scholarly journals Creating a sense of ‘CLOSURE’: Providing confidence intervals on some recent estimates of indigenous populations

2006 ◽  
Vol 33 (1) ◽  
pp. 1 ◽  
Author(s):  
Boyd H. Hunter ◽  
Mardi H. Dungey

The error of closure is the population growth that cannot be accounted for by either natural increase or quantifiable non-demographic factors, and is an issue that is particularly pronounced for indigenous peoples. This paper estimates Australia’s indigenous population using the dual system estimation method, and compares these to those produced using the standard undercount method. The main conclusion is that dual system estimates of the indigenous population appear to be reasonably accurate at the national level, which provide an appreciation of the reliability of existing estimates. Notwithstanding, policy makers need to take into account that population statistics are merely estimates.

Author(s):  
Robyn K Rowe ◽  
Jennifer D Walker

IntroductionThe increasing accessibility of data through digitization and linkage has resulted in Indigenous and allied individuals, scholars, practitioners, and data users recognizing a need to advance ways that assert Indigenous sovereignty and governance within data environments. Advances are being talked about around the world for how Indigenous data is collected, used, stored, shared, linked, and analysed. Objectives and ApproachDuring the International Population Data Linkage Network Conference in September of 2018, two sessions were hosted and led by international collaborators that focused on regional Indigenous health data linkage. Notes, discussions, and artistic contributions gathered from the conference led to collaborative efforts to highlight the common approaches to Indigenous data linkage, as discussed internationally. This presentation will share the braided culmination of these discussions and offer S.E.E.D.S as a set of guiding Indigenous data linkage principles. ResultsS.E.E.D.S emerges as a living and expanding set of guiding principles that: 1) prioritizes Indigenous Peoples’ right to Self-determination; 2) makes space for Indigenous Peoples to Exercise sovereignty; 3) adheres to Ethical protocols; 4) acknowledges and respects Data stewardship and governance, and; 5) works to Support reconciliation between Indigenous Peoples and settler states. S.E.E.D.S aims to centre and advance Indigenous-driven population data linkage and research while weaving together common global approaches to Indigenous data linkage. Conclusion / ImplicationsEach of the five elements of S.E.E.D.S interweave and need to be enacted together to create a positive Indigenous data linkage environment. When implemented together, the primary goals of the S.E.E.D.S Principles is to guide positive Indigenous population health data linkage in an effort to create more meaningful research approaches through improved Indigenous-based research processes. The implementation of these principles can, in turn, lead to better measurements of health progress that are critical to enhancing health care policy and improving health and wellness outcomes for Indigenous populations.


1995 ◽  
Vol 26 (2) ◽  
pp. 227-241 ◽  
Author(s):  
Gerrit Knaap

In modern Indonesia the demographic study of the population has become a major field of academic interest. The reason is obvious: the endeavour to develop the nation's economy in order to give every citizen a proper standard of living and to guarantee this in the future, bears a strong relation to the size of the population and the desire to stem the tide of excessive population growth. Demographic studies are only recent and the same is true for the statistical material with which these studies work: censuses at a national level and regular registrations of births, marriages and deaths at the basic local level. In Indonesia the first, still imperfect, censuses date from the final decades of the nineteenth century, while regular registration of births, deaths and marriages for the indigenous population has only taken place from the 1930s onwards.


Author(s):  
Heba Shahaed ◽  
Guneet Sandhu ◽  
Eric Seidlitz

Research has shown that Indigenous peoples in Canada experience health inequities when compared to the non-Indigenous population. High quality primary care has been described in literature; however, this has not been explored through the lens of Indigenous health. A scoping review was performed in order to investigate the quality of primary care received by indigenous peoples in Ontario. To conduct this review, a search of current literature on primary care in Indigenous communities in Ontario was performed. The studies examined in this review were derived from four different databases and many evaluated specific communities using a qualitative and quantitative approach. Several themes were identified including inadequate preparation and training of health care providers, physician and nursing shortages, strategies associated with improved quality of care, management of mental health, disparities in health service delivery station types and ineffective primary care impacts on hospitalizations. This literature search demonstrated a clear gap in the literature on the quality of primary care received by the Indigenous population in Ontario. Thus, further research is necessary in order to outline the current state of primary care being delivered to Indigenous populations in Ontario, and develop strategies to enhance the quality of care for this population.  


2022 ◽  
pp. 174077452110691
Author(s):  
Valerie Umaefulam ◽  
Tessa Kleissen ◽  
Cheryl Barnabe

Background Indigenous peoples are overrepresented with chronic health conditions and experience suboptimal outcomes compared with non-Indigenous peoples. Genetic variations influence therapeutic responses, thus there are potential risks and harm when extrapolating evidence from the general population to Indigenous peoples. Indigenous population–specific clinical studies, and inclusion of Indigenous peoples in general population clinical trials, are perceived to be rare. Our study (1) identified and characterized Indigenous population–specific chronic disease trials and (2) identified the representation of Indigenous peoples in general population chronic disease trials conducted in Australia, Canada, New Zealand, and the United States. Methods For Objective 1, publicly available clinical trial registries were searched from May 2010 to May 2020 using Indigenous population–specific terms and included for data extraction if in pre-specified chronic disease. For identified trials, we extracted Indigenous population group identity and characteristics, type of intervention, and funding type. For Objective 2, a random selection of 10% of registered clinical trials was performed and the proportion of Indigenous population participants enrolled extracted. Results In total, 170 Indigenous population–specific chronic disease trials were identified. The clinical trials were predominantly behavioral interventions (n = 95). Among general population studies, 830 studies were randomly selected. When race was reported in studies (n = 526), Indigenous individuals were enrolled in 172 studies and constituted 5.6% of the total population enrolled in those studies. Conclusion Clinical trials addressing chronic disease conditions in Indigenous populations are limited. It is crucial to ensure adequate representation of Indigenous peoples in clinical trials to ensure trial data are applicable to their clinical care.


2021 ◽  
pp. e20190042
Author(s):  
Joanne Heritz

The relationship between local government and urban Indigenous Peoples in Ontario is understudied, even though over half of Canada’s Indigenous population live in urban centres, one in five of Canada’s Indigenous population live in Ontario, and the Six Nations of the Grand River has the largest reserve population in Canada. Brantford, Hamilton, and Niagara were selected to build on previous research that mapped Municipal-Indigenous relations in seven municipalities across Canada. Studies regarding Municipal-Indigenous relations indicate the degree of inclusion of Indigenous Peoples in policy processes is as unique as each municipality. Some municipalities are urban Indigenous policy innovators with formal mechanisms for Indigenous inclusion in policy processes while others lag. An investigation of three Ontario municipalities is pivotal in partially supporting the finding that larger urban centres with proportionately smaller Indigenous populations are moving toward substantive Indigenous relationship building when compared to smaller municipalities with proportionately higher Indigenous populations.


2018 ◽  
Vol 2 (1) ◽  
pp. 1-13 ◽  
Author(s):  
Francis Markham ◽  
Nicholas Biddle

Background  The Indigenous population of Australia has grown very rapidly since the first tabulation of census statistics about Indigenous people in the 1971 ABS Census of Population and Housing (Census). Understanding the size and location of the Indigenous Australians is important to the State for service delivery and policy, and for Indigenous peoples themselves. Aims  This paper summarises changes to population geography of Indigenous Australians between 2011 and 2016. It describes the growth in the estimated population, and its changing geographic distribution. The paper derives a measure of ‘unexpected population change’: the spatial mismatch between demographic projections from the 2011 and 2016 Census counts. Data and methods  Census data and population projections are tabulated and mapped. Results  Indigenous people now comprise 3.3 per cent of the total Australian population, or 798,381 persons. This population grew by 3.5 per cent each year between 2011 and 2016, a rate of growth 34 per cent faster than that explained by natural increase alone. Both aspects of growth were concentrated in more urban parts of the country, especially coastal New South Wales and southeast Queensland. For the first time, fewer than 20 per cent of Indigenous people were recorded as living in remote areas. Conclusions  Indigenous population growth continues to be remarkably rapid. Future research is required to understand the correlates and causes of population growth beyond that explained by natural increase.


Author(s):  
Robyn Rowe ◽  
Stephanie Russo Carroll ◽  
Chyloe Healy ◽  
Desi Rodriguez-Lonebear ◽  
Jennifer D Walker

IntroductionGlobally, the ways that Indigenous data are collected, used, stored, shared, and analyzed are advancing through Indigenous data governance movements. However, these discussions do not always include the increasingly sensitive nature of linking Indigenous population health (IPH) data. During the International Population Data Linkage Network Conference in September of 2018, Indigenous people from three countries (Canada, New Zealand, and the United States) gathered and set the tone for discussions around Indigenous-driven IPH data linkage. ObjectivesCentering IPH data linkage and research priorities at the conference led to budding discussions from diverse Indigenous populations to share and build on current IPH data linkage themes. This paper provides a braided summary of those discussions which resulted in the SEEDS principles for use when linking IPH data. MethodsDuring the Conference, two sessions and a keynote were Indigenous-led and hosted by international collaborators that focused on regional perspectives on IPH data linkage. A retrospective document analysis of notes, discussions, and artistic contributions gathered from the conference resulted in a summary of shared common approaches to the linkage of IPH data. ResultsThe SEEDS Principles emerge as collective report that outlines a living and expanding set of guiding principles that: 1) prioritizes Indigenous Peoples' right to Self-determination; 2) makes space for Indigenous Peoples to Exercise sovereignty; 3) adheres to Ethical protocols; 4) acknowledges and respects Data stewardship and governance, and; 5) works to Support reconciliation between Indigenous nations and settler states. ConclusionEach of the elements of SEEDS need to be enacted together to create a positive data linkage environment. When implemented together, the SEEDS Principles can lead to more meaningful research and improved Indigenous data governance. The mindful implementation of SEEDS could lead to better measurements of health progress through linkages that are critical to enhancing health care policy and improving health and wellness outcomes for Indigenous nations.


2019 ◽  
Vol 26 (4) ◽  
pp. 437-456
Author(s):  
María Julia Ochoa Jiménez

Abstract:In Latin America, conflict-of-law norms have not appropriately considered the cultural diversity that exists in their legal systems. However, developments towards the recognition of Indigenous peoples’ human rights, at the international and national levels, impose the task of considering such diversity. In that regard, within the conflict-of-law realm, interpersonal law offers a useful perspective. This article proposes a conflict-of-law rule that can contribute to clarity and legal certainty, offering a sound way of dealing at the national level with Indigenous peoples’ claims for restitution of property with a cultural value for them, which is framed in international instruments on human rights.


Author(s):  
Cathie Martin ◽  
Tom Chevalier

Why did historical anti-poverty programs in Britain, Denmark and France differ so dramatically in their goals, beneficiaries and agents for addressing poverty? Different cultural views of poverty contributed to how policy makers envisioned anti-poverty reforms. Danish elites articulated social investments in peasants as necessary to economic growth, political stability and societal strength. British elites viewed the lower classes as a challenge to these goals. The French perceived the poor as an opportunity for Christian charity. Fiction writers are overlooked political agents who engage in policy struggles. Collectively, writers contribute to a country's distinctive ‘cultural constraint’, or symbols and narratives, which appears in the national-level aggregation of literature. To assess cross-national variations in cultural depictions of poverty, this article uses historical case studies and quantitative textual analyses of 562 British, 521 Danish and 498 French fictional works from 1770 to 1920.


Water ◽  
2021 ◽  
Vol 13 (15) ◽  
pp. 2092
Author(s):  
Songbai Song ◽  
Yan Kang ◽  
Xiaoyan Song ◽  
Vijay P. Singh

The choice of a probability distribution function and confidence interval of estimated design values have long been of interest in flood frequency analysis. Although the four-parameter exponential gamma (FPEG) distribution has been developed for application in hydrology, its maximum likelihood estimation (MLE)-based parameter estimation method and asymptotic variance of its quantiles have not been well documented. In this study, the MLE method was used to estimate the parameters and confidence intervals of quantiles of the FPEG distribution. This method entails parameter estimation and asymptotic variances of quantile estimators. The parameter estimation consisted of a set of four equations which, after algebraic simplification, were solved using a three dimensional Levenberg-Marquardt algorithm. Based on sample information matrix and Fisher’s expected information matrix, derivatives of the design quantile with respect to the parameters were derived. The method of estimation was applied to annual precipitation data from the Weihe watershed, China and confidence intervals for quantiles were determined. Results showed that the FPEG was a good candidate to model annual precipitation data and can provide guidance for estimating design values


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