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Characterizing the Lower Paleolithic bone industry from
Sch€
oningen 12 II: A multi-proxy study
Marie-Anne Julien
a
,
b
,
c
,
*
, Bruce Hardy
d
, Mareike C. Stahlschmidt
c
, Brigitte Urban
e
,
Jordi Serangeli
f
, Nicholas J. Conard
f
,
g
a
Centre for the Archaeology of Human Origins, Archaeology Department, University of Southampton, Avenue Campus, Southampton SO17 1BF, UK
b
Unit
e Histoire Naturelle de l'Homme Pr
ehistorique (UMR 7194), Sorbonne Universit
es, Mus
eum national d'Histoire naturelle, CNRS, 1 rue Ren
e Panhard,
75013 Paris, France
c
Institute for Archaeological Sciences, University of Tübingen, Rümelinstr. 23, 72070 Tübingen, Germany
d
Department of Anthropology, Palme House, Kenyon College, Gambier, OH 43022, USA
e
Institute of Ecology, Subject Area Landscape Change, Leuphana University Lüneburg, Scharnhorststraße 1, 21335 Lüneburg, Germany
f
Department of Early Prehistory and Quaternary Ecology, University of Tübingen, Schloss Hohentübingen, 72070 Tübingen, Germany
g
Senckenberg Centre for Human Evolution and Palaeoecology, University of Tübingen, Schloss Hohentübingen, 72070 Tübingen, Germany
article info
Article history:
Received 24 June 2015
Accepted 12 October 2015
Available online 1 December 2015
Keywords:
Middle Pleistocene
Lower Paleolithic
Geoarcheology
Zooarcheology
Taphonomy
Use-wear analysis
Bone tools
abstract
Although preservation of Paleolithic faunal assemblages from open-air settings is often poor, the Lower
Paleolithic sites of Sch€
oningen provide exceptionally well-preserved mammalian faunal material for
investigating hominin/animal relationships. Pleistocene fossil assemblages, however, usually reflect a
complex taphonomic history in which natural and anthropogenic processes are often superimposed. A
number of examples of osseous finds that resemble tools were recently discovered in the MIS 9 deposits
of Sch€
oningen 12 II. Non-anthropogenic agents are known to produce surface modifications mimicking
human artifacts and the identification of osseous remains used and/or deliberately modified by ancient
hominins is often controversial in such old contexts. Multiple lines of evidence are thus useful for dis-
tinguishing between osseous artifacts and “eco-facts”.
In this paper, the recognition of the use of bone for different technological purposes by late Middle
Pleistocene hominins is addressed through a multi-proxy study combining geoarcheology, bone
taphonomy, zooarcheology, and use-wear analysis. This allowed the identification of the processes and
agents responsible for the formation and modification of the different bone assemblages of Sch€
oningen
12 II. Our analysis points to different types of bones having been likely used as tools. These results expand
the diversity of the organic technological repertoire of the Middle Pleistocene hominins, making
Sch€
oningen 12 II a remarkable new source of information on osseous technology long before the Upper
Paleolithic, the period traditionally viewed as the start of the systematic use of bone tools. Together with
other observations of bone tools documented during the Lower and Middle Paleolithic, the results from
Sch€
oningen show that archeologists may have underestimated the diversity and importance of osseous
technology among archaic hominins.
©2015 Elsevier Ltd. All rights reserved.
1. Introduction
Bone is a raw material extensively used in the Upper Paleolithic,
however pre-Upper Paleolithic evidence of the use of bone tools is a
disputed topic. Usually without clear evidence of manufacturing,
the identification of bone tools in Lower and Middle Paleolithic
contexts depends on the recognition of wear from use alone. The
identification of such objects can therefore be difficult, especially in
contexts where other taphonomic agents may have been involved
in the formation and modification of the bone assemblages. The
misrecognition of Early and Middle Paleolithic bone artifacts is
particularly worrisome since the publication of Dart's (1957)
‘Osteodontokeratic’culture and Brain's (1981) taphonomical
studies warning about the variety of natural processes that can
create pseudo-tools. With the exception of the geographically and
chronologically widespread and easily distinguishable bone re-
touchers (e.g., Martin, 1907; Taute, 1965; Auguste, 2002; Malerba
*Corresponding author.
E-mail addresses: m.julien@soton.ac.uk,majulien@mnhn.fr (M.-A. Julien).
Contents lists available at ScienceDirect
Journal of Human Evolution
journal homepage: www.elsevier.com/locate/jhevol
http://dx.doi.org/10.1016/j.jhevol.2015.10.006
0047-2484/©2015 Elsevier Ltd. All rights reserved.
Journal of Human Evolution 89 (2015) 264e286
and Giacobini, 2002; Patou-Mathis, 2002; Schwab, 2002; Valensi,
2002a, b; Verna and d'Errico, 2011; Mallye et al., 2012; Tartar, 2012;
Blasco et al., 2013; Smith, 2013; Daujeard et al., 2014; Moigne et al.,
2015; Rosell et al., 2015), Paleolithic specialists tend to be cautious
in the recognition of the use of bone as a raw material in pre-Upper
Paleolithic European context.
Advances in taphonomic and technological analysis in recent
years have allowed for the identification of bone tools in the Lower
and Middle Paleolithic European and extra-European record (e.g.,
Tromnau, 1983; Gaudzinski,1999; Backwell et al., 2008; Burke and
d'Errico, 2008; Rosell et al., 2011; Soressi et al., 2013; Hardy et al.,
2014; Boschian and Sacc
a, 2015; Romandini et al., 2015), and
bones have been recognized to have been used as early as 1.5e2.0
million years in South Africa at sites such as Drimolen, Swartkrans,
and Sterkfontein (Backwell and d'Errico, 2001; Backwell and
d'Errico, 2008; d'Errico and Backwell, 2009). Expedient tools, or
“minimally modified bone artifacts”(Villa and d'Errico, 2001), are
typical of Lower and Middle Paleolithic bone industries (Patou-
Mathis, 1999). At the famous ‘spear horizon’of Sch€
oningen 13 II-4,
numerous long bones used as retouchers, distal epiphyses of un-
gulate metapodials likely used for hammering, and other activities
that appear to be unrelated to butchery have been reported
(Voormolen, 2008; Van Kolfschoten et al., 2015).
This paper focuses on the mammal remains from recent exca-
vations of the Sch€
oningen 12 II locality (excavated between 2008
and 2009), located about 800 m from Sch€
oningen 13 II (Serangeli
et al., 2015a;Fig. 1A). The goal of the present study is to discuss
the possible presence of bone tools in the different assemblages of
Sch€
oningen 12 II with special attention to the assemblage from
sedimentary cycle 4, geologically contemporaneous to the Spear
Horizon of Sch€
oningen 13 II-4, also known as the Horse Butchery
Site. Due to the emergency nature of the excavation (Serangeli et al.,
2015a), assessment of the context of deposition of the different
archeological collections from Sch€
oningen 12 II was limited in the
field, but a detailed study involving palynological, sedimentolog-
ical, and micromorphological analysis was performed in the
southern part of 12 II-4 (Fig. 1D). The exceptional preservation of
the bones allowed a detailed study of the bone surfaces, notably
through taphonomic and use-wear analysis. The results of this
multi-proxy study led to the identification of the processes and
agents (both natural and/or anthropogenic) responsible for the
formation and modification of the different bone assemblages of
this locality, and allowed the recognition of different kinds of bone
tools at Sch€
oningen 12 II.
In addition to bone retouchers and percussors that are also
frequent in Sch€
oningen 13 II-4 (Voormolen, 2008; Van Kolfschoten
et al., 2015), at least three possible new types of bone tools have
been recognized here: used-tip and smoothed-tip objects, anvil (or
anvil/retoucher?), as well as multiple-purpose tools. We also pre-
sent an intriguing piece of elephant ivory, on which the distinction
between natural or anthropogenic origin of the modifications is still
not entirely clear.
This study substantially increases the number of tool types
known so far for this key late Lower Paleolithic site, and shows,
without ambiguity, that Middle Pleistocene hominins, likely Homo
heidelbergensis, were using bones for a large range of activities. The
recognition of these organic technologies contributes to our un-
derstanding of the behavioral diversity and complex cognitive
abilities of pre-modern hominins.
2. Schöningen 12 II: context
Sch€
oningen is a complex of sites, composed of at least twenty
archeological sites as well as some more paleontological localities,
mostly belonging to the MIS 9 (Thieme, 2007a; Richter and
Krbetschek, 2015; Serangeli et al., 2015a). The site complex
became world famous after the discovery of the remains of
numerous butchered large Middle Pleistocene horses in association
with several Lower Paleolithic wooden spears (Thieme, 1997).
This paper focuses on material from the Plateau 4, 5, and 6 (P4,
P5, and P6) of Sch€
oningen 12 II, located between 800 and 1000 m
north of the well-known ‘spear horizon’of Sch€
oningen 13 II-4
(Fig. 1A, B). The P4, P5, and P6 areas, with a surface of some thou-
sands of square meters, were excavated between 2008 and 2009
with spade and shovel in the context of a rescue work. Constrained
by time pressure, the sediments were not sieved. During this
fieldwork, concentrations and scattered bone finds distributed
between five distinct sedimentary cycles (numbered from 1 to 5,
i.e., Sch€
oningen 12 II-1 to 5) have been discovered (cf. Serangeli
et al., 2015a;Table 1). Each sedimentary cycle consist of layers of
silty and clayish to calcareous muds that grade upwards into dark
brown organic muds (Table 1). The terminology used is as follow:
12 II-4c1 refers to locality 12, channel II, sedimentary cycle 4, layer
c, and sub-layer 1.
Bones are associated with Lower Paleolithic lithic artifacts in
12 II-1, 12 II-2 and 12 II-4 (Table 1;Serangeli and Conard 2015).
The remains discussed in detail in this paper come mostly from
12 II-4. Sch€
oningen 12 II-4 is geologically and stratigraphically
similar to the spear horizon of Sch€
oningen 13 II-4. For these
reasons, the geoarcheological, taphonomical, and zooarcheological
description will primarily focus on the sedimentary cycle 4 of
Sch€
oningen 12 II.
3. Materials and methods
3.1. Geoarcheological methods and materials
Sediments of profile Sch€
oningen 12 II-4, x 899, y 615 exposed
between 102.05 m and 103.25 m above sea level, encompassing
layers and sub-layers 4c, 4a1/b, and 4b (Figs. 1D and 2A, B, Table 2),
have been sampled using 25 75 cm sized steel boxes during
the excavation campaign of 2009. Subsampling for palynological,
sedimentological, and micromorphological investigations was
conducted at the Institute of Ecology, Subject Area Landscape
Change of Leuphana University Lüneburg. The material has been
subject to geochemical and botanical analysis. Samples have been
analyzed for carbon and nitrogen using a Perkin Elmer 2400 Series
II CHNS/O Elemental Analyzer, for their carbonate content
following gasometric determination with the Scheibler apparatus,
and for soluble salts (Electrical Conductivity, EC) according to
VDLUFA (1991). Sediment color has been determined with
MUNSELL Soil Color Charts. For palynological analysis, including
charcoal particles, 10e20 g samples were treated by standard
palynological methods (Faegri et al., 1989; Moore et al., 1991). The
remaining blocks were transferred to the Geoarchaeological Lab-
oratory, at the Institute for Archaeological Sciences, University of
Tübingen, Germany for micromorphological study (cf.
Stahlschmidt et al.[2015a] for a full description of the method). Six
thin sections were available for this study, with two thin sections
produced from each block sample Sch€
oningen 12 II-4 2009/20,
Sch€
oningen 12 II-4 2009/21, and Sch€
oningen 12 II-4 2009/22
(Table 2). The petrographic thin sections come from sub-layers
4c1 and 4c2, which contain archeological material. An additional
thin section of an encrusted bone sample from sub-layer 4c3-
Plateau 6 (ID 17897) was also produced. Analysis was conducted
with a petrographic microscope under plane-polarized, cross-
polarized, and UV-light at magnifications of 25to 500.Ter-
minology follows Courty et al. (1989), Stoops (2003),andStoops
et al. (2010).
M.-A. Julien et al. / Journal of Human Evolution 89 (2015) 264e286 265
Figure 1. (A) Location of Sch€
oningen 12 locality within the Sch€
oningen basin. (B) Extension of the archeological rescue excavation (indicated by the black lines) on Plateaus 4, 5, and
6 (P4, P5, and P6) of Sch€
oningen 12 II. (C) Plan of the northern part of the excavated area of Plateau 6, sub-layers 4c1 to 4c3, with the distributions of bones and bone artifacts. Lithic
remains include four retouched and two unretouched flints (not represented). (D) Cluster of bone remains Plateau 4-layer 4c, almost exclusively belonging to a single aurochs
carcass. A lithic retouched artifact was found in the vicinity (gray diamond). The location of the block samples Sch€
oningen 12 II-4 2009/20 to 24 is indicated on the bottom left
corner of the excavated area (modified from plans from J. Lehmann).
M.-A. Julien et al. / Journal of Human Evolution 89 (2015) 264e286266
3.2. Zooarcheological and use wear methods
The faunal material studied come from Sch€
oningen 12 II-1 to
Sch€
oningen 12 II-5. The study integrated all large mammal remains,
with the exception of beaver remains that were the focus of a
specific study. The nature of the excavation did not allow sieving of
the sediments and small elements are likely to be
underrepresented.
The mammal bones were identified using recent and fossil
mammalian collections from the Department of Archaeological
Science and the Department of Biology of the University of Tübin-
gen. When species identification was not possible, size classes were
considered (adapted from Brain,1981). Age and sex recognition was
performed on available cranial elements (i.e., antlers, teeth).
Refitting and matching right and left elements was also attempted
for bones and teeth, within and between layers or sub-layers.
All bone surfaces were observed for taphonomic modifications,
using a 10magnification lens with a low-angled light and a var-
iable magnification binocular microscope when necessary. Tapho-
nomic observations were based on the descriptions provided in
Table 1
Summary of sedimentary and archeological context of the Sch€
oningen 12 II sequence (excavation 2008 and 2009).
Sedimentary, depositional context
a
Surrounding/local environment
a
Lithic remains
b
Fauna (NSP)
12 II-5 Grayish brownish, laminated silt and silty
slightly organic mud and humus free silt
towards the top (plateau 4)
Unstable, nearly treeless landscape, steppe-
tundra; onset of a glacial
01
12 II-4
c
Dark brown organic mud (II-4b), gray
calcareous silty mud (II-4c), deposited inside
the lake (plateau 4)d
Lake level drop, increased territoriality (II-4b);
and high lake level stand, swampy (II-4c), open
steppe forest
5/2 570
12 II-3 Grayish to dark grayish calcareous silty, sandy
mud, mollusks and thin layer of strongly
weathered fen peat (plateau 4)
Lake level rise, riparian forest stands (Betula/
Alnus), swampy, climatic deterioration
025
12 II-2
c
Dark gray mud, with intercalated layers of peat
(plateau 2)
Swampy and boggy environment, decrease of
thermophilous trees, opening of landscape
3/4 442
12 II-1
c
Gray to brown mud, peaty layers intercalated,
plant residues, mollusk shells (plateau 2)
Full interglacial conditions, back swamp forest,
territoriality of the lakeshore towards the top of
level II-1
5/1 522
a
Data: this study and Urban and Sierralta (2012), Kunz et al. (Submitted for publication), Urban and Bigga (2015), Serangeli et al. (2015).
b
Retouched/unretouched lithic artifacts.
c
Our analysis focuses mainly on the material from Sch€
oningen 12 II-4, contemporaneous of the “Spear horizon”of Sch€
oningen 13 II-4, and includes comparisons and
elements from Sch€
oningen 12 II-1 and 12 II-2.
Figure 2. (A) Profile description of Sch€
oningen 12 II-4, x 899, y 615 (2009). (B) Profile photo at Sch€
oningen 12 II-4 (P4) with the block samples Sch€
oningen 12 II-4 2009/20 to 24
and the indicated layers.
M.-A. Julien et al. / Journal of Human Evolution 89 (2015) 264e286 267
different works (e.g., Binford, 1981; Marshall, 1989; Villa and
Mahieu, 1991; Lyman, 1994; Fisher, 1995; Blumenschine et al.,
1996; Dominguez-Rodrigo et al., 2012). Observations of the
morphology of the potential modifications followed the approaches
proposed by Johnson (1985) and Legrand and Sidera (2007). All
deformations of the volume of the piece were recorded, as well as
possible wear patterns in the form of striations, polish, and micro-
flake scarring. In addition, the analysis of micro-wear patterns of
the polish and striation details, and residue analysis were per-
formed on seven bone remains from Sch€
oningen 12 II-4 (ID 17868,
17870, 17875, 17896, 17910, 18091, and 18109), in order to consider
their possible anthropogenic vs. natural origins and/or as sup-
porting evidence in making a functional interpretation. The
methods used here are well-established, particularly with regard to
macro and micro-wear and functional analysis of bone tools (e.g.,
Backwell and d'Errico, 2004; Gates St-Pierre and Walker, 2007;
Legrand and Sidera, 2007; Burke and d'Errico, 2008; d'Errico and
Backwell, 2009; Buc, 2011; Soressi et al., 2013). The bones were
examined under reflected light using Dino-Lite Digital Microscopes
(AD-413ZT, magnification 20e220; AM4013ZT4, magnification
430e490) and images recorded using DinoCapture 2.0 software.
Residues that can be identified include hair, feathers, skin, bone,
plant tissue, wood, and starch grains (Hardy and Garufi, 1998;
Hardy et al., 2013).
Data are reported in number of identified specimens (NISP),
number of unidentified specimens (UNID), and total number of
specimens (NSP sensu Lyman [2008] with NSP ¼UNID þNISP). As
far as possible, the minimum number of elements (MNE) and
minimum number of individuals (MNI) take into account siding, as
well as age and sex identifications. Unless otherwise mentioned,
the frequency of taphonomic observations was calculated for the
NSPm, corresponding to the NSP excluding bones with unobserv-
able surfaces.
4. Results
4.1. Results of the geoarcheological study
4.1.1. Macroscopic description The sedimentary sequence of
Sch€
oningen 12 II-4 is composed of gray clay (sub-layers 4c2 and
4c1) followed by a dark organic rich sub-layer (4b); it shows clear
similarities to Sch€
oningen 13 II-4 (B€
ohner et al., 2005;Lang et al.,
2012;Urban and Sierralta, 2012; Kunz et al., Submitted for
publication). The general sedimentological features of this part of
the Sch€
oningen 12 II sequence are described in Figure 2A. Layer
4c at Sch€
oningen 12 II presents a calcareous mud, which was
subdivided in the field into sub-layers 4c1, 4c2 (Fig. 2A, B), and
4c3. 4c3 has a gravelly to sandy component and 4c2 and 4c1 is
sandy. On site, sedimentary distinctions were not always possible
and thus specimens were sometimes attributed only to the layer
or to the sedimentary cycle. As the excavation of 12 II was a
rescue excavation, the available sedimentary description is
limited, and the following description is derived from the block
samples from Plateau 4 (Figs. 1D and 2B).
In the block samples from Plateau 4 (Fig. 2) that encompass
most of layer 4b and 4c, the lowermost part is a dark grayish brown
to light brownish gray calcareous silt with some remains of mol-
lusks, corresponding to sub-layer 4c2. The overlying sub-layer 4c1
is a very dark grayish brown to very dark gray to dark gray
calcareous mud. The overlying sub-layer 4b (including 4b1/a
respectively) is a black fine organic silt.
4.1.2. Sedimentological and palynological characteristics of
Schöningen 12 II-4 Sediments from Sch€
oningen 12 II-4 are
continuously fine-grained and composed of variable amounts of
calcium carbonate and organic matter (Fig. 3). The sedimentary
sequence can be subdivided into three main sub-layers (cf. Table 2):
- a silty, slightly carbonate containing basal part, which corre-
sponds to sub-layer 4c2,
- a middle part consisting of a strong calcareous mud rich in
organic matter, corresponding to sub-layer 4c1,
- and a topmost part of fine organic detritus mud, sub-layer 4b
(4a1/b included; B€
ohner et al., 2005; Thieme, 2007b; Urban
et al., 2011).
The palynological analysis shows evidence for two major local
pollen assemblage zones (LPAZ) that could be correlated with
LPAZ RP4 and RP5 of reference profile Sch€
oningen 13 II of 2003
described in Urban and Bigga (2015) and reflecting plant associa-
tion growing in and at the margin of the paleo-lake (Kunz et al.,
2015). Sub-layer 4c2 and 4c1 are characterized by high amounts
of aquatic plants, grasses, and birch (Betula sp.) among the wooden
species, whereas layer 4b (including 4a1/b) is indicative of a phase
of increasing terrestriality dominated locally by sedges (Carex sp.)
and increased amounts of pine (Pinus sp.), while birch and willow
(Salix sp.) are local elements. The pollen zones reflect late phases of
the Reinsdorf Interglacial (MIS 9) defined at the Sch€
oningen 13 II
locality (Urban, 2007; Urban et al., 2011; Urban and Bigga, 2015).
4.1.3. Micromorphology of Schöningen 12 II-4 The two thin sec-
tions from sub-layers 4c2 and 4c1 display a dense grain supported
groundmass of silty quartz grains (Fig. 3A). Other coarse
components are mica, plant residues, shell fragments, ostracods,
and sand-sized quartz grains. The fine material includes clay and
amorphous organic fine material. There are areas with coarser
material than the general composition and erosional contacts are
present (Fig. 3B). Plant residues are mainly amorphous organic
fine material; elongated larger plant tissue residues mostly show
a tendency of horizontal alignment. Localized domains of
calcareous fine material were observed in low density. The
number of calcareous localized domains increases as you move
up and they mainly represent chara and shell remains. On the
other hand, the amount of clay decreases in this direction as does
the amount of silty quartz grains. This upward change presents a
clear transition to sub-layer 4c1.
The thin sections from sub-layer 4c1 show a very different
picture. Here the groundmass is calcareous, dominantly consisting
of chara remains and shell fragments (Fig. 3C). As in sub-layer 4c2,
plant residues are mainly present as amorphous organic fine ma-
terial, a few larger, well-preserved plant tissue residues are present
as well; elongated plant tissue residues show a tendency for hori-
zontal alignment. Silty quartz grains are present in lower density
than in 4c2. Occasional lenses of pure silty quartz were observed.
The number of plant residues gradually increases with height.
4.2. Depositional and environmental context of the Schöningen 12
II-4 faunal assemblage: archeological implications
The results of the thin section analysis performed on sediments
from Plateau 4 of Sch€
oningen 12 II indicate lacustrine deposition for
layer 4c. The horizontal clay and plant residue lamina, the hori-
zontal bedding of elongated plant residues, shell, and well-
Table 2
Sample list of micromorphology samples.
Sample Square z-value Units
Sch€
o 12 II-4 2009/22 899/615 102.5e102.75 4c1
Sch€
o 12 II-4 2009/21 899/615 102.25e102.5 4c1
Sch€
o 12 II-4 2009/20 899/615 102.05e102.3 4c1 to 4c2
Sch€
o 12 II-4 ID 17897 864/656 100.34 4c3
M.-A. Julien et al. / Journal of Human Evolution 89 (2015) 264e286268
Figure 3. (A) Dense silty quartz-rich groundmass with plant residues in sub-layer 4c2. Note the horizontal clay lamina in the middle of the picture with calcareous chara remains
(yellow arrow). Crossed-polarized light (XPL), scale on the bottom left ¼0.5 mm. (B) Erosional contact in sub-layer 4c2. Fine material increases upwards with a sharp contact in the
middle of the photo (blue lines). Well-preserved ostracod remains (yellow arrow) are present. Plane-polarized light (PPL), scale at right bottom ¼1 mm. (C) Calcareous groundmass
of sub-layer 4c1 with many chara remains (yellowarrows)and shell fragments (blue arrows). XPL, scale at lower left ¼2 mm. (D) Sub-layer 4c1 exhibiting a calcareous groundmass
with preserved shell fragments (blue arrow) and chara remains (yellow arrows), which still contain plant tissue. Note the high amount of amorphous plant residues in the matrix.
PPL, scale at lower left ¼0.5 mm. (E) Carbonate content and soluble salts of profile Sch€
oningen 12 II-4 (P4), x 899, y 615. (F) Carbon and nitrogen content of profile Sch€
oningen 12
II-4 (P4), x 899, y 615.
preserved chara remains in layer 4c are characteristic of a shallow,
open water lacustrine deposition under constant water cover
(Treese and Wilkenson, 1982; Bouma et al., 1990; Tucker et al.,
1990; Wallace, 1999).
The pyrite crust on the bone sample (Sch€
oningen 12 II-4, ID
17897) from sub-layer 4c3 reflects anoxic conditions for the for-
mation of the crust (Berner, 1970, 1984; Marnette et al., 1993; Suits
and Wilin, 1998). The formation of hematite presents a recent
feature of the weathering of the pyrite due to exposure (Challis,
1975). Sub-layer 4c3 was noted as sandy in the field, matching
the presence of sandy grains in the crust.
The sedimentary change from sub-layers 4c2 to 4c1 reflects a
shift from a relative higher to lower energy setting. The strong
quartz silt component in sub-layer 4c2 (thin section Sch€
o 12 II-4
2009/20A) might suggest that this sub-layer formed closer to the
deltaic source of the paleo-lake (see Lang et al., 2012) than the
upper sub-layer 4c1. The presence of clay lamina in sub-layer 4c2
suggests episodes of low energy deposition. Erosional contacts,
local absence of fine material, and the presence of slumps of silty
quartz in thin sections from 4c2 possibly indicate wave action. Sub-
layer 4c2 was therefore most likely deposited in the constantly
water covered, sub-littoral zone of the paleo-lake subjected to
episodic wave action.
Micromorphological analyses reveal a gradual change from sub-
layer 4c2 to 4c1 with a decrease in silty quartz and an increase in
plant residues and calcareous sedimentation. The dominantly
calcareous groundmass of sub-layer 4c1, mainly composed of chara
remains and shell fragments, reveals lower energy sedimentation
than sub-layer 4c2 and little post depositional disturbances. Sub-
layer 4c1 was most likely deposited in the sub-littoral zone of the
paleo-lake. The upward increase of plant residue in sub-layer 4c1
and its dominance in sub-layer 4b possibly indicate a greater
proximity to the shore (Dobrowski et al., 2001). Similarly, the
absence of calcite precipitation in sub-layer 4b might reflect
decreased water coverage (Dean, 1981; Brochier, 1983).
Deduced from the sedimentological as well as botanical in-
vestigations, the sediments of the basal part of sub-layer 4c2 mark
the onset of a change within the hydrological system of the lake
with a strong rise of the water table and with an increasing inflow
of carbonate rich water. Botanical, palynological, and macro re-
mains analyses (Urban et al., 2011; Urban and Sierralta, 2012; Bigga
et al., 2015; Urban and Bigga, 2015) show high amounts of non-
arboreal pollen and of rather low amounts of tree pollen (Betula and
Pinus <10%), indicative of a rather open landscape during deposi-
tional times. Nonarboreal pollen is mainly composed of grasses
(Poaceae 60%), which include substantial amounts of Phragmites
and of aquatic plants, (e.g., Potamogeton, aquatic buttercup
plantseRanunculus spec.), as reported by Jechorek (2000). Sub-
layer 4c1 is still characterized by tessellated open water condi-
tions (a.o. Potamogeton). Furthermore, pollen and spores indicate
growth of plants such as Sphagnum at slightly higher nutrient-poor
raised bog stands. The amount of Betula pollen has increased
pointing to local birch swamps.
Within layer 4b (12 II-4a1/b, respectively), the hydrological
conditions at the site have changed back and a lower lake level can
be deduced. Sediments are again carbonate free with a relatively
high amount of organic matter (Fig. 3). A variety of remains of local
plants indicate the onset of a phase of terrestrialization (a.o.
Cyperaceae, Pinus). The landscape around the lake and swampy
environments was quite open and covered by herbs and grasses
with scattered groups of trees and shrubs as Pinus, Betula, locally
Salix, single trees of Larix, and Juniper. A leaf of Sphagnum magel-
lanicum in the upper part of sub-layer 4c1 at a depth of
102.82e102.835 m (identification A. Hoelzer) points to persistent
raised bog growth in the vicinity of the swamp.
The highest micro-charcoal amounts (Stahlschmidt et al.,
2015a,b; Urban and Bigga, 2015) have been found in the transi-
tion between 4c1 and 4a1/b, peaking at 102.78 m, which might be
interpreted as another indicator for open landscape conditions and
spontaneous fire at climatic changes, or relate to human impact.
Table 3
Composition of the large mammal assemblages from Sch€
oningen 12 II-1, 2 and 4, Plateaus 4, 5, and 6 (castor excluded).
a
12 II-1 12 II-2 12 II-4
NISP MNE MNI NISP MNE MNI NISP MNE MNI
Palaeoloxodon antiquus 21 5 3 eee 111
Stephanorhinus sp. 136 16 3 43 9 1 2 2 1
Palaeoloxodon/Stephanorhinus ee e16 1 e11e
Equus cf. mosbachensis 68 22 3 25 12 2 53 27 3
Bos primigenius ee e eee287 109 1
Bos/Bison 94 19 2 95 14 2 35 11 1
cf. Megaloceros giganteus ee e 111 2 11
Cervus elaphus 14 5 1 12 5 1 35 8 1 þ2
b
Capreolus capreolus ee e 111 2 21
Cervidae 18 2 eeee15 6 e
Ungulate un. 23 5 e30 9 e40 6 e
Ursus sp. 5 5 1 eee e ee
Panthera (Leo) sp. 2 2 1 eee e ee
Meles meles 11 1 eee e ee
Carnivora 4 ee eee e ee
Anatomically identified bones (NSPa) 79 ee18 ee 44 ee
Unidentified bones (UNID) 57 ee202 ee 52 ee
TOTAL 522 82 15 443 52 8 569 174 12
Total number of specimens (NSP), of elements (MNE) and individuals (MNI) are indicated in bold.
a
NISP ¼number of identified specimens, MNE ¼minimum number of elements, MNI ¼minimum number of individuals. For identifications that did not reach the species
level, MNE and MNI were integrated when elements were complementary, supernumerary, or clearly different (in age, sex, or size) to specimens represented in related
taxonomic categories.
b
Indicates MNI based on shed antlers.
M.-A. Julien et al. / Journal of Human Evolution 89 (2015) 264e286270
4.3. Results of the zooarcheological and use wear study
4.3.1. Composition of the faunal assemblages from Schöningen 12
II A total of 1,560 bones (NSP) from Sch€
oningen 12 II-1 to 5 were
examined with standard zooarcheological methods, including
examination of surface modifications for the recognition of
natural and anthropogenic agents. Sch€
oningen 12 II-3 (25
unidentified fragments) and Sch€
oningen 12 II-5 (one unidentified
fragment) have small assemblages and will not be discussed any
further here (Table 1). The three other assemblages provide
roughly the same quantity of faunal material, with a total number
of remains reaching 522 NSP (12 II-1, MNE 82), 443 NSP (12 II-2,
MNE 52), and 569 NSP (12 II-4, MNE 174; Table 3). Refitting or
matching right and left elements was possible for faunal remains
from the same layer or sub-layer but never between different
layers, confirming the integrity of the stratigraphic division. The
faunal assemblage from Sch€
oningen 12 II-4, geologically
contemporaneous to the Sch€
oningen 13 II-4 spear horizon, will be
discussed in more detail here and compared to the faunal
assemblages from Sch€
oningen 12 II-1 and 2.
Large bovids represent more than 60% of the NISP of the
Sch€
oningen 12 II-4 faunal assemblage, followed by equids and
cervids (representing 11.2% and 11% of the NISP, respectively).
Elephant and rhinoceros are both represented by only a few re-
mains, corresponding to less than 1% of the NISP (Fig. 4A). However,
the horse is the most numerous species in terms of MNI with at
least three individuals represented, followed by the red deer with
three individuals (two represented by shed antlers only [Table 3]).
This over-representation of large bovids in both NISP and MNE is
due to the presence of a concentration of aurochs remains on
Plateau 4 (P4; Fig. 1D, Serangeli et al., 2012). A large amount of
refitting and matching was possible, yielding a sub-complete
skeleton of an adult male, of which the remains were dispersed
over a height of 40 cm embedded in layer 4c. If this specimen is not
considered, the assemblage is dominated by horse (28.3% of the
NISP) and cervid remains (with a total of 27.8% of the NISP), fol-
lowed by large bovid remains not belonging to the aurochs from P4
(with 19.3% NISP; Fig. 4B).
The fauna present in 12 II-2 and 12 II-4 are quite similar, with
equids (Equus mosbachensis) and large bovids (Bos/Bison)domi-
nating the faunal spectrums (Table 3). In 12 II-1, equids and large
bovids are also well-represented, but rhinoceros remains (Ste-
phanorhinus sp.) are the most numerous (at least for NISP).
Straight tusk elephant (Palaeoloxodon antiquus) is also relatively
well-represented in 12 II-1. A number of carnivore species (rep-
resented only by a few remains) were identified in 12 II-1
including Ursus sp., Panthera (Leo) sp, and Meles meles, while
carnivores are totally absent in 12 II-2 and 12 II-4 (Tab le 3).
4.3.2. Taphonomy of the Schöningen 12 II faunal assemblages
Sch€
oningen 12 II-1 and 4 have similar proportions of identified
specimens with 89.1 and 90.9% of bones at least anatomically
identified (Table 3). In 12 II-2, by contrast, 54.3% of the specimens
were identified to anatomical element (Table 3). Despite this
difference, the high frequency of identification indicates that the
three faunal assemblages are very well-preserved, though small
elements may be underrepresented due to the lack of sieving.
Bone surfaces are generally well-preserved in all layers,
although bones and teeth presented different colors ranging from
Figure 4. (A) Proportion of the different taxa from Sch€
oningen 12 II-4 in percentage of identified specimens ¼%NISP. (B) Sch€
oningen 12 II-4 faunal diversity expressed in %NISP,
excluding remains belonging to the sub-complete skeleton of aurochs from Plateau 4. (C) Sch€
oningen 12 II-4 faunal diversity expressed in percentage of individuals ¼%MNI.
M.-A. Julien et al. / Journal of Human Evolution 89 (2015) 264e286 271
mostly gray/beige-brownish in 12 II-4 to mostly brown/blackish
color in 12 II-1 and 2. This difference of color is typical of remains
deposited in anaerobic conditions (e.g., Rabinovich and Biton,
2011). In all sedimentary units, a few remains have surfaces that
are partly damaged by acidic water typical of chemical erosion
caused by acidic sedimentary conditions.
Carnivore action is limited in all the faunal assemblages
considered here. In 12 II-1 and 2, only three elements (MNE ¼3)
have carnivore marks (Table 4). In 12 II-4, ten elements (MNE ¼10,
NISP ¼14) present possible marks attributable to carnivore action
(Table 4), including a horse distal metacarpal that presents typical
tooth punctures on the epiphysis associated with probable claw
marks on each side of the diaphysis (ID 17902; Fig. 5A).
Hominin-induced marks in the form of cut or scraping marks
were recorded on six elements (MNE) from 12 II-1 (N ¼56) and two
from 12 II-2 (N ¼47). Sch€
oningen 12 II-4 has the largest number of
anthropogenic modification with 36 elements (N ¼43) presenting
scraping and/or cut marks (Table 4). The cut marks are varied, deep
or very shallow, short or long, and some cut marks present a double
bottom in the striation (like for the specimen 17470-Fig. 6B), sug-
gesting that the tool used was either not sharp or retouched, or
made of a somehow “coarse”material. Intentional green bone
breakage (identified through typical flakes, percussion pits, and
large percussion notches, cf. Villa and Mahieu, 1991) was observed
on eight specimens (MNE) from 12 II-4. The aurochs bones from
Plateau 4 are almost all complete, however, and no human inflicted
damage has been recognized on those remains. Generally long
bones presenting green bone breakages scars also have cut or
scraping marks. Cut marks and bone breakage attest to different
steps of butchery, including skinning, dismemberment, disarticu-
lation, defleshing, and likely marrow extraction (cf. Binford, 1981;
Figs. 6 and 7). No burned bones were recognized.
In the three main bone assemblages from Sch€
oningen 12 II,
several bones present different degrees of smoothing and rounding
of the edges or the surface. Five remains from 12 II-1 (ca. 1% NSP),
two (0.5% NSP) from 12 II-2, and 16 (2.8% NSP) from 12 II-4, present
relatively high degrees of smoothing of the surface and/or the
edges. In 12 II-4, those remains come mostly from sub-layer 4c3,
where three completely rounded bones are atypical in the collec-
tion, with rounding on all areas of the bone including the inner or
medullar part: a fragment of large bovid metatarsal (ID 18098), a
cervid phalanx (ID 18096), and a large bovid calcaneum (ID 17802)
dthis last one also shows a more advanced stage of weathering
than the rest of the bones from the collection. Those specimens
may also show randomly oriented striations of various lengths and
widths (also variable along the striations themselves) and with a
flat or uneven bottom at the base of the striation (Fig. 5AeE). Such
characteristics are typical of bones transported and/or abraded by
water and sediment particles (Andrews and Cook, 1985; Lyman,
1994; Fernandez-Jalvo and Andrews, 2003; Boschian and Sacc
a,
2010). However, most faunal remains from 12 II-4 belong to sub-
layer 4c1 (NSP ¼369), with a limited number of faunal remains
reported from sub-layers 4c2 and 4c3 (NSP ¼22 and 29,
respectively).
In the overall collection, long bones and long bone fragments
were the best-represented elements, followed by ribs and verte-
brae, while cranial remains were relatively limited. Comparison of
the proportion of MNE for the aurochs of Plateau 4 and the large
herbivores from Plateaus 5 and 6 shows different patterns. While
the aurochs from P4 is reflecting a complete skeleton, the herbi-
vores from P5-P6 4c3, 4c2, and 4c1 show relatively lower repre-
sentation of bones from Group I (composed mostly of ribs and
vertebrae) and a higher proportion of bones from Group II (i.e.,
principally long bones), which could account for a partial sorting of
the remains (Table 5). Remains from 4c3 and 4c2 are however too
few to be representative (Table 5).
Other remains from the 12 II-4 faunal collections present clearly
different patterns of smoothing than the one discussed above, with
a localized smoothing of their tips associated with different fea-
tures that could suggest that at least part of them may have been
used by hominins. They will be described in more details bellow.
4.3.3. Schöningen 12 II bone tools In the overall bone collections
from Sch€
oningen 12 II-1, 2, and 4, a number of remains present
highly localized mark and wear traces that suggest those
specimens may have been used by hominins. The morphology of
the specimens, the type of marks, and their localization allow us
to propose the recognition of different categories as follows:
retouchers, percussors, bones with used tip, possible smoothers,
and also anvil-like and multi-purpose bone tools.
By convention, active ends are described as distal ends.
Specimens are figured either anatomically oriented or with the
active end oriented upward. No residues were preserved on the
bones.
Percussor. A distal metatarsal of a horse from Sch€
oningen 12 II-4c1
(ID 18122) has two areas with short and deep incisions above the
articular surface on the anterior part of the metaphysis (Fig. 8A) that
could correspond to skinning and/or disarticulation marks (Binford,
1981). A chop-like mark associated with a large flake removal is
located on the edge of the distal epicondyle (Fig. 8B-C). These marks
are similar to other metapodial specimens described at Sch€
oningen
Table 4
Biological modifications related to human and carnivore activities recorded on the
surface of thebones of the large mammalassemblages from Sch€
oningen 12 II-1, 2, and
4.
a
12 II-1 12 II-2 12 II-4
N MNE N MNE N MNE
Cut and scraping
marks
56 6 47 2 43 36
Percussion damages
(perc. notches,
flakes, etc.)
21 ee10 8
Green bone breakage 19 e18 e55 e
Carnivore induced
marks
5 3 48 3 14 10
a
N¼number of specimens, MNE ¼minimum number of elements. No burned
bones have been recognized in the assemblages.
Table 5
Comparison of the representation (in MNE) of Voorhies Dispersal Groups for
Sch€
oningen 12 II-4 large herbivores from Plateaus 4, 5, and 6.
a
Plateau, Layer Dispersal groups
IIeII II IIeIII III
P4, 4c Aurochs 69 15 5 0 2
P5eP6, 4c1 Equid 0 0 11 2 1
P5eP6, 4c1 Bovid 3 1 3 0 1
P5eP6, 4c1 Cervid (medium-large) 1 1 4 0 0
P5eP6, 4c1 NSPa þþ eþþþ eþ
P5eP6, 4c2 Cervid 0 0 2 0 0
P5eP6, 4c3 Large herbivores 3 6 2 0 0
MNE was not possible to be calculated for anatomically identified specimens (NSPa),
relative proportions are indicated with the “þ”signs.
a
Dispersal groups after Voorhies (1969) in Lyman (1994).
M.-A. Julien et al. / Journal of Human Evolution 89 (2015) 264e286272
13 II-4 as possible hammers or percussors (Voormolen, 2008;Van
Kolfschoten et al., 2015). The helical fractures on the distal shaft
may result either from butchering, from the breakage of the bone
during use, or from another origin. Considering the angularity of the
distal end of large ungulate metapodials as well as their rigidness,
they may have been used as percussors for stone tool production
and/or curation, or for breaking bones for dismembering and/or
marrow extraction (see Van Kolfschoten et al., 2015).
Bone retoucher and multi-purpose tool. From Sch€
oningen 12 II-
2c1, a very distinctive double retoucher has been identified (spec-
imen 17938-Fig. 9). The piece is a fragment of shaft of a metapodial
of a large cervid (possibly Megaloceros). The fracture seems to have
occurred on a semi-fresh bone. A group of long superficial V-shaped
striations parallel to the length of the bone are located on the
central part of the piece. Two groups of sub parallel deep V-shaped
depressions, perpendicular to the length of the bones, are located
on the two extremities of the piece. These marks are typical of
bones used for retouching lithic artifacts (Patou-Mathis, 2002),
while the long striations correspond to scraping marks likely to
remove the periosteum or adhering tissue prior to the use of the
bone. The retouch marks are clustered and well delimited near both
ends of the piece with some marks partly covering the edge of the
fracture, likely indicating that the piece was used after the breakage
occurred and is likely “complete.”
From Sch€
oningen 12 II-4c1, a fragment of mid-shaft from a
metapodial of a medium size ungulate (likely a cervid-ID 17855)
shows a variety of marks of anthropogenic origin (Fig. 10). This
relatively small piece (6.6 cm long for 2.6 cm wide) presents several
short cut-like marks on the caudal side of the bone and a group of
longer marks on the opposite side that could all result from
butchery (Fig. 10D). The long marks are partly covered by two short
deep marks that resemble retouching marks. The helical fractures
suggest the shaft of the bone was broken while the bone was fresh.
In the middle part of the piece, two areas characterized by more
superficial though numerous and sometimes crossing marks,
correspond to scraping marks, likely from removing the perios-
teum. On the most proximal part, those marks seem to partly cover
Figure 5. Examples of taphonomical modifications observed on the bones from Sch €
oningen 12 II. (A) Carnivore modifications: possible claw marks (A1e2) and tooth marks (A3); (B)
Plant root etching; (CeD) Modifications resulting from sedimentary abrasion and/or water action. (Modified from pictures from A. Blanco, M.A. Julien).
M.-A. Julien et al. / Journal of Human Evolution 89 (2015) 264e286 273
a group of deep striations (Fig. 10B), as well being partially trun-
cated by V-shaped obliquely oriented depressions typical of bones
used as retouchers (Fig. 10C). The distal tip shows cortical micro-
flakes associated with localized smoothing and polishing, not
visible on any other parts of the piece, with the exception of a
highly localized polished area on the proximal tip (Fig. 10). These
marks likely result from a longitudinally applied force against the
distal tip of the bone (against both soft and hard material) and
handling at the proximal end. On the side of the piece, on the
exposed fractured edge, long longitudinal V-shaped striations are
visible. Made after the breakage of the bone, these are unlikely to be
related to butchering activities, but could result from the same
longitudinal movement that resulted in the creation of the flaking
and slight smoothing of the tip. Such localized wear patterns are
typically produced by the use of the tip of the bone (cf. Johnson,
1985).
In both cases, the fracture pattern seems to have occurred
prior to use on a fresh (17866) and a semi-fresh bone (17938).
The presence of scraping marks, likely corresponding to removal
of the periosteum prior to use, as well as the absence of cortical
scaled areas on the area used for retouching, tend to indicate
both bone blanks were also likely used while fresh or interme-
diately fresh (cf. Mallye et al., 2012; Abrams et al., 2014), while
the variety of types of wear patterns suggests multiple uses for
specimen 17866.
Anvil/Retoucher. From Sch€
oningen 12 II-4, a large proximo-medial
fragment of a radius of a large bovid (ID 17814) bears different
localized marks. On the cranial part of the proximal diaphysis, a
few short scraping marks seem to be associated with percussion
pits and several large notches with partially detached percussion
flakes (Fig. 11A). A large notch associated with a helical fracture is
also visible on the medio-caudal side (Fig. 11B). This seems to
indicate the bone was put on an anvil and fractured in a fresh
state. On the same caudal side, two possible short oblique cut-
marks are located on the epiphysis and the proximal part of the
diaphysis. On the anterior mid-shaft, numerous cut or scraping
marks are visible and seem to at least partly pre-date numerous
deep and very short V-shaped depressions that cover this area
(Fig. 11C). The depressions are not tightly clustered (unlike the
marks from the two retouchers described previously), though they
are restricted to the medial part of the bone and are clearly
distinct from natural taphonomic modifications by their V-shaped
cross sections, similar to thin and shallow retouching marks. A
distinctive smoothed edge is visible between the mid-part of the
impact area and the distal tip of the specimen, and a slightly
smoothed area is also present on both sides of the large caudal
notch. Other localized features include cortical flaking and
smoothing of the lower end (Fig. 11D).
These marks could result from the use of the bone as a passive
piece with actions of ‘chopping’as well as possible cutting with
sharp lithic material on the surface of the bone, though retouching
is also possible. The presence of the smoothed edges could result
from the rubbing of some material on the surface while chopping
occurred, or from a more active use of this piece in a grinding-like
movement.
Figure 6. Examples of ribs of large ungulates with cut marks from Sch€
oningen 12 II. Left (A): Horse rib (ID 17441) from Sch€
oningen 12 II-4, with three main areas presenting groups
of different kind of cut marks: A1 and A3) external side: deep, parallel, and short marks; A2) internal side: small, superficial, and oblique marks. Right (B): Large bovid rib (ID 17470)
from Sch€
oningen 12 II-2 with group of cut marks located on and near the neck of the rib; B1) internal side: group of long shallow oblique marks; B2) external side: group of deep
and short marks. Though not located on the same area on the ribs, the cut marks on specimens 17441 and 17470 likely correspond to similar butchery gestures, i.e., possibly from
evisceration (A2, B1) and defleshing (A1, A3, B2). (Modified from photos from W. Gerber, Uni. Tübingen; bar scales ¼2cm).
M.-A. Julien et al. / Journal of Human Evolution 89 (2015) 264e286274
Used-tip, smoothed-tip objects and pseudo-tools. Different ele-
ments with localized smoothing and flaking of the tip have been
recognized in the collections from Sch€
oningen 12 II-1 and 12 II-4.
Smoothed- and used-tip elements from 12 II-4 are composed
mostly of fragments of long bones of equids, but also of large bovid
and cervid long bones (Figs. 12 and 13). A single specimen coming
from 12 II-1 presents a localized flaked and polished tip, a distal
shaft of a cervid tibia (ID 17890) that resembles specimens from
12 II-4.
The specimens have the same elongated morphology, with
pointed or convex-smoothed tips (Figs. 12 and 13), with either
numerous cut and/or scraping marks on the cortical surface of the
bones (cf. Fig. 13A, B) or randomly oriented striations (e.g., 17868-
Fig. 13C) that suggest likely sedimentaryabrasionprior to the use of
some specimens.
Distinguishing polish/smoothing due to use versus taphonomic
origins can be challenging. Thus, determining if the bone was used
as a tool requires the differentiation of wear patterns created by
natural processes/taphonomic agents (such as water movement
and trampling) from anthropogenic modification. To establish a
possible anthropogenic connection, we examined the morphology,
as well as the macroscopic and microscopic patterning of use-wear.
Criteria of identification followed those based on experimental data
and archeological collections described in different studies, notably
d'Errico and Backwell (2003), Backwell and d'Errico (2008), and
Romandini et al. (2015).
Pointed elements present the same kind of pattern observed on
the distal end of specimen 17855 (Fig. 10), with small cortical and/
or medullar flakes; i.e., likely utilization flaking associated with
highly localized smoothing on the tip (Fig. 10A, B). As for specimen
17855, localized slight smoothing of the proximal ends was noticed
for specimens 17896 and 17816 (Fig. 13A, B). Convex-smoothed tip
elements show both low and high angled beveled tip edges (cf. ID
17870-Fig. 12; ID 17806, 17868, 18093-Fig. 13C). In most cases, the
proximal end is fresh (i.e., not abraded), but can also present a saw-
like breakage pattern (e.g., ID 17806, Fig. 13C) suggesting secondary
breakage on dry bone. The distal tips, by contrast, are highly
rounded and polished on both the external and internal surfaces,
but usually the smoothing is more clearly extended onto one of the
surfaces.
The use-wear present on the distal tips of the rounded-tip bones
shows a heterogeneous micro-topography with crossing and
transverse striations. Upon microscopic examination of the differ-
ential wear at high magnification (470), the polished surfaces
reveal fine parallel to sub-parallel striations (cf. Fig. 12A1 for
ID 17870; Fig. 13C for ID 17868). The patterning of the polish and
striations, confined to ½to 1 cm of the tip of each object, suggests
that these areas are polished due to anthropogenic action. This
pattern is similar to experimental bones used to rub hides (Buc,
2011). Although specimen 17896 is classified as a possible bone
tool, this specimen did not present microscopic scars that could
derive from anthropogenic use.
Micro-flaking, striations, differential polish, and loss of angu-
larity (or smoothing) correspond to use-wear categories usually
resulting from unintentional damage during use (Johnson, 1989),
while the slight smoothing present on opposite ends of some
specimens could correspond to unintentional wear while handling
the bones (cf. Figs. 10 and 13A, B).
A few other remains showing surface abrasion or polish have
been recognized as ‘pseudo-tools.’In these cases, contrary to the
specimens described previously as possible bone-tools, the
morphology of the break of the pseudo-tools was not changed by
the abrasion. Three of these bones for which the surface smoothing
was likely of natural origin did not reveal any microscopic evidence
of anthropogenic origin other than possible cut-marks: ID 17875,
17910 (both from 12 II-4c3), and 18109 (from 12 II-4c1). These
specimens were clearly distinguishable from the proposed bone
tools, and showed randomly oriented striations typical of sedi-
mentary abrasion (cf. Fig. 5 C, D).
Figure 7. Example of long bone with cut marks and spiral-like fracturefrom Sch€
oningen
12 II-4:cervid distal tibia (ID 18128) with parallel incisions on the medialmalleolus, likely
left during dismemberment. (Modified from photos from W. Gerber, Uni. Tübingen).
M.-A. Julien et al. / Journal of Human Evolution 89 (2015) 264e286 275
Figure 8. Horse distal metatarsal from Sch€
oningen 12 II-4c1 (ID 18122) showing deep incisions above the articular surface (A) likely left during skinning or disarticulation. On the
lateral side of the epicondyle, deep hack and flaking marks (B, C) likely result from the use of the bone as a percussor for stone tool production or maintenance. (Modified from
photos from J. Becher and W. Gerber, Uni. Tübingen).
Figure 9. Double retoucher on a fragment of metapodial of a large cervid from Sch€
oningen 12 II-2c1 (ID 17938), with close up on the areas used for retouching stone artifacts (A and
B). (Modified from photos from J. Becher, Uni. Tübingen).
M.-A. Julien et al. / Journal of Human Evolution 89 (2015) 264e286276
An interesting piece from Sch€
oningen 12 II-4c should also be
mentioned here: a large fragment of ivory bearing significant polish
(ID 17530, Fig. 14). In cross section, this ivory fragment shows
highly visible Schreger lines forming an angle characteristic of ivory
from the peripheral area of the tusk (Abelova, 2008). The general
shape of this ivory piece seems to indicate that it comes from the
mid part of a large tusk, rather than the tip or the proximal part. The
cementum is missing, suggesting that this piece was already dry or
fossilized and that some splits fell off before the different traces
visible on the surface occurred.
The specimen shows two axial breaks on each of the side. Ex-
amples of large pieces of ivory broken by elephants during theirlife
are known in the modern record (Palombo et al., 2010), and thick
fragments from the medial part of the tusk have been observed in
such situations (Haynes, 1988, 2006). However those show
different patterns, with less wrinkly flat fracture surfaces and more
helical-like general morphology of the break in comparison to the
present specimen, although quite long and flat specimens have
been reported in the fossil record (Villa and d'Errico, 2001). Both
surfaces are rough with no signs of post-breakage dentine growth;
there is no evidence that this ivory may have healed from a
breakage during the elephant's lifetime. The ripple texture of the
larger flat surface seems more characteristic of axially split tusks
from drying rather than from human induced-splitting (cf.
Khlopachev, 2006; Khlopachev and Girya, 2010). The outer split
surface is more difficult to interpret, though it might result from the
same process (i.e., drying out of the tusk). This split is not complete
and ends with a bending fracture on the lower half of the piece.
Although it cannot be totally excluded that this ivory piece might
have been intentionally broken from a sub-fossil tusk, the specimen
shows no clear evidence of it. No grooving or knapping traces are
visible on the surface.
The piece presents different degrees of polish over much of the
outermost and flat innermost surfaces. The proximal internal
surface is relatively unmarked. By contrast, the distal portion is
heavily polished on both the flat innermost and particularly the
outermost surface. The polish is mainly located but not restricted
to elevated areas, and this suggests contact against a relatively soft
material. The tip is highly polished and slightly beveled, with no
signs of chipping or fracture, suggesting that the polish took place
under static or low dynamic loading and in contact with a rela-
tively soft or fine material. Heavy dynamic loading such as impact
would likely have left visible fracturing or flaking of the ivory
surface, features that are absent here, however parallel micro-
striations observed on both sides of the tip (Fig. 14 A, B1) could
indicate use.
Figure 10. Mid-shaft of a metapodial of a medium size ungulate from Sch€
oningen 12 II-4c1 (ID 17855) showing a possibly utilized tip (distal part-A1, A2), an area used as a
retoucher (proximal part-C), as well as deep (B) and shallow incisions (D) and interpreted as a multi-purpose tool. (Modified from photos from J. Becher, Uni. Tübingen).
M.-A. Julien et al. / Journal of Human Evolution 89 (2015) 264e286 277
On the proximal portion of the outermost surface, there is a cluster
of thin parallel striations that are not associated with the polish seen
toward the distal end,as well as randomlyoriented marks(Fig. 14 C, D).
Their appearance matches well with sedimentary abrasion observed
on other specimens from the site. If we assume this specimen could
have been only partly buried, the marks observed seem to at least
partly result from the action of sedimentary particles in a moving
water environment on the part exposed.
Figure 11. Large bovid radius from Sch €
oningen 12 II-4c3, Plateau 6 (ID 17814) showing two opposed percussion marks on the anterior (A) and posterior (B) sides, typical of human
impact fractures. Note the percussion flake attached to percussion area A and the probable percussion pits just below the percussion area A, probably resulting from previous failed
attempts to break the bone open (indicated by the arrows). On the mid-shaft (C), numerous deep and short depressions associated to a localized smooth edge could indicate the
bone was used as an anvil and/or as a retoucher. The distal tip (D) shows large cortical flaking and smoothing. Scale bars ¼2 cm. (Modified from photos from J. Becher and W.
Gerber, Uni. Tübingen).
M.-A. Julien et al. / Journal of Human Evolution 89 (2015) 264e286278
5. Discussion
The Sch€
oningen Middle Pleistocene archeological deposits
provide a well-preserved faunal and environmental record that
allows a detailed, multi-proxy analysis of this Lower Paleolithic
archeological locality. The combination of geoarcheological, taph-
onomic, zooarcheological, and use-wear investigations at the
Lower Paleolithic site complex of Sch€
oningen 12 II allow the
identification of the processes and agents implicated in the for-
mation and modification of the different faunal accumulations at
this interglacial lakeshore, and the identification of bones used as
possible tools by pre-modern hominins.
5.1. Schöningen 12 II faunal assemblages
The faunal assemblages from Sch€
oningen 12 II-1, 2, and 4 are
typical of interglacial Middle Pleistocene contexts from north-
western Europe (Schreve, 2001). They are similar to the ones re-
ported for the nearby site complex of Sch€
oningen 13 II, confirming
the geological recognition of the layers and overall geological
synchrony of the deposition of the bones (cf. Van Kolfschoten, 2014;
Starkovich and Conard, 2015). The three main assemblages studied
show a clear anthropogenic input, but greater in 12 II-4 (Table 4).
Different mammal species (at least cervid, large bovid, and equids)
were processed and likely consumed, and some bones possibly
used as tools, showing an intense exploitation of the animal car-
casses. The lack of burned bones could be partly due to the specific
dark coloration of the remains, making the recognition of possible
burned bones difficult (cf. Rabinovich and Biton 2011) and/or to the
lack of the smallest fragments from the collection (due to the
absence of sieving). In Sch€
oningen 13 II, however, where sieving has
been performed, no burned remains have been recognized as well,
and recent examination of the sediments and artifacts from 13 II-4
shows that evidences of controlled fire is lacking on the excavated
area (Stahlschmidt et al., 2015b). The micro charcoal record seems
to indicate however that burning may have occurred at some dis-
tance from the depositional site (Urban and Bigga, 2015; Kunz et al.,
Submitted for publication). We propose that the lack of burned
material at Sch€
oningen 12 II could therefore result from 1) a spatial
or taphonomical bias, 2) the consumption of rawproducts, or 3) the
absence of consumption of the carcasses at the site (which is more
unlikely considering ethnographical accounts of butchering
events).
The different bone assemblages from Sch€
oningen 12 II-4 provide
evidence for slightly different taphonomic histories, which is in
agreement with the information deduced from the geo-
archeological study (cf. supra). Moreover, the limited number of
faunal remains in sub-layers 4c3 and 4c2 in comparison to 4c1
could account for either (1) a difference in function or intensity of
use of this area of the paleolake by humans, (2) a location at the
margin of the human occupation, or (3) a partial removal of the
remains by water or other taphonomic agents.
No remains from the Plateau 4e12 II-4 present signs of abra-
sion or rounding that would account for water action. Conversely
in Plateaus 5 and 6, sub-layer 4c3 has indications of water
modification of some of the bones, which could account for
multiple sources of the remains, i.e., a mix of anthropogenic and
natural origin (with possible water transport), or to a different
Figure 12. Possible bone artifact from Sch €
oningen 12 II-4c1, Plateau 6 (ID 17870) on a horse radius fragment,interpreted as a smoother. The cortical surface presents different marks
of various size and orientation (B(-black arrows indicate large chop-like incisions)), as well as two (possibly three) notches corresponding to impact areas (B-black stars). On the
distal tip, a heavily smoothed and polished area is restricted to the medullary side of the bone and does not extend over 15 mm (A2); parallel micro-striations are visible at high
magnification (A1). The cortical side of the tip is slightly rounded but does not present clear smoothing. (Modified from photos from J. Becher, C. Fuchs, B. Hardy).
M.-A. Julien et al. / Journal of Human Evolution 89 (2015) 264e286 279
hydrological system at the time of sedimentary deposition, as
suggested by the more gravelly to sandy component reported in
4c3 (cf. supra). Considering the estimated original topography of
the hydrological basin (Lang et al., 2015), the geoarcheological
data, and the clustering observed for the remains of aurochs in
layer 4c (P4), it is likely that P6 was closer to the lakeshore than
was P4. Assuming that human activities originally took place on
the shore, this could account for some relocation of the bones and
Figure 13. Possible bone artifacts from Sch€
oningen 12 II-4c1 (ID 17896, 17816, 17868, 17806) and 4c1/c3 (ID 18093), Plateau 6 exhibiting features characteristic of human-induced
modification through use. (A, B) Specimens with pointy-tips, showing flaking associated with localized smoothing. Note the slight smoothing on the opposite side, likely resulting
from handling. (C) Convex-smoothed tip elements, with detail of micro-wear observation of ID 17868 showing parallel micro-striations. Note the similar size and shape of the
blanks of the three specimens, likely chosen for their handiness. (Modified from photos from J. Becher, W. Gerber).
M.-A. Julien et al. / Journal of Human Evolution 89 (2015) 264e286280
possibly repeated movement of some of the bones by waves for
P6, particularly for 4c3. If water movements affected the bones
from the other layers and sub-layers studied, the intensity was
likely less than the one recorded in 4c3, which is in agreement
with the apparent sub-littoral lacustrine depositional environ-
ment recovered particularly from the above sub-level 4c1.
The 4c remains, however, are likely only a part of what would
have been the original site. Some of the remains could have been
abandoned on the shore and washed up by the former lake “tides.”
It is also possible that they correspond at least partly to refuse that
was thrown into the lake. In light of the evidence collected so far,
we consider the second and last hypothesis (or a mix of them) as
the more likely here. This could also at least partly explain the
limited amount of stone artifacts recovered at the site. However,
special purpose sites such as kill and butchery sites are also known
to offer limited amounts of lithic artifacts in relation to bone re-
mains (cf. Isaac, 1971; Julien, 2007; Julien and Krotova, 2008).
Recent investigations of the Horse Butchery Site of Sch€
oningen
13 II-4 have proposed that the bone bed resulted from the accu-
mulation of different events (Julien et al., 2015; Rivals et al., 2015).
Here, the limited proportion of remains, and particularly the low
proportion of dental remains, did not allow investigation of the
seasonality of death of the animals, but our analysis highlights the
integrity of the different sub-layers recognized in the field that
represent different taphonomical histories and slightly different
modes of accumulation. Moreover, the possible use of sub-fossil
remains and the different nature of the depositional events recor-
ded at Sch€
oningen 12 II-4 (with a mix of both, natural and
anthropogenic bone accumulation) allows us to propose that the
bone assemblages of at least 12 II-4c results from multiple accu-
mulation events.
In this context, and considering the relatively limited number of
remains examined here, the exact function of the site is difficult to
ascertain. Nonetheless, the activities represented suggest that
butchering, processing, and likely primary consumption of animals
occurred (with at least marrow snacking), corresponding in all
likelihood to a butchering/processing site. The different activities,
the apparent repetitive use of the site, and the use of bones for
different kinds of activities suggest that hominins used the area for
a realtively long period of time, and likely repeatedly (at least
during the time record that corresponds to the deposition of the
different layers and sub-layers considered here).
5.2. Toward the definition of the diversity of the Lower Paleolithic
bone industry
Bone retouchers, percussors, and possible anvils have been
identified in the material from Sch€
oningen 12 II-2 and 12 II-4. In
addition, numerous specimens from 12 II-1 and 12 II-4, for which
morphology and marks characteristic of use have been observed,
are considered here as possible tools and described as ‘used-tip’
and ‘smoothed-tip’objects.
Legrand and Sidera (2007) note that different marks are visible
after only a few minutes of use (scratches, surface polish or color-
ation, and flaking), while deformation and smoothing of the shape
of the object occur after a longer period of use. Therefore, it could be
proposed that the differential wear observed on the used- and
smoothed-tip objects reflects different intensity of use of the bones
for a similar gesture or task, with smoothed-tip objects corre-
sponding to a more advanced stage of modification of the
morphology of the tip of the objects. However the morphology of
those two types of remains is quite different, with the used-tip
Figure 14. Large ivory fragment with flat ‘removals’and smoothed tip from Sch€
oningen 12 II-4c, Plateau 5 (ID 17530) and details of use wear analysis. The specimen measures ca.
31.9 7.3 cm for 516 g. Smoothing and polishing are common on the outermost side (A) and limited to the tip of the specimen in the most internal side (B1eB2), parallel micro-
striations are visible at high magnification. Sedimentary abrasion is visible on the largest outermost area (C, D). Surface modifications of this specimen result likely from a complex
taphonomical history. (Photos: C. Fuchs, NLD, and B. Hardy).
M.-A. Julien et al. / Journal of Human Evolution 89 (2015) 264e286 281
objects clearly less elongated than the smoothed-tip ones. On the
used-tip objects, the micro-flaking also suggests a more heavy
dynamic loading involving some kind of impact against hard ma-
terial, while smoothing involves contacts against a soft material.
Therefore, a different function of those objects is more likely.
Similar broken bones to the ‘used-tip’objects have been success-
fully used as expedient tools for butchery activities, notably for
detaching muscles or slicing frozen meat, producing the same kind
of wear patterns on the tip of the bone as those from here (cf.
Stanford et al., 1981; Frison, 1991; Johnson and Bement, 2009).
The smoothed-tip artifacts are similar in morphology and wear
patterning to the bone tool type known as smoothers (or lissoirs).
Usually, but not always, made of rib fragments, smoothers are most
often considered tools used to smooth hides in order to make them
tougher, less permeable, and more burnished (Semenov, 1964;
Julien et al., 2011; Soressi et al., 2013). Smoothers are known
from Upper Paleolithic (late Upper Paleolithic: Averbouh and
Buisson, 2003; Gravettian: Lacarri
ere et al., 2015; Aurignacian:
Leroy-Prost, 1975, 1979; Ploux and Soriano, 2004;Proto-
Aurignacian: Julien et al., 2002; Tejero and Grimaldi, 2015; Cha-
telperronian: d'Errico et al., 1998; Baffier and Julien, 1990) and
Middle Paleolithic (Soressi et al., 2013) contexts but have rarely
been reported from the Lower Paleolithic (for a possible exception,
see Stekelis, 1967). All used- and smoothed-tip bones from
Sch€
oningen 12 II were located in the same area of P6 in the sub-
layer 4c1; none of them were found inside or near the main con-
centration of aurochs remains in area P4 (Fig. 1B).
Other specimens (including a large smoothed fragment of ivory)
could have been used by hominins, but result more likely from
natural modifications or a mix of the two. The large ivory fragment
was located in an area of lower concentration of remains (in P5)
between the aurochs bones concentration (in P4) and the main the
main area P6 (Fig. 1B). With the exception of flaking on large pieces
of ivory discovered in late Middle Paleolithic layers of the Barma
Grande cave at Grimaldi, no clear tools made on ivory have thus far
been recognized for assemblages pre-dating the Early Upper
Paleolithic (Onoratini et al., 2012). Identifying anthropogenic
modification on ivory is more difficult than on bone and no
comparative experimental use of large ivory fragments exists. This
specimen could have been used as suggested by the use-wear
analysis, but considering the complexity of the piece (at the
macro-scale), the context of discovery (i.e., isolated element found
in proximity to an apparently naturally deposited carcass), and the
difference in size and morphology with the other possible bone
tools identified, we cannot exclude that at least part of the traces
observed are of natural origin.
Known bone tools from Lower and Middle Paleolithic contexts
seem largely found in large mammal and megafaunal butchering
sites and related to butchery activities (e.g., Stout et al., 2014;
Boschian and Sacc
a, 2015; Zutovski and Barkai, 2015). If at least
part of the bone tools reported here were used during butchery
and carcass processing (or related activities), this could partially
explain the limited amount of lithic remains recovered at
Sch€
oningen, though this does not account for the relatively large
quantity of cut marks identified on the surface of the bones.
Different types of materials, including shells, ‘hard’plants, or
bones, are known to be suitable for butchering activities (e.g.,
Toth and Woods, 1989; Choi and Driwantoro, 2007; West and
Louys, 2007; Johnson and Bement, 2009). Such material may
have been available to and used by Sch€
oningen hominins, which
could at least partly explain the variety of cut mark shapes
recognized on the bone surfaces. Similarly, considering the lack of
large stones on the excavated area of Sch€
oningen, bones with
robust ends may have been used for breaking up other skeletal
material for dismemberment and/or marrow extraction, which
could explain the occurrence of intentional green bone breakage
at the site.
In the Sch€
oningen 12 II assemblage, none of the described ob-
jects have been clearly manufactured by hominins. Fresh and semi-
fossilized bones seem to have been used as raw material for
expedient use. Use-wear analyses performed on the flint artifacts
from Sch€
oningen demonstrate woodworking, hide working,
butchery, and plant processing. A few artifacts show possible use on
bone, but this could occur during butchery or from the use of a bone
retoucher (Rots et al., 2015). However, a number of the specimens
identified as bone tools show scraping marks and clear percussion
notches. This repeated evidence of scraping off the periosteum
prior to percussion and/or use could suggest that breakage was
performed with the intention of producing a blank, a cutting edge
and/or a pointed break. If this were the case, this would account for
some intentionality and potentially signify ‘manufacturing’here. In
addition, the deep striations located on the proximal end of spec-
imen 17855 (Fig.10B) seem to have occurred prior to the retouching
marks. Such deep parallel striations have not been recorded on any
other bones from the studied collection and could correspond to a
preparation of the functional area of the tool, prior to the use as a
retoucher, or to the cleaning or preparation of the edge of the lithic
tool itself. Moreover, specimen 17938, the only remain of very large
cervid from layer 12 II-2, seems to have been collected and broken
in a semi-fresh state, and possibly brought into the site as a blank.
Soft hammers, percussors, and retouchers made of bone (more
rarely antler) are frequent in the Middle and Lower Paleolithic re-
cords, and notably in Sch€
oningen 13 II-4 (Voormolen, 2008; Van
Kolfschoten et al., 2015; Serangeli et al., 2015b), but bone tools
from the Lower and Middle Paleolithic are usually quite isolated
finds. Here, in addition to the typical percussor and retoucher, at
least three new types of bone tools have been recognized (i.e.,
anvil-like, used-tip and smoothed-tip objects, as well as multi-
purpose tools), making of Sch€
oningen 12 II likely the most
diverse pre-Upper Paleolithic bone tool assemblage. For the large
fragment of ivory reported here could correspond to the earliest
possible evidence of the use of this raw material, though a more
detailed study involving experimentation will be necessary before
rejecting the possibility that it is an ecofact. So far, no typical Lower
Paleolithic bifacially retouched bone has been recognized at
Sch€
oningen. Those elements are usually made on and associated
with proboscidean remains (Segre and Ascenzi, 1984; Boschian and
Sacc
a, 2015; Zutovski and Barkai, 2015). The scarcity of probosci-
dean remains at Sch€
oningen may explain the absence of this typical
Lower Paleolithic bone tool in this assemblage.
The artifacts reported here are considered expedient tools since
most of them show no evidence of clear shaping of the bones.
However, we argue for a degree of intentionality in the choice and
possible transport and shaping or preparation of certain specimens.
Middle Pleistocene hominins seem to have taken advantage of the
different properties of the bones, using dense and sharp epiphyses
for flint knapping or breaking bones, rounded surfaces of long
bones for retouching lithic tools, pointy elements for defleshing
and/or processing soft materials, flat surfaces for cutting and/or
chopping (and rubbing?), and when needed, even used the same
element for performing at least two different tasks (Fig. 15). This
corresponds (to our knowledge) to the earliest evidence of the use
of multi-purpose bone tools. In addition, the diversity of types of
bone tools, likely corresponding to the possible diversity of use,
suggests that these elements, although expedients, might form an
industry in the same way as Lower Paleolithic lithic tools. More
work, especially experimentation and systematic use-wear anal-
ysis, will be needed to fully understand the chaîne op
eratoire and
possible multiple functions of those different objects. However, the
current study suggests that Late Lower Paleolithic hominins' bone
M.-A. Julien et al. / Journal of Human Evolution 89 (2015) 264e286282
tool repertoire may have been more diverse than previously
thought.
6. Conclusion
In this paper, we have examined multiple lines of evidence to
investigate the processes involved in the formation and mod-
ificaton of the faunal assemblages from the Middle Pleistocene
open-air locality of Sch€
oningen 12 II. The quality of the preservation
of organic material, including osseous remains, provided the op-
portunity to examine the possible use of bone as raw material
during the late Lower Paleolithic.
Some elements of the collection, including a concentration of
aurochs bones located on Plateau 4 of Sch€
oningen 12 II-4, were
inferred to have a natural origin as suggested by their restricted
spatial distribution (i.e., clustered in one area) and the absence of
clear human intervention. On the other hand, the material found in
Plateau 6 of Sch€
oningen 12 II-4, 2, and 1 were primarily of
anthropogenic origin, as deduced from the occurrence of butchery
marks, intentional green bone breakage, and the presence of
possible bone tools. The combined evidence suggests that intense
butchery and carcass processing occurred at the sites.
We propose that bone was used for different domestic activ-
ities, including stone tool production and curation, as well as
butchering and processing activities. While most remains seem to
represent expedient tools, a clear choice is manifested in the se-
lection of raw material depending on the anticipated use, and a
basic shaping or preparation of some artifacts is possible here.
This conclusion is supported by the substantial number of bone
tools and tool types that represent what we propose as a Lower
Paleolithic bone industry. The outstanding context and preserva-
tion of the faunal remains at Sch€
oningen foster the high quality
observations needed to identify previously unrecognized kinds of
artifacts.
Bone has undoubtedly been used for a variety of purposes at
Sch€
oningen (Voormolen, 2008; Van Kolfschoten et al., 2015) and
additional investigations of the material from the many sites at
Sch€
oningen and other Lower Paleolithic localities will provide
further insights into the diversity of organic technologies that were
part of the daily life of Middle Pleistocene hominins. Such well-
preserved archeological assemblages continue to allow us to
refine our understanding of the complex nature of human/animal
relationships during the Middle Pleistocene. While the use of bone
tools does not, in and of itself, prove advanced cognitive evolution
of the Sch€
oningen hominins, the new artifacts presented here
greatly expand the number and range of bone tools known from the
Middle Pleistocene. In this way, they open new avenues for the
study of the technology and economic behavior during this period.
Assuming that these technologies are not entirely unique to
Sch€
oningen, we suspect that future research will document com-
parable finds from other sites of similar age.
Acknowledgments
M.-A. Julien received support from the Fyssen Foundation and
the Arts and Humanities Research Council (AHRC grant AH/
K000378X/1). Analyses were supported by the Deutsche For-
schungsgemeinschaft (DFG) reasearch project CO 226/22-1, the
Lower Saxony State Service for Cultural Heritage and the Ministry of
Science and Culture, Hannover, Germany (B. Urban,
Figure 15. Proposition of typo-functional categorization of the possible osseous artifacts from Sch€
oningen 12 II. Soft materials include animal (skin, meat, viscera, tendons, etc.) and
vegetal (bark, fibers, etc.) resources. White ¼bone, gray ¼ivory, ? ¼specimen with unclear anthropogenic origin of the modifications.
M.-A. Julien et al. / Journal of Human Evolution 89 (2015) 264e286 283
PRO*Niedersachsen, Projekt: 74ZN1230). Many thanks to L.
Bement, K. Carlson, E. David, N. Goutas, G. Haynes, C. Houmard, G.
Khlopatchev, M. Patou-Mathis, S. Parfitt, S. P
ean, Starkovich, E.
Tartar, C. Vercout
ere, and S. Wolf for the helpful discussions. We
would like to thank S. Ali, J. Becher, A. Blanco-Lapaz, C. Fuchs, W.
Gerber, T. Rein, and T. Schmid for their assistance and help with the
organization of the bone material and the figures. We thank two
anonymous reviewers for their useful comments on an earlier draft
of the manuscript.
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