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WEST KIMBERLEY PLACE REPORT - Department of Sustainability ...

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Analyses <strong>of</strong> the botanical remains recovered from Carpenters Gap 1 indicates long<br />

term shifts in flora composition with changes in the climate, and provides evidence<br />

that much <strong>of</strong> the macroscopic plant remains were deposited by Aboriginal plant food<br />

procuring activities (McConnell 1997; McConnell and O'Connor 1997, 1999). In<br />

support <strong>of</strong> this view, Wallis (2001) points to the selective burning patterns on some<br />

plant remains; the lack <strong>of</strong> rodent gnaw marks on seeds; the fact that most <strong>of</strong> the plant<br />

remains are culturally useful; and a botanic trapping exercise carried out at the shelter<br />

that did not show significant botanic deposition by animal, wind or water action.<br />

Grasses constitute about 50 per cent <strong>of</strong> the overall phytolith (microscopic bits <strong>of</strong> silica<br />

stored in plant structures) assemblage throughout the Carpenter's Gap 1 sequence. The<br />

grassland communities <strong>of</strong> 40,000 years BP appear to be similar to those seen in the<br />

area today. Around 33,000 years BP, there was a reduction in the grass species<br />

diversity, perhaps due to decreasing temperatures and water availability. Interestingly,<br />

there are no obvious changes to these grassland communities through the last glacial<br />

maximum. From about 17,000 years BP there is again an increase in grass species<br />

diversity (Wallis 2001).<br />

While there are no palm species growing in the Napier Range today, 40,000 years ago<br />

the palms Livistona loriphylla and L. victoriae were present in considerable<br />

abundance. This continued up until about 30,000 years BP, after which the palms<br />

survived in smaller numbers until just prior to the last glacial maximum, when they<br />

disappear from the record. Palms require a permanent water source to survive, and in<br />

the Kimberley today they are commonly found on the edges <strong>of</strong> vine thickets and in<br />

sheltered gorges and gullies along more northerly ranges (Kenneally et. al. 1996). As<br />

climatic conditions deteriorated, i.e. got drier with the approach <strong>of</strong> the last glacial<br />

maximum, the palms contracted to smaller areas and the southerly boundary <strong>of</strong> their<br />

distribution moved northwards.<br />

Also <strong>of</strong> interest are the sedge (Cyperaceae) remains. Macroscopic stem fragments<br />

have been recovered from most levels <strong>of</strong> the site, except the uppermost Holocene<br />

levels. Ethnographic evidence <strong>of</strong> the use <strong>of</strong> sedges by Aboriginal people as a late dry<br />

season food source (Crawford 1982; Smith and Kalotas 1985), Wallis (2001) suggests<br />

that these large pieces <strong>of</strong> sedge were culturally deposited.<br />

The palaeobotanical record indicates that the Aboriginal inhabitants <strong>of</strong> Carpenter's<br />

Gap 1 did not abandon this region during the last glacial maximum, but instead<br />

adapted their survival strategies to cope with the changes. Other Pleistocene sites in<br />

the Kimberley show a hiatus in occupation during the last glacial maximum (Riwi:<br />

Balme 2000; Widgingarri and Koolan Island: O'Connor 1995, 1996, 1999).<br />

Evidence <strong>of</strong> Pleistocene occupation occurs elsewhere in the Australian archaeological<br />

record. Occupation sites from around the continent with dates <strong>of</strong> around 40,000 years<br />

include: Puritjarra in central Australia (39,000 BP: Smith et al. 1997); Allen's Cave in<br />

South Australia (40,000 BP: Roberts et al. 1996); Willandra Lakes in New South<br />

Wales (46,000 to 50,000 BP: Bowler et al. 2003); GRE8/Lawn Hill in Queensland<br />

(41,500 BP: O'Connell and Allen 2004); and Devil's Lair in southwest Western<br />

Australia (41,000 to 46,000 BP: Turney et al. 2001).<br />

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