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  <front>
    <journal-meta><journal-id journal-id-type="publisher">CP</journal-id><journal-title-group>
    <journal-title>Climate of the Past</journal-title>
    <abbrev-journal-title abbrev-type="publisher">CP</abbrev-journal-title><abbrev-journal-title abbrev-type="nlm-ta">Clim. Past</abbrev-journal-title>
  </journal-title-group><issn pub-type="epub">1814-9332</issn><publisher>
    <publisher-name>Copernicus Publications</publisher-name>
    <publisher-loc>Göttingen, Germany</publisher-loc>
  </publisher></journal-meta>
    <article-meta>
      <article-id pub-id-type="doi">10.5194/cp-17-1181-2021</article-id><title-group><article-title>2400 years of climate and human-induced environmental change recorded in sediments of Lake Młynek in northern Poland</article-title><alt-title>2400 years of climate change recorded in sediments of Lake Młynek​​​​​​​</alt-title>
      </title-group><?xmltex \runningtitle{2400 years of climate change recorded in sediments of Lake M{\l}ynek​​​​​​​}?><?xmltex \runningauthor{F. Welc et al.}?>
      <contrib-group>
        <contrib contrib-type="author" corresp="yes" rid="aff1">
          <name><surname>Welc</surname><given-names>Fabian</given-names></name>
          <email>f.welc@uksw.edu.pl</email>
        <ext-link>https://orcid.org/0000-0001-6122-1884</ext-link></contrib>
        <contrib contrib-type="author" corresp="no" rid="aff2">
          <name><surname>Nitychoruk</surname><given-names>Jerzy</given-names></name>
          
        </contrib>
        <contrib contrib-type="author" corresp="no" rid="aff3">
          <name><surname>Marks</surname><given-names>Leszek</given-names></name>
          
        <ext-link>https://orcid.org/0000-0002-4507-1828</ext-link></contrib>
        <contrib contrib-type="author" corresp="no" rid="aff3">
          <name><surname>Bińka</surname><given-names>Krzysztof</given-names></name>
          
        </contrib>
        <contrib contrib-type="author" corresp="no" rid="aff2">
          <name><surname>Rogóż-Matyszczak</surname><given-names>Anna</given-names></name>
          
        </contrib>
        <contrib contrib-type="author" corresp="no" rid="aff4">
          <name><surname>Obremska</surname><given-names>Milena</given-names></name>
          
        <ext-link>https://orcid.org/0000-0002-3465-1894</ext-link></contrib>
        <contrib contrib-type="author" corresp="no" rid="aff5">
          <name><surname>Zalat</surname><given-names>Abdelfattah</given-names></name>
          
        </contrib>
        <aff id="aff1"><label>1</label><institution>Institute of Archaeology, Cardinal Stefan Wyszynski University in Warsaw, Warsaw, Poland</institution>
        </aff>
        <aff id="aff2"><label>2</label><institution>Faculty of Economic and Technical Sciences, Pope John Paul II State
Higher School of Education, Biała Podlaska, Poland​​​​​​​</institution>
        </aff>
        <aff id="aff3"><label>3</label><institution>Faculty of Geology, University of Warsaw, Warsaw, Poland</institution>
        </aff>
        <aff id="aff4"><label>4</label><institution>Institute of Geological Sciences, Polish Academy of Sciences, Warsaw, Poland</institution>
        </aff>
        <aff id="aff5"><label>5</label><institution>Faculty of Science, Tanta University, Tanta, Egypt​​​​​​​</institution>
        </aff>
      </contrib-group>
      <author-notes><corresp id="corr1">Fabian Welc (f.welc@uksw.edu.pl)</corresp></author-notes><pub-date><day>14</day><month>June</month><year>2021</year></pub-date>
      
      <volume>17</volume>
      <issue>3</issue>
      <fpage>1181</fpage><lpage>1198</lpage>
      <history>
        <date date-type="received"><day>22</day><month>March</month><year>2020</year></date>
           <date date-type="rev-request"><day>30</day><month>June</month><year>2020</year></date>
           <date date-type="rev-recd"><day>7</day><month>April</month><year>2021</year></date>
           <date date-type="accepted"><day>6</day><month>May</month><year>2021</year></date>
      </history>
      <permissions>
        <copyright-statement>Copyright: © 2021 Fabian Welc et al.</copyright-statement>
        <copyright-year>2021</copyright-year>
      <license license-type="open-access"><license-p>This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this licence, visit <ext-link ext-link-type="uri" xlink:href="https://creativecommons.org/licenses/by/4.0/">https://creativecommons.org/licenses/by/4.0/</ext-link></license-p></license></permissions><self-uri xlink:href="https://cp.copernicus.org/articles/17/1181/2021/cp-17-1181-2021.html">This article is available from https://cp.copernicus.org/articles/17/1181/2021/cp-17-1181-2021.html</self-uri><self-uri xlink:href="https://cp.copernicus.org/articles/17/1181/2021/cp-17-1181-2021.pdf">The full text article is available as a PDF file from https://cp.copernicus.org/articles/17/1181/2021/cp-17-1181-2021.pdf</self-uri>
      <abstract><title>Abstract</title>
    <p id="d1e163">In the densely forested Warmia and Masuria region (northern Poland) there
are many small endorheic lakes characterized by their low sedimentation
rate, which makes them excellent archives of Holocene environmental and
palaeoclimatic change. Lake Młynek, located near the village of Janiki
Wielkie, was selected for multi-faceted palaeoenvironmental research
supported with radiocarbon dates. Sediments from this lake also contain
unique information about human impact on the environment, because a
stronghold has been operating on its northern shore since the early Iron Age
to the early Medieval period, giving the opportunity to correlate
palaeoenvironmental data with the phases of human activity over the last
2400 years. During the second and third centuries BCE the lake was
surrounded by a dense deciduous forest. From the first century BCE to
second century CE the forest around the lake was much reduced, which can
be associated with the first pre-Roman (La Tène) and Roman occupation phase
evidenced by the construction of the stronghold located close to the lake.
From the second up to ninth century CE gradual restoration of the
forest and a decline in human activity took place, along with lake deepening
and the onset of a colder and humid climatic phase which corresponded to the
global cooling episode known as the Bond 1 event (1.5 ka BP). The next
intensive phase of forest clearing around the lake occurred between the
9th–13th century CE as result of human activity (Middle
Age settlement phase of the stronghold). Whilst this period is marked by a
warming, the human impact which has transformed the landscape likely
overprints any signals of climate-driven environmental changes.</p>
  </abstract>
    </article-meta>
  </front>
<body>
      

<sec id="Ch1.S1" sec-type="intro">
  <label>1</label><title>Introduction</title>
      <p id="d1e175">Lake sediments are a useful source of proxies of past environmental and
climate changes in the Holocene (see Brauer, 2004; Brauer et al., 2009; Zolitschka, 2007; Wanner
et al., 2008; Francus et al., 2013; Ojala et al., 2013; Welc, 2017). The
main advantage of lakes for environmental reconstruction is the continuous
and uninterrupted accumulation of their sediments. Well-dated lake
sedimentary records allow for tracing of both long- and short-term climate
changes in the Holocene (Smol et al., 2001; Tiljander et al., 2002; Valpola
and Ojala, 2006; Czymzik et al., 2010; Elbert et al., 2012; Tylmann et al.,
2012; Welc, 2017). Particularly valuable for palaeoclimate reconstructions
are sequences from lakes without river inflow and outflow (Wetzel, 2001;
Stankevica et al., 2015). As in most of Europe, many lakes in Poland have
been heavily impacted by human activities within their catchments, resulting
in many of them becoming eutrophic in terms of their nutrient status (Cooke
et al., 2005). Such intensive bio-productivity arising from nutrient
enrichment results in the deposition of thick organic sedimentary sequences,
mostly of organic gyttja composed of the remains of aquatic plants, plankton and
benthic organisms transformed by bacteria and mixed with mineral components
supplied<?pagebreak page1182?> from the lake basin (Stankevica et al., 2015).
There are ca. 1000 freshwater lakes of different sizes in the Warmia and
Mazury region in northern Poland (Fig. 1). Most of them are located within
past glacial tunnel valleys formed by meltwater erosion at the termination
of the Vistulian (Weichselian) glaciation (ca. 115–12 ka BP). After
deglaciation at the end of the Pleistocene these glacial tunnel valleys were
partly filled with deposits and water, which persisted throughout the Holocene. Such
lake basins have steep slopes and their bottom deposits are underlain by either glaciofluvial sand, gravel and silt or glacial till (Kondracki, 2002; Gałązka, 2009). Many of these lakes are small (<inline-formula><mml:math id="M1" display="inline"><mml:mo lspace="0mm">&lt;</mml:mo></mml:math></inline-formula> 1 ha), with stable
sedimentation rates and without river inflow or outflow making them
excellent sites for palaeoclimate reconstructions. Indeed, most of the
climate reconstruction studies based mainly on pollen analysis are
undertaken in this area (e.g. Kupryjanowicz, 2008; Kołaczek et al.,
2013).</p>

      <?xmltex \floatpos{t}?><fig id="Ch1.F1" specific-use="star"><?xmltex \currentcnt{1}?><?xmltex \def\figurename{Figure}?><label>Figure 1</label><caption><p id="d1e187"><bold>(A)</bold> Location of Lake Młynek in the Warmia and Mazury Region (north-eastern Poland) (drawing: Fabian Welc). <bold>(B)</bold> View of Młynek Lake from the north-west (photo: Fabian Welc). <bold>(C)</bold> Satellite image of the lake (open source: © Google Earth: <uri>http://www.google.com/intl/pl/earth</uri>, last access: 10 June 2021). <bold>(D)</bold> Lidar image of the lake: <bold>(a)</bold> lake basin, <bold>(b)</bold> Janiki Wielkie
archaeological site established in early Iron Age (©
Geoportal Poland: <uri>http://www.geoportal.gov.pl</uri>, last access: 10 June 2021).</p></caption>
        <?xmltex \igopts{width=469.470472pt}?><graphic xlink:href="https://cp.copernicus.org/articles/17/1181/2021/cp-17-1181-2021-f01.png"/>

      </fig>

      <p id="d1e220">Lake Młynek is located near the village of Janiki Wielkie and was
selected for multi-faceted palaeoenvironmental research (pollen analysis,
diatom, chrysophyte cysts and geochemistry). It is hypothesized that the
bottom sediments of this lake contain a unique record of human impact on the
surrounding environment, as a result of the location of an Iron Age
stronghold on the northern shore, which was active (though not continuously)
up until the early Middle Ages (Fig. 1). Due to archaeological research,
stratigraphic units distinguished on this site were divided into seven main
settlement phases: early Iron Age (I), stronghold abandoned after the early
Iron Age (II), early Middle Ages (III), stronghold abandoned in the early
Middle Ages (IV), settlement activity in the 11th–13th
centuries (V), stronghold definitely abandoned in the 14th century (VI)
(Nitychoruk and Welc, 2017; Rabiega et al., 2017).</p>
      <p id="d1e224">This study provides an opportunity to reconstruct the transformation of the
vegetation around the lake that occurred under the influence of the climate
(regional significance) and as a result of human activity. Our results were
correlated with geoarchaeological data to determine mutual relations between
environmental and climatic changes with development of human settlement
phases in the Warmia and Mazury (northern Poland) region during the last
2400 years.</p>
</sec>
<sec id="Ch1.S2">
  <label>2</label><title>Study area</title>
      <p id="d1e235">Lake Młynek is a small water body that occupies a glacial tunnel valley
since the Holocene. The lake is located in the Iława Lakeland in northern
Poland, it is about 720 m long and 165 m wide. The lake has an area of 7.5 ha, with its water level at <inline-formula><mml:math id="M2" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 101 m a.s.l., and the maximum
depth is just over 2 m. Lake Młynek is surrounded by a morainic plateau at
120–130 m a.s.l, and its catchment is occupied by a dense forest
(Fig. 1). In general, most of the Ilawa Lakeland is covered with forest
(41.5 %), whereas meadows and synanthropic communities have a smaller
share. Among the habitats, a highly productive mixed forest prevails. The
basic components of the Iława forest are pine (<italic>Pinus</italic>), oak (<italic>Quercus)</italic>, beech (<italic>Fagus</italic>), alder
(<italic>Alnus</italic>) and birch (<italic>Betula</italic>), and in smaller amounts there are spruce (<italic>Picea</italic>), larch (<italic>Larix</italic>), ash
(<italic>Fraxinus</italic>), hornbeam (<italic>Carpinus</italic>), maple (<italic>Acer</italic>) and linden (<italic>Tilia</italic>). Currently, the lake sits in a
catchment that is characterized by a transitional climate with an influence from continental and maritime circulation. The growing season lasts about 206 d, and the snow cover remains for 70–90 d. Average temperature values
range from approximately <inline-formula><mml:math id="M3" display="inline"><mml:mo>-</mml:mo></mml:math></inline-formula>4.0 <inline-formula><mml:math id="M4" display="inline"><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup></mml:math></inline-formula>C in February to above
17.0 <inline-formula><mml:math id="M5" display="inline"><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup></mml:math></inline-formula>C in July. Due to significant influence of the polar air
masses and a large number of natural water reservoirs, air humidity is
relatively high, ranging from 72 % to 89 %. Total annual precipitation
ranges from 500 to 550 mm yr<inline-formula><mml:math id="M6" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula>. South-western winds dominate throughout the year, with westerly winds stronger in winter and the highest wind speeds recorded during the winter months (Jutrzenka-Trzebiatowski et al., 1997; Stopa-Boryczka at al., 2013). It is important to note that from the
north a small stream flows into the lake Młynek, which is active in
winter and dries up almost completely in summer (Fig. 1D). The stream is a
result of irrigation related to the construction of a mill in the 15th
century, somewhere in the vicinity of the medieval stronghold located on the
northern shore of the lake (Semrau, 1939; Bińka et al., 2020).</p>
</sec>
<sec id="Ch1.S3">
  <label>3</label><title>Material and methods</title>
<sec id="Ch1.S3.SS1">
  <label>3.1</label><title>Bathymetry</title>
      <p id="d1e332">The determination of lake bathymetry and thickness of bottom sediments is
extremely important in palaeolimnological research to help locate
appropriate coring sites. This can be achieved through the use of GPR
sounding (Lin et al., 2009; Sambuelli et al., 2009; Sambuelli and Silvia,
2012). In Poland, winter is a particularly convenient season as the lake is
covered with ice, making GPR profiling much easier and improving access and the
speed of data collection (Hunter et al., 2003). Measurements along and
across the lake were carried out in 2017, directly on the lake ice (Fig. 2).
We used the radar system ProEx of the Malå Geoscience
(<uri>http://www.malagpr.com.au/mala-professional-explorer.html</uri>, last access: 23 May​​​​​​​ 2021). A radar pulse was
generated at a regular distance interval of 0.02 m (900 samples were
recorded from a single pulse). The time window of recording was between 250
and 300 ns. Prospection was done with use of a shielded monostatic antenna
with 250 MHz nominal frequency of the electromagnetic wave.</p>

      <?xmltex \floatpos{t}?><fig id="Ch1.F2" specific-use="star"><?xmltex \currentcnt{2}?><?xmltex \def\figurename{Figure}?><label>Figure 2</label><caption><p id="d1e340">GPR reflection profile across Lake Młynek (see Fig. 2): <bold>(a)</bold> drilling M1, <bold>(b)</bold> upper boundary of the so-called hard bottom, <bold>(c)</bold> stratified glaciofluvial sandy-gravel beds beneath the lake sediments, <bold>(d)</bold> attenuation zone of electromagnetic waves connected with occurrence of organic sediment (gyttja) (measurements, processing and interpretation: Fabian Welc).</p></caption>
          <?xmltex \igopts{width=341.433071pt}?><graphic xlink:href="https://cp.copernicus.org/articles/17/1181/2021/cp-17-1181-2021-f02.png"/>

        </fig>

</sec>
<sec id="Ch1.S3.SS2">
  <label>3.2</label><title>Coring and sampling</title>
      <p id="d1e369">Based on the results of the GPR sounding, four drillings were undertaken a ca.
2 m water depth (Fig. 3) following the Givelet et al. (2004) collecting
protocol. A piston sampler was used during drilling, which is very<?pagebreak page1183?> suitable
for sampling in moderately cohesive sediments to a depth of 5 m. The sampler
set consists of a 200 cm long sonde, which is constructed from a
thin-walled, 40 mm diameter, stainless steel tube
(<uri>https://en.eijkelkamp.com/products/sediment-samplers/Piston-Sampler-set.html</uri>, last access: 10 June 2021).
Sediment cores were film-wrapped in 1 m plastic tubes and transported to the
laboratory. The cores (M1 to M4) were then subjected to magnetic susceptibility
measurements which enabled the selection of the core M1, the longest and
most continuous, to carry out detailed analysis. The 3.5 m long core M1
(geographic coordinates: 53.82486<inline-formula><mml:math id="M7" display="inline"><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup></mml:math></inline-formula> N, 19.72419<inline-formula><mml:math id="M8" display="inline"><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup></mml:math></inline-formula> E) was sub-sampled at 5 cm
intervals and used for multi-proxy laboratory analyses.</p>

      <?xmltex \floatpos{t}?><fig id="Ch1.F3"><?xmltex \currentcnt{3}?><?xmltex \def\figurename{Figure}?><label>Figure 3</label><caption><p id="d1e395">Młynek Lake: location of drillings M1–M4 and transect of GPR
sounding (© Google Earth: <uri>http://www.google.com/intl/pl/earth</uri>).</p></caption>
          <?xmltex \igopts{width=170.716535pt}?><graphic xlink:href="https://cp.copernicus.org/articles/17/1181/2021/cp-17-1181-2021-f03.png"/>

        </fig>

</sec>
<?pagebreak page1184?><sec id="Ch1.S3.SS3">
  <label>3.3</label><title>Magnetic susceptibility (MS)</title>
      <p id="d1e415">The cores from Lake Młynek were subjected to MS measurements using a SM-30
magnetic susceptibility meter (ZH Instruments). Due to very high sensitivity
(1 <inline-formula><mml:math id="M9" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<inline-formula><mml:math id="M10" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">7</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula> SI units) this device was provided with an 8 kHz linear integrated circuit oscillator,
and its pick-up coil sensor was large enough to measure sufficiently high
volume of sediments with very low MS. The measurements were made every 5 cm along each core (M1–M4).</p>
</sec>
<sec id="Ch1.S3.SS4">
  <label>3.4</label><title>Radiocarbon dating and age–depth model</title>
      <p id="d1e445">Radiocarbon dating was performed on four bulk samples from the core M1,
collected either from organic-rich gyttja or gyttja with dispersed organic
matter (Table 1). The organic matter seems to have been derived from both
aquatic and terrestrial sources. AMS dating was carried out by the
Poznań Radiocarbon Laboratory in Poland (for methodology see Goslar et
al., 2004). The construction of age–depth models required an assessment of
several factors that could disturb constant accumulation of bottom deposits
in Lake Młynek, such as those from sedimentary and post-sedimentary
processes (including a varied rate of deposition and compaction, and the
impact of bioturbation). The varied influx of material delivered to the lake
from the adjacent area is a very important factor of disturbance. Therefore,
a Bayesian age–depth model was chosen as it takes into account the
sedimentation rate and its variability (Blaauw et al., 2007) (Fig. 4). The model was based on default settings,
except for section thickness, which was set at 0.05 cm given the length of
this core. The Bacon software uses the IntCal3 curve (Reimer et al., 2013) to
calibrate the radiocarbon data.</p>

<?xmltex \floatpos{t}?><table-wrap id="Ch1.T1" specific-use="star"><?xmltex \currentcnt{1}?><label>Table 1</label><caption><p id="d1e451">List of radiocarbon determinations.</p></caption><oasis:table frame="topbot"><oasis:tgroup cols="6">
     <oasis:colspec colnum="1" colname="col1" align="left"/>
     <oasis:colspec colnum="2" colname="col2" align="right"/>
     <oasis:colspec colnum="3" colname="col3" align="left"/>
     <oasis:colspec colnum="4" colname="col4" align="right"/>
     <oasis:colspec colnum="5" colname="col5" align="left"/>
     <oasis:colspec colnum="6" colname="col6" align="left"/>
     <oasis:thead>
       <oasis:row>
         <oasis:entry colname="col1">No.</oasis:entry>
         <oasis:entry colname="col2">Depth (m)</oasis:entry>
         <oasis:entry colname="col3">Lab. reference</oasis:entry>
         <oasis:entry colname="col4"><inline-formula><mml:math id="M11" display="inline"><mml:msup><mml:mi/><mml:mn mathvariant="normal">14</mml:mn></mml:msup></mml:math></inline-formula>C BP</oasis:entry>
         <oasis:entry colname="col5">Age calibrated</oasis:entry>
         <oasis:entry colname="col6">Material dated</oasis:entry>
       </oasis:row>
       <oasis:row rowsep="1">
         <oasis:entry colname="col1"/>
         <oasis:entry colname="col2"/>
         <oasis:entry colname="col3"/>
         <oasis:entry colname="col4"/>
         <oasis:entry colname="col5">95 % probability</oasis:entry>
         <oasis:entry colname="col6"/>
       </oasis:row>
     </oasis:thead>
     <oasis:tbody>
       <oasis:row>
         <oasis:entry colname="col1">1</oasis:entry>
         <oasis:entry colname="col2">0.95–1.00</oasis:entry>
         <oasis:entry colname="col3">S/JW 1/2015/A</oasis:entry>
         <oasis:entry colname="col4">435 <inline-formula><mml:math id="M12" display="inline"><mml:mo>±</mml:mo></mml:math></inline-formula> 30</oasis:entry>
         <oasis:entry colname="col5">1418–1494 CE</oasis:entry>
         <oasis:entry colname="col6">Bulk of gyttja</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1">2</oasis:entry>
         <oasis:entry colname="col2">1.65–1.70</oasis:entry>
         <oasis:entry colname="col3">S/JW 1/2015/B</oasis:entry>
         <oasis:entry colname="col4">1015 <inline-formula><mml:math id="M13" display="inline"><mml:mo>±</mml:mo></mml:math></inline-formula> 30</oasis:entry>
         <oasis:entry colname="col5">971–1048 CE</oasis:entry>
         <oasis:entry colname="col6">Bulk of gyttja</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1">3</oasis:entry>
         <oasis:entry colname="col2">2.40–2.45</oasis:entry>
         <oasis:entry colname="col3">S/JW 1/2015/C</oasis:entry>
         <oasis:entry colname="col4">1730 <inline-formula><mml:math id="M14" display="inline"><mml:mo>±</mml:mo></mml:math></inline-formula> 30</oasis:entry>
         <oasis:entry colname="col5">236–386 CE</oasis:entry>
         <oasis:entry colname="col6">Bulk of gyttja</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1">4</oasis:entry>
         <oasis:entry colname="col2">3.45–3.50</oasis:entry>
         <oasis:entry colname="col3">S/JW 1/2015/D</oasis:entry>
         <oasis:entry colname="col4">2275 <inline-formula><mml:math id="M15" display="inline"><mml:mo>±</mml:mo></mml:math></inline-formula> 30</oasis:entry>
         <oasis:entry colname="col5">401–351 BCE</oasis:entry>
         <oasis:entry colname="col6">Bulk of gyttja</oasis:entry>
       </oasis:row>
     </oasis:tbody>
   </oasis:tgroup></oasis:table></table-wrap>

      <?xmltex \floatpos{t}?><fig id="Ch1.F4" specific-use="star"><?xmltex \currentcnt{4}?><?xmltex \def\figurename{Figure}?><label>Figure 4</label><caption><p id="d1e643">Age–depth model of the core M1 from the Lake Młynek sediments.
Good runs of a stationary distribution are shown in panel <bold>(a)</bold>;
green curves and grey histograms in panel <bold>(b)</bold> present
distributions for the sediment accumulation rate. Panel <bold>(c)</bold>
shows the calibrated <inline-formula><mml:math id="M16" display="inline"><mml:msup><mml:mi/><mml:mn mathvariant="normal">14</mml:mn></mml:msup></mml:math></inline-formula>C dates (transparent blue) and the age–depth model
(darker grey areas), which indicate calendar ages. Grey stippled lines
show 95 % confidence intervals and the red curve shows the “best” model
based on the weighted mean age for each depth. The model was created by Fabian Welc using the open Bacon software (Blaauw and Christen, 2011).</p></caption>
          <?xmltex \igopts{width=341.433071pt}?><graphic xlink:href="https://cp.copernicus.org/articles/17/1181/2021/cp-17-1181-2021-f04.png"/>

        </fig>

</sec>
<sec id="Ch1.S3.SS5">
  <label>3.5</label><title>Palaeobotanical analysis</title>
<sec id="Ch1.S3.SS5.SSS1">
  <label>3.5.1</label><title>Pollen</title>
      <p id="d1e686">The core M1 was sampled every 5 cm for pollen analysis. A total of 70 samples (ca. 10 g each) were treated with 5 % HCl and boiled in 5 % KOH and hot 30 % Hf.
They were washed with 15 % HCl and treated by the standard Erdtman's
acetolysis. In each sample about 1000 pollen grains were counted using an
optical microscope at 400<inline-formula><mml:math id="M17" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> magnification.</p>
</sec>
<sec id="Ch1.S3.SS5.SSS2">
  <label>3.5.2</label><title>Diatom and chrysophyte cyst analysis</title>
      <p id="d1e704">A total of 70 samples were prepared for the analysis of diatoms and chrysophyte cysts.
They were extracted from 1 g of dry sediment of using the disintegration
method in HCl and H<inline-formula><mml:math id="M18" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">2</mml:mn></mml:msub></mml:math></inline-formula>O<inline-formula><mml:math id="M19" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">2</mml:mn></mml:msub></mml:math></inline-formula>, according to the technique proposed by
Zalat and Vildary (2005). For slide preparation, 0.1 mL of the final
suspension was dried on coverslips and then mounted onto slides using
Naphrax. Diatoms were identified to species level using a Leica
photomicroscope with a digital camera and equipped with differential
interference contrast (DIC) optics at 1000<inline-formula><mml:math id="M20" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> magnification with oil
immersion. Identification and ecological information of the diatom species
were based primarily upon the published literature (e.g. Kilham et al.,
1986; Douglas and Smol, 1999; Witkowski et al., 2000; Hofmann et al., 2011).
Recent taxonomic advances split many diatom taxa of the former genus
<italic>Fragilaria</italic> sensu lato into several new genera, including <italic>Fragilaria</italic>, <italic>Pseudostaurosira, Staurosira</italic> and <italic>Staurosirella</italic> spp. (Williams and Round, 1987);
these new names are herein collectively referred to as <italic>Fragilaria</italic> sensu lato. Chrysophyte cysts were
described and enumerated following Duff et al. (1995, 1997) and
Wilkinson et al. (2002). Preliminary results of the diatom studies based on
the core M1 were already published by Zalat et al. (2018).</p>
</sec>
</sec>
<sec id="Ch1.S3.SS6">
  <label>3.6</label><title>Geochemical analysis</title>
      <p id="d1e757">ICP-OES (inductively coupled plasma–optical emission spectrometry) was used for determination of basic (Al, Ca, Mg, Na, K,
Fe, P) and trace elements (As, Cd, Mn, Th, Ti, U, V, Zn). Powdered samples
were mineralized in a closed microwave Anton Paar Multiwave PRO reaction
system. The mineralization procedure was based on the procedure of Lacort and
Camarero (2004). Characteristics of lake sediments were determined by the
extraction method of elements that are soluble in aqua regia (according to
European Standard CEN/TC 308/WG 1/TG 1, slightly modified). Dry samples of
about 0.2 g weight were transferred to the PTFE vessel and HNO<inline-formula><mml:math id="M21" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula>, and
HCL Merck Tracepur<sup>®</sup> was added. The vessels were placed in a
rotor and loaded to a microwave.<?pagebreak page1185?> Finally, the samples were analysed in the
Spectro Blue ICP-OES spectrometer at the Regional Research Centre for
Environment, Agricultural and Innovative Technologies, Pope John II State
School of Higher Education, in Biała Podlaska. A Bernd Kraft Spectro Genesis
ICAL solution and VHG SM68-1-500 Element Multi Standard 1 in 5 % HNO<inline-formula><mml:math id="M22" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> were used.</p>
      <p id="d1e781">Total organic carbon (TOC) analysis was done after sample acidification to
remove carbonates in the SHIMADZU SSM 5000A analyser with a solid sample
combustion unit. The method was the catalytically aided combustion oxidation
at 900 <inline-formula><mml:math id="M23" display="inline"><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup></mml:math></inline-formula>C with pre-acidification and oven temperature
200 <inline-formula><mml:math id="M24" display="inline"><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup></mml:math></inline-formula>C. A measuring range TC was 0.1 to 30 mg carbon. The sample amount was 1 g and aqueous content <inline-formula><mml:math id="M25" display="inline"><mml:mo>&lt;</mml:mo></mml:math></inline-formula> 0.5 g, with repeatability at SD <inline-formula><mml:math id="M26" display="inline"><mml:mo>±</mml:mo></mml:math></inline-formula>1 % of the full-scale range
(<uri>http://www.ssi.shimadzu.com/products/toc-analyzers/ssm-5000a</uri>, last access: 10 June 2021).</p>
      <?pagebreak page1186?><p id="d1e819">All selected samples were analysed using a scanning electron microscope
(SEM) HITACHI TM3000 with an energy dispersive spectrometer (EDS) SWIFT ED
3000 from Oxford Instruments. The samples were not covered with any conductive
material. Magnification range was used 20<inline-formula><mml:math id="M27" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> to 30 000<inline-formula><mml:math id="M28" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula>. This method was used
to perform basic microscopic observations of samples of the core M1 with
point determination of their chemical composition of major elements.</p>
</sec>
</sec>
<sec id="Ch1.S4">
  <label>4</label><title>Results</title>
<sec id="Ch1.S4.SS1">
  <label>4.1</label><title>Bathymetry</title>
      <p id="d1e852">A georadar transect across the lake reflects both its bathymetry and
composition of its bottom (Figs. 2–3). The superficial layer of the
transect is represented by lake ice that is ca. 25 cm thick, and although it is
almost not visible on radar images due to its thickness being smaller than a
vertical resolution of measurements, beneath there are multiple abundant horizontal
reflections of energy from the bottom of the ice. Two narrow and
vertical zones with small diffraction hyperboles at 23 and 29 m of the
transect indicate upward deformation of bottom sediments at the location
sites of the sounding core and the core M1 (Fig. 2a). The top of the
underlying mineral deposits (so-called hard bottom) is indicated as a
distinct downward-deflected reflection surface (Fig. 2b). In the central
part of the lake, it occurs at 2.6 m depth (two-way travel time 290 ns) and
indicates the top of the Holocene organic sediments. Unfortunately, beneath
there is a signal-absorption zone (Fig. 2d), resulting from the fact that
most sediments are composed of fine-grained organic material (gyttja).
However, the thickness of this layer was determined by drillings to about 5 m. A
relief of the lake bottom in the GPR image reflects a cross section of a
buried glacial tunnel valley that was eroded mainly in sandy and
sandy-gravel deposits. Close to the lake shore (0 to 20 m in the north-west
and 110 to 140 m in the south-east), there are numerous oblique and
chaotically parallel reflection surfaces dipping towards the channel axis.
They reflect bedding of the Pleistocene sandy-gravel series that partly
filled a subglacial channel (Fig. 2c).</p>
</sec>
<sec id="Ch1.S4.SS2">
  <label>4.2</label><title>Magnetic susceptibility</title>
      <p id="d1e863">MS is highly dependent on lithology and grain size of deposits (Dearing,
1994; Sandgren and Snowball, 2001). It reflects the presence and size of
ferromagnetic particles in a sample (Verosub and Roberts, 1995). Increased
content of ferromagnetic minerals such as magnetite, Fe-Ti oxides or
pyrrhotite generates higher MS whereas biotite, pyrite, carbonates and
organics result in its lower values. The total volume of magnetic minerals in
lake sediments mostly reflects climatic changes in a catchment (Bloemdal and
deMenocal, 1989; Snowball, 1993; Peck et al., 1994). MS in the core M1 is
varied but due to the organic character of the sediments, its values are
relatively low, from 0.002 to 0.034 <inline-formula><mml:math id="M29" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<inline-formula><mml:math id="M30" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">7</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula> units SI. In
grey-brown gyttja with organic matter at 3.50–2.58 m depth, MS rises and
drops in turn from 0.01 to 0.02 <inline-formula><mml:math id="M31" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<inline-formula><mml:math id="M32" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">7</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula> SI. MS drops from
2.60 m depth, reaching a minimum at 1.63 m. Higher up, MS rises again, with
the highest value at 1.35 m; then there is a minimum at 1.05 m, and the next
maximum is at 0.69 m depth (Fig. 6).</p>
</sec>
<sec id="Ch1.S4.SS3">
  <label>4.3</label><title>Chronology, lithology and sedimentation rate</title>
      <p id="d1e912">The age–depth model of the core M1 from Lake Młynek indicates (Fig. 4)
that the M1 core chronologically covers the last 2400 years. Bottom
deposits of Młynek Lake are organic-rich. The core M1 is composed of
grey-brown gyttja at 1.8–3.6 m depth (Fig. 5). At 1.45–1.80 m depth
there is grey-brown gyttja detritus, and at 1.10–1.45 m depth algal gyttja
is recorded. The uppermost part of the core is composed of grey-brown (depth
0.4–1.1 m) and detritus gyttja (0.0–0.4 m). The sedimentation rate was
calculated based on the age–depth model. Results reflect quite a stable
sedimentary environment with a general rate of 1.5 mm yr<inline-formula><mml:math id="M33" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula>. The rate is
stable at 3.40–1.77 m depth and equal to ca. 1.5 mm yr<inline-formula><mml:math id="M34" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula>. It drops to 1 mm and then rises to 1.3–1.8 mm yr<inline-formula><mml:math id="M35" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula> at 1.77–0.30 m. At 0.0–0.3 m the
sedimentary rate is the highest and equal to ca. 3 mm yr<inline-formula><mml:math id="M36" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula> (Fig. 5).</p>

      <?xmltex \floatpos{t}?><fig id="Ch1.F5"><?xmltex \currentcnt{5}?><?xmltex \def\figurename{Figure}?><label>Figure 5</label><caption><p id="d1e965">Lithology of the M1 borehole with radiocarbon determinations with
95 % confidence, close up – photo of the log at 2.6–3.0 m depth and
sedimentary rate (mm yr<inline-formula><mml:math id="M37" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula>) estimated based on the age–depth model.
Description of LOG: 1 – hydrated, detritus-type gyttja; 2 – very plastic, algal gyttja; 3 – grey-brown peaty, detritus gyttja; 4 – grey-brown gyttja (photo and drawing: Fabian Welc).</p></caption>
          <?xmltex \igopts{width=241.848425pt}?><graphic xlink:href="https://cp.copernicus.org/articles/17/1181/2021/cp-17-1181-2021-f05.png"/>

        </fig>

      <?xmltex \floatpos{t}?><fig id="Ch1.F6" specific-use="star"><?xmltex \currentcnt{6}?><?xmltex \def\figurename{Figure}?><label>Figure 6</label><caption><p id="d1e988">Concentration depth curves for selected elements and TOC in the core
M1 of Lake Młynek sediments. Description of LOG: 1 – hydrated, detritus-type gyttja; 2 – very plastic, algal gyttja; 3 – grey-brown peaty,
detritus gyttja; 4 – grey-brown gyttja (drawing: Fabian Welc).</p></caption>
          <?xmltex \igopts{width=412.564961pt}?><graphic xlink:href="https://cp.copernicus.org/articles/17/1181/2021/cp-17-1181-2021-f06.png"/>

        </fig>

</sec>
<sec id="Ch1.S4.SS4">
  <label>4.4</label><title>Pollen</title>
      <p id="d1e1005">Based on percentage contents of main trees and terrestrial herbs five local
pollen assemblage zones (LPAZ M1-M5) were established in the pollen sequence
of the Lake Młynek. The pollen contents were determined based on changes
in the percentage of individual taxa, confirmed by a cluster analysis (Table 2, Fig. 9).</p>

<?xmltex \floatpos{t}?><table-wrap id="Ch1.T2" specific-use="star"><?xmltex \currentcnt{2}?><label>Table 2</label><caption><p id="d1e1011">Local pollen assemblage zones of the Lake Młynek.​​​​​​​</p></caption><oasis:table frame="topbot"><oasis:tgroup cols="3">
     <oasis:colspec colnum="1" colname="col1" align="left"/>
     <oasis:colspec colnum="2" colname="col2" align="left"/>
     <oasis:colspec colnum="3" colname="col3" align="justify" colwidth="11cm"/>
     <oasis:thead>
       <oasis:row rowsep="1">
         <oasis:entry colname="col1">Zone</oasis:entry>
         <oasis:entry colname="col2">Depth (m)</oasis:entry>
         <oasis:entry colname="col3">Main features of pollen spectra</oasis:entry>
       </oasis:row>
     </oasis:thead>
     <oasis:tbody>
       <oasis:row rowsep="1">
         <oasis:entry colname="col1">LPAZ M1</oasis:entry>
         <oasis:entry colname="col2">345–315 cm</oasis:entry>
         <oasis:entry colname="col3">Pollen grains of <italic>Carpinus</italic> reached 33.5 % and <italic>Alnus</italic> 25 %, <italic>Pinus</italic> and <italic>Betula</italic> are <inline-formula><mml:math id="M38" display="inline"><mml:mo>&lt;</mml:mo></mml:math></inline-formula> 20 %. A top border of this zone is indicated by decline of <italic>Carpinus.</italic></oasis:entry>
       </oasis:row>
       <oasis:row rowsep="1">
         <oasis:entry colname="col1">LPAZ M2</oasis:entry>
         <oasis:entry colname="col2">315–265 cm</oasis:entry>
         <oasis:entry colname="col3">The share of <italic>Carpinus</italic> drops significantly (<inline-formula><mml:math id="M39" display="inline"><mml:mo lspace="0mm">&lt;</mml:mo></mml:math></inline-formula> 10 %), contents of <italic>Betula</italic>, <italic>Quercus</italic> and <italic>Corylus</italic> are slightly raised. The percentages of Gramineae significantly increased up to 7.5 %. There are continuous curves of <italic>Cannabis/Humulus,</italic> Chenopodiaceae, <italic>Plantago lanceolate</italic>, <italic>Rumex acetosella</italic> and <italic>Secale cereale</italic>, and a top boundary is indicated by a decline of Gramineae.</oasis:entry>
       </oasis:row>
       <oasis:row rowsep="1">
         <oasis:entry colname="col1">LPAZ M3</oasis:entry>
         <oasis:entry colname="col2">195–265 cm</oasis:entry>
         <oasis:entry colname="col3">At the beginning the curve of <italic>Betula</italic> rises to 24 % but then drops <inline-formula><mml:math id="M40" display="inline"><mml:mo>&lt;</mml:mo></mml:math></inline-formula> 10 %. The share of <italic>Carpinus</italic> and <italic>Fagus</italic> rises to 19 % and 27 %, respectively. Gramineae content decreased by <inline-formula><mml:math id="M41" display="inline"><mml:mo>&lt;</mml:mo></mml:math></inline-formula>  2 %, and the curves of <italic>Secale cereale</italic>, <italic>Plantago lanceolate</italic> and <italic>Rumex acetosella</italic> disappear. There are only single pollen grains of Chenopodiaceae and <italic>Cannabis/Humulus.</italic> A top boundary is indicated by a rise in Gramineae.</oasis:entry>
       </oasis:row>
       <oasis:row rowsep="1">
         <oasis:entry colname="col1">LPAZ M4</oasis:entry>
         <oasis:entry colname="col2">195–145 cm</oasis:entry>
         <oasis:entry colname="col3">Content of <italic>Fagus</italic> pollen begins to gradually decrease. The share of pollen grains of <italic>Betula</italic> increases and becomes stable at 22 %–27 %. Content of the Gramineae pollen grains increases again to 7 %. Curves of <italic>Cannabis/Humulus</italic>, <italic>Plantago lanceolate</italic>, <italic>Rumex acetosella</italic> and <italic>Secale</italic> raise, and a top boundary is marked by a rapid rise in <italic>Cannabis/Humulus.</italic></oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1">LPAZ M5</oasis:entry>
         <oasis:entry colname="col2">145–15 cm</oasis:entry>
         <oasis:entry colname="col3">Curves of main deciduous trees decline: <italic>Carpinus</italic> <inline-formula><mml:math id="M42" display="inline"><mml:mo>&lt;</mml:mo></mml:math></inline-formula> 9 %, <italic>Fagus</italic> <inline-formula><mml:math id="M43" display="inline"><mml:mo>&lt;</mml:mo></mml:math></inline-formula> 5 %, <italic>Quercus</italic> <inline-formula><mml:math id="M44" display="inline"><mml:mo>&lt;</mml:mo></mml:math></inline-formula> 5 %, <italic>Alnus</italic> <inline-formula><mml:math id="M45" display="inline"><mml:mo>&lt;</mml:mo></mml:math></inline-formula> 15 %, <italic>Betula</italic> <inline-formula><mml:math id="M46" display="inline"><mml:mo>&lt;</mml:mo></mml:math></inline-formula> 14 %. <italic>Pinus</italic> content increases to 40 %. There is a significant rise in Gramineae up to 15 %. Percentages of <italic>Cannabis/Humulus</italic> reach absolute maxima (25 %), but close to middle part of this zone their strong decline is observed (below 2 %–3 %). The continuous curves of <italic>Cerealia</italic> undiff., <italic>Centaurea cyanus</italic>, <italic>Plantago lanceolate</italic>, <italic>Rumex acetosella</italic> and<italic>Rumex acetosella</italic> appeared, and single pollen grains of <italic>Polygonum dumetorum</italic>, <italic>Polygonum aviculare</italic> and <italic>Urtica</italic> were present.</oasis:entry>
       </oasis:row>
     </oasis:tbody>
   </oasis:tgroup></oasis:table></table-wrap>

</sec>
<sec id="Ch1.S4.SS5">
  <label>4.5</label><title>Diatoms</title>
      <p id="d1e1306">Studies of the Lake Młynek bottom sediments revealed the presence of more than
200 diatom taxa belonging to 54 genera (Zalat et al., 2018) (Fig. 8).
Diatoms were generally abundant and well to moderately preserved in most
samples, although with a mixture of mechanically broken valves, especially in
the topmost part of the core. The results of the diatom analysis and relative
abundance of the most dominant taxa enabled subdivision of the M1 core
section into 11 diatom assemblage zones (Fig. 8) that reflected six phases
of lake development (Zalat et al., 2018). Moreover, changes in chrysophyte
cysts distributions along with variation in diatom composition could be
related to changes in pH, climate and trophic status. Stomatocysts can be
used as the index of lake-level changes, habitat availability, metal
concentrations and salinity.</p><?xmltex \hack{\newpage}?>
</sec>
<?pagebreak page1187?><sec id="Ch1.S4.SS6">
  <label>4.6</label><title>Geochemistry</title>
      <p id="d1e1318">Various factors influence distribution and accumulation of geochemical
elements in lake sediments. Most important are texture, mineral composition,
oxidation/reduction state, absorption/desorption and physical transportation
processes (Ma et al., 2016). Curves of representative elements are generally
used to characterize sedimentary environments. Most analysed elements do not
indicate any clear trend with depth in Lake Młynek. The curves of S
and TOC show significant increases at 2.0–1.4 m depth that are slightly
correlated with decreased Al, Fe, K, Ca, Mg and MS (Fig. 6).
Sulfur content is correlated with the existence of iron sulfides. In the
studied core, Fe is positively correlated with Al and Ti (Fig. 7). Fe–Ti
oxides are noted in SEM (scanning electron microscopy) EDS (energy dispersive spectroscopy) analysis. They are resistant to surface
weathering and carry trace elements (Bauer and Velde, 2014). At ca. 3 m,
high-frequency peaks of Al, K, Ca, Na, Mg, Fe and S occur (Fig. 6).</p>

      <?xmltex \floatpos{t}?><fig id="Ch1.F7" specific-use="star"><?xmltex \currentcnt{7}?><?xmltex \def\figurename{Figure}?><label>Figure 7</label><caption><p id="d1e1323">Scatter plot showing the correlation in the core M1 between S and
TOC, Al and TOC, Ti and Fe, and Ti and Fe (drawing: Anna Rogóż-Matyszczak).</p></caption>
          <?xmltex \igopts{width=412.564961pt}?><graphic xlink:href="https://cp.copernicus.org/articles/17/1181/2021/cp-17-1181-2021-f07.png"/>

        </fig>

</sec>
</sec>
<sec id="Ch1.S5">
  <label>5</label><title>Discussion</title>
      <p id="d1e1342">Magnetic susceptibility is generally low in biogenic sediments such as gyttja,
which is composed mainly of microfossil skeletons, e.g. diatoms and
radiolarians (Thompson and Oldfield, 1986). In Lake Młynek there is an
apparent negative relationship between TOC and MS. Several intervals show
both higher percentages of TOC and lower MS values. Changes in MS in Lake
Młynek sediments most probably record an input of clay into the lake and
diagenetic conditions in bottom sediments. Iron oxides are presumably of
detrital origin and were delivered to the basin through deep valleys incised
at the north-western shore. Concentration of ferromagnetic minerals is
connected with periodical intensive soil erosion around the lake. Their
higher content also depends on diagenetic processes in bottom sediments.
Oxidation of organic matter in anoxic conditions (by iron-oxide-reducing
bacteria) results usually in an increase in ferromagnetic particles
(small particles are removed first). Conversely, oxygenation by heavy floods
stops this process, and small magnetic particles are preserved (Jelinowska et
al., 1997). At 1.40 m depth, TOC suddenly drops, probably due to
deforestation, and then MS rises significantly due to the increasing input of
terrestrial (non-organic) material to the lake. Such a coincidence clearly
indicates that TOC is both of autochthonous and allochthonous derivation
(Fig. 6).</p>
      <p id="d1e1345">The highest contents of detrital elements like Al, K, Ca and Mg are to be
associated with sudden delivery of clastic material to the lake, e.g. during
increased flooding or rainfall (Wirth et al., 2013). Aluminium is extremely
immobile, that<?pagebreak page1188?> is why it should be regarded as a typical lithogenic element
(Price et al., 2007). Additionally, Al is a major constituent of soils and
other sediments as a structural element of clays. It has a strong positive
correlation with many major elements (Fig. 7). The association between Al
and other elements can be therefore used as the basis to compare natural
elemental contents in sediments and soils. Calcium is well correlated with
Al and likely originated from terrigenous bicarbonate inputs and deposited
in a lake as a solid carbonate (Miko et al., 2003). Calcium is evidently
more easily removed in solution from a mineral material and it is highly
concentrated in highly erosional periods (Mackereth, 1965).</p>
      <p id="d1e1348">The Fe <inline-formula><mml:math id="M47" display="inline"><mml:mo>/</mml:mo></mml:math></inline-formula> Ca ratio is considered as a eutrophication proxy. The highest values are found in low-oxygenation, eutrophic or dystrophic reservoirs (i.e. Kraska and
Piotrowicz, 2000; Holmes and De Decker, 2012), whereas the low Fe <inline-formula><mml:math id="M48" display="inline"><mml:mo>/</mml:mo></mml:math></inline-formula> Ca ratio
in bottom sediments indicates the oligotrophic character of a lake. In the
studied core sediments, Fe <inline-formula><mml:math id="M49" display="inline"><mml:mo>/</mml:mo></mml:math></inline-formula> Ca ratio varies from 0.80 (depth 3.05 m) to 3.67
(1.2 m). The ratio is low, indicating oligotrophic conditions in bottom
sediments, which gives conflicting results with other data. The Fe <inline-formula><mml:math id="M50" display="inline"><mml:mo>/</mml:mo></mml:math></inline-formula> Ca ratio
can be disturbed by detrital input to the lake (Fig. 6). The dysaerobic
conditions in the lake are confirmed by Th <inline-formula><mml:math id="M51" display="inline"><mml:mo>/</mml:mo></mml:math></inline-formula> U ratios (0.03–0.41) which are
lower than the critical value of 2 as indicated by Myers and Wignall (1987). The ratio of total Fe to total P ranges from 13.91 (1.6 m depth) to 30.82 (0.55 m). The values are typical for other lakes in
northern Poland, which vary from 3 to 180 according to Bojakowska (2016).
The release of P follows in reducing conditions. According to Ahlgren et al. (2011) it can be up to 10 times greater than in aerobic conditions.
However, there is a poor correlation with other redox proxies, i.e. Th <inline-formula><mml:math id="M52" display="inline"><mml:mo>/</mml:mo></mml:math></inline-formula> U
(<inline-formula><mml:math id="M53" display="inline"><mml:mi>R</mml:mi></mml:math></inline-formula> <inline-formula><mml:math id="M54" display="inline"><mml:mo>=</mml:mo></mml:math></inline-formula> 0.08), which may be caused by the presence of Al which forms
Al(OH)<inline-formula><mml:math id="M55" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula>. In such systems, even though the redox state favours the release of
P from iron minerals, the P is immobilized by binding with hydroxides. Thus,
the presence of Al(OH)<inline-formula><mml:math id="M56" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:math></inline-formula> can stop the release of P even in an
anoxic hypolimnion (Hupfer and Lewandowski, 2008). This could be the case in
the studied sediments as Al shows positive correlation with P content
(<inline-formula><mml:math id="M57" display="inline"><mml:mi>R</mml:mi></mml:math></inline-formula> <inline-formula><mml:math id="M58" display="inline"><mml:mo>=</mml:mo></mml:math></inline-formula> 0.49). Except for Fe <inline-formula><mml:math id="M59" display="inline"><mml:mo>/</mml:mo></mml:math></inline-formula> Ca, all counted ratios point to anoxic
conditions in all studied samples, which is typical in eutrophic lakes.
Nevertheless, as all proxies are characterized by extreme values at the 3.05 m depth, they seem to depend on an external load of terrigenous material. It is
confirmed with very good positive correlation between Fe and Al (0.95), Fe
and Ti (0.64), Mn and Al (0.46), or Mn and Ti (0.78).</p>
      <p id="d1e1448">The periphytic diatom species dominate throughout the core. A high
proportion of periphyton to plankton assemblages was reported as indicative
of long-lasting ice cover (Karst-Riddoch et al., 2005), whereas a shift
from benthic to planktonic diatom taxa is considered an ecological
indicator, which is interpreted in high-altitude lakes as a record of shorter
winters and increased temperatures. The common occurrence of benthic forms
represented by a <italic>Staurosira venter/Staurosirella pinnata</italic> diatom assemblage indicates circumneutral to slightly
alkaline shallow water with lowering lake levels and prolonged ice cover.
However, <italic>Aulacoseira</italic> is the most dominant planktonic genus followed by <italic>Cyclotella</italic> and low
frequency of <italic>Cyclostephanos</italic>. Diatom preservation in the upper part of the core (depth 1.40–0.15 m) is moderate to relatively poor, and the recognized assemblage was
represented by the occurrence of some dissolved and teratological diatoms
valves, in particular the topmost part of the core section (0.30–0.15 m)
(Zalat et al., 2018).</p>
</sec>
<sec id="Ch1.S6">
  <label>6</label><?xmltex \opttitle{Phases of the Lake M{\l}ynek development}?><title>Phases of the Lake Młynek development</title>
      <p id="d1e1472">Based mostly on the results of palynological studies, five main phases of the
Lake Młynek development in relation to the climate and human-induced
environmental change were distinguished (Fig. 10).</p>
<sec id="Ch1.S6.SS1">
  <label>6.1</label><?xmltex \opttitle{Phase 1: 2300--2100\,cal\,BP (ca. 4--1\,BCE), depth: 3.45--3.15\,m}?><title>Phase 1: 2300–2100 cal BP (ca. 4–1 BCE), depth: 3.45–3.15 m</title>
      <p id="d1e1483">This phase is recorded in LPAZ M1, which represents closed forest
communities dominated by hornbeam and alder, which colonized marshlands near
lake shores. Plants of open stands are only rarely noted as well as
indicators of anthropogenic activity (e.g. <italic>Plantago lanceolata</italic>). Vegetation at that time was
relatively natural and not disturbed. The diatom assemblage at the start of
this record (3.45–3.40 m depth) was distinguished by diatom subzone DZ1a
(Fig. 8) dominated by the periphytic taxa such as <italic>Staurosira construens</italic>, <italic>Staurosira venter</italic>, <italic>Staurosirella pinnata</italic>, <italic>Gyrosigma acuminatum</italic> associated with the
planktonic <italic>Aulacoseira granulata</italic>, <italic>A. ambigua</italic> and <italic>Puncticulata radiosa</italic>, which indicates a shallow and slightly alkaline lake. This
interval was followed by a great abundance of the planktonic <italic>Alkaliphilus</italic> diatoms of subzone DZ 1b (3.35–3.15 m, Fig. 8) dominated by <italic>Aulacoseira granulata</italic>, <italic>Cyclotella</italic> sensu lato species,
<italic>Cyclostephanos dubius</italic> and <italic>Stephanodiscus</italic> species. The diatom assemblage suggests a rising lake level with
increasing nutrients (Douglas and Smol, 1999; Zalat, 2015). The predominance
of <italic>A. granulata</italic> suggests a high trophic status and slightly alkaline freshwater
environment with high silica<?pagebreak page1190?> concentration (Kilham et al., 1986; Zalat et
al., 2018). Magnetic susceptibility is high and corresponds to high contents
of Fe, Ti and Al, indicating an increasing influx of terrigenous material,
presumably activated by intensive rainfall.</p>

      <?xmltex \floatpos{t}?><fig id="Ch1.F8" specific-use="star"><?xmltex \currentcnt{8}?><?xmltex \def\figurename{Figure}?><label>Figure 8</label><caption><p id="d1e1532">Diatom stratigraphy of the core M1, showing diatom zones and lake
phases and relative water level changes estimated based on the relation between
planktonic and benthonic diatom taxa (interpretation and drawing:
Abdelfattah Zalat).</p></caption>
          <?xmltex \igopts{width=369.885827pt}?><graphic xlink:href="https://cp.copernicus.org/articles/17/1181/2021/cp-17-1181-2021-f08.png"/>

        </fig>

      <?xmltex \floatpos{t}?><fig id="Ch1.F9" specific-use="star"><?xmltex \currentcnt{9}?><?xmltex \def\figurename{Figure}?><label>Figure 9</label><caption><p id="d1e1544">Percentage pollen diagram from core M1 – selected taxa.</p></caption>
          <?xmltex \igopts{width=497.923228pt}?><graphic xlink:href="https://cp.copernicus.org/articles/17/1181/2021/cp-17-1181-2021-f09.png"/>

        </fig>

      <?xmltex \floatpos{t}?><fig id="Ch1.F10" specific-use="star"><?xmltex \currentcnt{10}?><?xmltex \def\figurename{Figure}?><label>Figure 10</label><caption><p id="d1e1555">Diagram with selected palaeoenvironmental proxies including
lithology (1 – hydrated, detritus type gyttja; 2 – very plastic, algal
gyttja; 3 – grey-brown peaty, detritus gyttja; 4 – grey-brown gyttja) with phases of human activity in the vicinity of Lake Młynek, supplemented by an archaeological chronology for Poland (drawing: Fabian Welc).</p></caption>
          <?xmltex \igopts{width=497.923228pt}?><graphic xlink:href="https://cp.copernicus.org/articles/17/1181/2021/cp-17-1181-2021-f10.png"/>

        </fig>

</sec>
<sec id="Ch1.S6.SS2">
  <label>6.2</label><?xmltex \opttitle{Phase 2: 2100--1830\,cal\,BP (ca. 1\,BCE--2\,CE), depth: 3.15--2.65\,m}?><title>Phase 2: 2100–1830 cal BP (ca. 1 BCE–2 CE), depth: 3.15–2.65 m</title>
      <p id="d1e1573">During this phase changes in the environment around the lake were caused by
significant human impact. This phase corresponds with the LPAZ M2,
characterized by the reduction and fragmentation of the hornbeam-dominated
forest. Birch, pine and hazel expanded under better lighting conditions in a
partly open forest. Mid-forest pastures occupied rather small-scale open
areas, as can be inferred from higher percentages of <italic>Plantago lanceolata</italic> and other herbaceous
plants, e.g. Gramineae, <italic>Artemisia</italic> and <italic>Rumex</italic> <italic>acetosa/acetosella</italic>. Cultivated plants such as <italic>Cannabis</italic> and <italic>Secale</italic> are rare;
however, their occurrence is entirely consistent with other human indicators
present during this phase. This phase is commonly noted and similarly
expressed in numerous palynological sequences in neighbouring areas (see for
example Noryśkiewicz, 1982, 1987; Bińka et al., 1991;
Ralska-Jasiewiczowa et al., 1998). Pollen data indicate that societies of
that time cultivated rye and probably hemp. It is the oldest settlement
phase at Janiki Wielkie stronghold and corresponds to the termination of the
La Tène and the time of the early Roman period. Human communities in the
vicinity of the lake can be connected with settlements of the eastern Baltic
Kurgan culture (Rabiega et al., 2017). During this phase, planktonic diatoms
were replaced by benthic taxa, (DZ2) such as <italic>Staurosira construens</italic>, <italic>S. venter</italic> and <italic>Staurosirella pinnata</italic> accompanied by a
significant abundance of <italic>Gyrosigma acuminatum</italic> indicating a lower lake level and dominance of a
mesotrophic alkaline freshwater environment. The lower stands were
interrupted by a short rise in water level at 2.90–2.85 m (ca. 1930–1896 cal BP) where the abundance of planktonic eutrophic indicator
<italic>Aulacoseira</italic> spp. increased suddenly at the expense of the benthic taxa. During this phase
climatic conditions were still similar to ones in the previous phase, but it
was drier than is reflected by shallowing of the lake. This phase can be
correlated with the so-called Roman Climatic Optimum (see McCormick et al.,
2012).</p>
</sec>
<?pagebreak page1191?><sec id="Ch1.S6.SS3">
  <label>6.3</label><?xmltex \opttitle{Phase 3: 1830--1150\,cal\,BP (ca. 2--9\,CE), depth: 2.65--1.95\,m}?><title>Phase 3: 1830–1150 cal BP (ca. 2–9 CE), depth: 2.65–1.95 m</title>
      <p id="d1e1620">This phase corresponds to LPAZ M3 when a forest restoration occurred.
Absence of human indicator plants suggest that the settlement in the
catchment was abandoned. There are also no traces of human activity nearby
(Rabiega et al., 2017). Reduction of human impact and human-generated
semi-open habitats allowed for a short-term expansion of birch into empty,
open areas, which were later replaced by hornbeam that rebuilt its position to the
level it was at in the LPAZ M1. Elm also expanded again in a riparian forest. This
restoration of the natural forest was followed by abrupt expansion of beech
in the second half of the LPAZ<?pagebreak page1192?> M3. The area of open herbaceous plants
communities, previously widespread, was limited.</p>
      <p id="d1e1623">Abundant planktonic diatoms including <italic>Aulacoseira</italic> spp. and <italic>Puncticulata radiosa</italic> and the common occurrence of
small <italic>Cyclotella</italic> spp. occurred in the lake (Fig. 8), which indicates its deepening,
enhanced thermal stratification, reduced mixing and increased thermal
stability (Zalat et al., 2018). Intensified development of vegetation
cover and higher lake levels are indicated by geochemical indices. A gradual
drop of MS corresponds with decreased content of detrital elements such us
Fe, Ti, Al and K, accompanied by a gradual increase in TOC and the Fe <inline-formula><mml:math id="M60" display="inline"><mml:mo>/</mml:mo></mml:math></inline-formula> Ca
ratio. Lower MS and Al content (acting as a major constituent of soils)
accompanied by the higher TOC suggest limited erosion, in spite of gradually
higher precipitation in the lake catchment and therefore a rise in its
water level (Fig. 6). The climate in this phase has become more humid.
Increased rainfall and decreased evaporation are reflected in lake
sedimentation as the lake got deeper, resulting in reduced deposition and
greater stability. This phase could be associated with a global cooling of
the Bond 1 event (1.5 ka BP) (Bond et al., 1997; Welc, 2019).</p>
</sec>
<sec id="Ch1.S6.SS4">
  <label>6.4</label><?xmltex \opttitle{Phase 4: 1150--780\,cal\,BP (ca. 9--13\,CE), depth: 1.95--1.45\,m}?><title>Phase 4: 1150–780 cal BP (ca. 9–13 CE), depth: 1.95–1.45 m</title>
      <p id="d1e1651">This phase is correlated with the LPAZ M4 and is divided into two sub-phases
4a and 4b (Fig. 10). The sub-phase 4a marks the onset of another settlement
phase, resulting in forest clearing. Disturbances took place firstly in a
beech forest and less in a hornbeam-dominated one. The anthropogenic
activity is reflected by presence of <italic>Gramineae</italic>, <italic>Artemisia</italic>, <italic>Cannabis/Humulus</italic>, <italic>Plantago lanceolata</italic>, <italic>Rumex acetosella</italic>, <italic>Secale</italic> and <italic>Cerealia</italic> undiff.
Diatom assemblages suggest a deepening of the lake (Zalat et al., 2018) as
indicated by the abundance of <italic>Aulacoseira</italic> associated with <italic>Puncticulata radiosa</italic> in the upper part of the diatom
zone 5 at 1.85–1.70 m depth (ca. 1070–941 cal BP). The diatom
assemblage suggests a rising lake level, higher trophy and stronger
turbulent mixing conditions (Rühland et al., 2008; Zalat et al., 2018).
Moreover, the greatest reduction of abundant <italic>Fragilaria</italic> sensu lato accompanied by abundant <italic>A. granulata</italic>,
could be a result of forest clearing around the lake. Higher TOC corresponds
with lower content of detrital material (Fe, Ti, Al and K) and lower MS, and
it can reflect a progressing humidity (Fig. 6). This phase can be correlated
with the Migration Period and the early Middle Ages. A wooden-loamy defence
rampart was raised at the end of the phase in a settlement close to the lake
(archaeological phase III), after removal of a natural soil developed during
abandonment of the<?pagebreak page1193?> site in the early Roman Period. After a short period,
this stronghold was destroyed. Charcoal from a fired wall that represents
destruction at the end of the archaeological phase IIIA was dated at 1245 <inline-formula><mml:math id="M61" display="inline"><mml:mo>±</mml:mo></mml:math></inline-formula> 25 cal BP (i.e. 682–870 CE; 95.4 % probability) and 1090 <inline-formula><mml:math id="M62" display="inline"><mml:mo>±</mml:mo></mml:math></inline-formula> 30 cal BP (i.e. 892–1014 CE; 95.4 % probability) (Rabiega et
al., 2017).</p>
      <p id="d1e1703">Human impact declines during the subphase 4b (1.70–1.45 m depth, ca. 940–782 cal BP). At this time birch and less intensively poplar occupied
temporarily abandoned open areas, especially toward the end of the zone,
when human activity was less intensive. Alder became more abundant,
probably expanding into exposed marginal areas of the lake. The sub-phase
4b corresponds to the diatom zone 6 (Fig. 8), which is characterized by
abundant benthic <italic>Fragilaria</italic> sensu lato with sporadic occurrence of planktonic taxa. A high
proportion of benthic to plankton assemblages was reported as indicative of
long-lasting ice cover (Karst-Riddoch et al., 2005). As well as this, a great
abundance of the benthic <italic>Staurosira venter</italic> and <italic>Staurosira construens</italic> with marked decline in the planktonic diatoms
such as <italic>Aulacoseira</italic> spp. and <italic>Puncticulata radiosa</italic> reflects lowering water levels and slightly alkaline
freshwater, lower nutrient concentrations and low silica content (Kilham et
al., 1986; Stevens et al., 2006; Zalat et al., 2018).</p>
      <p id="d1e1721">In the stronghold at the lake shore, the next phase of human activity took
place at the end of the 11th century CE when a new rampart was
raised. Wooden constructions were also built, traces of which were excavated
in the gate passage. The settlement was finally abandoned, presumably in the
first half of the 13th century, and then its ramparts were strongly
eroded, with their material moving towards a yard and the moat (Rabiega et
al., 2017). The sub-phase 4b is characterized by a gradual warming, which
correlates with a gradual shallowing of the lake and increased rate of
sedimentation. Human impact on the environment in this sub-phase is already
so great that reconstruction of a climate change is not clear. There is no
doubt; however, that this is a warm period, which should be correlated with
the Medieval Warm Period (MWP) (Mann et al., 2009).</p>
</sec>
<sec id="Ch1.S6.SS5">
  <label>6.5</label><?xmltex \opttitle{Phase 5: 780--0\,cal\,BP (13\,CE--present time), depth: 1.45--0\,m}?><title>Phase 5: 780–0 cal BP (13 CE–present time), depth: 1.45–0 m</title>
      <p id="d1e1733">This phase starts about 1200 CE and is connected with the early Modern
Period. Cultivation and treatment of hemp has been terminated but
cultivation of cereals and presence of synanthropic plants indicate human
activity near the lake. The water level changes only slightly and is not high, which is evidenced by a great abundance of benthic
diatom taxa over the planktonic forms (DZ 8–10, Fig. 8). There is a drop in TOC
and rise in MS caused by increasing input of terrestrial material at 1.4 m
depth (ca. 751 cal BP), resulting presumably from human deforestation.
The small watercourse which enters the lake from the north-east appeared
most probably during this phase and had a strong impact on its water
environment (see, Bińka et al., 2020). As previously mentioned, in the 15th century CE a mill was built near the lake, and damming of the water in the
mill reservoir probably contributed to periodical blooms of dinoflagellate
populations in Lake Młynek. Major blooms of <italic>Tetraedron</italic>, which usually precede blooms
of the dinoflagellate, were most probably the main factor that contributed
to the decline of settlement at the stronghold (Bińka et al., 2020). This
zone is also characterized by increased precipitation which is reflected by
more intensive terrestrial inflow to the lake and is confirmed by
quasi-linear correlation of MS with contents of Fe and Ti in sediments (Fig. 6). The modern lake is shallow (2–3 m) and gradually overgrowing. Summing
up, the phase 5 is marked by intensive human activity around the lake, and
therefore most “natural” environmental and climate changes are
obliterated.</p>
</sec>
</sec>
<sec id="Ch1.S7">
  <label>7</label><?xmltex \opttitle{Development of Lake M{\l}ynek -- a regional background}?><title>Development of Lake Młynek – a regional background</title>
      <p id="d1e1749">The above scenario seems to be confirmed by earlier palaeoenvironmental
research carried out in the south-western part of the Warmia–Masuria
lake lands (Kupryjanowicz, 2008; Kołaczek et al., 2013). Previous studies of
the lake sediments in this region were based mainly on pollen analysis and
enable the comparison of the Lake Młynek record with other sequences.</p>
      <p id="d1e1752">The closest records from Lake Woryty (Pawlikowski et al., 1982;
Noryśkiewicz and Ralska-Jasiewiczowa, 1989; Ralska-Jasiewiczowa and
Latałowa, 1996), just 35 km to the east, is a reference one.
Palaeoenvironmental records inferred from the Lake Młynek core are very
similar to the Woryty palynological succession with distinctive human impact
during the Roman Period and the Medieval Ages, however, a detailed
comparison is difficult, because of the low resolution of the pollen
spectrum obtained at Woryty.</p>
      <p id="d1e1755">The second site is Lake Drużno, located in the Vistula Delta, 35 km to
the north of Młynek Lake (Zachowicz et al., 1982; Zachowicz and
Kępińska, 1987; Miotk-Szpiganowicz et al., 2008). Unfortunately, the
low resolution and the lack of reliable age–depth models of the lake make
comparison difficult. Despite habitat differences between Lake
Drużno and Lake Młynek, pollen records obtained at both sites are very
similar and comprise human indicators during the Roman Period and human
impact during the Medieval times.</p>
      <p id="d1e1759">The pollen spectrum from Lake Łańskie (Madeja, 2013), located 55 km to
the south-east from Lake Młynek, shows higher pine content and lower
share of beech than in the case of Lake Młynek. Such divergences are
probably not only due to different location and environmental conditions in
the lake vicinity but also depend on different size of these lakes. Lake Młynek is a very small (0.7 km<inline-formula><mml:math id="M63" display="inline"><mml:msup><mml:mi/><mml:mn mathvariant="normal">2</mml:mn></mml:msup></mml:math></inline-formula>) mid-forest basin, whereas Lake
Łańskie is over 10 km<inline-formula><mml:math id="M64" display="inline"><mml:msup><mml:mi/><mml:mn mathvariant="normal">2</mml:mn></mml:msup></mml:math></inline-formula> large and contains mostly a regional pollen
record. Based on periodical<?pagebreak page1194?> appearances of human plant indicators and
archaeological data between 300 BCE and 800 CE, three human phases of the West
Baltic Barrow, Wielbark and Prussian cultures were distinguished (Madeja,
2013). In the pollen diagram from Lake Młynek (phase 2), the first culture
is indicated, including termination of the La Tène and the Roman Period.
Significant growth of human indicators from the beginning of the 11th
century CE, are visible in diagrams from both sites. A more local record from
Lake Młynek is especially marked by high <italic>Humulus/Cannabis</italic> content (to 25 %) in the
13th–15th centuries CE. In the sediments of Lake Łańskie, hemp
occurred discontinuously and was <inline-formula><mml:math id="M65" display="inline"><mml:mo>&lt;</mml:mo></mml:math></inline-formula> 1 %.</p>
      <p id="d1e1790">The pollen records from Lake Młynek are similar to the ones from the
Masurian lakes, Wojnowo, Miłkowskie and Jędzelek, located over 100 km
to the east (Wacnik et al., 2014). Recorded episodes of human impact on
vegetation during the Roman Period and Medieval times are separated by
500–600-year-long intervals without cultivation and with natural
reforestation (indicated by a strong presence of birch, which is a pioneer
species). A similar period of human withdrawal in the Lake Młynek section
began and terminated earlier than recorded in the lakes Wojnowo and Miłkowskie. Another history of human activity is represented in a record from
Lake Salęt (Szal et al., 2014b). Pollen grains of cultivated and ruderal
plants are noted continuously from the early Iron Age to the early Medieval
times. In contrast to the pollen record from lakes Młynek, Wojnowo and Miłkowskie, the suggested continuous settlement in the neighbourhood of the
Lake Salęt was interrupted by a single very short decline of human
impact between 880–980 CE (Szal et al., 2014a). Numerous pollen data are
available from the area adjacent in the south-west in the Brodnica Lake
District, including Strażym Lake (Noryśkiewicz, 1987;
Noryśkiewicz and Ralska-Jasiewiczowa, 1989), Oleczno Lake
(Filbrandt-Czaja, 1999; Filbrandt-Czaja et al., 2003) and the Chełmno
Lakeland (Noryśkiewicz, 2013). Pollen records from this region also
suggest intensive settlements during La Tène, Roman and Medieval periods.</p>
      <p id="d1e1793">Pollen records from other sites located to the east of Lake Młynek
indicate differences in the representation of beech content. The <italic>Fagus sylvatica</italic> content
changes to the north-east, and its significantly high content in Lake Młynek sediments represents a very local record in a small lake. The decline of
<italic>Fagus sylvatica</italic> depends on a continental climate and is noted in pollen diagrams from the
lakes Salęt (Szal et al., 2014a), Mikołajki (Ralska-Jasiewiczowa,
1989), Żabińskie (Wacnik et al., 2016) and Wigry (Kupryjanowicz,
2007). A decline of beech is accompanied by a rise in <italic>Picea abies</italic>. A record of human
activity in pollen spectra from eastern Poland was noted at many sites.</p>
</sec>
<sec id="Ch1.S8" sec-type="conclusions">
  <label>8</label><title>Conclusions</title>
      <p id="d1e1813">Based on the results of laboratory analysis, supplemented with
archaeological data, five main environmental phases of the Lake Młynek
development were distinguished (Fig. 10). Radiocarbon ages enabled detailed
chronology, whereas pollen data and stratigraphy of the stronghold to the
north-east of the lake made correlation possible between human activity for the last 2300 years and environmental
data. From the first century BCE to
second century CE the forest around the lake was much reduced, which can be
associated with pre-Roman and Roman occupation phases (confirmed also by the
stronghold located close to the lake). From the second to ninth century
CE there is a gradual restoration of the forest and decline in human
activity along with a deepening of the lake as a result of wetter climatic
conditions. This colder and humid phase corresponded to the Bond 1 event
(1.5 ka BP) cooling episode. Intensive forest clearing around the lake
occurred in the 9th–13th centuries CE as result of another phase of
human activity. This period is marked by warming, confirmed by a gradual
shallowing of the lake (Middle Age Warm Period). Since the 14th century
CE strong human impact transformed the local landscape, especially through
the construction and activity associated with the mill and the creation of a
small artificial lake in the 15th century CE. This results in potential
climate-driven environmental changes being obscured by the direct impact of
humans on the lake and its catchment. It is important to add here that
transformations of Lake Młynek, reconstructed based on diatom analysis,
not only indicate changes of the lake water level and correspond with a
human impact but also determine episodes of more humid climate during
coolings.</p>
      <p id="d1e1816">We can conclude that environmental transformations recorded in bottom lake
sediments of Lake Młynek were highly dependent on human activity and were
especially intensive in the Roman and Middle Age periods due to favourable
climatic conditions</p>
</sec>

      
      </body>
    <back><notes notes-type="dataavailability"><title>Data availability</title>

      <p id="d1e1823">All data will be made available on request.</p>
  </notes><notes notes-type="authorcontribution"><title>Author contributions</title>

      <p id="d1e1829">FW, JN, and LM conceptualized the study. FW, JN, KB, ARM, MO, and AZ designed the methodology. Formal analysis was performed by FW, JN, LM, KB, ARM, MO, and AZ. The investigation was carried out by FW and JN. FW and JN provided resources and wrote the original draft. FW, JN, and LM reviewed and edited the paper. Visualization was carried out by FW, KB, ARM, MO, and AZ. JN and FW acquired the funds.​​​​​​​</p>
  </notes><notes notes-type="competinginterests"><title>Competing interests</title>

      <p id="d1e1835">The authors declare that they have no conflict of interest.</p>
  </notes><?xmltex \hack{\newpage}?><ack><title>Acknowledgements</title><p id="d1e1843">The research was funded by the National Science Centre in Poland in the
project UMO-2016/21/B/ST10/03059: “Correlation of prehistoric and early medieval settlement phases in north-east Poland with the changes of the natural environment in the light of lacustrine sediments study”.</p></ack><notes notes-type="financialsupport"><title>Financial support</title>

      <p id="d1e1848">This research has been supported by the National Science Centre in Poland – Narodowe Centrum Nauki (grant no. UMO-2016/21/B/ST10/03059).</p>
  </notes><notes notes-type="reviewstatement"><title>Review statement</title>

      <p id="d1e1854">This paper was edited by Keely Mills and reviewed by Daniel Schillereff and one anonymous referee.</p>
  </notes><ref-list>
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    <!--<article-title-html>2400 years of climate and human-induced environmental change recorded in sediments of Lake Młynek in northern Poland</article-title-html>
<abstract-html><p>In the densely forested Warmia and Masuria region (northern Poland) there
are many small endorheic lakes characterized by their low sedimentation
rate, which makes them excellent archives of Holocene environmental and
palaeoclimatic change. Lake Młynek, located near the village of Janiki
Wielkie, was selected for multi-faceted palaeoenvironmental research
supported with radiocarbon dates. Sediments from this lake also contain
unique information about human impact on the environment, because a
stronghold has been operating on its northern shore since the early Iron Age
to the early Medieval period, giving the opportunity to correlate
palaeoenvironmental data with the phases of human activity over the last
2400 years. During the second and third centuries BCE the lake was
surrounded by a dense deciduous forest. From the first century BCE to
second century CE the forest around the lake was much reduced, which can
be associated with the first pre-Roman (La Tène) and Roman occupation phase
evidenced by the construction of the stronghold located close to the lake.
From the second up to ninth century CE gradual restoration of the
forest and a decline in human activity took place, along with lake deepening
and the onset of a colder and humid climatic phase which corresponded to the
global cooling episode known as the Bond 1 event (1.5&thinsp;ka&thinsp;BP). The next
intensive phase of forest clearing around the lake occurred between the
9th–13th century CE as result of human activity (Middle
Age settlement phase of the stronghold). Whilst this period is marked by a
warming, the human impact which has transformed the landscape likely
overprints any signals of climate-driven environmental changes.</p></abstract-html>
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