SONJA B. GRIMM · BERIT VALENTIN ERIKSEN · SASCHA KRÜGER
TOBIAS REUTER · MARKUS WILD · MARA-JULIA WEBER
LATE GLACIAL OCCUPATION OF NORTHERN GERMANY
AND ADJACENT AREAS. REVISITING THE ARCHIVES
Abstract
This contribution presents the status quo of research on the Final Palaeolithic occupation of Schleswig-Holstein. Over
the last two decades new insights became possible based on isotopic, genetic, biostratigraphic, tephrochronologic, and
archaeological analyses. Some of these projects and studies are still on-going. The material on which these analyses
were performed was mainly uncovered during the 20th century. We particularly focus on the chronology and the different challenges associated with the Late Glacial record. To do so, we review the radiocarbon dating record of SchleswigHolstein and adjacent areas, especially Denmark, including 11 new radiocarbon dates from the sites of Stellmoor and
Meiendorf. At present, in particular, the period of the Federmessergruppen (i. e., curve-backed point industries) appears
poorly represented in this record. This shortage is due to preservational conditions on the one hand, as well as the
often uncertain attribution of osseous single finds to archaeological entities on the other. Hence, a synoptic analysis of
osseous remains of Late Glacial northern Germany and southern Scandinavia is desirable.
The recently introduced partially laminated biostratigraphic lake sequence from Nahe LA 11 contains three cryptic
tephra layers including the first geochemically identified evidence of the Laacher See Tephra in Schleswig-Holstein. The
palynological analysis of this archive interlinks palaeoenvironmental with archaeological research questions. Amongst
other implications, the data provided here suggest a continuity of human and reindeer presence in the area until the
early Holocene. This result lines up with observations of shifting ecological zones throughout the Weichselian Late
Glacial in Schleswig-Holstein.
Keywords
Schleswig-Holstein, Final Palaeolithic, Weichselian Late Glacial, chronology, osseous material
INTRODUCTION
At the MONREPOS Archaeological Research Centre and Museum for Human Behavioural Evolution Elaine
Turner and Martin Street represented the well-established field of zooarchaeology to inform us about past
human settlement and land use behaviour (Turner, 2004; Street et al., 2006; Street and Turner, 2013). Their
studies in the Central Rhineland were made possible by the excellent preservation of organic material underneath the ignimbrites and pumices of the Laacher See volcanic eruption. The organic preservation further
allowed for the establishment of a reliable chronology of the Late Glacial re-settlement of north-western
central Europe after the Last Glacial Maximum (Street et al., 1994; Housley et al., 1997; Terberger and
Street, 2002; Street and Terberger, 2004; Stevens et al., 2009; Fiedel et al., 2013). With the increasing industrial exploitation of the Laacher See pumice in the 1950s and 1960s, Late Glacial / Allerød surfaces were
uncovered and thereby revealing archaeological remains from Late Magdalenian and Federmessergruppen
(FMG) contexts which accordingly became a focus of research (Bosinski, 1979; Baales, 2002). Besides the
excellent preservation conditions, these relatively recent discoveries also paved the way to apply modern
standards of excavation, documentation, and archiving. These conditions allowed for some of the most
In: S. Gaudzinski-Windheuser · O. Jöris (Eds.), The Beef behind all Possible Pasts. The Tandem-Festschrift in Honour of
The
Beefand
behind
Possible
Pasts – The
in Honour
of Elaine Turner and Martin Street
Elaine
Turner
Martinall
Street.
Monographien
desTandem-Festschrift
RGZM 157 (Mainz 2021).
DOI: 10.11588/propylaeum.950.c12572
433
detailed insights into the reconstruction of Late Upper and Final Palaeolithic lifeways. Furthermore, the
Laacher See volcano – like many of the volcanic craters in the Eifel volcanic field – has transformed into a
maar lake. Laminated sequences from these natural sediment traps were used to build up a stacked record
of Late Glacial climatic and environmental change, which is in large parts annually laminated (ELSA; Sirocko,
2016). Hence, for the Late Glacial and early Holocene periods, a detailed vegetation history with relevance
for the wider region was also established (Litt and Stebich, 1999; Sirocko et al., 2016). These high-resolution
records helped to contextualise the archaeological findings of the Central Rhineland. Researchers in other
areas aimed to synchronise their records with these high-resolution archives through the use of archaeological comparison or by bio- or tephrochronology (Housley et al., 2013). The Laacher See tephra (LST) has
been of particular interest as a short-term chronostratigraphic marker horizon (Litt et al., 2001; Blockley
et al., 2008; Wulf et al., 2013).
Recently, the LST has been geochemically confirmed for the first time in Schleswig-Holstein (Krüger and van
den Bogaard, 2021). In contrast to the Rhineland, research on the Late Glacial in Schleswig-Holstein has
been more or less continuous since the 19th century, with numerous collections but few excavations and
variable standards of documentation (Schwantes, 1923, 1928, 1933; Schwabedissen, 1944; Taute, 1968;
see below). Hence, to understand the occupation history of the region and attempting to base this on a
solid chronostratigraphic framework, this area offers a large amount of legacy data and all the challenges
that come with it. In the last years, some new analyses were made, especially at the Centre for Baltic and
Scandinavian Archaeology (ZBSA) and in the context of the subproject “Pioneers of the North” of the DFGfunded collaborative research centre 1266 “Scales of Transformation”. The results allow new insights that
are outlined in the following, with a focus on the Late Glacial chronology of Schleswig-Holstein, supplemented with data from adjacent areas.
RESEARCH HISTORY
The excavations of Alfred Rust and his interdisciplinary team in the Ahrensburg tunnel valley in the 1930s,
1940s, and early 1950s (Fig. 1; Rust, 1937, 1943, 1958) provide a first milestone in the Palaeolithic archaeology of Schleswig-Holstein. In these campaigns, Palaeolithic organic material uncovered from Late Glacial
lake deposits included the oldest wooden arrows (unfortunately lost during World War II; cf. Hartz et al.,
2019). Especially the excavations at Stellmoor (Ahrensburg LA 1 78.1) provided the stratigraphic evidence
that the Hamburgian preceded the Ahrensburgian. Furthermore, these technocomplexes were associated
with the palynologically well-defined bio zones that were (later) named Meiendorf and Younger Dryas (i. e.,
Dryas 3) (Menke, 1968; cf. Krüger et al., 2020) and allowed for a first general chronostratigraphy. Following this pioneering work, few systematic excavations of Late Glacial material have been conducted in the
Ahrensburg tunnel valley and in entire Schleswig-Holstein. This research will be shortly presented in the
following.
In the late 1960s / early 1970s Gernot Tromnau excavated different concentrations of Late Glacial archaeological material on the sandy Teltwisch ridge in the Ahrensburg tunnel valley. This showed the potential
for further excavations of Late Glacial organic material by corings and test trenches in nearby kettle holes
(Tromnau, 1975). Besides Hamburgian and Ahrensburgian material, he also identified two small concentrations with FMG material. In the Vierbergen area in the northern part of the Ahrensburg tunnel valley,
1
LA = Landesaufnahme (register of prehistoric and historic artefacts and archaeological sites and monuments of Schleswig-Holstein).
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Fig. 1 Map of northern Germany and southern Scandinavia during GI-1c-a with major glacial valleys and drainage
channels indicated (darker green) and sites mentioned in
the text and the tables (map: www.epha.zbsa.eu – Allerød
map with the addition of drainage systems). 1 Ahrensburg
tunnel valley; 2 Lasbek; 3 Nahe; 4 Lüdersdorf; 5 Klein Nordende; 6 Eggstedt; 7 Schalkholz; 8 Alt Duvenstedt; 9 Ahrenshöft; 10 Klappholz; 11 Endingen; 12 Krogsbølle; 13 Trollesgave; 14 Fensmark Skydebane; 15 Bromme; 16 Arreskov;
17 Odense Kanal; 18 Slotseng; 19 Fogense Enge; 20 Tyrsted;
21 Køge Bugt; 22 Bara Mosse; 23 Hässelberga; 24 Mickelsmosse (Munkarp); 25 Nørre Lyngby; 26 Rissen; 27 Melbeck;
28 Grabow 15; 29 Hämelsee; 30 Querenstede.
200 km
km
east of the Borneck site (Ahrensburg LA 76), in 1985 Klaus Bokelmann could not find any archaeological
remains in a 6-7 m deep survey trench and hence identified the limits of the concentration of Palaeolithic
sites that he assumed was due to the geomorphology of the Late Glacial landscape (Bokelmann, 1996). In
2008 Ingo Clausen conducted a survey of test trenches and corings (Ahrensburg LA 78.2) to locate A. Rust’s
Stellmoor excavation trenches more precisely and to test if archaeological material was still present and
preserved (Clausen, 2010). In January 2010, most of the Ahrensburg tunnel valley became a “Natura 2000”
conservation area within the EU Habitats Directive (92/43/EEC) and the accompanying management plan
prohibited any further penetration into the ground. However, in the context of the planned expansion of the
railway line S4 through the Ahrensburg tunnel valley, further test pits and trenches on the mineral soils near
Stellmoor (Stellmoor-Lusbusch, Ahrensburg LA 105, 160, 162, and 187), around Meiendorf (Ahrensburg LA
79 and 140), and into the Hamburgian area of the tunnel valley became possible in summer 2015 (Clausen
and Guldin, 2016, 2017). These identified the limits of the accumulation of Late Glacial sites around Meiendorf, which was almost congruent with the modern border of the federal states of Schleswig-Holstein and
Hamburg. Furthermore, corings in Late Glacial lake sediments south of Stellmoor (Ahrensburg LA 187-191)
revealed the preservation of bone and antler material in an area larger than hitherto known. New palynological samples were taken during these efforts (Krüger, 2015) and, most importantly, Sascha Krüger could
obtain access to the archival data of the region collected by Hartmut Usinger.
Outside the Ahrensburg tunnel valley, Hermann Schwabedissen’s work in 1948 at the site of Rissen 14/14a
to the west of Hamburg, where an Ahrensburgian horizon was underlain by a FMG horizon, clarified the
chronostratigraphic sequence of the northern German Final Palaeolithic (Schwabedissen, 1954): The Hamburgian present during the Meiendorf period was followed by the FMG during the Allerød period and in
turn was followed by the Ahrensburgian during the Dryas 3. In 1959, Wolfgang Taute excavated typical
Ahrensburgian material associated with long and large blades in Eggstedt (LA 50), but only some material
was recovered in situ as previous amateur excavations had disturbed the area (Taute, 1968). In 1960 he
excavated Ahrensburgian material including a few faunal remains in an area of the Lieth Moor near Klein
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Nordende (LA 2; Taute, 1968). South-west of this site, K. Bokelmann and the amateur Alfred Rasmussen
uncovered several concentrations of FMG and faunal material in the 1970s (Klein Nordende LA 37: Bokelmann et al., 1983). In 2013, Ingo Clausen and Annette Guldin tested an area north-west of this and west
of W. Taute’s site because – over the course of several decades – collectors had reported (mainly) Ahrensburgian artefacts from there, and geologists had reconstructed Late Glacial wetlands in the vicinity. However,
only fragmented stratigraphic sequences were found that showed significant movement of sediment due to
various natural processes such as water level changes or cryoturbation. This was explained by the very complex geomorphological situation in the region that often included significant changes over short distances.
Furthermore, in 1970 another Hamburgian site was rescue excavated in a single day by A. Rust and G. Tromnau at the limits of a gravel pit near Schalkholz (LA 116; Tromnau, 1974). Nearby, Volker Arnold found a
partially destroyed FMG concentration (Schalkholz LA 65) that was also uncovered in a rescue excavation
by K. Bokelmann and Dieter Stoltenberg in late 1975 (Bokelmann, 1978). From the mid-1980s to the early
1990s I. Clausen and Sönke Hartz – excavating near Alt Duvenstedt – uncovered a total of nine Late Glacial
concentrations of lithic material that in some cases centred around a still identifiable hearth (Clausen and
Hartz, 1988; Clausen, 1995, 1996a; Kaiser and Clausen, 2005). Most assemblages were attributed to the
FMG but two were of a very early Ahrensburgian origin (Clausen and Schaaf, 2015). In the mid-1990s two
sites with Hamburgian material were excavated at Ahrenshöft in the context of a renaturalisation program
(Clausen, 1997). Especially the site Ahrenshöft LA 73 has major relevance for the Late Glacial chronology
as, for the first time, a horizon containing an inventory dominated by classic Hamburgian shouldered points
was overlain by a horizon with mostly Havelte tanged points. Palynological analyses further showed that
both horizons were deposited at different stages within the Meiendorf period (Usinger, 1997). In 2008
Mara-Julia Weber extended the excavation area at the Havelte concentration Ahrenshöft LA 58 D (Weber
et al., 2010). Finally, the most recently identified area of finds is situated around the north-western outlet of
the modern Lake Itzstedt where Thomas Poelmann had collected Ahrensburgian and Hamburgian material
since 1986 (Nahe LA 11). In 2003, I. Clausen made some test trenches in the wetlands of the present-day
Rönne valley and found some faunal material dominated by reindeer (Weber et al., 2011; Wild, 2017).
I. Clausen’s work was complemented by 68 sediment cores that H. Usinger took along and across the valley. The results of these corings helped S. Krüger to identify the basin of a former incision lake (palaeolake
Nahe) and to locate the currently best Late Glacial environmental archive of Schleswig-Holstein. This was
cored in October 2017 (Dreibrodt et al., 2021; Krüger, 2020; Krüger and van den Bogaard, 2021; Krüger
et al., 2020). In addition, H. Usinger has left a large archive of palaeoenvironmental information from his
coring campaigns in different locations throughout Schleswig-Holstein. This material is currently under
revision.
In summary, most excavated sites with Late Pleistocene archaeology are clustered in seven find areas: the
Ahrensburg tunnel valley, Rissen, Klein Nordende, Nahe, Alt Duvenstedt, Schalkholz, and Ahrenshöft. Therefore, most research was focused on these areas, making predictive modelling across most of Schleswig-Holstein rather difficult (Hamer et al., 2019). Furthermore, in total very few pieces of faunal material were
found after the Ahrensburg tunnel valley excavations of the 1930s to 1950s, no further wooden artefacts
could be detected. In addition, some mostly single faunal remains were collected during different dredging
works. Hence, the material from A. Rust’s excavations remained the most relevant assemblages and have
been re-analysed on different occasions (Grønnow, 1985; Bratlund, 1990, 1996; Weinstock, 2000a, 2000b;
Pasda, 2009; Wild, 2020). In contrast to the Central Rhineland, a documentation record that allows each
artefact to be located precisely within the site is mostly missing; this is partially due to the excavation standards at the time and partially due to difficult excavation circumstances underneath the groundwater table
(cf. Slotseng; Wild, 2020). The exclusive preservation of organic material in discard zones or as single finds
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from waterlogged contexts makes the approach to understanding the occupation history and settlement
behaviour through zooarchaeological analyses for the Final Palaeolithic of Schleswig-Holstein impossible.
Nevertheless, especially in combination with palynological data, this material allows for further chronological considerations. In a few publications, radiocarbon dates from northern German sites were compiled
and re-evaluated, in collaborations including researchers from both MONREPOS and Schleswig (Grimm and
Weber, 2008; Riede et al., 2010; Weber et al., 2011). Based on these and on additional studies and analyses
of the last decade, we will establish a more detailed chronology of the Final Palaeolithic of this region and
discuss human-environment interactions during the Weichselian Late Glacial.
ARCHIVES
As the research history in Schleswig-Holstein encompasses more than 150 years, a wealth of material and
data is known. It can roughly be divided into two categories: on the one hand the actual material that
was collected from surface surveys or during excavations and coring programs, and on the other hand the
documentation and reports of such activities or materials. Archaeological sites in Schleswig-Holstein including those of single finds are reported in the register of prehistoric and historic artefacts and archaeological sites and monuments of Schleswig-Holstein (Landesaufnahme, see footnote 1). This collection of sites,
their location, reports about their discovery, and description of the identified features and archaeological
material is maintained at the Archaeological State Office Schleswig-Holstein (Archäologisches Landesamt
Schleswig-Holstein: ALSH). The actual archaeological material as well as the documentation that does not
remain with the collector is archived at the State Museum for Archaeology in Schloss Gottorf (Museum für
Archäologie: MfA). These archives allow queries on authenticity, spatial and chronological attribution, and
different new approaches, but they also require different lines of source criticism. Many of the archaeological excavations and collections and / or their documentation do not conform to modern standards. Before
the reliability of the data can be assessed, meticulous comparisons with the old documentation and the
results of modern analytical methods and techniques are necessary so that further information from the
material can be extracted (e. g., Groß et al., 2021; Hinrichs, 2020).
For the identification of potential taphonomic processes and possible palimpsests, more precise documentation of the context and location of artefacts is necessary. However, this is rarely available for older excavations. For instance, A. Rust recorded the spatial position of artefacts in two dimensions only during his later
excavations, and only on a square metre basis (Rust, 1958). Although there are some uncertainties with the
available coarse-grained 2D spatial information, it does allow some testing of the integrity of assemblages
and implications for understanding settlement behaviour (Hinrichs, 2020). A general outline of the stratigraphy is also usually given and frequently accompanied by a palynological analysis allowing insights into the
chronostratigraphic development of the site. 3D documentation of artefact positions and of higher resolution stratigraphic data became standard much later in Schleswig-Holstein, but proved that many of the sites
studied with these refined methods were affected by complex geomorphological processes (Bokelmann
et al., 1983; Kaiser and Clausen, 2005; Wild, 2017).
Usinger’s palaeoenvironmental archive – comprising the documentation of analysed stratigraphic sequences – includes information on their location, counting sheets of the samples taken from these sequences, as well as occasional personal comments. In general, remains of the sediment cores or samples are
preferably stored in cooling chambers, while prepared samples (such as the material from palaeolake Nahe)
are stored in the archives of the respective laboratories.
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RECENT CONTRIBUTIONS TO LATE GLACIAL CHRONOLOGY
AND ARCHAEOLOGY
The general stratigraphic succession of the Palaeolithic archaeological units in Schleswig-Holstein has been
known for over 70 years (see above research history); also, the vegetation history of the region has been well
established for several decades (Usinger, 1985). Yet the biostratigraphic terminology occasionally causes
some confusion and discussion. For the Rhineland, this was settled by the definitions based on the nearby
maar sequences from the Eifel (Litt and Stebich, 1999), whereas in northern Germany and especially in
Denmark the use of the term Bølling remained controversial, depending on which part of Iversen’s classical
palynological definition (Iversen, 1942) was used: “the first spread of tree birch” in the sense of a “biozone”
(Usinger, 1978, 1985) or “the temperate climatic oscillation that preceded the Allerød” in the sense of a
“chronozone” (Krüger and Damrath, 2020). Hence, in the following the INTIMATE event stratigraphy with
its recognition of Greenland Stadials (GS) and Interstadials (GI) will be used in a chronozone and event
stratigraphy approach (Tab. 1; Rasmussen et al., 2014). In a recently published article about a sequence
from the Lake Bølling type locality (Krüger and Damrath, 2020), one of the authors highlighted the problem
of the double characterisation of Bølling that was previously addressed (Usinger, 1997; De Klerk, 2004).
Nevertheless, with the new stratigraphy from the palaeolake Nahe, some new considerations about the
development of the biozones in Lower Saxony, Schleswig-Holstein, and southern Denmark became possible
(Krüger et al., 2020). Inter-regional comparison of three high-resolution palaeoenvironmental archives from
these regions showed different onsets, durations, and appearances of woodland phases shifting from south
to north (Krüger et al., 2020: fig. 7). This puts Schleswig-Holstein in a transitional zone for most of the Late
Glacial, making precise palaeoenvironmental studies accompanying archaeological research important tools
for locating the sites not only chronologically but also ecologically. Furthermore, it indicates that chronoand biozones must be clearly differentiated when discussing this area.
The record of palaeolake Nahe comprises a robust age-depth model based on radiocarbon dates, three crypto-tephra layers including the first geochemical finger-print of the LST from the region (Krüger and van den
Bogaard, 2021), and a laminated section covering the period of GI-1c3 to GI-1a (Dreibrodt et al., 2021). The
palaeoenvironmental data from the palaeolake Nahe reflects the developments in southern Schleswig-Holstein with relevant find areas such as the Ahrensburg tunnel valley, Klein Nordende, the immediate surroundings of the palaeolake itself, and the Hamburg area of Rissen. Based on lithological, geochemical, and
palynological data, the Dryas 3 biozone has been bisected in this stratigraphy into an upper, more humid,
and a lower, drier part at around the fallout deposition of the Islandic Vedde Ash (Krüger et al., 2020), a
distinction that was already observed in other archives (Overbeck, 1975; Bakke et al., 2009; cf. Weber et al.,
2011). Although the generally accepted development of the vegetation in Schleswig-Holstein is confirmed
by the palaeolake Nahe sequence, the development within the biostratigraphically defined Allerød period
can be further refined here. Furthermore, the Meiendorf period proves to be more complex than generally
considered. When comparing the onset of these biozones to the onsets in the western German Meerfelder
Maar (Litt and Stebich, 1999) with the chronozones based on the current INTIMATE event stratigraphy
(Rasmussen et al., 2014), we find offsets that can only partially be explained with the successive ecological
reaction to general climatic changes, reflecting the complexity of regional environmental transformations
(Krüger et al., 2020). Yet, the palaeolake Nahe sequence also demonstrates that charcoal particles and
non-pollen palynomorphs (NPPs) can help answering archaeological questions (Krüger, 2020).
The palaeoenvironmental studies were embedded in the previously mentioned large scale cooperation project (CRC 1266), in which also some archaeological and genetic studies were accomplished (Burau, 2019;
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The Beef behind all Possible Pasts – The Tandem-Festschrift in Honour of Elaine Turner and Martin Street
INTIMATE event
stratigraphy
Palaeolake Nahe
Palynological characteristics of NAH PAZ
lower boundaries
Age estimate
NAH biofor boundaries stratigraphic
[yrs cal BP]
terminology
Betula pub.-type ↑, Filipendula, Typha lat.-type ↗
Poaceae, Artemisia, Empetrum, other NAP-types ↘
Preboreal
Dryas 3
Poaceae, Artemisia, other NAP-types ↗
Allerød 3
Allerød 2 /
Dryas 2
Allerød 1
Dryas 1
GI-1c1-1a
GI-1c2
GI-1c3
GI-1d
Meiendorf
GI-1e
Pleniglacial
GS-2.1
Betula, Pinus ↓, Salix ↑
NAP-types ↑
12,680
Pinus, Filipendula ↑
NAP-types, Artemisia ↓
Allerød
13,350
Betula ↓
Artemisia ↑
Older Dryas
13,650 **
Betula ↑
NAP-types, Artemisia ↓
Bølling
13,780 **
Betula, Salix ↓
NAP-types ↑
Oldest Dryas
13,910 **
Meiendorf
14,642
14,510
Palynological characteristics of
MFM PAZ lower boundaries
Betula, Pinus ↑,
Juniperus ↓, NAP-types ↓
Younger Dryas
14,025
13,940
Pinus ↘, Betula pub.-type, B. nana-type ↗
Artemisia, Hippophaë ↗
GS-1
Age estimate
for boundaries
[varve yrs BP]
11,590
13,904
13,830
Hippophaë, AP ↘
Poaceae, Helianthemum, Rumex acet.-type ↗
Preboreal
13,610
13,710
Betula pub.-type ↑, Hippophaë ↗
Poaceae, Helianthemum ↘
Holocene
13,550
13,610
Betula pub.-type ↘, Juniperus ↗
Poaceae ↗
MFM biostratigraphic
terminology
12,846
12,540
Betula pub.-type ↗, Juniperus ↘
Poaceae, other NAP-types ↘
Mean Age
for boundary
[yrs cal BP]
11,653
11,560 *
Betula pub.-type ↘, B. nana-type ↗
Meerfelder Maar
end of lamination: Pinus ↓, Betula, Salix,
14,560 **
Juniperus ↑
unknown
Pleniglacial
439
Tab. 1 Comparison of terminology and age estimate of the Meerfelder Maar (MFM; Litt and Stebich, 1999: Tab. 2), the Palaeolake Nahe (NAH; Dreibrodt et al., 2021: Tab. 2 modified according to
Krüger et al., 2020 for boundaries and terminology), and the INTIMATE event stratigraphy (Rasmussen et al., 2014). PAZ Pollen assemblage zones.
* age estimate (varve yrs cal BP; cf. Merkt and Müller, 1999) used to create present age- depth modelling.
** original age estimates of Litt and Stebich (1999) have been shifted by 110 years to the older, considering a hiatus according to Brauer et al. (2001).
Hamer et al., 2019; Grimm et al., 2020; Hinrichs, 2020). Additionally, a number of dissertations and smaller
cooperation projects increased our knowledge of the Late Glacial in the last decade (Rivals et al., 2020;
Wild, 2020; Wild et al., in press). Results from all these projects are combined in the following overview.
Classic Hamburgian / Havelte Group
The available radiocarbon dates have been discussed in a previous review of the Hamburgian (Grimm and
Weber, 2008). Since then 20 new radiometric results have been obtained in the course of various projects
(Tab. 2). Five additional dates on worked reindeer antler (T2: 15-17, 19-20 2) confirmed the thus far accepted dating range for the Meiendorf site (Ahrensburg LA 79) in an early phase of GI-1e, which cannot be
defined chronologically more precisely due to a radiocarbon plateau during this interval (Wild, 2020). Two
new results (KIA-53517; KIA-53518; T2: 12-13) obtained on petrous bones in the framework of a genetic
study of reindeer confirm this picture and even extend the dating range into GS-2.1, whereas a third one
(KIA-53519; T2: 21) prolongs the range to mid-GI-1e (cf. Tab. 1), which corresponds to the occupation
of the neighbouring Poggenwisch site (Ahrensburg LA 101 and 137; Wild, 2020). The genetic study considerably enlarged the radiocarbon record for Stellmoor by seven new dates (T2: 3-9), which, when calibrated, show a similar distribution to the dates from Meiendorf. Another five measurements were made on
reindeer bones attributed to the classic Hamburgian sites of Stellmoor (n = 3) and Meiendorf (n = 2), but
produced dates that fall into the Ahrensburgian (T2: 47, 50, 52, 69-70; cf. Rivals et al., 2020; see below
Ahrensburgian). Hence, in total we currently know of 61 dates that are associated with the Hamburgian in
Schleswig-Holstein, of which 32 appear to be reliable (cf. Pettitt et al., 2003).
In Denmark, two further dates were obtained on a modified reindeer antler and bone dredged from the
Køge Bugt, where another worked reindeer antler had already been found that was dated to the Hamburgian (Tab. 3; Fischer and Jensen, 2018; Wild, 2020). The new date on the antler from the Køge Bugt
(AAR-18732; T3: 13) is very similar to the previous one (AAR-1036; T3: 14), and the date on a reindeer bone
(AAR-18733; T3: 12) is only slightly older. Both dates support a presence of hunter-gatherers in eastern Denmark during the second half of GI-1e. Altogether 13 radiocarbon dates are published and judged as reliable
for the Hamburgian in Denmark mostly coming from Slotseng in eastern Jutland (n = 10; Grimm and Weber,
2008). In addition to the radiocarbon dates, the excavation of the new site Krogsbølle – containing material
attributable to the Havelte Group – substantiated the corpus of Havelte Group material in Denmark (Riede
et al., 2019). After correction of the marine reservoir effect, a gull (Larus sp.) from a palaeolake adjacent to
Krogsbølle dates to GI-1e, but cannot be linked to human activity (AAR-17464: 12,710 ± 55 14C-BP; Riede
et al., 2019).
In sum, the calibrated radiocarbon dates for the Hamburgian indicate that hunter-gatherers visited the area
of Schleswig-Holstein throughout GI-1e and GI-1d. According to isotope analyses on reindeer bone and
micro-wear analyses on reindeer molars from Meiendorf and Stellmoor, the GI-1e environment of these animals presented little soil maturation and provided limited lichen availability, but more than in other European
regions (Drucker et al., 2011; Rivals et al., 2020). The Havelte Group occupation at Ahrenshöft LA 58 D may
even be attributed to GI-1c3, which would correspond to the palynological characterisation of the occupation layer confirmed by analyses in 2008 and 2009 (Weber et al., 2010). Nevertheless, the calibrated date
(AAR-2784; T2: 32) also spans into GI-1d and the site underwent considerable post-depositional processes.
2
References to specific radiocarbon dates listed in Table 2 and in Table 3 are referred to in the following format: T2 / 3: #ID#, where it
is specified whether Table 2 or Table 3 are meant, followed by the reference to the ID(s) within that table.
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S.B. Grimm et al. · Late Glacial Occupation of Northern Germany and Adjacent Areas
At a chronological micro-scale, the combination of zooarchaeological and technological observations on different Hamburgian sites and on the French Magdalenian site of Verberie led to a model of hunter-gatherer
economy and settlement throughout different phases of the autumn season (Wild, 2020).
Federmessergruppen (FMG)
The number of radiocarbon dates associated with the FMG in Schleswig-Holstein is limited (n = 12). Some
dates have previously been revised, highlighting the frequently problematic association of the dated material and the archaeological remains (Riede et al., 2010). In total, only eight dates can be associated with
human occupation during the time of the FMG (Tab. 2). The uncertain association with the FMG is partially
due to the generally limited and / or poor preservation of organic material from this period and the subsequent lack of identified human modification of the material, and partially due to the lack of knowledge
about what happened to the Hamburgian groups as well as about how the Brommean and Ahrensburgian
developed. Only charcoal from Alt Duvenstedt LA 120 b (AAR-2244; T2: 38) was found in association with
lithic material (Kaiser and Clausen, 2005); a bone sample from the same site lacked collagen and resulted in
a much too young age (AAR-2243-3: 4,420 ± 70 14C-BP; Kaiser and Clausen, 2005), and was consequently
excluded from our compilation.
The faunal material from Borneck was mostly recovered in wetland excavations adjacent to the site where
Hamburgian, FMG, and Ahrensburgian material had been excavated (Rust, 1958). Although the dated
specimens from box trench (“Kammer”) III display no cut-marks, their position near the accumulation of
archaeological remains at Borneck suggests a connection to human activities, yet a natural origin (background fauna) cannot be excluded. The dates (Riede et al., 2010) rule out an attribution to the Ahrensburgian but an association of a reindeer humerus (KIA-33949; T2: 36) with a very late Hamburgian is still
possible though not likely (see above Classic Hamburgian / Havelte Group). Rudolf Schütrumpf conducted
a palynological analysis of the stratigraphy in this trench and attributed the lower horizon from which the
faunal material originated to the Older Dryas period (Rust, 1958: 88; Allerød 2 / Dryas 2 according to: Krüger
et al., 2020; Tab. 1). This attribution fits well with the calibrated results but makes an attribution to the late
Hamburgian very unlikely (see above).
For Klein Nordende LA 37, the fish remains seem to form part of a natural thanatocoenosis (Benecke and
Heinrich, 2003), and the previously dated twigs (T2: 33-34) also reflect a natural event that was stratigraphically correlated with the lower archaeological deposits of the area CR (Bokelmann et al., 1983). However,
the stratigraphy in the area of Klein Nordende is highly complex not only due to halokinetic processes but
also due to soil creep and displacing of layers due to changing water levels, sediment admixture at the
banks, freezing and thawing processes. Hence, the relation of the dated samples to the archaeological material remains uncertain but likely determines a terminus post quem for the human presence at the locality
(cf. Riede et al., 2010). Hence, only the cut-marked elk bone from the Allerød gyttja in the area D unambiguously dates human activity at Klein Nordende (KIA-33951; T2: 35), but in this area no lithic archaeology
was found, potentially allowing its attribution to the FMG or to the early Ahrensburgian. A conventional
radiocarbon date (Y-442: 11,220 ± 350 14C-BP; Barendsen et al., 1957) from the site of “Lieth” (i. e., Klein
Nordende LA 33) was obtained from a peat sample but was excluded from the study for technical reasons,
although the top of the dated peat-lens within dune deposits produced a curve-backed point indicative of
a FMG context. Certainly, the area of the Lieth Moor around Klein Nordende was visited repeatedly during
the Late Glacial by different groups, but in order to reconstruct the settlement history more radiocarbon
dates would be required.
The Beef behind all Possible Pasts – The Tandem-Festschrift in Honour of Elaine Turner and Martin Street
441
Outside of Schleswig-Holstein, five dates were measured in the late 1950s on samples from the Rissen area
in Hamburg that is known for its FMG material. Unfortunately, the association of the sample material with
the archaeology remained uncertain and the results are technically questionable. Moreover, two samples
were dated from Grabow 15 (T3: 15-16), which is located near to the well-known site of Weitsche (Veil and
Breest, 2002; Veil et al., 2012), and yielded some evidence of amber working and amber artefacts besides a
rich FMG assemblage (Tolksdorf et al., 2013). The Grabow samples originated from archaeological features
associated with FMG artefacts similar to the lithic material found in Weitsche (Tolksdorf et al., 2013). The
sedimentation as well as the palynological analysis suggests that the site dates to the transition from the
Dryas 1 to the Allerød period. This attribution matches with the calibrated ages. The dates are slightly older
than the dates correlated with the lower horizon of Klein Nordende CR and, hence, represent the earliest
FMG in northern Germany. Two dates on bulked samples of cremated bones from Weitsche are slightly
younger. The younger date (T3: 18) had a sufficient amount of carbon preserved (5.2 mg), whereas the
older date (T3: 17) yielded small amounts only (0.5 mg). But the very similar results indicate no significant
source of contamination affected the samples. Both dates further support the presence of FMG in northern
Germany during this period.
In total, the FMG radiocarbon record reflects discontinuous settlement in northern Germany and Schleswig-Holstein. However, the appearance of this discontinuous record may result from the poor preservation
of datable material from this period. This contrasts with the amount and the distribution of sites associated
with FMG material; both suggest a wide extent over a period of noticeable duration. Additionally, the major
results of a modelling approach indicate that the FMG were rather well established in their local environments (Hamer et al., 2019), from which we can cautiously conclude that they knew their environments well,
supporting a more continuous presence in the landscape. In contrast, the number of Danish FMG (lithic)
assemblages is small. Association of lithic assemblages with radiocarbon dates is not given in a single case
(Pedersen, 2009; Petersen, 2009). Hence, this could well reflect the only occasional presence of FMG groups
in this area (Eriksen, 2000, 2002).
Furthermore – due to their radiocarbon dates pointing into the Late Glacial Interstadial – two artefacts made
of reindeer antler have to be mentioned in the context of the FMG occupation of the region: the double
bevelled point from Lasbek LA 14 (T2: 73; Wild and Weber, 2017; ZooMS-determination by Th.T.Z. Jensen)
and the so-called antler axe (Lyngby type artefact) from Klappholz LA 63 (T2: 72; Clausen, 2004). However,
the technological habitus in which these specimens were made resembles other Final Palaeolithic technocomplexes, namely the Hamburgian in the case of the Lasbek piece (Wild and Weber, 2017), and the Brommean or Ahrensburgian for the Klappholz specimen (Clausen, 2004).
This discrepancy may suggest (i) problems with the radiometric results, (ii) that our current knowledge about
the presence of the various archaeological entities is incomplete, or (iii) that the osseous industry may have
developed asynchronously to the lithic industries. The first aspect does not appear very likely in view of increasingly rigorous protocols at the radiocarbon laboratories. That our knowledge is incomplete should become apparent in this contribution and also the desideratum for osseous studies from Late Glacial northern
Germany and southern Scandinavia. In fact, several other osseous artefacts were dated to this overlapping
period of the FMG, the Brommean, and, possibly, the early Ahrensburgian.
For Denmark, some further dates in this age range need to be discussed in this context (Tab. 3), although the
sampled material is usually associated with the Brommean. In particular, results from Nørre Lyngby were frequently mentioned in this context, since one of the first Bromme points was found and described from this
site; also the eponymous Lyngby antler artefact has been defined at this locality (Eriksen, 1999; Fischer et al.,
2013a; cf. Petersen, 2021). However, these finds were not made together and, although the new palaeontological investigation focused on the same freshwater deposits, there is no established connection with the
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S.B. Grimm et al. · Late Glacial Occupation of Northern Germany and Adjacent Areas
previous artefact finds. From the new investigations, only one specimen showed traces of possible human
modification and was dated to the GI-1c1 (AAR-1511; T3: 28; Aaris-Sørensen, 1995). The original Lyngby
antler artefact dates to the early Holocene (AAR-8919: 9,110 ± 65 14C-BP), which is comparable to the antler
artefact from the Swedish Bara Mosse (OxA-2793: 9,090 ± 90 14C-BP; Larsson, 1996; Fischer et al., 2013a);
yet, both were subject to contamination with conservation material and considered as potentially too young.
The date from Arreskov (OxA-3173; T3: 32) was made on a single find of a reindeer antler artefact (Fischer,
1996). It dates slightly later than the Brommean dates from Denmark (see below). The slightly older Lyngby
antler artefact from Odense Kanal (AAR-9298; T3: 30; Stensager, 2006) dates close to the dates from Alt
Duvenstedt LA 121 (AAR-2245-1; AAR-2245-2; T2: 40-41) and 123 (AAR-2246; T2: 39) and, hence, could
be viewed in an early Ahrensburgian context. The bone point from Fogense Enge (AAR-15025; T3: 31)
dates between these two implements (Petersen, 2021), and can also be discussed within FMG, early Ahrensburgian as well as Brommean contexts (Jensen et al., in prep). An antler club from Mickelsmosse in southern
Sweden (OxA-2791; T3: 29) was dated to a similar period as the Odense Kanal specimen (Larsson, 1996),
but – due to its geographical position – should rather be discussed within the Brommean.
This short review reveals some important points: firstly, reindeer seems to have been used as a resource
throughout the Final Palaeolithic, thus revising a long obsolete picture of FMG as only elk hunters (Clausen,
2004; Riede et al., 2010, Wild and Weber, 2017; Weber and Wild, 2019). Further, newly dated reindeer
antler artefacts suggest that in Denmark reindeer antler may even have been used predominantly as osseous
raw material during the Allerød (Wild et al., in press). Secondly, the transitional character of the environment in Schleswig-Holstein and southern Scandinavia may have played a role in the potential co-occurrence
of groups adapted to different environments (cf. Eriksen, 2000, 2002; Mortensen et al., 2014; Burau, 2019;
Krüger et al., 2020).
Moreover, in northern Germany and southern Scandinavia, remains of giant deer (Megaloceros giganteus)
were found occasionally (Bratlund, 1993; Street, 1996; Aaris-Sørensen and Liljegren, 2004), and at least the
northern German specimens from Lüdersdorf (Bratlund, 1993) and Endingen, Horst VI showed traces of human modification (Street, 1996). Both were directly dated but the Lüdersdorf date (OxA-3615: 11,600 ± 105
14C-BP; Hedges et al., 1993) might be subject to technical problems (column resin bleed; Burky et al., 1998)
and – as the δ13C value was considerably low for Late Glacial giant deer – this date has been rejected. The
Endingen date (ETH-13585; T3: 27) fell well within GI-1c1; hence, giant deer was probably also a prey of the
Final Palaeolithic hunters as an increasing number of identified Late Glacial specimens suggest (Immel et al.,
2015; Baales et al., 2019). However, the cultural association remains also a matter of debate for these finds.
Furthermore, we do not yet know enough about the variability and development of the lithic technology of
the FMG in Schleswig-Holstein to be certain about the distinction to the material of the late Hamburgian,
the Brommean, and early Ahrensburgian. Currently this desideratum is approached by an on-going dissertation (Reuter, in prep.). Only a better understanding of this chronologically intermediate group will facilitate
more precise interpretations of the cultural developments during the Late Glacial in northern Germany and
southern Scandinavia.
Brommean
The Brommean forms the most uncertain archaeological unit in Schleswig-Holstein. Although large Brommean points are well known from this region, their relation to the FMG assemblages remains unclear. Inventories that were stratigraphically attributed to the Allerød period and thought to represent the Brommean
or FMG in Alt Duvenstedt (LA 85, 86, and 89; Clausen and Hartz, 1988; Kaiser and Clausen, 2005: fig. 2)
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443
became subject to discussion when very early Ahrensburgian material was found in Allerød sediments of
the same site (LA 121 and 123). Besides the lack of knowledge about the variability of the FMG (see above),
the small numbers of datable material from archaeological sites limits our understanding of the presence
and possible development of the Brommean in Schleswig-Holstein. Due to these uncertainties, there are no
14C-dates that are reliably connected with the Brommean in the region, and we cannot reach conclusions
regarding their presence and / or duration (see above FMG).
In contrast, Brommean presence and preferences are well established in Denmark (Eriksen, 1991, 1999, 2000;
Mortensen et al., 2014), but the development there also remains a matter of debate (Eriksen, 2002). Although
single finds of the prominent Bromme tanged point may result in a biased picture of the settlement activity, the
number of reliable settlement sites remains significant (cf. Eriksen, 1999; Fischer et al., 2013b). The small number of radiocarbon dates (n = 6) originates from only three, geographically close Brommean sites (Bromme,
Fensmark Skydebane, Trollesgave; cf. Fischer et al., 2013b). A further sample of a reindeer antler fragment
from Bromme lacked collagen and delivered no result (AAR-4538; Heinemeier and Rud, 2000).
In addition, reindeer antler material was found near Tyrsted in a kettle hole in a well-preserved Late Pleistocene / Early Holocene palaeoenvironmental sequence with lithic material that was partially washed in from a
small concentration on the north-western shore of the kettle hole (Borup and Nielsen, 2017; Eriksen et al.,
2018). The lithic material can be attributed to the Brommean. Some characteristics of the archaeological
material may already suggest a very late date and possibly displays even Ahrensburgian resemblance. Geophysical investigations have shown additional kettle holes in this area with high potential for Late Glacial
archaeology (Corradini et al., 2020). Palaeoenvironmental and archaeological analyses are still on-going.
The limited amount of datable faunal remains and the lack of information on osseous typo-technology restricts the insights in Denmark as in Schleswig-Holstein. A project on reindeer in Denmark during the ice age
aimed to revisit the faunal material and to record and study the potential human modifications. This project
increased the corpus of modified osseous material significantly (Wild et al., in press).
The reliable dates assigned to the Brommean span a relatively short period. Compared to the considerable
number of Brommean sites over most of Denmark (Eriksen, 1999), this would speak for intensive settlement
activities and / or a particularly well-preserved section of the Late Glacial. In light of the generally difficult
preservation conditions for this period, such an interpretation appears highly unlikely. Moreover, the samples of the few reliable dates come from one region only and possibly represent just one stage of a longer
development (Fischer et al., 2013b). However, the numerous Brommean sites indicate the first established
settlement of southern Scandinavia.
Ahrensburgian
In total we currently know of 44 dates that are associated with the Ahrensburgian in Schleswig-Holstein. Of
these we consider 32 dates to be reliable (Tab. 2).
In comparison to a previous evaluation (Weber et al., 2011), eleven more dates can be attributed to the
Ahrensburgian in Schleswig-Holstein. Three measurements were carried out on mammal bones from species other than reindeer recovered at Stellmoor: a date on bison (KIA-3331; T2: 62; Benecke, 2004) was
overlooked in the previous evaluation, a date on elk (KIA-51382; T2: 56; Wild and Weber, 2017) was obtained in order to check if the remains of this species are intrusive into the Ahrensburgian horizon or not
(cf. Bratlund, 1999), and a date on horse (KIA-48960; T2: 54; Drucker et al., 2016; Rivals et al., 2020) was
made in the context of a project on understanding Late Glacial reindeer migrations. The remaining new
dates on reindeer also originate from this project (T2: 46-49, 51-52, 61; Rivals et al., 2020) as well as from
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S.B. Grimm et al. · Late Glacial Occupation of Northern Germany and Adjacent Areas
ongoing genetic studies (T2: 50). Four Ahrensburgian dates (T2: 46-49) confirmed a date which was produced at Yale University during the early years of the development of the radiocarbon method (Y-159.2:
10,320 ± 250 14C-BP; Barendsen et al., 1957), which is not considered here due to its large standard deviation but which points to Ahrensburgian presence in Stellmoor at around the middle of GS-1.
Five further samples from Stellmoor (n = 3; KIA-48959; KIA-53523; KIA-47378; T2: 47, 50, 52) and Meiendorf (n = 2; KIA-46301; KIA- 47380; T2: 69-70) were attributed to the classic Hamburgian but resulted in
Ahrensburgian dates (cf. Rivals et al., 2020). In Stellmoor this can be explained by the mixture of material
during its recovery or during the following storage period. However, no younger horizon has been suggested
for Meiendorf thus far, although a barbed point from the pond has been discussed as an Ahrensburgian
specimen (Tromnau, 1992). This attribution is further strengthened by different studies indicating that various bone point types that were previously attributed only to the Mesolithic seem to have a longer tradition
and to originate in the Final Palaeolithic (Cziesla and Pettitt, 2003; Groß et al., 2020). Wild (2020) showed
that collagen was preserved in the aforementioned barbed point from the site of Meiendorf, but in contrast
to other faunal remains from the site the collagen yield was so low that currently a too large sample would
be necessary to date the specimen directly. Another sample from Meiendorf was previously considered as a
falsely labelled specimen from the Stellmoor site when it was dated to the Ahrensburgian (K-4330; T2: 71;
Fischer and Tauber, 1986; Weber et al., 2011). Yet, this date and the two additional Ahrensburgian dates
from Meiendorf as well as the barbed point could alternatively indicate that the Meiendorf pond preserved
a second, younger archaeological horizon which remained undetected during the early excavations.
In the context of Ahrensburgian chronology, a series of seven radiocarbon measurements intended to determine the age of two potential arrow shaft fragments found in A. Rust’s legacy need to be mentioned
(Meadows et al., 2018). As their provenance remains unknown and both items have been contaminated
with consolidants, the dates cannot serve as evidence for the Ahrensburgian settlement. The oldest and reliable results of the seven dates (KIA-49753: 10,050 ± 90 14C-BP; KIA-49754: 9,915 ± 45 14C-BP; Meadows
et al., 2018) fall into the range of the accepted Ahrensburg dates obtained from faunal remains.
At Nahe LA 11, four radiocarbon dates indicate the presence of Ahrensburgian hunters at both the beginning and the end of GS-1 (Weber et al., 2011). Continued human presence into the Preboreal period is indicated from sediment cores retrieved in the vicinity of the archaeological site within the palaeolake (Krüger,
2020; Krüger et al., 2020). This indication consists of charcoal particles most likely to originate from anthropogenic fires at the shores of the lake. The situation at Nahe thereby corresponds to that at Poggenwisch
where reindeer remains were found in peat attributed to the Preboreal period (Herre and Requate, 1958),
and to that at Stellmoor where the uppermost Ahrensburgian horizon can be associated with the early
Preboreal period on the basis of the partly revised biostratigraphy (Krüger, 2020). In addition, the Stellmoor
radiocarbon dates confirm a continuation of the Ahrensburgian into the early Holocene, and a comparison
of Ahrensburgian and Mesolithic radiocarbon dates shows that in northern Germany the transition between
the two archaeological entities only occurred at the end of the GH-11.4 ka event (Grimm et al., 2020). Considering all reliable radiocarbon dates for Schleswig-Holstein, the presence of Ahrensburgian groups from
possibly as early as GI-1b throughout GS-1 into GH-11.4 can be suggested.
The most restrained explanation for the continuation of the Ahrensburgian into the early Preboreal would
lie in the development of favourable feeding conditions for reindeer during this period. For GS-1, the results
of isotope and micro- / meso-wear analyses of reindeer remains suggest that a tundra landscape with a considerable amount of lichen was present in southern Schleswig-Holstein (Drucker et al., 2011; Rivals et al.,
2020). At the onset of the Preboreal period, an increasing availability of young birch shoots can be observed
in the Nahe record, where they coincide with maximum values of coprophilous fungal spores (originating
from fungi that germinated on reindeer feces). This coincides with the highest frequency of larger charcoal
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445
particles indicative of local anthropogenic fires (Krüger, 2020), leading to the hypothesis that longer seasonal stays of reindeer herds led to the intensification of human presence at the site.
Groups classified as Mesolithic due to techno-typological criteria seem to have established earlier in Denmark than in Schleswig-Holstein (Jessen et al., 2015; Jensen et al., 2020). However, the Ahrensburgian
technological tradition has continued in the osseous material adapted to different faunal species (Wild
et al., in press).
At an annual scale, seasonal migrations in east-west direction of the reindeer hunted at Stellmoor and
Meiendorf are suggested on the basis of further isotope analyses carried out within the abovementioned
reindeer project (Price et al., 2017). An even smaller temporal scale was aimed at by attempts to refit the
lithic material from two neighbouring Ahrensburgian units at Borneck. The analysis showed, however, that
a contemporaneous occupation of both units under study can be excluded (Hinrichs, 2020).
CONCLUSION
If we focus on the chronological indications of the material and their relation to human activity, we can identify the presence of humans throughout most of the Late Glacial in Schleswig-Holstein and their frequent
presence in Denmark. However, if we try to link the dating evidence to specific technocomplexes defined
on the basis of lithic material (Hamburgian, FMG, Brommean, Ahrensburgian), we clearly see the limits of
our legacy data and single finds. For several sites in Schleswig-Holstein we must admit that much desirable
information is forever lost with respect to old excavations or collections. Nonetheless, material studies of this
old material are still possible and new analyses show the potential of these old finds to speak for themselves
beyond chronological considerations. Furthermore, the surveys showed that at a site such as Stellmoor more
material is still preserved in the ground. Although hydrological changes and interventions occasionally lead
to the destruction of archaeological organic remains which had preserved until now (e. g., Star Carr, Satrup),
demanding archaeological rescue, so long as natural protection remains high and the hydrology of this area
is monitored, the archaeological remains seem well protected and waiting for future investigations requiring
only minimal invasive and destructive measures.
The lack of additional data makes it difficult to correlate archaeological and palaeoenvironmental data.
The need of this correlation becomes particularly relevant in transitional areas of different ecological zones
such as in Schleswig-Holstein during the Late Glacial. A potential step forward for bringing together the
palaeoenvironmental and archaeological data lies in the examination of additional charcoal particles, as the
palaeolake Nahe data showed (Krüger, 2020). The observation of shifting ecological zones implies that in
different parts of Schleswig-Holstein different habitats existed contemporaneously during the Late Glacial,
which might explain observed temporal overlaps of different technocomplexes, such as the Hamburgian in
northern Schleswig-Holstein and the FMG in southern Schleswig-Holstein (Burau, 2019). Comparably, in
later phases the geological and pedological differences could explain different developments of the landscapes and subsequent cultural phenomena in a roughly east-west direction (Mortensen et al., 2014). The
picture is further complicated by species that are not restricted to one of these ecological zones. Hence, a
simple eco-deterministic correlation is not possible in these areas.
Finally, another consequence of these shifting ecological zones is the irregular offset of chronozones (as in
the INTIMATE event stratigraphy) and biozones documented for Schleswig-Holstein and most of northern
Europe during the Late Glacial. This calls for rigorous considerations of the chronology of archaeological
sites to allow comparison on a supra-regional European scale.
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S.B. Grimm et al. · Late Glacial Occupation of Northern Germany and Adjacent Areas
ID site
species
method lab. no.
The Beef behind all Possible Pasts – The Tandem-Festschrift in Honour of Elaine Turner and Martin Street
Age 14C
±
[BP]
[BP]
district
material
1 Stellmoor (Ahrensburg LA 78.1)
Stormarn
bone, bulked material x
conv.
KN-2223
12,590
2 Stellmoor (Ahrensburg LA 78.1)
Stormarn
bone / antler,
bulked material
conv.
KN-2224
12,530
Age
[cal BP **]
δ13C
[‰]
80 15,200-14,560
15,258-14,453
-
classic Hamburgian Grimm and Weber, 2008
160 15,340-14,060
15,291-14,126
-
classic Hamburgian Grimm and Weber, 2008
Age
[cal BP *]
comment
references
Hamburgian
Cervidae
3 Stellmoor (Ahrensburg LA 78.1)
Stormarn
bone
R. tarandus
AMS
KIA-53524
12,510
55 15,060-14,420
15,072-14,352
-20.0 classic Hamburgian this contribution
4 Stellmoor (Ahrensburg LA 78.1)
Stormarn
bone
R. tarandus
AMS
KIA-53520
12,485
55 15,000-14,360
15,011-14,317
-19.2 classic Hamburgian this contribution
5 Stellmoor (Ahrensburg LA 78.1)
Stormarn
bone
R. tarandus
AMS
KIA-53522
12,485
55 15,000-14,360
15,011-14,317
-20.1 classic Hamburgian this contribution
6 Stellmoor (Ahrensburg LA 78.1)
Stormarn
bone
R. tarandus
AMS
KIA-53525
12,460
55 14,970-14,290
14,973-14,308
-17.8 classic Hamburgian this contribution
7 Stellmoor (Ahrensburg LA 78.1)
Stormarn
bone
R. tarandus
AMS
KIA-53527
12,450
55 14,950-14,270
14,962-14,297
-20.0 classic Hamburgian this contribution
8 Stellmoor (Ahrensburg LA 78.1)
Stormarn
bone
R. tarandus
AMS
KIA-53521
12,305
50 14,600-14,000
14,812-14,081
-19.8 classic Hamburgian this contribution
9 Stellmoor (Ahrensburg LA 78.1)
Stormarn
bone
R. tarandus
AMS
KIA-53526
12,210
55 14,350-13,910
14,772-13,887
-19.4 classic Hamburgian this contribution
10 Stellmoor (Ahrensburg LA 78.1)
Stormarn
antler
R. tarandus
AMS
K-4261
12,190
125 14,650-13,730
14,835-13,792
-18.6 classic Hamburgian Fischer and Tauber, 1986
11 Stellmoor (Ahrensburg LA 78.1)
Stormarn
bone
R. tarandus
AMS
K-4328
12,180
130 14,630-13,710
14,838-13,787
-18.0 classic Hamburgian Fischer and Tauber, 1986
12 Meiendorf (Ahrensburg LA 79)
Stormarn
bone
R. tarandus
AMS
KIA-53517
12,525
55 15,080-14,480
15,112-14,371
-20.6 classic Hamburgian this contribution
13 Meiendorf (Ahrensburg LA 79)
Stormarn
bone
R. tarandus
AMS
KIA-53518
12,520
55 15,060-14,460
15,101-14,361
-19.5 classic Hamburgian this contribution
14 Meiendorf (Ahrensburg LA 79)
Stormarn
bone
conv.
KN-2220
12,470
250 15,480-13,760
15,521-13,817
15 Meiendorf (Ahrensburg LA 79)
Stormarn
antler, humanly
modified
R. tarandus
AMS
KIA-52178
12,455
55 14,960-14,280
14,967-14,304
-18.3 classic Hamburgian Wild, 2020
16 Meiendorf (Ahrensburg LA 79)
Stormarn
antler, humanly
modified
R. tarandus
AMS
KIA-52180
12,425
55 14,920-14,200
14,938-14,260
-18.7 classic Hamburgian Wild, 2020
17 Meiendorf (Ahrensburg LA 79)
Stormarn
antler, humanly
modified
R. tarandus
AMS
KIA-52176
12,405
55 14,880-14,160
14,896-14,208
-19.2 classic Hamburgian Wild, 2020
18 Meiendorf (Ahrensburg LA 79)
Stormarn
antler
R. tarandus
AMS
K-4329
12,360
110 14,940-13,940
14,948-14,077
-18.3 classic Hamburgian Fischer and Tauber, 1986
19 Meiendorf (Ahrensburg LA 79)
Stormarn
antler, humanly
modified
R. tarandus
AMS
KIA-52177
12,355
55 14,770-14,050
14,841-14,115
-19.2 classic Hamburgian Wild, 2020
20 Meiendorf (Ahrensburg LA 79)
Stormarn
antler, humanly
modified
R. tarandus
AMS
KIA-52179
12,355
55 14,770-14,050
14,841-14,115
-19.1 classic Hamburgian Wild, 2020
21 Meiendorf (Ahrensburg LA 79)
-
classic Hamburgian Grimm and Weber, 2008
Stormarn
bone
R. tarandus
AMS
KIA-53519
12,270
50 14,520-13,960
14,805-14,056
-20.2 classic Hamburgian this contribution
22 Poggenwisch (Ahrensburg LA 101) Stormarn
bone
R. tarandus
AMS
K-4332
12,570
115 15,280-14,320
15,268-14,299
-18.6 classic Hamburgian Fischer and Tauber, 1986
conv.
KN-2754
12,470
95 15,090-14,170
15,077-14,213
conv.
GrN-11254
12,460
60 14,990-14,270
14,982-14,297
23 Poggenwisch (Ahrensburg LA 101) Stormarn
bone
24 Poggenwisch (Ahrensburg LA 101) Stormarn
wood
25 Poggenwisch (Ahrensburg LA 101) Stormarn
bone
R. tarandus
AMS
K-4331
12,440
115 15,090-14,050
15,069-14,135
-18.8 classic Hamburgian Fischer and Tauber, 1986
26 Poggenwisch (Ahrensburg LA 101) Stormarn
bone, humanly
modified
R. tarandus
AMS
K-4577
12,440
115 15,090-14,050
15,069-14,135
-17.4 classic Hamburgian Fischer and Tauber, 1986
27 Poggenwisch (Ahrensburg LA 101) Stormarn
antler, humanly
modified
R. tarandus
AMS
KIA-32926
12,365
60 14,790-14,070
14,848-14,138
-20.4 classic Hamburgian Grimm and Weber, 2008
Betula sp.
-
classic Hamburgian Grimm and Weber, 2008
-28.6 classic Hamburgian Tromnau, 1992: 81,
Anmerk. 8
447
Tab. 2 Reliable radiocarbon dates of Final Palaeolithic material from Schleswig-Holstein. * 95 % confidence interval, using the CalPal-2019-Hulu calibration curve in CalPal program, Version 2020.2
(Weninger and Jöris, 2008) ** 95,4 % confidence interval, unmodelled, using IntCal 20 (Reimer et al., 2020) in the OxCal program, version 4.4 (Bronk Ramsey, 2009)
448
ID site
district
method lab. no.
Age 14C
±
[BP]
[BP]
Age
[cal BP *]
Age
[cal BP **]
δ13C
[‰]
S.B. Grimm et al. · Late Glacial Occupation of Northern Germany and Adjacent Areas
material
species
comment
28 Poggenwisch (Ahrensburg LA 101) Stormarn
antler with attached
cranial bone
R. tarandus
AMS
KIA-32927
12,330
55 14,700-14,020
14,829-14,091
-21.3 classic Hamburgian Grimm and Weber, 2008
29 Poggenwisch (Ahrensburg LA 101) Stormarn
antler, humanly
modified
R. tarandus
AMS
KIA-32925
12,265
55 14,490-13,970
14,804-14,051
-21.6 classic Hamburgian Grimm and Weber, 2008
30 Ahrenshöft LA 73 South, layer I
Nordfriesland
charcoal
Pinus sp.
AMS
KIA-3605
12,200
60 14,340-13,900
14,777-13,871
-
Havelte Group
31 Ahrenshöft LA 73 North, layer II
Nordfriesland
charcoal
Salix /
Populus
AMS
KIA-3833
12,130
60 14,170-13,850
14,153-13,807
-
classic Hamburgian Clausen, 1997
and Havelte Group
32 Ahrenshöft LA 58 D
Nordfriesland
charcoal
AMS
AAR-2784
12,030
60 14,050-13,730
14,050-13,794
33 Klein Nordende LA 37 C
Pinneberg
wood, twigs
Hippophaë
sp.
conv.
KI-2124
12,035
110 14,180-13,620
14,166-13,607
-
archaeological con- Bokelmann et al., 1983
nection uncertain
34 Klein Nordende LA 37, erosion
channel (south of A)
Pinneberg
wood, twigs
Hippophaë
sp.
conv.
KI-2152
11,990
100 14,070-13,590
14,075-13,607
-
archaeological con- Bokelmann et al., 1983
nection uncertain
35 Klein Nordende LA 37 D
Pinneberg
bone, femur
proximal sin.
A. alces
AMS
KIA-33951
11,035
50 13,090-12,810
13,086-12,840
-20.5 with cut-marks
36 Borneck Kammer III
(Ahrensburg LA 76)
Stormarn
bone, humerus
distal sin.
R. tarandus
AMS
KIA-33949
11,940
50 13,950-13,630
14,025-13,609
-17.5 archaeological con- Riede et al., 2010
nection uncertain
37 Borneck Kammer III
(Ahrensburg LA 76)
Stormarn
bone, tibia distal
sin.
A. alces
AMS
KIA-33950
11,770
55 13,750-13,430
13,766-13,502
-19.5 archaeological con- Riede et al., 2010
nection uncertain
38 Alt Duvenstedt LA 120 b
Rendsburg- charcoal
Eckernförde
AMS
AAR-2244
11,780
110 13,880-13,360
14,003-13,430
-
Clausen, 2004
39 Alt Duvenstedt LA 123
Rendsburg- charcoal
Eckernförde
AMS
AAR-2246
11,060
110 13,150-12,750
13,161-12,761
-
Clausen, 2004
40 Alt Duvenstedt LA 121
Rendsburg- charcoal
Eckernförde
AMS
AAR-2245-1
10,810
80 12,900-12,660
12,920-12,627
-
Clausen, 1996b
41 Alt Duvenstedt LA 121
Rendsburg- charcoal
Eckernförde
AMS
AAR-2245-2 10,770
60 12,820-12,660
12,830-12,679
-
Clausen, 1996b
42 Nahe LA 11
Segeberg
bone, humic acid,
humerus
R. tarandus
AMS
KIA-23369
10,610
80 12,820-12,340
12,747-12,336
-
Weber et al., 2011
43 Nahe LA 11
Segeberg
antler with cranial
bone attached
R. tarandus
AMS
KIA-23372
10,544
49 12,740-12,340
12,699-12,473
-20.5
Weber et al., 2011
44 Nahe LA 11
Segeberg
bone, lumbar
vertebra
R. tarandus
AMS
KIA-23370
10,172
45 11,930-11,650
11,969-11,620
-19.3
Weber et al., 2011;
Wild, 2017
45 Nahe LA 11
Segeberg
bone, lumbar
vertebra
R. tarandus
AMS
KIA-23371
10,142
49 11,900-11,540
11,943-11,406
-16.7
Weber et al., 2011;
Wild, 2017
46 Stellmoor (Ahrensburg LA 78.1)
Stormarn
bone, mandibula
R. tarandus
AMS
KIA-46300
10,445
40 12,680-12,080
12,614-12,102
-16.3
Rivals et al., 2020
47 Stellmoor (Ahrensburg LA 78.1)
Stormarn
bone, tibia sin.
R. tarandus
AMS
KIA-48959
10,335
30 12,350-11,870
12,461-11,949
-18.6 attributed to classic Rivals et al., 2020
Hamburgian
48 Stellmoor (Ahrensburg LA 78.1)
Stormarn
bone, mandibula dext., R. tarandus
human modification
(part of the so-called
Kultpfahlschädel)
AMS
KIA-51367
10,294
54 12,340-11,740
12,461-11,830
-17.9
-25.7 Havelte Group
references
Clausen, 1997
Clausen, 1997
Federmessergruppen (FMG)
Riede et al., 2010
Ahrensburgian
Tab. 2 (continued)
Rivals et al., 2020
The Beef behind all Possible Pasts – The Tandem-Festschrift in Honour of Elaine Turner and Martin Street
Age
[cal BP **]
δ13C
[‰]
32 12,040-11,760
12,095-11,818
-18.5
40 11,980-11,700
12,001-11,741
-18.4 attributed to classic this contribution
Hamburgian
10,200
40 11,970-11,690
11,998-11,739
-17.0
10,195
40 11,960-11,680
11,996-11,655
-19.2 attributed to classic Rivals et al., 2020
Hamburgian
KN-2222
10,160
90 12,130-11,330
12,433-11,338
-
AMS
KIA-48960
10,155
35 11,880-11,640
11,940-11,626
-21.9
R. tarandus
AMS
K-4326
10,140
105 12,140-11,260
12,432-11,274
-
Fischer and Tauber, 1986
A. alces
AMS
KIA-51382
10,136
51 11,900-11,500
11,941-11,405
-20.1
Wild and Weber, 2017:
Anm. 1
antler
R. tarandus
AMS
K-4327
10,130
105 12,110-11,230
12,429-11,269
-17.7 attributed to classic Fischer and Tauber, 1986
Hamburgian
Stormarn
antler
R. tarandus
AMS
K-4262
10,110
105 12,040-11,240
12,098-11,261
-
Fischer and Tauber, 1986
Stormarn
bone
R. tarandus
AMS
K-4578
10,100
100 12,000-11,240
12,001-11,266
-
Fischer and Tauber, 1986
60 Stellmoor (Ahrensburg LA 78.1)
Stormarn
bone / antler, bulked
material
Cervidae
(R. tarandus?)
conv.
KN-2221
10,080
80 11,900-11,260
11,934-11,317
-
Grimm and Weber, 2008
61 Stellmoor (Ahrensburg LA 78.1)
Stormarn
bone, mandibula
R. tarandus
AMS
KIA-47379
10,080 +45 / 11,850-11,330
-40
11,821-11,399
-17.0
method lab. no.
Age 14C
±
[BP]
[BP]
ID site
district
material
species
49 Stellmoor (Ahrensburg LA 78.1)
Stormarn
bone, tibia dext.
R. tarandus
AMS
KIA-48958
10,245
50 Stellmoor (Ahrensburg LA 78.1)
Stormarn
bone
R. tarandus
AMS
KIA-53523
10,205
51 Stellmoor (Ahrensburg LA 78.1)
Stormarn
bone, mandibula
R. tarandus
AMS
KIA-46299
52 Stellmoor (Ahrensburg LA 78.1)
Stormarn
bone, mandibula
R. tarandus
AMS
KIA-47378
53 Stellmoor (Ahrensburg LA 78.1)
Stormarn
bone,
bulked material
conv.
54 Stellmoor (Ahrensburg LA 78.1)
Stormarn
bone, costa sin.,
possible human
modification
Equus sp.
55 Stellmoor (Ahrensburg LA 78.1)
Stormarn
bone
56 Stellmoor (Ahrensburg LA 78.1)
Stormarn
bone, scapula
57 Stellmoor (Ahrensburg LA 78.1)
Stormarn
58 Stellmoor (Ahrensburg LA 78.1)
59 Stellmoor (Ahrensburg LA 78.1)
Age
[cal BP *]
comment
references
Rivals et al., 2020
Rivals et al., 2020
Grimm and Weber, 2008
Drucker et al., 2016;
Rivals et al., 2020
Rivals et al., 2020
449
62 Stellmoor (Ahrensburg LA 78.1)
Stormarn
bone
Bison sp.
AMS
KIA-3331
10,070
50 11,830-11,310
11,820-11,351
-
Benecke, 2004
63 Stellmoor (Ahrensburg LA 78.1)
Stormarn
bone
R. tarandus
AMS
K-4325
10,010
100 11,850-11,170
11,872-11,238
-
Fischer and Tauber, 1986
64 Stellmoor (Ahrensburg LA 78.1)
Stormarn
antler
R. tarandus
AMS
K-4581
9,990
105 11,830-11,150
11,829-11,218
-
Fischer and Tauber, 1986
65 Stellmoor (Ahrensburg LA 78.1)
Stormarn
antler
R. tarandus
AMS
K-4579
9,980
105 11,830-11,150
11,821-11,218
-
Fischer and Tauber, 1986
66 Stellmoor (Ahrensburg LA 78.1)
Stormarn
antler
R. tarandus
AMS
K-4323
9,930
100 11,760-11,120
11,805-11,196
-
Fischer and Tauber, 1986
67 Stellmoor (Ahrensburg LA 78.1)
Stormarn
antler
R. tarandus
AMS
K-4324
9,900
105 11,760-11,080
11,811-11,166
-
Fischer and Tauber, 1986
68 Stellmoor (Ahrensburg LA 78.1)
Stormarn
antler
R. tarandus
AMS
K-4580
9,810
100 11,520-10,960
11,687-10,794
-
Fischer and Tauber, 1986
69 Meiendorf (Ahrensburg LA 79)
Stormarn
bone, mandibula
R. tarandus
AMS
KIA-46301
10,350
45 12,420-11,860
12,471-11,951
-18.3 attributed to classic Rivals et al., 2020
Hamburgian
70 Meiendorf (Ahrensburg LA 79)
Stormarn
bone, mandibula
R. tarandus
AMS
KIA-47380
10,145
55 11,940-11,500
11,946-11,404
-19.0 attributed to classic Rivals et al., 2020
Hamburgian
71 Meiendorf (Ahrensburg LA 79)
Stormarn
bone
R. tarandus
AMS
K-4330
10,110
85 11,990-11,270
11,971-11,315
-18.3 attributed to classic Fischer and Tauber, 1986
Hamburgian, considered as falsely
labelled Stellmoor
72 Klappholz LA 63
SchleswigFlensburg
Lyngby antler
artefact
R. tarandus
AMS
AAR-2785
11,560
110 14,180-13,620
13,731-13,179
-
73 Lasbek LA 14
Stormarn
antler artefact:
double bevelled point
R. tarandus
AMS
KIA-51380
11,169
64 13,190-12,910
13,181-12,910
-18.7
Osseous artefacts
Tab. 2 (continued)
Clausen, 2004
Wild and Weber, 2017
450
ID
site
country
material
species
method
lab. no.
Age 14C
[BP]
±
[BP]
Age
[cal BP *]
Age
[cal BP **]
δ13C
[‰]
conv.
KN-2707
12,650
320
16,020-13,780
15,988-13,879
-
comment
references
Hamburgian
Lanting and Van der
Plicht, 1996
Hamburgian
S.B. Grimm et al. · Late Glacial Occupation of Northern Germany and Adjacent Areas
1
Querenstede
D (Lower Saxony)
charcoal
2
Slotseng, kettle hole
DK (South Jutland)
antler / bone,
humanly modified
R. tarandus
AMS
AAR-906
12,520
190
15,400-13,960
15,365-14,069
-18.6
Havelte Group
Holm and Rieck, 1992;
Holm, 1991
3
Slotseng, kettle hole
DK (South Jutland)
antler
R. tarandus
AMS
AAR-8159
12,410
70
14,920-14,120
14,938-14,191
-19.6
Havelte Group
Aaris-Sørensen et al.,
2007
4
Slotseng, kettle hole
DK (South Jutland)
antler, humanly
modified
R. tarandus
AMS
AAR-8157
12,299
41
14,540-14,020
14,806-14,083
-19.1
Havelte Group
Aaris-Sørensen et al.,
2007; Grimm and
Weber, 2008
5
Slotseng, kettle hole
DK (South Jutland)
bone, vertebra with R. tarandus
flint projectile
AMS
AAR-8165
12,290
75
14,660-13,940
14,831-14,050
-19.4
Havelte Group
Aaris-Sørensen et al.,
2007
6
Slotseng, kettle hole
DK (South Jutland)
bone, vertebra with R. tarandus
flint projectile
AMS
AAR-8160
12,240
50
14,400-13,960
14,782-14,042
-19.0
Havelte Group
Aaris-Sørensen et al.,
2007
7
Slotseng, kettle hole
DK (South Jutland)
antler
R. tarandus
AMS
AAR-8162
12,220
100
14,610-13,810
14,822-13,809
-18.9
Havelte Group
Aaris-Sørensen et al.,
2007
8
Slotseng, kettle hole
DK (South Jutland)
bone, tibia
R. tarandus
AMS
AAR-8163
12,205
65
14,370-13,890
14,795-13,863
-19.5
Havelte Group
Aaris-Sørensen et al.,
2007
9
Slotseng, kettle hole
DK (South Jutland)
bone, costa
R. tarandus
AMS
AAR-8164
12,190
50
14,290-13,890
14,311-13,881
-18.6
Havelte Group
Aaris-Sørensen et al.,
2007
10
Slotseng, kettle hole
DK (South Jutland)
antler / bone,
humanly modified
R. tarandus
AMS
AAR-8158
12,165
55
14,240-13,880
14,305-13,813
-19.0
Havelte Group
Aaris-Sørensen et al.,
2007
11
Slotseng, kettle hole
DK (South Jutland)
antler, humanly
modified
R. tarandus
AMS
AAR-8161
12,065
80
14,130-13,730
14,113-13,781
-19.7
Havelte Group
Aaris-Sørensen et al.,
2007
12
Køge Bugt
DK (Zealand)
bone, humanly
modified
R. tarandus
AMS
AAR-18733
12,238
46
14,390-13,950
14,769-14,045
-
Final Palaeolithic
(Hamburgian?)
Fischer and Jensen,
2018; Wild, 2020
13
Køge Bugt
DK (Zealand)
antler, humanly
modified
R. tarandus
AMS
AAR-18732
12,170
45
14,210-13,890
14,301-13,866
-
Final Palaeolithic
(Hamburgian)
Fischer and Jensen,
2018; Wild, 2020
14
Køge Bugt 1 (also: off- DK (Zealand)
shore Solrød Strand)
Federmessergruppen (FMG)
antler, humanly
modified
R. tarandus
AMS
AAR-1036
12,140
110
14,440-13,720
14,801-13,770
-
Final Palaeolithic
(Hamburgian)
Fischer, 1996; Petersen
and Johansen, 1996
15
Grabow 15
D (Lower Saxony)
charcoal
Betula sp.
AMS
KIA-41862
12,125
50
14,130-13,850
14,113-13,810
-27.7
from archaeological
feature (FMG)
Tolksdorf et al., 2013
16
Grabow 15
D (Lower Saxony)
bone, calcined, one
fragment unburnt
AMS
KIA-41861
12,070
100
14,200-13,680
14,218-13,614
-23.8
from archaeological
feature (FMG)
Tolksdorf et al., 2013
17
Weitsche
D (Lower Saxony)
bone, cremated,
bulked sample
C. fiber &
unidentified
AMS
KIA-26439
11,980
120
14,120-13,520
14,108-13,591
-
from lithic (FMG) and
amber concentration
Veil et al., 2012
18
Weitsche
D (Lower Saxony)
bone, cremated,
bulked sample
C. fiber &
unidentified
AMS
KIA-35664
11,755
50
13,720-13,440
13,756-13,501
-
from lithic (FMG) and
amber concentration
Veil et al., 2012
Brommean
19
Trollesgave
DK (Zealand)
charcoal
Salix sp.
AMS
AAR-16021
11,126
44
13,130-12,890
13,155-12,916
-28.0
Brommean
Fischer et al., 2013b
20
Trollesgave
DK (Zealand)
charcoal
Salix sp.
conv.
K-2509
11,100
160
13,270-12,710
13,298-12,750
-24.6
Brommean
Fischer, 1996: 158;
Fischer et al., 2013b
Tab. 3 Reliable radiocarbon dates of Final Palaeolithic material from adjacent areas. * 95 % confidence interval, using the CalPal-2019-Hulu calibration curve in CalPal program, Version 2020.2
(Weninger and Jöris, 2008) ** 95,4 % confidence interval, unmodelled, using IntCal 20 (Reimer et al., 2020) in the OxCal program, version 4.4 (Bronk Ramsey, 2009)
The Beef behind all Possible Pasts – The Tandem-Festschrift in Honour of Elaine Turner and Martin Street
method
lab. no.
Age 14C
[BP]
±
[BP]
Age
[cal BP *]
Age
[cal BP **]
δ13C
[‰]
comment
references
Salix / Betula /
Populus
conv.
K-2641
11,070
120
13,180-12,740
13,166-12,761
-24.5
Brommean
Fischer, 1996: 158;
Fischer et al., 2013b
Salix sp.
AMS
AAR-16019
10,826
49
12,860-12,700
12,838-12,722
-27.0
Brommean
Fischer et al., 2013b
OxA-3614
10,810
120
12,990-12,590
13,071-12,510
-25.5
Brommean
Fischer, 1996: 158 f.
AAR-4539
10,720
90
12,810-12,570
12,835-12,491
-20.4
Brommean
Heinemeier and Rud,
2000: 302
Hv-17306
10,515
95
12,790-12,030
12,722-12,060
-
Long Blade
Technology
Richter, 1992
ID
site
country
material
species
21
Trollesgave
DK (Zealand)
charcoal, bulked
material
22
Trollesgave
DK (Zealand)
charcoal
23
Fensmark Skydebane
DK (Zealand)
charcoal
x
AMS
24
Bromme
DK (Zealand)
bone fragment,
vertebra lumbalis
A. alces
AMS
D (Lower Saxony)
charcoal
Pinus
sylvestris?
conv.
Ahrensburgian
25
Melbeck
Osseous artefacts
26
Endingen, Horst VI
D (MecklenburgWest Pomerania)
bone, blade-like
shaped rib
Equus sp.
AMS
UtC-5681
11,830
50
13,820-13,500
13,792-13,526
-
Final Palaeolithic
(FMG / Brommean)
Kaiser et al., 1999: 115
27
Endingen, Horst VI
D (MecklenburgWest Pomerania)
antler with groove
and splinter technique remain
M. giganteus
AMS
ETH-13585
(UZ-3798)
11,555
100
13,560-13,200
13,601-13,186
-
Final Palaeolithic
(FMG / Brommean)
Terberger, 1996; Kaiser
et al., 1999
28
Nørre Lyngby,
new investigations
DK (North Jutland)
bone, costa,
cut-marks
R. tarandus
AMS
AAR-1511
11,570
110
13,600-13,200
13,737-13,182
-17.9
Final Palaeolithic
(FMG / Brommean)
Aaris-Sørensen, 1995:
358
29
Mickelsmosse (Munkarp)
S (Scania)
antler club
R. tarandus
AMS
OxA-2791
10,980
110
13,110-12,710
13,094-12,749
-19.4
Final Palaeolithic
(FMG / Brommean /
Ahrensburgian)
Hedges et al., 1995;
Larsson, 1996
30
Odense Kanal
DK (Funen)
Lyngby antler
artefact
R. tarandus
AMS
AAR-9298
10,815
65
12,880-12,680
12,890-12,700
-
Final Palaeolithic
(FMG / Brommean /
Ahrensburgian)
Stensager, 2006
31
Fogense Enge
DK (Zealand)
bone rod
A. alces
AMS
AAR-15025
10,726
27
12,760-12,680
12,747-12,698
-
Final Palaeolithic
(FMG / Brommean /
Ahrensburgian)
Petersen, 2021
32
Arreskov
DK (Funen)
Lyngby antler
artefact
R. tarandus
AMS
OxA-3173
10,600
100
12,840-12,240
12,756-12,105
-18.4
Final Palaeolithic
(FMG / Brommean /
Ahrensburgian)
Fischer, 1996:
158-162
Tab. 3 (continued)
451
Acknowledgements
We would like to thank Kristina Hüntemeyer for her help
with literature search and editing. The research was mainly
conducted and financed in the context of subproject B1
“Pioneers of the North” within the Collaborative Research
Centre 1266 “Scales of Transformation – Human-environmental interaction in prehistoric and archaic societies” of
the German Research Foundation (DFG, German Research
Foundation, project number 2901391021-SFB 1266).
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Sonja B. Grimm
Berit Valentin Eriksen
Mara-Julia Weber
Schleswig-Holstein State Museums Foundation
Schloss Gottorf
Centre for Baltic and Scandinavian Archaeology
Collaborative Research Centre 1266 Project B 1
“Pioneers of the North“
Schlossinsel
D - 24837 Schleswig
sonja.grimm@zbsa.eu
Sascha Krüger
The National Museum of Denmark
Environmental Archaeology and Materials Science
I. C. Modewegsvej
DK - 2800 Kongens Lyngby
and
Kiel University
Institute of Prehistoric and Protohistoric Archaeology
Johanna-Mestorf-Straße 2-6
D - 24106 Kiel
lithic antler assemblages from northern Germany, southern
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Tobias Reuter
Schleswig-Holstein State Museums Foundation
Schloss Gottorf
Centre for Baltic and Scandinavian Archaeology
Schlossinsel
D - 24837 Schleswig
Markus Wild
Schleswig-Holstein State Museums Foundation
Schloss Gottorf
Centre for Baltic and Scandinavian Archaeology
Schlossinsel
D - 24837 Schleswig
and
Kiel University
Cluster of Excellence ROOTS
Ohlshausenstraße 80 h
D - 24118 Kiel
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