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For thousands of years Aboriginal and Torres Strait Islander people nurtured their young, allowing natural skills to develop. Education using the powers of observation and listening was the most important process used with information being delivered to the child when they were ready to receive it. Most times this information was delivered by several members of the community. Prominent Australian Aboriginal scholar Kaye Price (2012) affirms that ‘right from the beginning there was a specialised education and for each child there was a teacher, a mentor and a peer with whom to learn … who ensured that history and the essentials of life were taught’ (p. 4). Aboriginal society was based on an egalitarian system that was holistic and emphasised belonging, spirituality, and relatedness. Learning was viewed as a natural holistic process where education was centred on the land and children learned alongside adults (Martin, 2005). The traditional epistemological system that maintained Aboriginal Nations in Australia for millennia was disrupted upon colonisation in 1788 resulting in discrimination towards Aboriginal culture and traditions (Morgan, 2019).
On the surface, Australian metal music can be read—quite fairly—as a white, working-class, hypermasculine phenomenon. With further excavation, however, the way metal music materializes in local Australian scenes around the country in various ways reveals its power in negotiating complex structures of identity and belonging. Australian metal music is paradoxical and complex, and fans ‘use’ metal in a variety of political ways. Quite specific to Australian metal music, too, are the ways in which it has long been constructed as a frontier space—a space sitting ‘on the edge’ both geographically and politically, wherein metal’s tendency for extremes—its celebration of brutality, and its perpetuation of hegemonic white masculinity—is only matched by its potential for counter-hegemonic politics, radical change, and boundary-pushing. The Australian frontier functions symbolically in our reading, both as a space dominated by the centralizing figure of the colonial white man, but also as a precarious space in which women’s resilience and Aboriginal and Torres Strait Islander people’s agency in pushing back against colonial normativity rise to destabilize the accepted narratives of invasion politics.
The rock art of Australia is among the oldest, most complex, and most fascinating manifestations of human creativity and imagination in the world. Aboriginal people used art to record their experiences, ceremonies, and knowledge by embedding their understanding of the world in the landscape over many generations. Indeed, rock art serves as archives and libraries for Australia's Indigenous people. It is, in effect, its repository of memory. This volume explores Indigenous perspectives on rock art. It challenges the limits and assumptions of traditional, academic ways of understanding and knowing the past by showing how history has literally been painted 'on the rocks'. Each chapter features a biography of an artist or family of artists, together with an artwork created by contemporary artist Gabriel Maralngurra. By bringing together history, archaeology, and Indigenous artistic practice, the book offers new insights into the medium of rock art and demonstrates the limits of academic methods and approaches.
This paper presents new radiocarbon dates for two Aboriginal archaeological complexes situated on the cliff-lines of the Murray River in South Australia (SA); at Pooginook Flat and Tanamee. These dates represent the first age estimates for archaeological sites within the Upper Gorge section of the Murray River. The dates ranged from ca. 11 cal ka to the Late Holocene. The research supports previous evidence which has indicated that sites located along the Murray cliffs preserve much of the oldest evidence of Aboriginal peopling along the Murray River corridor in SA. The new dates also allow us to contribute to discussions concerning broader chronological trends in Aboriginal lifeways within the Murray-Darling Basin (MDB). Specifically, the new ages add some insight into the nature and timing of early Aboriginal occupation along the Murray River corridor in SA and further evidence that the LGM acted as a significant inhibitive factor for intensive occupation of this riverscape. The conservation of these significant and informative cliff-top sites remains precarious, however, and there is an imperative to continue to record and sample the extant sites.
Dr Jodi Edwards, an Aboriginal woman of Yuin and Dharawal kinship, wrote this chapter through her lens as an Elder connected to Country and the waters of the Illawarra coast of New South Wales. She explains how cultural knowledge-holders have seen, and continue to see and interpret, the natural environment through rich environmental play experiences that help shape cultural identity and strengthen Aboriginal Lore/Law. In a contemporary context, Jodi extends on these ways of understanding by sharing the rationale behind a children’s playscape and public art space being developed by the Shellharbour City Council in collaboration with the local Aboriginal community. The playscape is a play-based site for physical activity, and a place for storytelling and language learning, and for learning about bush tucker and bush medicines. It is intended to inform local young people and visitors alike about the multiple sustainable practices engaged in by the Aboriginal community of the area. At a broader level, the playscape also offers considerable potential for enhancing cultural and language reclamation, decolonisation and reconciliation.
Within a tidal wave of dispossession, Indigenous performers forged livings in scientific showmanship. In 1850, ‘Jemmy’, an Aboriginal boy, starred in a Melbourne lecture series that fused phrenology with mesmerism. During the mid 1860s, Tamati Hapimana Te Wharehinaki, chief of the Ngati Ruangutu hapū of the Tapuika Iwi, toured through the Australian colonies with the infamous Thomas Guthrie Carr. Supposedly mesmerised by the lecturers, these performers demonstrated actions that corresponded with particular phrenological organs, wrapping feigned subordination in displays of cultural difference that fascinated Europeans. An ethnographic history approach to these lecture reports reveals how these performers cannily shaped these representations for personal gain. Although serving colonial fantasies of control, the stage world nevertheless allowed them to push against the constraints that bound their daily lives. The fragile relations of power that made or broke a show enabled tactical choices for fleeting material or social benefit.
How did Aboriginal audiences experience popular science when it unfolded on stage in a mission site? This chapter considers phrenological visits to Yorta Yorta country in south-eastern Australia, and particularly the lectures of JB Thomas at Maloga Mission in 1884 and John Joseph Sheridan at nearby Cummeragunja in 1892. Like other scientists and medical men who visited here, these men perpetuated scientific racism. But newspaper reports also point to the possibility of these lectures – which also included lantern slides – as moments of nuanced interaction from which Yorta Yorta and other Aboriginal residents derived value and pleasure, rather than as straightforward impositions. As participatory entertainments, such shows hinged on uncertain moments with mixed emotions on both sides. This chapter considers the possible ways that, within the local context, phrenology and rational amusement might have become items for perusal and collection by Aboriginal people negotiating two-way living in a changing world.
The developed countries of the Australasian region have legislative and healthcare systems similar to the UK, consistent with their relatively recent colonial history. Australia and Aotearoa New Zealand both demonstrate varying approaches to provision of healthcare, disability support services and legislative frameworks for people with neurodevelopmental disabilities who commit offences. Particular areas of need are described, including the impact of the lack of capacity in neurodevelopmental disability healthcare and also the additional skills and understanding required to develop cultural competence to better support and work with the Indigenous people of both countries facing additional disadvantage. The challenges of service delivery across vast geographic areas of low population density are also discussed. Common features of both countries are discussed initially, then unique aspects in Australia andAotearoa New Zealand. Significant improvements have been made in recent years, but both countries still suffer from a lack of capacity in the workforce and sufficient funding to deliver high-quality services to people with neurodevelopmental disabilities who commit offences.
The contentious science of phrenology once promised insight into character and intellect through external 'reading' of the head. In the transforming settler-colonial landscapes of nineteenth-century Australia and Aotearoa New Zealand, popular phrenologists – figures who often hailed from the margins – performed their science of touch and cranial jargon everywhere from mechanics' institutions to public houses. In this compelling work, Alexandra Roginski recounts a history of this everyday practice, exploring how it featured in the fates of people living in, and moving through, the Tasman World. Innovatively drawing on historical newspapers and a network of archives, she traces the careers of a diverse range of popular phrenologists and those they encountered. By analysing the actions at play in scientific episodes through ethnographic, social and cultural history, Roginski considers how this now-discredited science could, in its own day, yield fleeting power and advantage, even against a backdrop of large-scale dispossession and social brittleness.
The British colonisation of Van Diemen’s Land (later Tasmania) began in 1803. There was an estimated 6,000 Aborigines (Palawa) living on the island with a history dating back over 40,000 years. By 1835, there were just over 100 Palawa living in forced exile on one of Tasmania’s smaller offshore islands. Only two residents remained when the government closed the Aboriginal Settlement in 1871. This chapter traces the history of Tasmania’s colonisation from 1803 to 1871 and finds that the British committed acts against the Palawa that meet the 1948 UN Convention on the Prevention and Punishment of the Crime of Genocide: killings, child removals, and creating conditions unconducive to sustaining life. Tasmania has been cited as one the ‘classical’ cases of genocide, but the finding has also stirred debate. This chapter surveys the historiography of Tasmanian genocide including Raphael Lemkin’s 1940s finding of a clear case of genocide; Henry Reynolds’ 2001 counter evidence of gubernatorial humanitarianism; and the subsequent histories that recognise genocide within the structure of settler colonialism. This chapter concludes that the British committed genocide in Tasmania with intent, but reported and framed that crime within the rhetoric, and even the guidelines, of contemporaneous humanitarian policies.
By 1837 the British government had been sending convicts, soldiers, and livestock entrepreneurs to Australia for almost fifty years. A committee of its own House of Commons, inspired by humanitarian principles, now reported the devastating effects on the indigenous inhabitants. Evidence of ‘extermination’ and ‘extirpation’ meant that the best minds of the Colonial Office were already exercised by the devastation of indigenous peoples inflicted by settlers who might have no clear aim of damaging them. When British government was extended to New Zealand, it was soon evident that Māori, for centuries sharing a largely common language and history, had a more effective capacity to resist than Aboriginal Australians, for millennia divided into hundreds of separate peoples and languages. In all Australian colonies and New Zealand, the determination of immigrants to ‘make productive’ land they knew belonged to others created disaster. Within twenty years of settlement, the Aboriginal population of Victoria declined by eighty percent. As the British spread over the whole continent, countless nations were extinguished. Across the Tasman the indigenous population was halved and the ‘passing of the Māori’ was still openly discussed even as adaptation, intermarriage and parliamentary representation saved it from genocide.
This chapter explores the notion of diachronic toponymy, which is the discipline that deals with the reconstruction of a place name in the context of undocumented languages/language families and in the absence of historical records. In many communities that do not have a writing system, oral stories and traditions become important sources of toponymic data, as place names are passed down orally, from one generation to another. Additionally, oral stories also commemorate the land and its namers, and are an ‘oral record’ of the physical territory and the changes made to it by human inhabitation. The chapter presents a step-by-step guide for studying place names according to a diachronic toponymy approach – one that also incorporates methods from anthropological linguistics, language documentation, and field linguistics. This is applied to a toponymic system in the Abui community on Alor Island, southeast Indonesia. The authors also demonstrate how historical semantics can complement the toponymic analysis by applying its criteria to a toponymic system which includes several Abui toponyms that show a semantic specialisation of the Abui term for ‘village’.
This chapter examines how we think about questions of plurality and the relations between legal orders. It does so through a specific history of the engagement between Indigenous legal orders and the Australian common law from the perspective of the latter. This chapter approaches legal plurality through the specific lens of thinking, both conceptually and practically, with jurisdiction. It looks at the ways in which the technology of jurisdiction has worked to obscure Indigenous legal orders and hence plurality. The chapter notes the increasing division between the approach of the High Court of Australia to plurality – as a matter to be contained or ignored –and the increasingly careful histories being written of our plural pasts and present.
The aim of this development paper is to inform the ongoing implementation of the partnership approach with Aboriginal families in Australia. As almost all Community Health Nurses employed by the Health Department of Western Australia, Country Health Service are non-Aboriginal, there are a number of factors that may, potentially, limit their capacity to work effectively with the primary caregivers of Aboriginal children.
Historically, much that has been written about the health and development of Aboriginal people in Australia has been negative and derogatory with wide criticism for their non-participation with health services and healthy lifestyle activities. Not only has this “deficit discourse” approach proved to be unhelpful in terms of improving the health and well-being of Aboriginal people but also there is mounting evidence that it has been detrimental to mental and physical health and capacity to achieve autonomy in all aspects of life.
In response to the voices of Aboriginal people, the partnership approach to care has been promoted for use by Community Health Nurses in Western Australia. However, the implementation of the approach is not always genuinely strength based, and it does not always focus on mutual goal setting within authentic partnership relationships. The partnership approach has the potential to improve the lives of Aboriginal people if it is implemented with appropriate cultural sensitivity, shared responsibility, dignity and respect.
Creating the conditions for meaningful relationships is essential to understanding Aboriginal worldviews and co-designing ways of working to achieve better health outcomes. Non-Aboriginal health professionals struggle to recognise the importance of social relationships to Aboriginal peoples and tensions emerge due to these different worldviews informed by different ontologies and epistemologies. This is more so in clinical settings where training and models of care are often inadequate for working with Aboriginal people. The impact of different understandings of relationships on the provision of health services to Aboriginal peoples remains under-researched. There is a critical need to reassess the way clinicians are supported by their organisations to engage with Aboriginal clients in competent and meaningfully ways.
Methods:
The paper provides key insights into an Aboriginal-led participatory action research project and the work of Aboriginal Elder co-researchers with non-Aboriginal mainstream service staff to better understand the importance of social relationships from an Aboriginal worldview. The paper critically engages literature on clinical service provision for Aboriginal peoples, along with an examination of the Australian Psychological Society Code of Conduct, to explore the tensions between professional training and the need to build relationships with Aboriginal clients.
Findings:
Through the Elders, non-Aboriginal service staff have expanded their understanding of Aboriginal culture, kinship and the importance of country to Aboriginal wellbeing. The Elders mentored staff to unpack the tensions between worldviews in clinical settings. The research resulted in a co-designed culturally safe framework for non-Aboriginal practitioners, which is building confidence, capacity and competence to work in partnership with Aboriginal peoples. The framework emphasis the need for culturally safe models of care. The Elders have supported non-Aboriginal staff to sit between the two worldviews to develop ways to work with Aboriginal clients and shift mainstream models of mental health care to improve the wellbeing of Aboriginal people.
In the crowded field of leadership research, Indigenous leadership remains under-researched. This article explores the Leadership Model of an Aboriginal Community Controlled Primary Health Care Organisation providing services to the Yolngu people of remote northern Australia: the Miwatj Health Aboriginal Corporation (Miwatj).
Background:
The limited research which does exist on Indigenous leadership points to unique challenges for Indigenous leaders. These challenges relate to fostering self-determination in their communities, managing significant community expectations, and navigating a path between culturally divergent approaches to management and leadership.
Methods:
Guided by Indigenous methodology and using a mixed methods approach, semi-structured interviews, self-reported health service data, organisational and publicly available documents, and literature were analysed using a framework method of thematic analysis to identify key themes of the Miwatj Leadership Model.
Findings:
The Miwatj Leadership Model is underpinned by three distinctive elements: it offers Yolngu people employment opportunities; it supports staff who want to move into leadership positions and provides capacity building through certificates and diplomas; and it provides for the physical, emotional, and cultural wellbeing of all Yolngu staff. Furthermore, the model respects traditional Yolngu forms of authority and empowers the community to develop, manage and sustain their own health. The Miwatj Leadership Model has been successful in providing formal pathways to support Indigenous staff to take on leadership roles, and has improved the accessibility and acceptability of health care services as a result of Yolngu employment and improved cultural safety.
Conclusions:
Translating the Miwatj Leadership Model into other health services will require considerable thought and commitment. The Miwatj Leadership Model can be adapted to meet the needs of other health care services in consideration of the unique context within which they operate. This study has demonstrated the importance of having a formal leadership model that promotes recruitment, retention, and career progression for Indigenous staff.
Brain injury, resulting from stroke and traumatic brain injury, is a common occurrence in Australia, with Aboriginal people affected at a significant rate and impact felt by individuals, families and communities. Access to brain injury rehabilitation services for Aboriginal people is reported to be often limited, with very little support outside the hospital environment. Our research involving Aboriginal brain injury survivors and their families to date has revealed that people often manage ‘on their own’ following such events. Following recommendations from survivors and their families, the Healing Right Way clinical trial, currently underway in Western Australia, has created the role of Aboriginal Brain Injury Coordinator (ABIC) to assist in navigating information and services, particularly after discharge from hospital. Eight positions for this role have been instigated across metropolitan and rural regions in the state. Healing Right Way’s aim is to enhance rehabilitation services and improve quality of life for Aboriginal Australians after brain injury. The ABIC’s role is to provide education, support, liaison and advocacy services to participants and their families over a six-month period, commencing soon after the participant’s stroke or injury has occurred. This paper outlines the development of this role, the partnerships involved, experiences to date and identifies some facilitators and barriers encountered that may impact the role’s ongoing sustainability. Details of components of the planned full Process Evaluation of Healing Right Way related to the ABIC role and the partnerships surrounding it are also provided. In combination with the trial’s ultimate results, this detail will assist in future service planning and provide a model of culturally secure care for stroke and brain injury services that can also inform other sub-acute and primary care models.
This chapter discusses the health of Aboriginal and Torres Strait Islander peoples from a gendered perspective, considering the different health needs and outcomes experienced by men and women. It begins by unpacking the construct of gender and discussing how gender and gender variations are viewed and accepted by Aboriginal and Torres Strait Islander communities. The Indigenous understandings of women’s business and men’s business are discussed from historical and contemporary perspectives, with a strong focus on the National Aboriginal Health Strategy’s definitions of the two. The chapter then discusses the differences in health outcomes between Indigenous and non-Indigenous men and women, and how the different views they have of health may affect them, before considering how nurses can best provide gender-appropriate care to their Aboriginal and Torres Strait Islander patients. The chapter concludes by considering how Australian policies have varied in meeting the gendered needs of Indigenous Australians, and how the health of Aboriginal and Torres Strait Islander men and women is changing and will continue to do so into the future.
This chapter focuses on the different health needs and outcomes of Indigenous children and their families. It begins by discussing the national policies aimed at improving Indigenous child health, including the National Framework for Health Services for Aboriginal and Torres Strait Islander Children and Families, and by considering the cultural and social considerations when providing healthcare to Indigenous children. The gap between mortality and morbidity rates of Aboriginal and Torres Strait Islander children and non-Indigenous children is established as the authors call for nurses and midwives to understand the stories behind these statistics, before considering the programs and initiatives aimed at improving health outcomes of Indigenous children. The chapter discusses ways to promote health, and considers common health issues experienced by Indigenous children, including poor nutrition, oral and ear health, and infections. The chapter provides concrete ways in which nurses and midwives can care for Indigenous children and also discusses examples of community programs working to reduce the rate of accidents and self-harm in Indigenous children.
The health outcomes and health needs of Aboriginal and Torres Strait Islander peoples living in remote communities are different to those living in regional and urban communities. This chapter discusses the role of remote area nurses (RANs) and their scope of practice, along with the challenges they may face while working in remote Indigenous communities. It establishes the need for RANs to integrate with the community and lead health initiatives. The work RANs may undertake is discussed, as well as the additional qualifications, including immunisation, sexual health endorsements and x-ray licences, which may be of benefit. The chapter discusses the different burden of disease and injury in remote Aboriginal and Torres Strait Island communities, and the holistic way these communities often perceive health. The chapter calls for cultural safety in remote area nursing, and suggests that respecting differences in culture, communication and health education is critical. The author concludes by reflecting on her own experience as a remote area nurse.