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Bennett’s wallaby marrow quality vs quantity: Evaluating human decision-making and seasonal occupation in late Pleistocene Tasmania Jillian Garvey Archaeology Program, La Trobe University, Victoria, Australia [email protected]

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Page 1: Bennett’s wallaby marrow quality vs quantityalexandriaarchive.org/bonecommons/archive/files/garvey-icaz-2010... · Bennett’s wallaby marrow quality vs quantity: Evaluating human

Bennett’s wallaby marrow quality vs quantity:Evaluating human decision-making and seasonal occupation in

late Pleistocene Tasmania

Jillian Garvey

Archaeology Program, La Trobe University, Victoria, Australia

[email protected]

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Archaeology of Late Pleistocene SW Tasmania

• First site identified during the late 1970s- KUTIKINA CAVE.

• Kutikina excavated by Rhys Jones and colleagues 1981 (Kiernan et al. Nature 1983:31).

• Followed by the Southern Forests Archaeological Project in 1990s by La Trobe University (Richard Cosgrove, Jim in 1990s by La Trobe University (Richard Cosgrove, Jim Allen and colleagues) excavated several more caves.

e.g. Nunamira, Bone Cave, Warreen, Pallawa Trounta

• In 2005 the Kutikina faunal assemblage was analysed.

• Recent Bennett’s wallaby teeth annuli studies indicate seasonal use of the landscape (Pike-Tay, Cosgrove & Garvey 2008 JAS).

Top left hand corner: map of

Australia with the southern island

state of Tasmania shaded.

Main figure: Tasmania with

southwest region indicated and

Kutikina Cave marked by the star. Kutikina

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SW Settlement Pattern &

Chronology (Uncal 14C)

35,000-10,000BP

Warreen 34,780-18,630

Parmerpar Meethaner 34,000 - 750

ORS 7 30,840 - 2,500

Nunamira 30,420 - 11,630

Bone Cave 29,000 - 13,700

Pallawa Trounta 29,800 - 13,410

Parmerpar MeethanerParmerpar Meethaner

Pallawa Trounta 29,800 - 13,410

Kutikina Cave 19,770 - 14,840

Mackintosh 17,000

• >950,000 bones analysed

• Bennett’s wallabies dominate

• Preference for the larger hindlimbs

• Femora and tibiae always split open

Southwest Tasmania characterised by:

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Kutikina Cave excavated 1981

Kutikina Cave:

•1m2 wide, 1.3m deep excavated

•Volume 0.583 cubic metres, wet sieved

(3mm)

•11 C14 dates- 22,000-15,000 (LGM)

Jones 1987

1981 Kutikina excavation

•11 C14 dates- 22,000-15,000 (LGM)

•Only published paper on Kutikina excavation

or analysis was preliminary report in 1983

Nature: approx 250,000 bones & 30,000 stone

tools.

• Unpublished preliminary report on faunal

sample by Geering 1983. Jones 1987

Jones 1987

Tasmania was joined to

mainland Australia during

the late Pleistocene

Inspecting Kutikina

Cave, 1981

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Similar:

• Stone tools

• Hearths (fireplaces)

Parallels between Northern and Southern

Hemisphere’s during LGM

• Hunting patterns

• Butchering patterns

Bennett’s wallaby Macropus rufogriseus

“The specific targetting onto reindeer by the European hunters bears comparison

with the similar emphasis on wallabies by subsub-Antarctic palaeo-Tasmanians”

(Kiernan et al. Nature 1983:31).

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Bennett’s wallaby (Macropus rufogriseus)

• Also known as the Red-necked wallaby

• Small wallaby weighing 10-15kg

• Found in SE mainland Australia & Tasmania

Male Red kangaroo (70kg) with

• In Tasmania:

– Seasonal breeders

– Widespread distribution

• Common in zoos and as pets in Europe & Nth America:

– quiet nature

– easy to breed

– excellent lawnmowers

Kangaroo skeleton

Male Red kangaroo (70kg) with

female grey (45kg) Female (10kg) Bennett’s wallaby

Tamar wallaby (8kg) with joey

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Typical spit from Kutikina- Bennett’s wallaby dominates

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• 269,459 bone fragments, weighing 46.11kg were analysed (Garvey 2006).

• 28,210 or 12% identified to taxon &/or element.

• 21 species identified, 13 of which are potential human prey taxa

(identified by Cosgrove & Allen 2001).

2005-2007 Kutikina results

(identified by Cosgrove & Allen 2001).

• Of the potential prey BW >92% (MNI 44), Wombats

<7% (MNI 10), minor medium elements.

• Emu and grey kangaroo identified.

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Kutikina Cave

small mammals medium mammals

bones relatively complete

= owls -humans?

-devil, thylacine

or quolls?

-natural death ?

Taphonomic history

Kutikina Cave

Bennett’s wallaby

( >75%)

Wombat (7%)

kangaroo & emu

humans selected

whole animals

humans selected certain elements

such as the lower long bones

humans selected

entire wombats

Images from Van Dyck & Strahan 2008

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Bennett’s wallaby represents

<92% of the identified fauna

MNI 44 (per Unit)

- Hindlimb dominates.

- Axial and manus under

Bennett’s wallaby

- Axial and manus under represented.

- Numerous cut marks on hindlimbs.

- Tibiae and femora always smashed open.

- 4th and 5th metatarsals, large phalanges, calcaneum often smashed open.

Garvey 2006

Percentage of Bennett’s wallaby body parts

represented at Kutikina Cave

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Kutikina wallaby bones

cut marks

percussion

access marrow

bone

point

A

A

A

B

A- distal tibia

Garvey 200x

chop? marks

size range

cut mark

location

D

A

C

A- distal tibia

B- fibula

C- pes phalange

D- distal humerus

access marrow

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Why the dominance of Bennett’s wallaby

split hindlimb longbones?

1. Marrow/meat quality?

and/orand/or

2. Marrow/meat quantity?

and/or

3. Processing time?

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• Marrow and meat quantity was evaluated by Garvey 2010

Quaternary International 211(1-2):144-156.

• It seemed that humans were not under selective pressure

concerning which parts of the animals they transported.

Marrow and meat quantity: economic utility

concerning which parts of the animals they transported.

• Ignored some of the larger ‘meaty’ elements such as the

sacrum, preferring the hindlimbs which were found to not

only carry large amounts of flesh but also the greatest volume

of bone marrow.

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40

50

60

70

80

90

100%MUI

BW1

BW2

BW3

BW4

Mean

Bennett’s wallaby economic utility:

Meat Utility Index (MUI)

The %MUI for the 4 wallabies and the mean.

indicates the highest body part.

0

10

20

30

Cranium

Mandible

Cervical

Thoracic

Rib

Sternum

Scapula

Clavicle

Humerus

Ulna & Radius

Manus

Lumbar

Pelvis

Femur

Tibia & Fibula

Pes

Sacral

Caudal

Mean

Garvey 2010, Quaternary International 211(1-2):144-156

WHERE: CAU- caudal, CER- cervical, CLA- clavicle, CRA- cranial, FEM- femur, HUM- humerus, LUM- lumbar, MAND-

mandible, MANU- manus, PEL- pelvis, PES- pes, RIB- rib, SAC- sacrum, SCA- scapula, STE- sternum, TIB- tibia, THO-

thoracic, ULN- ulna

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CRA

TIB

CAUPES

ULN

CERSCA

CLA

PELHUM

FEM

8

10

12

14

16

18

20MAU

Accounts for the possibility of riders: other body parts selected

along with preferred elements (Binford 1978, pp. XX). Where

RED- high in meat/marrow & common in Kutikina; BLUE- those

high in meat/marrow & rare in Kutikina

Bennett’s wallaby economic utility:

Modified Meat Utility Index (MMUI)

PEL

LUM

RIB

SAC

THO

HUM

MAND

STE

MANU

0

2

4

6

8

0 10 20 30 40 50 60 70 80 90 100

%MUI

WHERE: CAU- caudal, CER- cervical, CLA- clavicle, CRA- cranial, FEM- femur, HUM- humerus, LUM- lumbar, MAND-

mandible, MANU- manus, PEL- pelvis, PES- pes, RIB- rib, SAC- sacrum, SCA- scapula, STE- sternum, TIB- tibia, THO- thoracic,

ULN- ulna

Garvey 2010, Quaternary International 211(1-2):144-156.

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Marrow and meat quality: marrow composition

• Fatty acid analysis, in particular oleic acid (a monounsaturated omega-9 fatty acid), argued to be a good indicator of unsaturated fat quality (Binford 1978).

• It has been found that in caribou, and ungulates in general, unsaturated fats increase as you move away from the body core temperature or the heart(Meng et al. 1969; West and Shaw 1975).

• High % unsaturated fatty acids in the distal limbs causes lowering a of melting temperature and oiler marrow (Irving et al. 1957; Morin 2007).

• While extensive work has occurred on ungulates, there has been no analysis of marsupial bone marrow.

– Test to see if a similar pattern occurs in the Bennett’s wallaby.

– How does age, sex, altitude, and season effect bone marrow quality?

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Marrow and tissue composition

• Total Fat (FOLCH) and Fatty Acid Profile (FAMES) determined.

• 14 fatty acids measured per sample.

• Fatty acid concentration of wallaby bone marrow decreased in saturated fats distally

• Largest fatty acid changes occurred in the monounsaturated Oleic acid (C 18=1) and Palmitoleic (C16:1) both increased distally

• Saturated Palmitic acid (C16:0) and Stearic acid (C18:0) both decreased accordingly

• These results are similar to that identified in caribou Rangifer tarandus (Meng et al. 1969), Dall sheep Ovis dalli (West and Shaw 1975), and in the desert bighorn sheep Ovis canadensis cremnobates (Turner 1979).

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Distribution of unsaturated fatty acids in the

Bennett’s wallaby

After Hume et al. 1987

after Meng et al. 1969;

© 2010 Falling Pixel ltd

Morin 2007

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Bennett’s Wallaby Hindlimb

Note: the dark red saturated fat in the femur marrow, with the unsaturated

marrow very pale in the distal tibia, i.e. increase in unsaturated fatty acids as

you move away from the body core temperature or the heart.

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Wallaby Collection Areas

Buckland 90-150 m.a.s.l.

Western Tiers 900-1300 m.a.s.l.

-alpine grasslands & herbfields

Western Tiers

Buckland

Buckland 90-150 m.a.s.l.

-open dry sclerophyll

-variable climate

-warm to hot summers

-cool to cold winters

Maydena 190-240 m.a.s.l.

-wet sclerophyll

-high rainfall

-warm summers & cool

winters

-cool summers & cold winters

Tissue samples collected per wallaby

(where possible):

1) tibia marrow

2) brain tissue

3) femur tissue

Seasonal variation:

1) Summer collection- February 2008

2) Autumn collection- May 2008

3) Winter collection- July 2008

4) Spring collection- October 2008

Note: the same 3 control areas as wallaby seasonal teeth annuli study by

Pike-Tay, Cosgrove & Garvey 2008, JAS

Maydena

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Collecting road kill

27 individual wallabies tested:

8 Buckland (4M & 4F)

9 Maydena (4M & 5F)

10 Western Lakes (5M & 5F)

Collecting marrow sample

Collecting muscle sample10 Western Lakes (5M & 5F)

3 samples per wallaby

(where possible)

-Brain tissue

-Hindlimb muscle

-Distal tibia marrow

Collecting brain sample

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Fatty acid results for the

three collection areasmean max temperature (oC)

mean min temperature (oC)

mean rainfall (mm)

S- summer A- autumn

W- winter Sp- spring

Marrow

Meat

Brain

Numbers on graph bars refer to

individual wallabies

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Preliminary conclusions

• Bennett’s wallaby remained stable and reliable resource

throughout the year irrespective of:

– Season

– Rainfall– Rainfall

– Temperature

– Sex

– Age

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Future work

Then how do we explain hunting, butchery and seasonal patterns

observed in late Pleistocene SW Tasmania?

Future work:

• Processing time & butchery practices

– Ethnographic

– Experimental

• Other commodities

– Bone tools

– Fur

• Bone Density

– Scientific evaluation

– However tiny complete rodent bones indicates excellent preservation

• Human physiology & the role of fatty acids

– Environmental stress

– Sex, age, pregnancy, breastfeeding, etc

Photo: R. Cosgrove

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Acknowledgements

• Tasmanian Aboriginal Land & Sea Council (TALSC) and Tasmanian Museum & Art Gallery (TMAG), Hobart.

• Rudy Frank, Peter Saad & Wei Ming, LTU, for technical assistance.

• Tiffany Liew, Seema Siddiqui & Grammatis Tsintzoglou for dissecting the wallabies in 2007.

• Georgia Bennett, Tiffany Liew, Richard Cosgrove, Coral Montero Lopez & Anthony Dall’Oste for collecting roadkill in 2008/2009.

• Helpful discussions with Richard Cosgrove, Anne Warren, Mike Archer, Eugene Morin, Jim O’Connell and reviewers of JAS paper.

• 2008 La Trobe University Research Grant for the economic anatomy and fatty acid analysis.

• LTU Postdoctoral Fellowship 2006-2008

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References

• Binford, L.R., 1978. Nunamiut Ethnoarchaeology. New York, Academic Press.

• Garvey, J., 2006. Preliminary zooarchaeological interpretations from Kutikina Cave, southwest Tasmania. Australian Aboriginal Studies 2006(1), 58-63.

• Garvey, J., 2007. Surviving an Ice Age: the zooarchaeology from southwest Tasmania. Palaios 22, 583-585.

• Garvey, J., 2010. Economic anatomy of the Bennett’s wallaby (Macropus rufogriseus): implications for understanding human hunting strategies in late Pleistocene Tasmania. QuaternaryInternational 211, 144-256.

• Hume, I.D., Jarman, P.J., Renfree, M.B., Temple-Smith, P.D., 1987. Chapter 29: Macropodidae, in: Walton, D.W., Richardson, B.J. (Eds.), Fauna of Australia, Volume 1B Mammalia. Australian Government Publishing Service, Canberra, pp. 679-715.

• Jones, R., 1987 Ice-age hunters of the Tasmanian wilderness, Australian Geographic Oct/Dec 87:26-45.

• Jones, R., 1987 Ice-age hunters of the Tasmanian wilderness, Australian Geographic Oct/Dec 87:26-45.

• Kiernan, K., Jones, R., Ranson, D.. 1983 New evidence from Fraser Cave for glacial age man in south-west Tasmania, Nature 301:28-32.

• Meng, M.S., West, G.C., Irving, L., 1969. Fatty acid composition of caribou bone marrow. Comparative Biochemistry and Physiology 30, 187-191.,

• Morin, E., 2007. Fat composition and Nunamiut decision-making: a new look at the marrow and bone grease indices. Journal of Archaeological Science 34, 69-82.

• Pike-Tay, A., Cosgrove, R., Garvey, J. 2008. Systematic seasonal land use by late Pleistocene Tasmanian Aborigines. Journal of Archaeological Science. 35(9), 2532-2544.

• Van Dyck, S. Strahan, R., 2008. The mammals of Australia, 3rd Edition. Reed New Holland, Sydney .

• Turner, J.C., 1979. Adaptive strategies of selective fatty acid deposition in the bone marrow of desert bighorn sheep. Comparative Biochemistry and Physiology 62A, 599-604.

• West, G., Shaw, D., 1975. Fatty acid composition of Dall sheep bone marrow. Comparative Biochemistry and Physiology 50B, 599-601.