Table showing ethnic group statistics by aggregated groupings.
Categories covered:
Figures may not add exactly due to rounding. Numbers rounded to the nearest thousand.
Data is from the Annual Population Survey.
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This dataset was produced in the 1990s by Myron Gutmann and others at the University of Texas to assess demographic change in European- and Mexican-origin populations in Texas from the mid-nineteenth to early-twentieth centuries. Most of the data come from manuscript records for six rural Texas counties - Angelina, DeWitt, Gillespie, Jack, Red River, and Webb - for the U.S. Censuses of 1850-1880 and 1900-1910, and tax records where available. Together, the populations of these counties reflect the cultural, ethnic, economic, and ecological diversity of rural Texas. Red River and Angelina Counties, in Eastern Texas, had largely native-born white and black populations and cotton economies. DeWitt County in Southeast Texas had the most diverse population, including European and Mexican immigrants as well as native-born white and black Americans, and its economy was divided between cotton and cattle. The population of Webb County, on the Mexican border, was almost entirely of Mexican origin, and economic activities included transportation services as well as cattle ranching. Gillespie County in Central Texas had a mostly European immigrant population and an economy devoted to cropping and livestock. Jack County in North-Central Texas was sparsely populated, mainly by native-born white cattle ranchers. These counties were selected to over-represent the European and Mexican immigrant populations. Slave schedules were not included, so there are no African Americans in the samples for 1850 or 1860. In some years and counties, the Census records were sub-sampled, using a letter-based sample with the family as the primary sampling unit (families were chosen if the surname of the head began with one of the sample letters for the county). In other counties and years, complete populations were transcribed from the Census microfilms. For details and sample sizes by county, see the County table in the Original P.I. Documentation section of the ICPSR Codebook, or see Gutmann, Myron P. and Kenneth H. Fliess, How to Study Southern Demography in the Nineteenth Century: Early Lessons of the Texas Demography Project (Austin: Texas Population Research Center Papers, no. 11.11, 1989).
The world's population first reached one billion people in 1805, and reached eight billion in 2022, and will peak at almost 10.2 billion by the end of the century. Although it took thousands of years to reach one billion people, it did so at the beginning of a phenomenon known as the demographic transition; from this point onwards, population growth has skyrocketed, and since the 1960s the population has increased by one billion people every 12 to 15 years. The demographic transition sees a sharp drop in mortality due to factors such as vaccination, sanitation, and improved food supply; the population boom that follows is due to increased survival rates among children and higher life expectancy among the general population; and fertility then drops in response to this population growth. Regional differences The demographic transition is a global phenomenon, but it has taken place at different times across the world. The industrialized countries of Europe and North America were the first to go through this process, followed by some states in the Western Pacific. Latin America's population then began growing at the turn of the 20th century, but the most significant period of global population growth occurred as Asia progressed in the late-1900s. As of the early 21st century, almost two-thirds of the world's population lives in Asia, although this is set to change significantly in the coming decades. Future growth The growth of Africa's population, particularly in Sub-Saharan Africa, will have the largest impact on global demographics in this century. From 2000 to 2100, it is expected that Africa's population will have increased by a factor of almost five. It overtook Europe in size in the late 1990s, and overtook the Americas a few years later. In contrast to Africa, Europe's population is now in decline, as birth rates are consistently below death rates in many countries, especially in the south and east, resulting in natural population decline. Similarly, the population of the Americas and Asia are expected to go into decline in the second half of this century, and only Oceania's population will still be growing alongside Africa. By 2100, the world's population will have over three billion more than today, with the vast majority of this concentrated in Africa. Demographers predict that climate change is exacerbating many of the challenges that currently hinder progress in Africa, such as political and food instability; if Africa's transition is prolonged, then it may result in further population growth that would place a strain on the region's resources, however, curbing this growth earlier would alleviate some of the pressure created by climate change.
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Statistics illustrates consumption, production, prices, and trade of Portland cement, white, whether or not artificially coloured in Eastern Europe from 2007 to 2024.
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Employment rate of people from non-white ethnic groups Source: Annual Population Survey (APS) Publisher: Nomis Geographies: Local Authority District (LAD), County/Unitary Authority, Government Office Region (GOR), National Geographic coverage: England Time coverage: 2004 to 2009 Type of data: Survey
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The survey, commissioned by the newsmagazine Suomen Kuvalehti, charted attitudes in Finland towards immigrants from different countries as well as beliefs about race. First, the respondents were asked to state their position on a scale from 0 to 10, where 10 indicated they hoped that Finland would be populated as much as possible by people of Finnish origin sharing the national values, and 0 that they hoped Finland would be populated as much as possible by people from a diversity of countries and ethnic backgrounds. Next, opinions were studied regarding how desirable or undesirable the respondents thought it was that immigrants of certain nationalities would come to Finland. The nationalities mentioned were Swedes, Germans, Russians, Estonians, US Americans, Somalis, Kosovars, Iraqis, Afghans, Syrians, Chinese, Thai and Ukrainians. The respondents were also asked to what extent they agreed with the following four statements: 'The mental abilities of black Africans are lower than those of white people living in Western countries', ' All people have equal value regardless of the colour of their skin or ethnic background', 'The white European race should be prevented from being mixed with darker races because otherwise the original population of Europe will become extinct before long ', and 'There is no such thing as 'race' since all human beings are genetically very much alike'. One question studied whether the respondents thought the Finnish media reported more negatively or positively on the Perussuomalaiset party (the Finns Party) than on the other political parties. Background variables included the respondent's gender, age, region of residence (NUTS3), major region of residence (NUTS2), city or type of municipality, education, occupational status and economic activity, household composition, number and ages of children living at home, total gross annual income of the household, and type of housing.
At the end of the Revolutionary Period in United States history, the majority of white settlers in the United States of America had English heritage. The Thirteen Colonies, which claimed independence in 1776, was part of the British Empire until this point - English settlers and their descendants made up over 60 percent of the population by 1790. The English were the ethnic majority (among whites) in all states except Pennsylvania, which had a similarly-sized German population, while New York had a sizeable Dutch population as it was a former Dutch colony. The second-largest group was the Irish, where those from both the island's north and south made up a combined 10 percent of the population, followed by the Scottish and Germans at over eight percent each. Outside of the United States, the French and Spanish territories that would later be incorporated into the Union were majority French and Spanish - despite their large size they were relatively sparsely populated. The composition of the U.S. population would change drastically throughout the 19th century due largely to waves of migration from Europe.
Gaia-DR2 has provided an unprecedented number of white dwarf candidates of our Galaxy. In particular, it is estimated that Gaia-DR2 has observed nearly 400000 of these objects and close to 18000 up to 100pc from the Sun. This large quantity of data requires a thorough analysis in order to uncover their main Galactic population properties, in particular the thin and thick disc and halo components. Taking advantage of recent developments in artificial intelligence techniques, we make use of a detailed Random Forest algorithm to analyse an 8D space (equatorial coordinates, parallax, proper motion components, and photometric magnitudes) of accurate data provided by Gaia-DR2 within 100pc from the Sun. With the aid of a thorough and robust population synthesis code, we simulated the different components of the Galactic white dwarf population to optimize the information extracted from the algorithm for disentangling the different population components. The algorithm is first tested in a known simulated sample achieving an accuracy of 85.3 per cent. Our methodology is thoroughly compared to standard methods based on kinematic criteria demonstrating that our algorithm substantially improves previous approaches. Once trained, the algorithm is then applied to the Gaia-DR2 100pc white dwarf sample, identifying 12227 thin disc, 1410 thick disc, and 95 halo white dwarf candidates, which represent a proportion of 74:25:1, respectively. Hence, the numerical spatial densities are (3.6+/-0.4)x10^-3^pc^-3^, (1.2+/-0.4)x10^-3^pc^-3^, and (4.8+/-0.4)x10^-5^pc^-3^ for the thin disc, thick disc, and halo components, respectively. The populations thus obtained represent the most complete and volume-limited samples to date of the different components of the Galactic white dwarf population.
European white stork are long considered to diverge to eastern and western migration pools as a result of independent overwintering flyways. In relatively recent times, the western and northern distribution has been subject to dramatic population declines and country-specific extirpations. A number of independent reintroduction programs were started in the mid 1950s to bring storks back to historical ranges. Founder individuals were sourced opportunistically from the Eastern and Western European distributions and Algeria, leading to significant artificial mixing between eastern and western flyways. Here we use mitochondrial and microsatellite DNA to test the contention that prior to translocation, eastern and western flyways were genetically distinct. The data show a surprising lack of structure at any spatial or temporal scale suggesting that even though birds were moved between flyways, there is evidence of natural mixing prior to the onset of translocation activities. Overall a high retention of genetic diversity, high Nef, and an apparent absence of recent genetic bottleneck associated with early 20th century declines suggest that the species is well equipped to respond to future environmental pressures.
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European populations of the white-tailed eagle (Haliaeetus albicilla) suffered a drastic decline during the 20th century. In many countries, only a few dozen breeding pairs survived or the species disappeared completely. By today, the populations have recovered, naturally or through restocking (e.g. in Scotland or the Czech Republic). In the Carpathian Basin, which is now a stronghold in southern Europe for the species in the southern part of the distribution range with more than 500 breeding pairs, only about 50 pairs survived the bottleneck. This region provides important wintering places for individuals arriving from different regions of Eurasia. In the present study, we investigated 249 DNA samples from several European countries, using 11 microsatellites and mitochondrial control region sequences (499 bp), to answer two main questions: 1) Did the Carpathian Basin population recover through local population expansion or is there a significant gene flow from more distant populations as well? 2) Does the Czech population show signs in its genetic structure of the restocking with birds of unknown origin? Our microsatellite data yielded three genetically separate lineages within Europe: northern, central and southern, the latter being present exclusively in the Carpathian Basin. Sequencing of mitochondrial DNA revealed that there is one haplotype (B12) which is not only exclusive to the Carpathian Basin but it is frequent in this population. Our results suggest that in accordance with the presumably philopatric behaviour of the species, recovery of the Carpathian Basin population was mainly local, but some of the wintering birds coming from the northern and central populations contributed to its genetic composition as well. We detected considerably higher proportions of northern birds within the Czech Republic compared to the neighbouring areas, making it likely that parents of the reintroduced birds came from northern populations.
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The labour force participation rate is the percentage of economically active population aged 15-64 on the total population of the same age. According to the definitions of the International Labour Organisation (ILO) for the purposes of the labour market statistics people are classified as employed, unemployed and outside the labour force. The economically active population (also called labour force) is the sum of employed and unemployed persons. Persons outside the labour force are those who, during the reference week, were neither employed nor unemployed. The MIP Scoreboard indicator is the three-year change in percentage points, with an indicative threshold of -0.2 pp. In the table, values are expressed also as percentage of total population. The data source is the quarterly EU Labour Force Survey (EU LFS). The survey covers the resident population in private households.
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BackgroundSocio-economic position (SEP) and ethnicity influence type 2 diabetes mellitus (T2DM) risk in adults. However, the influence of SEP on emerging T2DM risks in different ethnic groups and the contribution of SEP to ethnic differences in T2DM risk in young people have been little studied. We examined the relationships between SEP and T2DM risk factors in UK children of South Asian, black African-Caribbean and white European origin, using the official UK National Statistics Socio-economic Classification (NS-SEC) and assessed the extent to which NS-SEC explained ethnic differences in T2DM risk factors. Methods and FindingsCross-sectional school-based study of 4,804 UK children aged 9–10 years, including anthropometry and fasting blood analytes (response rates 70%, 68% and 58% for schools, individuals and blood measurements). Assessment of SEP was based on parental occupation defined using NS-SEC and ethnicity on parental self-report. Associations between NS-SEC and adiposity, insulin resistance (IR) and triglyceride differed between ethnic groups. In white Europeans, lower NS-SEC status was related to higher ponderal index (PI), fat mass index, IR and triglyceride (increases per NS-SEC decrement [95%CI] were 1.71% [0.75, 2.68], 4.32% [1.24, 7.48], 5.69% [2.01, 9.51] and 3.17% [0.96, 5.42], respectively). In black African-Caribbeans, lower NS-SEC was associated with lower PI (−1.12%; [−2.01, −0.21]), IR and triglyceride, while in South Asians there were no consistent associations between NS-SEC and T2DM risk factors. Adjustment for NS-SEC did not appear to explain ethnic differences in T2DM risk factors, which were particularly marked in high NS-SEC groups. ConclusionsSEP is associated with T2DM risk factors in children but patterns of association differ by ethnic groups. Consequently, ethnic differences (which tend to be largest in affluent socio-economic groups) are not explained by NS-SEC. This suggests that strategies aimed at reducing social inequalities in T2DM risk are unlikely to reduce emerging ethnic differences in T2DM risk.
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System estimation coefficients: Ordinary least squares.
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Estimation results for the pooled series with cross-section fixed effects.
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Conversation style variables for latina and white-european mothers: Descriptive statistics and reliabilities.
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Background Osteoporosis presents a significant global health challenge, compromising bone quality and elevating fracture susceptibility. While dual-energy x-ray absorptiometry (DXA) stands as the gold standard for bone mineral density (BMD) assessment and osteoporosis diagnosis, its costliness and complexity impede widespread screening adoption. Predictive modeling of BMD, leveraging genetic and clinical data, emerges as a more viable and cost-effective approach for osteoporosis and fracture risk evaluation. Methods and Findings We developed BMD prediction models for the femoral neck (FNK) and lumbar spine (SPN) using various methods within a UK Biobank (UKBB) training set comprising 17,964 individuals from the British white population. Models based on Regression with Least Absolute Shrinkage and Selection Operator (LASSO), selected based on the coefficient of determination (R2) from a model selection subset of 5,973 individuals from the British white population, underwent testing on five UKBB test sets and 12 independent cohorts of diverse ancestries, totaling over 15,000 individuals. Furthermore, we assessed the correlation of predicted BMDs with fragility fractures in a distinct case-control set of over 287,000 participants lacking DXA-BMDs in the UKBB of the European white population. Incorporating genetic factors marginally improved predictions, capturing an additional 2.3% variation for FNK-BMD and 3% for SPN-BMD over clinical factors alone. Predicted BMDs exhibited significant associations with fragility fracture risk in the European white population. Nonetheless, the predictive model's performance varied between the UKBB population of other ethnic groups and the independent cohorts. Conclusions Our study yields novel insights into predicting osteoporosis and fracture risk. Genetic factors enhance BMD predictive performance beyond clinical factors alone. Adjusting inclusion thresholds for genetic variants (e.g., 5×10^(-6) or 5×10^(-7)) rather than solely considering genome-wide association study (GWAS)-significant variants may further refine the model's explanatory power for BMD variations. This study also underscores the imperative for training models on diverse population to bolster predictive performance across various ethnic and geographical populations.
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Studies of measured and estimated glomerular filtration rate in Africa and Europe.
Between 1500 and 1820, an estimated 2.58 million Europeans migrated to the Americas, namely from the British Isles, Portugal, Spain, France and Germany. Until the mid-1600s, the majority of European migrants were from the Iberian Peninsula, as Portugal and Spain had a 150 year head start over other European powers when building their overseas empires. However, by the end of the century, more settlers from the British Isles had emigrated to the New World than from Spain or Portugal; the majority of which migrated to British colonies in the Caribbean as indentured servants or prisoners. The 18th century also saw migrants from other European nations begin to migrate en masse, particularly those from France and the German states, although migration from the British Isles and Portugal remained at the highest levels.
In comparison to the almost 2.6 million Europeans migrants, it is estimated that over 8.6 million Africans were forced across the Atlantic during this time period, as part of the transatlantic slave trade. The first half of the 19th century saw the demise of the transatlantic slave trade, which was followed by an influx of white migration to the Americas from across Europe; this contributed heavily to reversing demographic trends and making those with African ancestry an ethnic minority in most American countries today.
In the middle of 2023, about 60 percent of the global population was living in Asia.The total world population amounted to 8.1 billion people on the planet. In other words 4.7 billion people were living in Asia as of 2023. Global populationDue to medical advances, better living conditions and the increase of agricultural productivity, the world population increased rapidly over the past century, and is expected to continue to grow. After reaching eight billion in 2023, the global population is estimated to pass 10 billion by 2060. Africa expected to drive population increase Most of the future population increase is expected to happen in Africa. The countries with the highest population growth rate in 2024 were mostly African countries. While around 1.47 billion people live on the continent as of 2024, this is forecast to grow to 3.9 billion by 2100. This is underlined by the fact that most of the countries wit the highest population growth rate are found in Africa. The growing population, in combination with climate change, puts increasing pressure on the world's resources.
Brazil and the United States are the two most populous countries in the Americas today. In 1500, the year that Pedro Álvares Cabral made landfall in present-day Brazil and claimed it for the Portuguese crown, it is estimated that there were roughly one million people living in the region. Some estimates for the present-day United States give a population of two million in the year 1500, although estimates vary greatly. By 1820, the population of the U.S. was still roughly double that of Brazil, but rapid growth in the 19th century would see it grow 4.5 times larger by 1890, before the difference shrunk during the 20th century. In 2024, the U.S. has a population over 340 million people, making it the third most populous country in the world, while Brazil has a population of almost 218 million and is the sixth most populous. Looking to the future, population growth is expected to be lower in Brazil than in the U.S. in the coming decades, as Brazil's fertility rates are already lower, and migration rates into the United States will be much higher. Historical development The indigenous peoples of present-day Brazil and the U.S. were highly susceptible to diseases brought from the Old World; combined with mass displacement and violence, their population growth rates were generally low, therefore migration from Europe and the import of enslaved Africans drove population growth in both regions. In absolute numbers, more Europeans migrated to North America than Brazil, whereas more slaves were transported to Brazil than the U.S., but European migration to Brazil increased significantly in the early 1900s. The U.S. also underwent its demographic transition much earlier than in Brazil, therefore its peak period of population growth was almost a century earlier than Brazil. Impact of ethnicity The demographics of these countries are often compared, not only because of their size, location, and historical development, but also due to the role played by ethnicity. In the mid-1800s, these countries had the largest slave societies in the world, but a major difference between the two was the attitude towards interracial procreation. In Brazil, relationships between people of different ethnic groups were more common and less stigmatized than in the U.S., where anti-miscegenation laws prohibited interracial relationships in many states until the 1960s. Racial classification was also more rigid in the U.S., and those of mixed ethnicity were usually classified by their non-white background. In contrast, as Brazil has a higher degree of mixing between those of ethnic African, American, and European heritage, classification is less obvious, and factors such as physical appearance or societal background were often used to determine racial standing. For most of the 20th century, Brazil's government promoted the idea that race was a non-issue and that Brazil was racially harmonious, but most now acknowledge that this actually ignored inequality and hindered progress. Racial inequality has been a prevalent problem in both countries since their founding, and today, whites generally fare better in terms of education, income, political representation, and even life expectancy. Despite this adversity, significant progress has been made in recent decades, as public awareness of inequality has increased, and authorities in both countries have made steps to tackle disparities in areas such as education, housing, and employment.
Table showing ethnic group statistics by aggregated groupings.
Categories covered:
Figures may not add exactly due to rounding. Numbers rounded to the nearest thousand.
Data is from the Annual Population Survey.