Abstract
The establishment of Tasmanian Palawa/Pakana communities ~40 thousand years ago (ka) was achieved by the earliest and farthest human migrations from Africa and necessitated migration into high-latitude Southern Hemisphere environments. The scarcity of high-resolution paleoecological records during this period, however, limits our understanding of the environmental effects of this pivotal event, particularly the importance of using fire as a tool for habitat modification. We use two paleoecological records from the Bass Strait islands to identify the initiation of anthropogenic landscape transformation associated with ancestral Palawa/Pakana land use. People were living on the Tasmanian/Lutruwitan peninsula by ~41.6 ka using fire to penetrate and manipulate forests, an approach possibly used in the first migrations across the last glacial landscape of Sahul.
Paleoecological records show that Aboriginal people burned wet forest to first settle in Tasmania 41,600 years ago.
INTRODUCTION
The establishment of ancestral Tasmanian Palawa/Pakana communities is the earliest evidence of human migrations into temperate latitude regions in the Southern Hemisphere. The oldest archaeological evidence of human occupation in Tasmania (Aboriginal given name: Lutruwita) is from excavated sediment layers in Warreen Cave (1) and Parmerpar Meethaner rock shelter (2), with the calibrated radiocarbon dates of 39,924 ± 1130 years and 38,680 ± 1400 years, respectively. Lutruwita was isolated from the mainland of Australia by high sea levels for much of the interval between 135 and 43 thousand years ago (ka), with the first sustained land bridge of the last glacial cycle occurring between 43 and 37 ka (3). Palawa/Pakana communities were able to traverse the partially exposed eastern Bassian Land Bridge to enter Lutruwita at this time (1–4). The land bridge became isolated from the Australian mainland as a result of rising sea levels during the early to mid-Holocene (3). While early evidence for the occupation of Lutruwita by Palawa/Pakana people is well documented through the archaeological record (1, 2, 5), the nature of fire use and effects on vegetation and fauna (including megafauna) remains speculative (2, 5) and at times contentious (6, 7). This is partly due to the scarcity of high-resolution paleoecological data that span the period between 50 and 40 ka in the region. Paleoecological records from the Australian mainland suggest that the arrival of Aboriginal peoples on the continent at least ~50 ka (8–13) was accompanied by changes in the biotic environment, including burning of vegetation and the replacement of closed woody vegetation by open vegetation communities, as well as the decline and extinction in megafaunal population (6, 14–18). Landscape management practices using fire are evident in Lutruwita at least after the Last Glacial Maximum (LGM) (19) and apparent in paleoenvironmental records from northern and eastern Australia during the past 11,000 years (20, 21). Given existing evidence documenting millennia of burning practices in mainland Australia (20–22), we would expect landscape burning to accompany the arrival of people in Lutruwita.
Our goal in this study was to use two well-dated deep sedimentary records: Emerald Swamp and laymina paywuta (Palawa meaning: lagoon from a long time ago) situated at the western and eastern extremes of the Bass Strait (Three Hummock Island and Clarke Island/lungtalanana; Figs. 1 and 2) to reconstruct past environmental change and landscape changes associated with human arrival. Three Hummock Island is situated in the presently wet (annual average rainfall, ~939 mm) western side of Bass Strait, and lungtalanana is on the drier (annual average rainfall, ~616 mm) eastern side. These long-term records provide a unique opportunity to understand the interplay of past climates across the Pleistocene land bridge (23), including floristic and fire-regime changes associated with the earliest evidence for people within Lutruwita in two contrasting bioclimatic zones of this landscape (dry and wet temperate) with millennia of reversing precipitation gradients (24). In the context of previous research from mainland Australia, we expect that Aboriginal arrival in Lutruwita was also accompanied by a shift in fire regimes as a result of an additional source of fire ignitions—namely, people (hypothesis 1). We also expect the greatest plant species turnover (measured by beta diversity) following the first evidence for human arrival to have occurred in the then wetter landscapes where more fire-sensitive plants would have been common compared to the then drier landscapes where plant assemblages were likely more adapted to fires (hypothesis 2). Increased burning by people would differentially disadvantage the fire-sensitive species in wet environments compared to the fire-tolerant species from drier and more naturally fire-prone environments.
Study area climate and vegetation
As with the broader Lutruwita landscape today, the variability in annual rainfall between western and eastern Bass Strait is dominantly controlled by the northward-southward shifts in the position of the Southern Westerlies (SW) known as the Southern Annular Mode (SAM), which creates an east-west rainfall anti-phasing pattern (25, 26). During summer, a positive SAM phase (southward position of the SW) results in higher chances of rainfall over eastern Lutruwita and eastern Bass Strait. Conversely, a negative SAM phase (northward position of the SW) results in greater chances of rainfall in western Lutruwita and western Bass Strait. In winter, a positive SAM phase is associated with reduced chances of rainfall over the entire region and the reverse is the case during a negative SAM phase (26). The warm Leeuwin Current (LC) that flows from the coast of Western Australia toward the western side of Lutruwita also contributes moisture to the western Bass Strait today (Fig. 1A) (27). Overall, western Lutruwita (including western Bass Strait) currently receives the highest annual rainfall in the region and is characterized by relatively less flammable wetter vegetation communities compared to eastern Lutruwita and eastern Bass Strait (Fig. 1, B to D). Emerald Swamp vegetation on Three Hummock Island, western Bass Strait, is dominated by dense Melaleuca ericifolia–Acacia melanoxylon swamp forest, while laymina paywuta vegetation on lungtalanana, eastern Bass Strait, is characterized by dry sclerophyll shrub and heathland, dominated by Eucalyptus, Casuarina, and Banksia.
The present-day SAM-driven rainfall anti-phasing over Lutruwita is thought to have also prevailed in the region during the LGM (23), the late glacial and early to mid-Holocene, weakening during the past 5000 years as El Niño–Southern Oscillation intensified (24). Our pollen records suggest that the climatic anti-phasing may have also prevailed during marine isotope stage 3 (MIS 3), which is discussed below.
RESULTS AND DISCUSSION
Aboriginal arrival accompanied by a shift in fire regime in Lutruwita ~41.6 ka (hypothesis 1)
The co-dominance of drought-tolerant Callitris and Eucalyptus at the base of the laymina paywuta record indicates possible variable to less-wet conditions in eastern Bass Strait during the beginning of MIS 3, with the latter expansion of wet Eucalyptus forest and rainforest marking a wetter phase with potentially easterly moisture flow (+SAM) from ~50 to 35 ka. Rainfall reconstruction for southeast Lutruwita also shows high values during this period (Fig. 3, A and C) (28). Aboriginal arrival on the eastern Bassian Land Bridge may have occurred around this wet climatic phase, with perhaps abundant vegetative and potentially freshwater resources for subsistence on the narrow land bridge (Fig. 3, A, C, and F). Fire would have been an important tool used by early Palawa/Pakana communities to penetrate and manage the dense wet forest to promote open vegetation supporting key prey species and to access different raw materials and shelter (29–31). We expect shifts in fire regime to precede vegetation change in Lutruwita following human arrival, and this is observed in the record from laymina paywuta in eastern Bass Strait. Charcoal accumulation rates (biomass burned: amount of vegetation consumed by fire at the site) (32) increased abruptly at the site at ~41.6 ka, and this was followed by a major vegetation change at ~40 ka as identified by pollen zone classification (CONISS; Figs. 3C and 4A). Biomass burned and fire frequency records suggest possible initial forest burns with frequent intense fires within the first two millennia of Aboriginal arrival on the land bridge (Fig. 3A). Given the absence of major climatic shifts in southern Australia during the interval between ~41.6 and 40 ka (Fig. 3A) (33), increased charcoal influx, erosional activity (i.e., sediment influx; Fig. 4A), and the transition of closed to open vegetation (vegetation discussed in hypothesis 2) likely indicate landscape changes associated with anthropogenic firing. The environmental impact, however, would have taken time to become observable in archaeological or sedimentary archives. Hence, we interpret the earliest evidence for Palawa/Pakana occupation of Lutruwita to be at ~41.6 ka, followed by a gradual vegetation response by ~40 ka, which is about 2000 years earlier than suggested by the archaeological evidence in the southwest of the island (2, 5).
At Emerald Swamp (hereafter “Emerald”), Eucalyptus forest expanded following the termination of the arid MIS 4 and beginning of MIS 3 but quickly declined by ~54 ka and was replaced by shrubland. This suggests a wet start (~57 to 54 ka) of MIS 3 in western Bass Strait, with drying and treeless vegetation expansion after 54 ka. Rainforest also declined in western Lutruwita during MIS 3 (Fig. 3, A and B) (34). The corresponding changes in Emerald Eucalyptus pollen to LC flow (33), which also bring moisture as far as western Bass Strait today (27), suggest that it may have influenced the rainfall pattern in the area as well during MIS 3 (Fig. 3A). LC was also strong at the beginning of MIS 3 and generally became weaker between 54 and 30 ka, as inferred from the declining trend of tropical foraminifera Globigerinoides ruber in southern Australia at this time (33). Biomass burned increased in the area at ~41.1 ka (500 years after fire-regime shift in laymina paywuta) but was muted compared to that of laymina paywuta, and minor vegetation changes were evident at ~40 ka (Fig. 3, B and C). Western Lutruwita, including Emerald, was likely under a drier climate with less arboreal vegetation when Aboriginal people arrived in Lutruwita. People likely spread to northwest Lutruwita by ~41.1 ka, also frequently burning vegetation (shrubland) but possibly with less-intense fires. The likely explanation for the relatively less landscape firing and minimal vegetation changes at Emerald compared to laymina paywuta is discussed below (hypothesis 2).
Aboriginal burning-drive vegetation turnover across climate gradient following arrival in Lutruwita (hypothesis 2)
Given the abundance of fire-intolerant rainforest communities of western Lutruwita today, we hypothesized greater vegetation turnover in areas under wetter climates in the region following the onset of anthropogenic landscape burning ~41.6 ka. The eastern Bassian Land Bridge was wetter than the western area at this time, with more fire-sensitive plants in the former, including rainforest taxa (Fig. 3, B, C, and F). Of the two study sites, our CONISS and turnover analysis detect the greatest vegetation turnover in laymina paywuta in response to Aboriginal burning following arrival (Figs. 3, B and C, and 5). Notable floristic changes include the marked decline in Callitris and the increase in Dodonaea by ~40 ka (Fig. 4A). The gradual replacement of preexisting Callitris-Eucalyptus woodland by wet Eucalyptus forest and rainforest at the site was already underway from ~50 ka before the first evidence of people in the landscape (Fig. 4A). There is a brief increase in Callitris ~41 ka, possibly due to infrequent anthropogenic fires suitable for regeneration that was favorable for this long-lived obligate seeder. However, by 40 ka, the permanent establishment of Palawa/Pakana communities occupying the Bassian Land Bridge (1) likely caused major increases in fire activity causing Callitris to quickly decline while favoring fire-adapted Eucalyptus. Callitris is both fire dependent and fire sensitive in that infrequent fires reduce competition with shade-tolerant trees, allowing canopy-stored serotinous seeds to establish, yet frequent fires can destroy seed sources and cause local extinction (35). Other fire-adapted taxa also became more abundant (~5%), including Banksia marginata and the Australian endemic species Beyeria (fig. S3). The shift in fire regime at this time likely opened existing forest/woodland canopy, as indicated by increases in understory shrubs, especially Dodonaea, given the taxon’s preference for light availability under open canopies (Fig. 4A) (35, 36).
There were no notable changes in preexisting vegetation in the Emerald area following human arrival (Figs. 3B and 4B). The already open dry shrubby vegetation in the area perhaps did not require substantial burning for access and use as reflected in the lower charcoal influx (biomass burned) following human arrival compared to laymina paywuta. The marked expansion of fire-adapted and serotinous Casuarinaceae was the key floristic change associated with anthropogenic burning in Emerald. Dense Monotoca-Leptospermum scrub (shrubland >2 m tall) and Melaleuca swamp forest largely characterized the site before evidence of anthropogenic burning (Fig. 4B). The small presence of native pepper Tasmannia (fig. S2) that thrives after disturbance likely also indicates some opening of existing scrub by burning (36), with perhaps more heathy vegetation type (shrubland <2 m tall). The Casuarinaceae species is likely Allocasuarina monilifera, which is an endemic dwarf heathland species. It is currently the only Casuarinaceae species recorded growing in the Fleurieu Group islands (37) but commonly found across the drier eastern Lutruwita (including the Furneaux Group) today in dry substrates (36). Dry conditions that prevailed when people arrived in the area, combined with landscape burning, likely drove its successful generation and expansion. It is possible that the recorded Casuarinaceae expansion at Emerald was part of a broader western Lutruwitan vegetation response following human occupation of the area. An existing pollen record from Lake Selina, 100 km to the south in western Lutruwita, spanning the past 30,000 to 52,000 years, also recorded Casuarinaceae pollen increase at ~42 ka, although the chronology is problematic (38). While increasing biomass burning intensity and fire frequency from ~35 ka would have resulted in the Casuarinaceae species decline due to fire regime outside species tolerance level (39), the onset of wetter conditions may have also reduced the species’ niche and outcompeted by wet-tolerant or mesophyllous species (Figs. 3B and 4B). Increased burning was likely driven by the desire to keep the landscape open in response to Eucalyptus expansion and vegetation thickening as conditions became wetter toward the end of MIS 3 and beginning of MIS 2. This may also reflect human occupation expansion in northwest Lutruwita, especially between ~30 and 27 ka upon the onset of the LGM when sea level reached minimum and the full extent of the western and eastern Bassian Land Bridge was exposed (Fig. 3G) (40). Although the onset of the LGM climate may have contributed to the marked vegetation change in northwest Lutruwita at ~28 ka, frequent Aboriginal burning that kept wet sclerophyll vegetation open at this time likely significantly contributed to a decline in Leptospermum in the understory while favoring the more stress/disturbance-tolerant Monotoca (Figs. 3G and 4B) (36, 37).
Our results suggest that Aboriginal people markedly burned the landscape when they first entered Lutruwita, a pattern consistent with other evidence from mainland Australia (14, 17). Landscapes characterized by fire-adapted vegetation types were also likely more resilient to anthropogenic burning following Aboriginal arrival in Australia. After comparing vegetation turnover in Lutruwita and sites from moist forest and dry woodland-shrubland biomes from the mainland, the lowest floristic turnover following the earliest evidence for Aboriginal occupation with major burning was observed in southern Australia, followed by Emerald (Fig. 5, A and C). Turnover value distribution was also not significantly different in comparable vegetation types, with similar distributions between southern Australia and Emerald, and between northeast Australia and laymina paywuta (Fig. 5, B and C). In southern Australia, from ~58 ka, people likely used fire to maintain herb-dominated landscapes already created by previous cooling between 75 and 60 ka (17, 41, 42) and to prevent tree biomass recovery when the climate warmed again between 60 and 45 ka (17), stabilizing vegetation composition. A similar pattern of prehuman arrival herbaceous woodland and arid savanna persistence with minimal response to cultural burning after human arrival has also been observed in northwestern and northern Australia, respectively (20, 43). Conversely, high turnover was recorded for tropical wet northeast Australia’s vegetation following Aboriginal migration and anthropogenic burning in the area from ~41 ka (Fig. 5) (14, 44). Existing mixed vegetation of sclerophyllous forest and rainforest communities became replaced by sclerophyllous forest at this time (14, 44). The sensitivity of vegetation in northeast Australia to anthropogenic burning may be due to the abundance of fire-intolerant wet forest communities, which is also the case at laymina paywuta, where wet forest also existed at the time of human arrival. Climate would have modulated Aboriginal landscape burning during the late Pleistocene, with people burning wet forested/wooded landscapes with high-intensity fires to promote open landscapes (19), and burned already open dry vegetation types with low-intensity fires to maintain desired conditions. The former likely resulted in high vegetation turnover with the decline in fire-intolerant plants, while the latter favored fire-adapted plants with low turnover. It is possible that Aboriginal people were able to modify and use wet forest communities, including rainforests, much more in the past than presently thought (31), creating community composition and/or structure very different from today’s wet forest communities (19).
MATERIALS AND METHODS
Coring sites: Emerald Swamp and laymina paywuta—Lagoon from a long time ago
Emerald Swamp [40°26′23.59″S, 144°54′48.15″E, 35 m above sea level (masl)] sits in the center of Three Hummock Island and is the largest catchment on the granite island at ~1 km2. The site is characterized by dense M. ericifolia–A. melanoxylon swamp forest, with sedgy and mossy forest floors. Old tall Eucalyptus trees are also present in the forest. Leptospermum and Banksia form stands in drier substrates away from the swamp forest (45). Laymina paywuta (40.542173°S, 148.217650°E, 10 masl) is on the eastern coastal margin of Clarke Island (lungtalanana), bounded by an easterly facing lunette and nestled within a granite catchment. The site is characterized by dry sclerophyll shrub and heathland, with Eucalyptus, Casuarina, and Banksia prominent components of the vegetation. The study areas on lungtalanana and Three Hummock Island have a major feature in common. Both catchments have existed in the landscape for a long period without being obliterated by eolian sand sheets, which elsewhere on both islands have both covered any old lagoons as well as forming newer ones.
Sediment core collection and analysis
A 2.9-m core was collected from Emerald Swamp and a 3.94-m sediment core from laymina paywuta (Fig. 1), and accelerator mass spectrometry (AMS) radiocarbon dates were obtained for 28 and 24 bulk sediment sample depths across respective cores. AMS radiocarbon dates were measured at DirectAMS, Washington and Australian Nuclear Science and Technology Organization, Sydney. An age-depth model was then built for the sediment cores based on the resulting AMS dates, using SHCal20 in “rbacon” (46, 47).
Pollen and macrocharcoal were also analyzed from the sediment cores to reconstruct vegetation and fire history, respectively. Pollen analysis follows the standard protocol involving HCl, KOH, and acetolysis treatment (48), and at least 300 terrestrial taxa were identified in each pollen sample and presented as percentages. Sediment cores were sampled for pollen at 0.5- to 4-cm intervals and for macrocharcoal at 1-cm interval. To identify major temporal changes in vegetation (pollen spectra), stratigraphically constrained CONISS cluster analysis was performed on terrestrial pollen records and within-cluster scores were used to identify the timing of greatest shifts in pollen assemblages (49). Pollen data were further analyzed for turnover using the squared chord dissimilarity (SCD) metric (50–53) in R “analogue” package (54) to further quantify the magnitude of vegetation change. Turnover refers to the amount of compositional change in vegetation (pollen spectra) through time. There are different dissimilarity metrics used in calculating turnover in pollen records, including but not limited to chord distance, SCD, detrended correspondence analysis, and chi-square coefficient; however, these metrics produce similar results (53, 55–57). Here, we used the SCD due to its better handling of signal-to-noise effects (53). Study sites’ turnover results were also compared to sites on the mainland, especially during the first 5000 years of human occupation of landscapes, and pairwise Wilcoxon tests were used to determine the differences in turnover distribution between sites.
Sediment cores were contiguously sampled for macrocharcoal, and samples were bleached overnight (~16 hours) using household bleach, washed through a 125-μm sieve, and manually counted under the stereoscope. Using the CharAnalysis program (32), macrocharcoal counts (charcoal particles per cubic centimeter) were converted to influx (charcoal pieces per square centimeter per year) with interpolation to a median time interval, a proxy for past biomass burned at the study sites (32). The peak component of charcoal influx, which is the frequency of above-average charcoal influx events, was then used to infer past fire frequency (58). Significant charcoal peaks were detected at a minimum count cutoff probability of 0.05, and the frequency of peaks was computed every 2000 years. Given the multi-millennial scale of this study, individual charcoal peaks are taken to represent aggregates of fire events (fire episodes) and not single fire events. Charcoal influx was further subjected to regime shift (P < 0.01, cutoff = 50, Huber’s weight parameter = 5) analysis to detect the timing of major shift in biomass burned (59).
Acknowledgments
Research on the Bass Strait islands is supported by the Aboriginal Land Council of Tasmania and the Tasmanian Aboriginal Centre. In the field, we thank the Working on Country rangers, truwana Rangers, and Palawa/Pakana rangers for guidance and advice while in their country. Sediment cores used for this study were collected from the Bass Strait islands of Clarke/lungtalanana and Three Hummock with the permission of the Department of Natural Resources and Environment Lutruwita and Aboriginal Heritage Tasmania. We also thank the Cradle Coast Authority for logistic assistance and A. Sculthorpe (Land and Heritage Coordinator), Tasmanian Aboriginal Centre, for helpful feedback on the paper. M. Bird from James Cook University assisted with hydropyrolysis pretreatment for radiocarbon analysis.
Funding: This research was made possible through an Australian Research Council Centre of Excellence for Australian Biodiversity and Heritage support grant CE170100015 (to S.G.H.) and in-country support from the Tasmanian Aboriginal Centre.
Author contributions: S.G.H., M.A.A., and F.H. co-developed study idea. All authors (except G.L.S.) participated in the fieldwork. M.A.A. conducted laboratory analysis on the Emerald Swamp sediment core, while F.H. and G.L.S. conducted laboratory analysis on the laymina paywuta sediment core. M.A.A. conducted all data analysis and wrote the original manuscript draft, and all authors contributed to manuscript revisions. Funding was acquired by S.G.H. and D.M.J.S.B.
Competing interests: The authors declare that they have no competing interests.
Data and materials availability: All data needed to evaluate the conclusions in the paper are present in the paper and/or the Supplementary Materials. Pollen and charcoal datasets used in this study have been deposited in the Dryad and Mendeley online data repository and can be publicly accessed via DOI: 10.5061/dryad.3n5tb2rsb and https://data.mendeley.com/datasets/k4c6kd3n5n/1, respectively.
Supplementary Materials
This PDF file includes:
REFERENCES AND NOTES
- 1.J. Allen, R. Cosgrove, “The southern forests archaeological project” in Report of the Southern Forest Archaeological Project. Volume 1. Site Descriptions, Stratigraphies and Chronologies (Archaeology Publications, School of Archaeology, La Trobe Univ., 1996).
- 2.Cosgrove R., Forty-two degrees south: The archaeology of Late Pleistocene Tasmania. J. World Prehist. 13, 357–402 (1999). [Google Scholar]
- 3.Lambeck K., Chappell J., Sea level change through the last glacial cycle. Science 292, 679–686 (2001). [DOI] [PubMed] [Google Scholar]
- 4.S. Bowdler, Hunter Hill, Hunter Island: Archaeological investigations of a prehistoric Tasmanian site. Terra Australis 8 (1984).
- 5.Jones R., Tasmanian archaeology: Establishing the sequences. Annu. Rev. Anthropol. 24, 423–446 (1995). [Google Scholar]
- 6.Turney C. S. M., Flannery T. F., Roberts R. G., Reid C., Fifield L. K., Higham T. F. G., Jacobs Z., Kemp N., Colhoun E. A., Kalin R. M., Ogle N., Late-surviving megafauna in Tasmania, Australia, implicate human involvement in their extinction. Proc. Natl. Acad. Sci. U.S.A. 105, 12150–12153 (2008). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Cosgrove R., Field J., Garvey J., Brenner-Coltrain J., Goede A., Charles B., Wroe S., Pike-Tay A., Grün R., Aubert M., Lees W., O’Connell J., Overdone overkill—The archaeological perspective on Tasmanian megafaunal extinctions. J. Archaeol. Sci. 37, 2486–2503 (2010). [Google Scholar]
- 8.Clarkson C., Jacobs Z., Marwick B., Fullagar R., Wallis L., Smith M., Roberts R. G., Hayes E., Lowe K., Carah X., Florin S. A., McNeil J., Cox D., Arnold L. J., Hua Q., Huntley J., Brand H. E. A., Manne T., Fairbairn A., Shulmeister J., Lyle L., Salinas M., Page M., Connell K., Park G., Norman K., Murphy T., Pardoe C., Human occupation of northern Australia by 65,000 years ago. Nature 547, 306–310 (2017). [DOI] [PubMed] [Google Scholar]
- 9.Roberts R. G., Jones R., Smith M. A., Thermoluminescence dating of a 50,000-year-old human occupation site in northern Australia. Nature 345, 153–156 (1990). [Google Scholar]
- 10.Roberts R. G., Jones R., Spooner N. A., Head M. J., Murray A. S., Smith M. A., The human colonisation of Australia: Optical dates of 53,000 and 60,000 years bracket human arrival at Deaf Adder Gorge, Northern Territory. Quat. Sci. Rev. 13, 575–583 (1994). [Google Scholar]
- 11.Bowler J. M., Johnston H., Olley J. M., Prescott J. R., Roberts R. G., Shawcross W., Spooner N. A., New ages for human occupation and climatic change at Lake Mungo, Australia. Nature 421, 837–840 (2003). [DOI] [PubMed] [Google Scholar]
- 12.Turney C. S. M., Bird M. I., Fifield L. K., Roberts R. G., Smith M., Dortch C. E., Grün R., Lawson E., Ayliffe L. K., Miller G. H., Dortch J., Cresswell R. G., Early human occupation at devil’s lair, southwestern Australia 50,000 years ago. Quat. Res. 55, 3–13 (2001). [Google Scholar]
- 13.O’Connell J. F., Allen J., Williams M. A. J., Williams A. N., Turney C. S. M., Spooner N. A., Kamminga J., Brown G., Cooper A., When did Homo sapiens first reach Southeast Asia and Sahul? Proc. Natl. Acad. Sci. U.S.A. 115, 8482–8490 (2018). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Rule S., Brook B. W., Haberle S. G., Turney C. S. M., Kershaw A. P., Johnson C. N., The aftermath of megafaunal extinction: Ecosystem transformation in pleistocene Australia. Science 335, 1483–1486 (2012). [DOI] [PubMed] [Google Scholar]
- 15.Miller G. H., Magee J. W., Johnson B. J., Fogel M. L., Spooner N. A., McCulloch M. T., Ayliffe L. K., Pleistocene extinction of Genyornis newtoni: Human impact on Australian megafauna. Science 283, 205–208 (1999). [DOI] [PubMed] [Google Scholar]
- 16.Brook B., Johnson C. N., Selective hunting of juveniles as a cause of the imperceptible overkill of the Australian Pleistocene “megafauna”. Alcheringa 30, 39–48 (2006). [Google Scholar]
- 17.Adeleye M., Andrew S., Gallagher R., van der Kaars S., De Deckker P., Hua Q., Haberle S. G., On the timing of megafaunal extinction and associated floristic consequences in Australia through the lens of functional palaeoecology. Quat. Sci. Rev. 316, 108263 (2023). [Google Scholar]
- 18.Constantine I. V., Mooney S., Hibbert B., Marjo C., Bird M., Cohen T., Forbes M., McBeath A., Rich A., Stride J., Using charcoal, ATR FTIR and chemometrics to model the intensity of pyrolysis: Exploratory steps towards characterising fire events. Sci. Total Environ. 783, 147052 (2021). [DOI] [PubMed] [Google Scholar]
- 19.Cooley S., Fletcher M.-S., Lisé-Pronovost A., May J.-H., Mariani M., Gadd P. S., Hodgson D. A., Heijnis H., Rainforest response to glacial terminations before and after human arrival in Lutruwita (Tasmania). Quat. Sci. Rev. 329, 108572 (2024). [Google Scholar]
- 20.Bird M. I., Brand M., Comley R., Fu X., Hadeen X., Jacobs Z., Rowe C., Wurster C. M., Zwart C., Bradshaw C. J. A., Late Pleistocene emergence of an anthropogenic fire regime in Australia’s tropical savannahs. Nat. Geosci. 17, 233–240 (2024). [Google Scholar]
- 21.Constantine M., Williams A. N., Francke A., Cadd H., Forbes M., Cohen T. J., Zhu X., Mooney S. D., Exploration of the burning question: A long history of fire in Eastern Australia with and without people. Fire 6, 152 (2023). [Google Scholar]
- 22.van der Kaars S., Miller G. H., Turney C. S. M., Cook E. J., Nürnberg D., Schönfeld J., Kershaw A. P., Lehman S. J., Humans rather than climate the primary cause of Pleistocene megafaunal extinction in Australia. Nat. Commun. 8, 14142 (2017). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Fletcher M.-S., Thomas I., A quantitative Late Quaternary temperature reconstruction from western Tasmania, Australia. Quat. Sci. Rev. 29, 2351–2361 (2010). [Google Scholar]
- 24.Fletcher M.-S., Moreno P. I., Have the Southern Westerlies changed in a zonally symmetric manner over the last 14,000 years? A hemisphere-wide take on a controversial problem. Quat. Int. 253, 32–46 (2012). [Google Scholar]
- 25.Saunders K. M., Kamenik C., Hodgson D. A., Hunziker S., Siffert L., Fischer D., Fujak M., Gibson J. A. E., Grosjean M., Late Holocene changes in precipitation in northwest Tasmania and their potential links to shifts in the Southern Hemisphere westerly winds. Glob. Planet. Change 92–93, 82–91 (2012). [Google Scholar]
- 26.Australian Government Bureau of Meteorology, Southern Annular Mode in Australia; www.bom.gov.au/climate/sam/images/SAM-in-Australia.pdf.
- 27.Ridgway K. R., Condie S. A., The 5500-km-long boundary flow off western and southern Australia. J. Geophys. Res. Oceans 109, C04017 (2004). [Google Scholar]
- 28.Deckker P., van der Kaars S., Macphail M., Hope G., Land-sea correlations in the Australian region: 460 ka of changes recorded in a deep-sea core offshore Tasmania. Part 1: The pollen record. Aust. J. Earth Sci. 66, 1–15 (2019). [Google Scholar]
- 29.Bowman D. M. J. S., The impact of Aboriginal landscape burning on the Australian biota. New Phytol. 140, 385–410 (1998). [DOI] [PubMed] [Google Scholar]
- 30.B. Gammage, The Biggest Estate on Earth: How Aborigines Made Australia (Allen & Unwin, 2012). [Google Scholar]
- 31.Roberts P., Buhrich A., Caetano-Andrade V., Cosgrove R., Fairbairn A., Florin S. A., Vanwezer N., Boivin N., Hunter B., Mosquito D., Turpin G., Ferrier Å., Reimagining the relationship between Gondwanan forests and Aboriginal land management in Australia’s “Wet Tropics”. iScience 24, 102190 (2021). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Higuera P. E., Brubaker L. B., Anderson P. M., Hu F. S., Brown T. A., Vegetation mediated the impacts of postglacial climate change on fire regimes in the South-Central Brooks Range, Alaska. Ecol. Monogr. 79, 201–219 (2009). [Google Scholar]
- 33.De Deckker P., Moros M., Perner K., Blanz T., Wacker L., Schneider R., Barrows T. T., O’Loingsigh T., Jansen E., Climatic evolution in the Australian region over the last 94 ka—spanning human occupancy—, and unveiling the Last Glacial Maximum. Quat. Sci. Rev. 249, 106593 (2020). [Google Scholar]
- 34.Van De Geer G., Heusser L. E., Lynch-Stieglitz J., Charles C. D., Paleoenvironments of Tasmania inferred from a 5-75 Ka marine pollen record. Palynology 18, 33–40 (1994). [Google Scholar]
- 35.J. Reid, R. Hill, M. Brown, M. Hovenden, Vegetation of Tasmania, Flora of Australia Supplementary Series (Commonwealth of Australia, 1999).
- 36.C. Howells, Tasmania’s Natural Flora (Australian Plant Society Tasmania Inc., Hobart Group, ed. 2, 2012). [Google Scholar]
- 37.J. B. Kirkpatrick, S. Harris, The Dissappearing Heath Revisited (Tasmanian Environment Centre, 1999). [Google Scholar]
- 38.Colhoun E. A., Pola J. S., Barton C. E., Heijnis H., Late Pleistocene vegetation and climate history of Lake Selina, Western Tasmania. Quat. Int. 57-58, 5–23 (1999). [Google Scholar]
- 39.Nicholson Á., Prior L. D., Perry G. L. W., Bowman D. M. J. S., High post-fire mortality of resprouting woody plants in Tasmanian Mediterranean-type vegetation. Int. J. Wildland Fire 26, 532–537 (2017). [Google Scholar]
- 40.Adeleye M. A., Haberle S. G., McWethy D., Connor S. E., Stevenson J., Environmental change during the last glacial on an ancient land bridge of southeast Australia. J. Biogeogr. 48, 2946–2960 (2021). [Google Scholar]
- 41.Kershaw A. P., McKenzie G. M., Porch N., Roberts R. G., Brown J., Heijnis H., Orr M. L., Jacobsen G., Newall P. R., A high-resolution record of vegetation and climate through the last glacial cycle from Caledonia Fen, southeastern highlands of Australia. J. Quat. Sci. 22, 481–500 (2007). [Google Scholar]
- 42.Harle K. J., Heijnis H., Chisari R., Kershaw A. P., Zoppi U., Jacobsen G., A chronology for the long pollen record from Lake Wangoom, Western Victoria (Australia) as derived from uranium/thorium disequilibrium dating. J. Quat. Sci. 17, 707–720 (2002). [Google Scholar]
- 43.van der Kaars S., De Deckker P., A Late Quaternary pollen record from deep-sea core Fr10/95, GC17 offshore Cape Range Peninsula, northwestern Western Australia. Rev. Palaeobot. Palynol. 120, 17–39 (2002). [Google Scholar]
- 44.Kershaw A. P., Bretherton S. C., van der Kaars S., A complete pollen record of the last 230 ka from Lynch’s Crater, North-Eastern Australia. Palaeogeogr. Palaeoclimatol. Palaeoecol. 251, 23–45 (2007). [Google Scholar]
- 45.Harris S., Balmer J., The vegetation and flora of Three Hummock Island, western Bass Strait. Pap. Proc. R. Soc. Tasmania 131, 37–56 (1997). [Google Scholar]
- 46.Hogg A. G., Heaton T. J., Hua Q., Palmer J. G., Turney C. S., Southon J., Bayliss A., Blackwell P. G., Boswijk G., Ramsey C. B., Pearson C., Petchey F., Reimer P., Reimer R., Wacker L., SHCal20 Southern Hemisphere calibration, 0–55,000 years cal BP. Radiocarbon 62, 759–778 (2020). [Google Scholar]
- 47.M. Blaauw, J. A. Christen, M. A. A. Lopez, J. E. Vazquez, O. M. Gonzalez V. T. Belding, J. Theiler, B. Gough, C. Karney, rbacon: Age-depth modelling using bayesian statistics, version 2.5.8 (2022); https://CRAN.R-project.org/package=rbacon.
- 48.K. Faegri, J. Iversen, Textbook of Pollen Analysis (Hafner Press, rev. ed. 3, 1975). [Google Scholar]
- 49.Bennett K. D., Determination of the number of zones in a biostratigraphical sequence. New Phytol. 132, 155–170 (1996). [DOI] [PubMed] [Google Scholar]
- 50.Adeleye M. A., Mariani M., Connor S., Haberle S. G., Herbert A., Hopf F., Stevenson J., Long-term drivers of vegetation turnover in Southern Hemisphere temperate ecosystems. Glob. Ecol. Biogeogr. 30, 557–571 (2021). [Google Scholar]
- 51.Connor S. E., Vannière B., Colombaroli D., Anderson R. S., Carrión J. S., Ejarque A., Gil Romera G., González-Sampériz P., Hoefer D., Morales-Molino C., Revelles J., Schneider H., van der Knaap W. O., van Leeuwen J. F., Woodbridge J., Humans take control of fire-driven diversity changes in Mediterranean Iberia’s vegetation during the mid–late Holocene. Holocene 29, 886–901 (2019). [Google Scholar]
- 52.Seddon A. W., Macias-Fauria M., Willis K. J., Climate and abrupt vegetation change in Northern Europe since the last deglaciation. Holocene 25, 25–36 (2015). [Google Scholar]
- 53.Overpeck J. T., Webb T., Prentice I. C., Quantitative interpretation of fossil pollen spectra: Dissimilarity coefficients and the method of modern analogs. Quat. Res. 23, 87–108 (1985). [Google Scholar]
- 54.G. L. Simpson, J. Oksanen, M. Maechler, Analogue: Analogue and weighted averaging methods for palaeoecology, version 0.17-6 (2021); https://CRAN.R-project.org/package=analogue.
- 55.Mottl O., Grytnes J.-A., Seddon A. W. R., Steinbauer M. J., Bhatta K. P., Felde V. A., Flantua S. G. A., Birks H. J. B., Rate-of-change analysis in paleoecology revisited: A new approach. Rev. Palaeobot. Palynol. 293, 104483 (2021). [Google Scholar]
- 56.Giesecke T., Wolters S., van Leeuwen J. F. N., van der Knaap P. W. O., Leydet M., Brewer S., Postglacial change of the floristic diversity gradient in Europe. Nat. Commun. 10, 5422 (2019). [DOI] [PMC free article] [PubMed] [Google Scholar]
- 57.Nogué S., Santos A. M. C., Birks H. J. B., Björck S., Castilla-Beltrán A., Connor S., de Boer E. J., de Nascimento L., Felde V. A., Fernández-Palacios J. M., Froyd C. A., Haberle S. G., Hooghiemstra H., Ljung K., Norder S. J., Peñuelas J., Prebble M., Stevenson J., Whittaker R. J., Willis K. J., Wilmshurst J. M., Steinbauer M. J., The human dimension of biodiversity changes on islands. Science 372, 488–491 (2021). [DOI] [PubMed] [Google Scholar]
- 58.Higuera P., Gavin D., Bartlein P., Hallett D., Peak detection in sediment–charcoal records: Impacts of alternative data analysis methods on fire-history interpretations. Int. J.Wildland Fire 19, 996 (2010). [Google Scholar]
- 59.Rodionov S. N., A sequential algorithm for testing climate regime shifts. Geophys. Res. Lett. 31, L09204 (2004). [Google Scholar]
- 60.Department of Natural Resources and Environment Tasmania, TASVEG—The Digital Vegetation Map of Tasmania; https://nre.tas.gov.au/conservation/development-planning-conservation-assessment/planning-tools/monitoring-and-mapping-tasmanias-vegetation-(tasveg)/tasveg-the-digital-vegetation-map-of-tasmania.
- 61.P. De Deckker, M. Moros, T. Blanz, R. R. Schneider, T. T. Barrows, K. Perner, Multidataset for sediment cores MD03-2611 and SS0206-GC15 taken offshore southern Australia, PANGAEA (2020); 10.1594/PANGAEA.911846. [DOI]
- 62.P. Morrison, QGIS sea level tool plugin (2023); https://github.com/patrick-morrison/qgis_sea_level_tool.
- 63.De Deckker P., van der Kaars S., Haberle S., Hua Q., Stuut J.-B. W., The pollen record from marine core MD03-2607 from offshore Kangaroo Island spanning the last 125 ka; implications for vegetation changes across the Murray-Darling Basin. Aust. J. Earth Sci. 68, 928–951 (2021). [Google Scholar]
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