, 2006</xref>).</p>
<p>After 800&#x2013;750 cal yrs BP, a marine core record located at 41&#xb0;S inferred a less humid interval as a result of the southward displacement of SWW (<xref ref-type="bibr" rid="B49">Lamy et&#xa0;al., 2001</xref>) in concordance with an increase of pollen types indicating drier conditions in Laguna El Calvario, Laguna Quebrada Parada and Laguna Corralito (<xref ref-type="bibr" rid="B64">Mayta and Maldonado, 2022</xref>). Superimposed on these long-term conditions, a high frequency of ENOS-modulated storms was recorded by different proxies in Laguna Aculeo (33&#xb0;S) and Laguna del Maule (36&#xb0;S; <xref ref-type="fig" rid="f1">
<bold>Figure&#xa0;1A</bold>
</xref>) (<xref ref-type="bibr" rid="B45">Jenny et&#xa0;al., 2002a</xref>; <xref ref-type="bibr" rid="B25">Frugone-&#xc1;lvarez et&#xa0;al., 2020</xref>, respectively). So, dry general climatic conditions under a high variability associated with the ENSO may have prevailed north of 32&#xb0;S but more marked southwards of 33&#xb0;S.</p>
<p>After 1800 AD, the higher temporal resolution of the Laguna El Calvario record, increasing from 0.02 to 0.13 cm yr<sup>&#x2212;1</sup>, provides quite detailed data for the last two centuries (<xref ref-type="supplementary-material" rid="SM1">
<bold>Figure&#xa0;2 Supplementary Material</bold>
</xref>). Drier than present conditions were replaced by colder ones as reflected by the increase in upper Andean belt elements (cold-tolerant taxa) around 1850 AD. This is synchronous to the last part of the Little Ice Age, recorded in central Chile lowlands as lower spring-summer temperatures (<xref ref-type="bibr" rid="B107">von Gunten et&#xa0;al., 2009b</xref>), glacial expansion in the high Andes at 35&#xb0;S (<xref ref-type="bibr" rid="B502">Espizua and Pitte, 2009</xref>) and increased precipitation in central Chile (33&#x2013;34.5&#xb0;S; <xref ref-type="bibr" rid="B503">LeQuesne et&#xa0;al., 2006</xref>). Between 1900 and 1950 AD, wet pollen indicators (Poaceae) abundance increased at the expense of cold tolerant taxa pollen. Besides, a synchronous higher variability of runoff indicators related to an upward shift of the zero-isotherm altitude might suggest an increase in liquid precipitation. This increasing trend of precipitation was also recorded by the low-frequency signal of three ring chronologies of central Chile (33&#xb0;&#x2013;34.5&#xb0;; <xref ref-type="bibr" rid="B503">LeQuesne et&#xa0;al., 2006</xref>).</p>
<p>During the last part of the 20<sup>th</sup> century, similar to modern dry conditions established in Laguna El Calvario synchronously to the mediterranean Andes (<xref ref-type="bibr" rid="B59">Martel-Cea et&#xa0;al., 2016</xref>) and the Altiplano (<xref ref-type="bibr" rid="B71">Morales et&#xa0;al., 2012</xref>). The recent decline of Poaceae and the increase of lowland shrubs (<italic>Ephedra</italic> and Chenopodiaceae) may represent an ongoing upward displacement of plant communities in the subtropical Andes. This process can be directly linked to the ongoing climate change characterized by the establishment of extreme drought conditions (also called Mega Drought; <xref ref-type="bibr" rid="B29">Garreaud et&#xa0;al., 2019</xref>) that broadly affects the Andean lake basins in central Chile (<xref ref-type="bibr" rid="B27">Fuentealba et&#xa0;al., 2021</xref>). Regarding regional warming, warmer autumns and springs (<xref ref-type="bibr" rid="B9">Burger et&#xa0;al., 2018</xref>) may have influenced the nutrient enrichment (high productivity, OM, and P) in Laguna El Calvario (<xref ref-type="fig" rid="f6">
<bold>Figure&#xa0;6D</bold>
</xref>; <xref ref-type="supplementary-material" rid="SM1">
<bold>Figure&#xa0;2 Supplementary Material</bold>
</xref>) but may have led in a drastic decline of primary productivity in the plant communities at the same time (<xref ref-type="bibr" rid="B87">Rudloff et&#xa0;al., 2021</xref>).</p>
<p>Climate variability in the subtropical Andes during the late Holocene, mainly after ~2000 cal yrs BP has been attributed to El Ni&#xf1;o Southern Oscillation, whose positive phase (El Ni&#xf1;o) originates rainy winters in central Chile (<xref ref-type="bibr" rid="B45">Jenny et&#xa0;al., 2002a</xref>; <xref ref-type="bibr" rid="B55">Maldonado and Villagr&#xe1;n, 2006</xref>; <xref ref-type="bibr" rid="B59">Martel-Cea et&#xa0;al., 2016</xref>; <xref ref-type="bibr" rid="B25">Frugone-&#xc1;lvarez et&#xa0;al., 2020</xref>). Wetter than present conditions around 2400 and 1500 cal yrs BP as well as colder conditions until 800 cal yrs BP in Laguna El Calvario is near concomitant with the increased El Ni&#xf1;o activity inferred by several tropical records from the Eastern Pacific with a range of ca. 2000 to ca. 1000 cal yrs BP (<xref ref-type="fig" rid="f6">
<bold>Figures&#xa0;6G, I</bold>
</xref>) (<xref ref-type="bibr" rid="B74">Moy et&#xa0;al., 2002</xref>: 2000&#x2013;1000 cal yrs BP; <xref ref-type="bibr" rid="B85">Rein et&#xa0;al., 2005</xref>: 2000&#x2013;1300 cal yrs BP; <xref ref-type="bibr" rid="B13">Conroy et&#xa0;al., 2008</xref>: 2000&#x2013;1500 cal yrs BP). Therefore, ENSO may have played a key role in the hydrological dynamics in the Laguna El Calvario at least between 2000 and 1500 cal yrs BP. Most ENSO paleorecords show a more weakened activity or La Ni&#xf1;a-like phase in the past 800 years that may explain the stable dry conditions displayed by the Laguna El Calvario record (<xref ref-type="bibr" rid="B74">Moy et&#xa0;al., 2002</xref>; <xref ref-type="bibr" rid="B85">Rein et&#xa0;al., 2005</xref>; <xref ref-type="bibr" rid="B13">Conroy et&#xa0;al., 2008</xref>). Some discrepancies among records of central Chile and the subtropical Andes during the last millennium (i.e., Laguna Aculeo, Laguna del Maule, and neoglacial advances) could be attributed to other large atmospheric anomalies such as Southern Annular Mode (SAM) that also could have played a key role in the past at the interannual scale (<xref ref-type="bibr" rid="B108">Vuille and Milana, 2007</xref>; <xref ref-type="bibr" rid="B16">D&#xe4;twyler et&#xa0;al., 2020</xref>). However, further studies are needed to elucidate the implications of the coupling SAM and ENSO modes of variability in the past by evaluating the sensibility of paleorecords of the semiarid Andes of central Chile.</p>
</sec>
</sec>
<sec id="s6" sec-type="conclusions">
<label>6</label>
<title>Conclusions</title>
<p>The Laguna El Calvario record reflects significant climate-driven changes at millennial to sub-centennial timescales during the past 2400 years in the semiarid Andes of central Chile based on sedimentological, geochemical, pollen, diatoms and chironomids data. The sediment deposition onset in Laguna El Calvario might have occurred after ice retreatment around 2600 cal yrs BP. Geochemical analyses provided a good approximation of the allochthonous clastic input where the Ti/coh ratio allowed us to estimate the long-term changes in the precipitation regime along with the pollen record. Maximum values of Ti/coh ratio evidenced an intense runoff period before 1400 cal yrs BP. Increased precipitation and colder than present conditions may have triggered a 200 m downward shift of the Andean vegetation belts whereas the aquatic biota records (algae, diatoms, and chironomids) suggested cold and shallow waters in El Calvario. Between 1500 and 800 cal yrs BP, the Laguna El Calvario record reflects wetter and colder conditions under a high centennial-to-multidecadal variability (wetter pulses) of precipitation. After 800 yrs BP, an increase of lowland pollen types in Laguna El Calvario suggests the establishment of drier conditions under a high variability associated with ENSO until 1850 AD when the dominance of upper Andean belt elements (cold tolerant taxa) indicates colder conditions synchronous to the last part of the Little Ice Age. Between 1900 and 1950 AD, an increase of wet pollen indicators at expenses of cold-tolerant taxa pollen synchronous to higher variability of runoff indicators might be related to an upward shift of the zero-isotherm altitude, and therefore a major proportion of liquid precipitation. The modern establishment of the drought regime and the increment of temperature have been shown since 1950 AD and accentuated in the last decade (Mega Drought). In addition, higher lake productivity, the presence of exotic plants, and the heavy metal enrichment of the sediments of Laguna El Calvario may be associated with transhumance practices and the establishment of the industrial mining companies in the area (Anthropocene) which have played a key role in the mid-to-long-term resilience of mountain communities.</p>
<p>The sedimentary record of Laguna El Calvario is not just the northernmost Andean record in central Chile but is unique in that it provides such a high temporal resolution for the last two centuries. The agreement between the Laguna El Calvario climatic trends during this period and the dendrochronological and instrumental data is surprising and confirms the robustness of this record for the whole 2400 cal yrs BP. Indeed, the regional comparison with other paleorecords allows us to confirm that even though there is a quite robust pattern of the dynamics of the northern edge of the SWW at the millennial-to-centennial scale, there are temporal (at shorter times scales)/latitudinal asynchronies that need to be further analyzed.</p>
</sec>
<sec id="s7" sec-type="data-availability">
<title>Data availability statement</title>
<p>The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.</p>
</sec>
<sec id="s8" sec-type="author-contributions">
<title>Author contributions</title>
<p>All authors have approved the final version of the manuscript and the individual contributions of each co-author to the article are: AM-C analyzed the pollen, diatom, chironomid, and sedimentological data and age-depth model, wrote and edited the manuscript with contributions from all coauthors. AM designed the study, retrieved the cores, obtained the funding and participated in writing and editing the manuscript. MdP retrieved the cores, obtained the funding and participated in writing and editing the manuscript. PM carried out the <sup>210</sup>Pb chronology, the analysis of ICP-MS data and participated in writing the manuscript. NM carried out the diatom analysis and participated in writing the manuscript. JM carried out the chironomid analysis and participated in writing the manuscript. KS carried out the XRF analysis and participated in writing the manuscript.</p>
</sec>
</body>
<back>
<sec id="s9" sec-type="funding-information">
<title>Funding</title>
<p>The author(s) declare financial support was received for the research, authorship, and/or publication of this article. The funding for this work was provided by the ANID-FONDECYT #1180413, ANID-Millennium Science Initiative Program-NCN19_153, and ANID-R20F0008.</p>
</sec>
<ack>
<title>Acknowledgments</title>
<p>We thank Andres Zamora for his assistance during the coring collection campaign, Leonardo D. Rios for assistance with <xref ref-type="fig" rid="f1">
<bold>Figure&#xa0;1</bold>
</xref>, Marigen Heise and Claudia Alca&#xed;no for their assistance with laboratory analysis, Alexander Rhein for the sedimentological description, and the Hospital P&#xfa;blico San Juan de Dios de La Serena for the digital X-ray images of the core.</p>
</ack>
<sec id="s10" sec-type="COI-statement">
<title>Conflict of interest</title>
<p>The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p>
</sec>
<sec id="s11" sec-type="disclaimer">
<title>Publisher&#x2019;s note</title>
<p>All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.</p>
</sec>
<sec id="s12" sec-type="supplementary-material">
<title>Supplementary material</title>
<p>The Supplementary Material for this article can be found online at: <ext-link ext-link-type="uri" xlink:href="https://www.frontiersin.org/articles/10.3389/fevo.2023.1227020/full#supplementary-material">https://www.frontiersin.org/articles/10.3389/fevo.2023.1227020/full#supplementary-material</ext-link>
</p>
<supplementary-material xlink:href="DataSheet_1.pdf" id="SM1" mimetype="application/pdf"/>
</sec>
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