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El sitio Pilauco, Pleistoceno tardío, Osorno, Chile.

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Mario Pino Ximena Navarro-Harris , Rafael Labarca , Martín Chavez-Hoffmeister , Omar Recabarren , Patricia
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Canales & Ricardo De Pol Instituto de Ciencias Ambientales & Evolutivas, Universidad Austral de Chile;; Departamento
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de Antropología, Universidad Católica de Temuco; Programa de Doctorado Universidad Nacional del Centro de la Provincia
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de Buenos Aires; University of Bristol, School of Earth Science, U..K; Departamento de Oceanografía, Universidad de
Concepción, ricdepol@udec.cl.
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E-mail: mariopino@uach.cl

Resumen. El sitio Pilauco está ubicado en la ciudad de In a new approach, “exit”, Dillehay (2008) proposed to
Osorno (40º34’12’’S, 73º06’13’’W). En el Pleistoceno tardío understand cultural developments between the late
estuvo dominado por una asociación vegetacional de Pleistocene and early Holocene analyzing the early
parque norpatagónico, tal como Monte Verde. Se han rhythms towards social complexity. In this approach, the
recuperado 718 huesos de vertebrados extintos y extantes,
emphasis is given to site location studies, paleo-faunal and
30 dientes y 11 coprolitos. Tafonómicamente se registran
procesos de carroñeo, pisoteo y reacomodación por -floral studies, seasonality, mobility and sedentism, and
crecidas fluviales esporádicas. principles of organization”. Our work, till in a primary
14 phase, is towards this direction.
El sitio comenzó a formarse hace 13.470±35 años C A.P.
Posteriormente se desarrolla un pantano sobre “ox-bow
lake”. La turba PB-7 contiene los restos paleontológicos y 2 Results
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arqueológicos (13.220±60 - 11.004±186 años C AP). Las
familias de vertebrados representadas son
2.1 Stratigraphy, Sedimentology and Age
Gomphotheriidae, Equidae, Camelidae, Cervidae,
Mylodontidae, Mephitidae, Muridae y Myocastoridae. Los
artefactos líticos de basalto, andesita y obsidiana que It is possible to recognize two geomorphologic units, each
registran los humanos tempranos se encuentran solamente one with their own sets of beds. To the north the site is
en algunas unidades de excavación, asociadas a altas limited by hills deposited by a major acid to intermediate
concentraciones de huesos. Se presentan la estratigrafía, volcanic Andean regional activity. These volcanic
sedimentología, paleontología, arqueología y tafonomía del processes deposited a series of volcanoclastic flows,
sitio, basado en un gran conjunto de fechas grouped under “Secuencia piroclástica – epiclástica San
radiocarbónicas. Pablo” (Pérez et al., 2003). The age of this unit is
equivalent to the Valdivia interglacial. In Pilauco six beds
Palabras Claves: norpatagonia chilena, megafauna,
compose the hill. The PB-1 to PB-6 layers correspond to
hombre temprano, paleontología, arqueología.
volcaniclastic and terrigenous sediments (Fig. 1). To the
south of the hill four sedimentary beds originated a
1 Introduction floodplain. Over the eroded and channelized top of PB-1
bed, well-sorted coarse gravel originate PB-6 layer. Above
In the Intermediate Depression of south-central Chile sites these PB-7, -8 and -9 layer are located, forming well-
containing megafauna are frequently found by chance, defined horizontal strata. The first two are composed by
(until today 13 sites, Recabarren 2007). Usually the only peat including gravel clasts (mode 2-3 cm diameter, 0.5 -
remains recovered are the molars and tusks of 16%) dispersed in a fine matrix (sand 13.4 – 36.9%; mud
gomphotheres. In 1986 a company was carrying out 33.1 - 53.4% and 11 - 32% total organic carbon mater).
excavations in Pilauco, a suburb of Osorno city (40°34’S- This kind of texture can originate in a swamp that has
73°07’ W). They found megafauna bones, classified as developed over a former ox-bow lake invaded sporadically
mastodon and horse, kept today at the History Museum of by river overfloods. No percussion marks were found in
Osorno. Recabarren (2007) concluded that molars and the aphanitic basalts, which is a typical indicator of high-
tusks of the Pilauco Gomphothere, as well as Gomphothere velocity energy and impact.
remains from the other 12 sites, belong to Stegomastodon The fossils of mammalian fauna and birds are associated
platensis. An exploratory project was developed between exclusively to the PB-7 layer, dated between 13.220 ± 60
November 2007 and November 2008, excavating 41 m2. and 11,122 ± 178 years B.P. The pure peat PB-9 layer
(Pino, 2008). Today we know a) the site is located in a seals the site.
wetland dating from late Pleistocene - early Holocene; b) a
large amount of this space (about 2 ha) was not used for 2.1 Record of vertebrates
house building and is then available for excavations; and c)
in the site individuals from 7 mammal families were Gomphotheriidae bones are the most abundant identified
registered. Megafauna was found coexisting with extant vertebrate remains. The specimens found in 1986
mammals. Bird bones, pollen, diatoms and parasites were correspond to a left hemimandible with m2 and m3
also recovered. inserted, a right hemimandible with m3 inserted, an

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isolated m2, a right humerus, three thoracic vertebrae, a
partial spinous process, and a fragment of skin. During the
2007-2008 campaign were obtained mostly vertebrae, the
atlas, ribs, two scapulae, and pelvic elements. During the
2010-2011 season, a high concentration of elements be was
found. Ribs exhibit the highest abundance. A tibia, tarsal,
vertebrae, molars and a skull were also excavated. It is
worth noting that small tusk fragments were found in the
surrounding grid squares, which suggests a high degree of
fragmentation or shattering. The finding of a second atlas
confirms the presence of at least two individuals in the
deposit. After Recabarren (2007) the Chilean
Gomphotheriidae remains registered south of 39º30’,
including the Pilauco specimens, and classified them as
Stegomastodon. platensis based on molar measurements
following Alberdi and Prado (1995) and Frassinetti and Figure 1. Schematic stratigraphy of the Pilauco site. PB-1:
Alberdi (2005) taxonomic proposal. Lapilli tuff. PB-2: Lapilli tuff with abundant volcanic ash matrix.
Ungulates are the second most abundant mammal remains PB-3: Lapilli tuff with medium sand matrix. PB-4: Volcanic ash.
found in the Pilauco site, represented by the families PB-5: Terrigenous coarse sand, with scattered angular pebbles.
Equidae, Camelidae and Cervidae. The horse record of the PB-6: Gravel composed by clasts ranging from 1 to 15 cm in
site includes 15 specimens attributed possibly to Equus diameter. PB-7: Peat with very dark brown matrix (10YR 3/1)
(Amerhippus) andium (Recabarren et al., 2011), belonging including isolated gravel clasts up to 7 cm, poorly selected. Rest
to at least three individuals. These are the southernmost with erosion unconformity over PB-2 and PB-6. PB-8: Peat very
records for the genus Equus, which expands its distribution similar to PB-7, but slightly more brown in color (2.5Y 4/2) and
without fossils. PB-9: Black peat (2.5 Y 2/0). PB-7 and 8
from 38º S to 40º S in the Chilean territory. interfinger with gravel and sand layers to the south.
Camelids are locally represented by skeletal and dental
remains including a metatarsal and metacarpal shaft, a
astragalus, a fragment of tibia, an isolated canine tooth, 2.2 Taphonomy
and a coxal. The fossils are temporarily assigned to cf.
Hemiacuhenia paradoxa Gervais & Ameghino 1880 There are clear field evidences of extinct and extant bone
(Labarca and Pino, 2010). Hemiauchenia has not been elements concentrating in the PB-7 level, between 350 and
recorded previously in Chile. 450 cm of local altitude, which is within the 14,680 and
An isolated vertebra is the only available record of 13,029 calibrated ages. Only one small rodent and two bird
Cervidae in the Pilauco site (Fig. 2). A detailed fragments were obtained. No fish, amphibian or reptile
morphological comparison with anatomical elements of remains have been found, although systematically search.
various representatives of the family suggests that the The local accumulation of large megafauna bones suggests
specimen belongs to Pudu puda, the only confirmed record that in PB-7, characterized by fine and organic textures,
of this species for the Pleistocene (González et al., there was no fluvial displacement of the carcass. This is in
unpublished results). accordance with the relative anatomical consistency of
Xenarthra is represented by isolated 11 sloths osteoderms. some bones (e.g. atlas and skull). An initial study of the
These dermal ossicles allow by first time confirmation of marks on the bones of mammals has been performed. At
the presence of this group in the region. least four types of modifications were possible to detect:
An isolated cranium belonging to the genus Conepatus carnivore marks, roots, trampling and abrasion (i.e.
represents the carnivores. This is the first fossil record of Labarca, 2009). Trampling marks are the most abundant
the family Mephitidae for the Pleistocene in Chile and are characterized for being mainly superficial, with
(González et al., 2010). Recently, an isolated molar with a irregular sides, winding forms and random orientations.
highly worn crown has also been registered. The Such marks are registered both on gomphotheres as
morphology of the molar discards the assignation to the ungulates bones. Carnivore marks concentrated exclusively
herbivores described in the site (Aguilera et al., 2011). on gomphotheres bones. The abrasion marks have been
According to the authors the molar presents considerable observed up to now only in the bones of camelids.
degree of wear on its occlusal surface, therefore it is not High buoyancy of small and pneumatic bones could
possible to recognize the metacones and paracones. explain the absence of remains of small animals. Another
Aguilera et al. (2011) assigned the molar to Ursidae indet. explanation is related to the acidic pH of the swamp water
The presence of rodents is limited to two taxa. Dental and peat, were the thin calcareous material can be
pieces confirm the presence of the genus Myocastor (Pino, dissolved. Predators could also have played a role in the
2008). The presence of Loxodontomys micropus has also distribution of body parts often seen on the site, consuming
been confirmed through a cranium fragment (Canales, small bones and / or moving anatomical units into their
2010). burrows (i.e. Martin, 2008). This scenario, however, does
not explain the absence of other large anatomical units of

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gomphothere in the site, such as tusk, humerus and femurs.
Considering the human presence on the site, actually it is Alberdi, M.T., Prado, J L. 1995. Los mastodontes de América del Sur,
In: M.T. Alberdi, G. Leone & E.P. Tonni (Eds.). Evolución
not possible discard the possibility of selective transport of
biológica y climática de la Región Pampeana durante los últimos
anatomical units by hunter-gatherers to other areas. 5 millones de años. Un ensayo de correlación con el
Mediterráneo occidental, Monografías, Museo Nacional de
2.3 Archaeology Ciencias Naturales, CSIC, Madrid. pp. 277-292.

Andrefsky, W. 1998. Lithics. Macroscopic approaches to analysis.


The Pleistocene human population that inhabited the Cambridge Manuals in Archaeology . Cambridge University
Pilauco region, within a north Patagonian park landscape, Press, Cambridge. 322p.
must have felt attracted by the presence of an enclave rich
in resources located in an ecotone of hills, floodplains and Canales, P. 2010. Identificación de roedor fósil del Pleistoceno
swamps. The archaeological analysis has allowed us to Superior, sitio paleontológico Pilauco, Osorno, Chile.
Unpublished Tesis, Licenciado en Ciencias Biológicas, UACH
isolate a total of 101 intentionally modified lithic pieces. 68 p.
These are represented by fine grain basalt and dacitic
obsidian cores; artifacts for scraping and cutting in basalt, Frassinetti, D., Alberdi, M. T. 2005. Presencia del género
quartzite and dacitic obsidian with unifacial marginal Stegomastodon entre los restos fósiles de mastodontes de Chile
trimming, and principal chipping waste material (i.e. (Gomphotheriidae), Pleistoceno Superior. Estudios Geológicos,
Andrefsky, 1998). The basalt and quartzite were selected 61: 101-107.
from pebbles available in the deposits of the ancient local González, E., Prevosti, F., Pino M. 2010. Primer registro de
river. In contrast, the dacitic obsidian was collected in the Mephitidae (Carnivora: Mammalia) para el Pleistoceno de Chile.
volcaniclastic deposits in the northern hill. The reduced Magallania, 38(2): 239-248.
lithic collection is coherent with records from other
Southern Cone and Patagonian early sites (i.e. Nuñez et González, E., Labarca, R., Chávez, M. Pino. Unpublished results.
al., 1994) First fossil record of the smallest deer Pudu puda Molina 1792
(Artiodactyla, Cervidae) in the late Pleistocene of South
America.
3 Conclusions and Discussion
Labarca, R. 2009. El yacimiento paleontológico "Kamac Mayu":
The PB-7 layer containing cultural and paleontological tafonomía y procesos de formación en el Cuaternario kárstico de
la cuenca de Calama (Región de Antofagasta-Chile).
remains in Pilauco was generated by a palustrine peat Ameghiniana 46 (1): 3-16.
deposition event, following the retreat of a meander of the
local ancient river. The swamp received fluvial overflows Labarca, R., Pino, M. 2010. Nuevos antecedentes sobre los Lamini
in many occasions, which resulted in presence of isolated fósiles (Artiodactyla: Camelidae) del Pleistoceno Superior en el
gravel in the peat matrix, within a low kinetic energy extremo sur de Chile (30º-42ºS). Resúmenes, II Simposio
environment. This simple stratigraphy in Pilauco, as well Paleontología en Chile (Concepción). p. 67.
as the described deposition environments, is more similar Martin, F.M. 2008. Bone crunching felids at the end of the
to Tagua-Tagua than Monte Verde. The faunal collection Pleistocene in Fuego-Patagonia, Chile. Journal of Taphonomy 6
present in Pilauco is consistent with the described millieu, (3-4): 337-372.
with dominance of animals associated to open
environments, presence of freshwater species and Nuñez, L.; Varela, J.; Casamiquela, R.; Schiappacasse, V.; Niemeyer,
H., Villagrán, C. 1994. Cuenca de Taguatagua en Chile: el
generalist species. Extant and extinct taxa overlap.
ambiente del Pleistoceno superior y ocupaciones humanas.
The cultural evidence presented in this study, shows a Revista Chilena de Historia Natural, 67: 503-519.
group of generalized foragers using energy saving and
technological strategies for the provision and production of Perez, Y., Milovic, J., Troncoso, R., Hanish, F., Helms, F., Toloczky,
lithic resources. M. 2003. Geología para el ordenamiento territorial: Área de
The geomorphological context of the site opens the Osorno, Región de los Lagos. Servicio Nacional de Geología y
Minería, Carta Geológica de Chile, Serie Geológica Ambiental
possibility to use it as prospective model in central and Nº6, 62 p, 7 mapas escala 1:100.000. Santiago.
south Chile.
Pino, M. 2008. Pilauco, un sitio complejo del Pleistoceno tardío.
Acknowledgments Osorno, norpatagonia chilena. Universidad Austral de Chile.
Valdivia, Chile.– Imprenta América. 164p.
This scientific contribution was partially supported by the Recabarren, O. 2007. Análisis de restos óseos de gonfoterios del área
project FONDECYT 1100555. Thank to all Pilauco team. comprendida entre los 39º 39' y 42º 49' S, Centro - Sur de Chile.
Unpublished Tesis, Licenciado en Ciencias Biológicas, UACH.
References 53 pp.

Aguilera, F.; Chávez, M; Pino, M. 2011. Análisis de un molar Recabarren, O., Pino, M., Cid, I. 2011. New record of Equus
perteneciente a la megafauna del Pleistoceno tardío, sitio Pilauco, (Mammalia: Equidae) from the Late Pleistocene of central-south
Osorno, Chile. IV Congreso Latinoamericano de Paleontología Chile. Revista Chilena de Historia Natural 84: 535-542
de Vertebrados. San Juna, Argentina, Actas del Congreso, p. 88.

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