The world's population first reached one billion people in 1803, and reach eight billion in 2023, and will peak at almost 11 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 live 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 decade 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.

The earliest point where scientists can make reasonable estimates for the population of global regions is around 10,000 years before the Common Era (or 12,000 years ago). Estimates suggest that Asia has consistently been the most populated continent, and the least populated continent has generally been Oceania (although it was more heavily populated than areas such as North America in very early years). Population growth was very slow, but an increase can be observed between most of the given time periods. There were, however, dips in population due to pandemics, the most notable of these being the impact of plague in Eurasia in the 14th century, and the impact of European contact with the indigenous populations of the Americas after 1492, where it took almost four centuries for the population of Latin America to return to its pre-1500 level. The world's population first reached one billion people in 1803, which also coincided with a spike in population growth, due to the onset of the demographic transition. This wave of growth first spread across the most industrially developed countries in the 19th century, and the correlation between demographic development and industrial or economic maturity continued until today, with Africa being the final major region to begin its transition in the late-1900s.

Between 1800 and 2021, the total population of each continent experienced consistent growth, however as growth rates varied by region, population distribution has fluctuated. In the early 19th century, almost 70 percent of the world's population lived in Asia, while fewer than 10 percent lived in Africa. By the end of this century, it is believed that Asia's share will fall to roughly 45 percent, while Africa's will be on course to reach 40 percent. 19th and 20th centuries Fewer than 2.5 percent of the world's population lived in the Americas in 1800, however the demographic transition, along with waves of migration, would see this share rise to almost 10 percent a century later, peaking at almost 14 percent in the 1960s. Europe's share of the global population also grew in the 19th century, to roughly a quarter in 1900, but fell thereafter and saw the largest relative decline during the 20th century. Asia, which has consistently been the world's most populous continent, saw its population share drop by the mid-1900s, but it has been around 60 percent since the 1970s. It is important to note that the world population has grown from approximately one to eight billion people between 1800 and the 2020s, and that declines in population distribution before 2020 have resulted from different growth rates across the continents. 21st century Africa's population share remained fairly constant throughout this time, fluctuating between 7.5 and 10 percent until the late-1900s, but it is set to see the largest change over the 21st century. As Europe's total population is now falling, and it is estimated that the total populations of Asia and the Americas will fall by the 2050s and 2070s respectively, rapid population growth in Africa will see a significant shift in population distribution. Africa's population is predicted to grow from 1.3 to 3.9 billion people over the next eight decades, and its share of the total population will rise to almost 40 percent. The only other continent whose population will still be growing at this time will be Oceania, although its share of the total population has never been more than 0.7 percent.

Throughout the Common Era, Western Europe's population development fluctuated greatly. The population was very similar at the beginning and end of the first millennium, at around 25 million people. The largest decline in this period occurred in the sixth century, due to the Plague of Justinian, which the source claims to have killed around one third of the continent's population (although recent studies dispute this). Similarly, the population fell by almost 17 million throughout the 14th century, due to the Black Death.

Improvements in agriculture and infrastructure then saw population growth increase once more from the 15th century onwards, before the onset of the demographic transition saw a population boom throughout the 19th and 20th centuries.

Between 1500 and 1800, London grew to be the largest city in Western Europe, with its population growing almost 22 times larger in this period. London would eventually overtake Constantinople as Europe's largest in the 1700s, before becoming the largest city in the world (ahead of Beijing) in the early-1800s.

The most populous cities in this period were the capitals of European empires, with Paris, Amsterdam, and Vienna growing to become the largest cities, alongside the likes of Lisbon and Madrid in Iberia, and Naples or Venice in Italy. Many of northwestern Europe's largest cities in 1500 would eventually be overtaken by others not shown here, such as the port cities of Hamburg, Marseilles or Rotterdam, or more industrial cities such as Berlin, Birmingham, and Munich.

By 1800, London had grown to be the largest city in Western Europe with just under one million inhabitants. Paris was now the second largest city, with over half a million people, and Naples was the third largest city with 450 thousand people. The only other cities with over two hundred thousand inhabitants at this time were Vienna, Amsterdam and Dublin. Another noticeable development is the inclusion of many more northern cities from a wider variety of countries. The dominance of cities from France and Mediterranean countries was no longer the case, and the dispersal of European populations in 1800 was much closer to how it is today, more than two centuries later.

South America has a complex demographic history shaped by multiple migration and admixture events in pre- and post-colonial times. Settled over 14,000 years ago by Native Americans, South America has experienced migrations of European and African individuals, similar to other regions in the Americas. However, the timing and magnitude of these events resulted in markedly different patterns of admixture throughout Latin America. We use genome-wide SNP data for 437 admixed individuals from 5 countries (Colombia, Ecuador, Peru, Chile, and Argentina) to explore the population structure and demographic history of South American Latinos. We combined these data with population reference panels from Africa, Asia, Europe and the Americas to perform global ancestry analysis and infer the subcontinental origin of the European and Native American ancestry components of the admixed individuals. By applying ancestry-specific PCA analyses we find that most of the European ancestry in South American Latinos is from the Iberian Peninsula; however, many individuals trace their ancestry back to Italy, especially within Argentina. We find a strong gradient in the Native American ancestry component of South American Latinos associated with country of origin and the geography of local indigenous populations. For example, Native American genomic segments in Peruvians show greater affinities with Andean indigenous peoples like Quechua and Aymara, whereas Native American haplotypes from Colombians tend to cluster with Amazonian and coastal tribes from northern South America. Using ancestry tract length analysis we modeled post-colonial South American migration history as the youngest in Latin America during European colonization (9–14 generations ago), with an additional strong pulse of European migration occurring between 3 and 9 generations ago. These genetic footprints can impact our understanding of population-level differences in biomedical traits and, thus, inform future medical genetic studies in the region.

This dataset is about books. It has 1 row and is filtered where the book is Population movements in modern European history. It features 7 columns including author, publication date, language, and book publisher.

The expansion of human settlements over the past few centuries is responsible for an unprecedented number of invasive species introductions globally. An important component of biological invasion management is understanding how introduction history and post-introduction processes have jointly shaped present-day distributions and patterns of population structure, diversity, and adaptation. One example of a successful invader is the European starling (Sturnus vulgaris), which was intentionally introduced to numerous countries in the 19th century, including Aotearoa New Zealand, where it has become firmly established. We used reduced-representation sequencing to characterise the genetic population structure of the European starling in New Zealand, and compared the population structure to that present in sampling locations in the native range and invasive Australian range. We found that population structure and genetic diversity patterns suggested restricted gene flow from the majority of New Zealand to the northmost sampling location (Auckland). We also profiled genetic bottlenecks and shared outlier genomic regions, which supported historical accounts of translocations between both Australian subpopulations and New Zealand, and provided evidence of which documented translocation events were more likely to have been successful. Using these results as well as historic demographic patterns, we demonstrate how genomic analysis complements even well-documented invasion histories to better understand invasion processes, with direct implication for understanding contemporary gene flow and informing invasion management. Methods Sample Collection A total of 106 starling specimen samples were obtained from various contributors within New Zealand from five geographically distinct locations between May 2022 and October 2023. Sampling covered three locations in the North Island, specifically in the Auckland region (AUK: n=18), the Manawatū-Whanganui region (WHA: n=12), the Wellington region (WEL: n=40) and two in the South Island in the Marlborough region (MRL: n=15) and Canterbury region (CAN: n=21). In addition to the newly obtained samples, we also incorporated sequence data from the native European range (Antwerp, Belgium; ANT: n=15, Newcastle, United Kingdom; NWC: n=15, Monks Wood, United Kingdom; MKW: n=15), as well as two locations from within the invasive Australian range (Orange; ORG: n=15, McLaren Vale; MLV: n=15) from a previously published Diversity Arrays Technology Pty Ltd sequencing (DArT-seq) dataset. DNA Extraction and Sequencing Extracted DNA from the newly collected New Zealand samples was sent to Diversity Arrays for sequencing. Sequencing was performed on an Illumina Hiseq2500/Novaseq6000. Raw Sequence Processing The previously published raw DArT-seq data, along with the MRL samples (January 2023 sequencing batch) were demultiplexed using stacks v2.2 process_radtags, while also discarding low quality reads (-q), reads with uncalled bases (-c), and rescuing barcodes and RAD-Tag cut sites (-r). It was not necessary to perform this step on the remainder of the new raw sequence data because DArT performed in-house demultiplexing using a proprietary bioinformatic pipeline. For all the data, we used fastp v0.23.2 to remove adapter sequences and in the same step filtered reads for a minimum Phred quality score of 22 (-q 22) and a minimum length of 40 (-l 40). Both batches of sequence data produced as part of this study were additionally length trimmed to reduce the read length of the newer sequence data to match the base length of the older sequence data (-b 69). Mapping, Variant Calling, and Filtering We used the program bwa v0.7.17 to index the reference genome S. vulgaris vAU1.0 and align the trimmed DArT reads using the bwa aln function (-B 5 to trim the first 5 base pairs of each read), which is optimised for single-end short reads. This was then followed by the bwa samse function for producing the SAM formatted output files containing the alignments and their respective base qualities. Alignments were then sorted and indexed using samtools v1.16.1, and single nucleotide polymorphisms (SNPs) were subsequently called and annotated using bcftools v1.16 with the mpileup (-a "DP,AD,SP", --ignore-RG) and call (-mv, -f GQ) functions. We removed known technical replicates and identified relatives from the data. vcftools v0.1.15 was used to remove indels (--remove-indels), and quality filter for a minimum site quality score of 30 (--minQ30), minimum genotype quality score of 20 (--minGQ 20), and minimum and maximum depth of coverage of 5 (--minDP 5) and 100 (--maxDP 100). Then, to account for batch effects that may impact the sequenced loci, we kept only SNPs present in at least 50% of the individuals in each sampling location. We ran one final filtering step to ensure appropriate levels of missingness and rare alleles using the following parameters: maximum missingness per site of 30% (--max-missing 0.7), minor allele count of 5 (--mac 5), and a minimum and maximum allele per locus of 2 (--min-alleles 2 --max-alleles 2), resulting in a dataset containing 19,174 SNPs and 141 individuals.

The population of Europe was estimated to be 742.2 million in 2023, an increase of around 2.2 million when compared with 2013. Over 35 years between 1950 and 1985, the population of Europe grew by approximately 157.8 million. But 35 years after 1985 it was estimated to have only increased by around 38.7 million. Since the 1960s, population growth in Europe has fallen quite significantly and was even negative during the mid-1990s. While population growth has increased slightly since the low of -0.07 percent in 1998, the growth rate for 2020 was just 0.04 percent.

Which European country has the biggest population? As of 2021, the population of Russia was estimated to be approximately 145.9 million and was by far Europe's largest country in terms of population, with Turkey being the second-largest at over 85 million. While these two countries both have territory in Europe, however, they are both only partially in Europe, with the majority of their landmasses being in Asia. In terms of countries wholly located on the European continent, Germany had the highest population at 83.9 million, and was followed by the United Kingdom and France at 68.2 million and 65.4 million respectively.

Characteristics of Europe's population There are approximately 386.5 million females in Europe, compared with 361.2 million males, a difference of around 25 million. In 1950, however, the male population has grown faster than the female one, with the male population growing by 104.7 million, and the female one by 93.6 million. As of 2021, the single year of age with the highest population was 34, at 10.7 million, while in the same year there were estimated to be around 136 thousand people aged 100 or over.

This database offers the legal populations of Ile-de-France municipalities in the population censuses of 1968, 1975, 1982, 1990, 1999, from 2006 to 2014.

The interpretation of changes must take into account changes introduced with the renovation of the census and which are specified in the definition of municipal population.

The results are not established with identical geographical perimeter, they are in the geography in force at the time of the corresponding census. Thus, since 1968, municipalities have for example merged: find all the municipal evolutions.

The database is used to calculate the intercensal population evolutions. It gives for each municipality the populations without double counts in the censuses from 1968 to 1999 and the "https://www.insee.fr/fr/metadonnees/definition/c1932">municipal population since the 2006 census< /a>.

Data for the commune of Paris are presented for each municipal arrondissement (75101 to 75120).

Alcobendas City Council. Relative population growth since 2003. Data obtained from the Municipal Padrón of Alcobendas

This dataset contains data on population by sex and age on the basis of the results of the Census Data of Estonia, which was carried out on 28 December 1922. Dataset "Estonian Population by Sex and Age in 1922 Census Data" was published implementing project "Historical Sociology of Modern Restorations: a Cross-Time Comparative Study of Post-Communist Transformation in the Baltic States" from 2018 to 2022. Project leader is prof. Zenonas Norkus. Project is funded by the European Social Fund according to the activity "Improvement of researchers' qualification by implementing world-class R&D projects' of Measure No. 09.3.3-LMT-K-712".

This table contains figures on the employment history of the Dutch population (aged 15 years or over) in the past 4 years that have been included in the population register of a Dutch municipality on 31 December of the year under review. The employment history figures over the past 4 years have been subdivided into continuous employment, partly employed and non-active and are based on a continuous period of 4 years. Data on employment history are further broken down by gender, age, migration background and region. Regional data are based on the regional classification of 1 January 2019. Persons working at international organisations are considered to be working in the current table. This applies from the 2011 level year.

Data available: 2004 to 2018

Status of the figures: The figures in this table are final, with the exception of the most recent year 2018. The results in this table are presented according to the municipal classification of 1 January 2019.

Changes as of 4 February 2021: None, this table has been discontinued.

When will there be new figures: No longer applicable. This table is followed by the table Labour past population last 4 years, region (2020 breakdown). See paragraph 3.

Understanding the biological processes involved in genetic differentiation and divergence between populations within species is a pivotal aim in evolutionary biology. One particular phenomenon that requires clarification is the maintenance of genetic barriers despite the high potential for gene flow in the marine environment. Such patterns have been attributed to limited dispersal or local adaptation, and to a lesser extent to the demographic history of the species. The corkwing wrasse (Symphodus melops) is an example of a marine fish species where regions of particular strong divergence are observed. One such genetic break occurred at a surprisingly small spatial scale (FSTÂ ~0.1), over a short coastline (<60Â km) in the North Sea-Skagerrak transition area in southwestern Norway. Here, we investigate the observed divergence and purported reproductive isolation using genome resequencing. Our results suggest that historical events during the post-glacial recolonization route can explain...

The Caribbean basin is home to some of the most complex interactions in recent history among previously diverged human populations. Here, we investigate the population genetic history of this region by characterizing patterns of genome-wide variation among 330 individuals from three of the Greater Antilles (Cuba, Puerto Rico, Hispaniola), two mainland (Honduras, Colombia), and three Native South American (Yukpa, Bari, and Warao) populations. We combine these data with a unique database of genomic variation in over 3,000 individuals from diverse European, African, and Native American populations. We use local ancestry inference and tract length distributions to test different demographic scenarios for the pre- and post-colonial history of the region. We develop a novel ancestry-specific PCA (ASPCA) method to reconstruct the sub-continental origin of Native American, European, and African haplotypes from admixed genomes. We find that the most likely source of the indigenous ancestry in Caribbean islanders is a Native South American component shared among inland Amazonian tribes, Central America, and the Yucatan peninsula, suggesting extensive gene flow across the Caribbean in pre-Columbian times. We find evidence of two pulses of African migration. The first pulse—which today is reflected by shorter, older ancestry tracts—consists of a genetic component more similar to coastal West African regions involved in early stages of the trans-Atlantic slave trade. The second pulse—reflected by longer, younger tracts—is more similar to present-day West-Central African populations, supporting historical records of later transatlantic deportation. Surprisingly, we also identify a Latino-specific European component that has significantly diverged from its parental Iberian source populations, presumably as a result of small European founder population size. We demonstrate that the ancestral components in admixed genomes can be traced back to distinct sub-continental source populations with far greater resolution than previously thought, even when limited pre-Columbian Caribbean haplotypes have survived.

The U.S. landscape has undergone substantial changes since Europeans first arrived. Many land use changes are attributable to human activity. Historical data concerning these changes are frequently limited and often difficult to develop. Modeling historical land use changes may be necessary. We develop annual population series from first European settlement to 1999 for all 50 states and Washington D.C. for use in modeling land use trends. Extensive research went into developing the historical data. Linear interpolation was used to complete the series after critically evaluating the appropriateness of linear interpolation versus exponential interpolation.Our objective was to develop an annual population data series from the first nonindigenous settlements to 1999 for each present day state that could be used to model landscape change presumed to be a direct result of activities associated with the settlement of nonindigenous people.

Alcobendas City Council. Population distribution data in the districts of the city, according to age and sixth criteria, since 2016

Phased haplotpyes -- callable regionsThe .tar archive contains phasing information for each sample. The files *.mask.bed.gz, indicate the genomic regions for each sample deemed to be callable. Files are based on the GRCh37 reference genome assembly. This release contains phased data generated by Song et al. as well as reprocessing of previously published data (samples NA20847 (KITZMAN et al. 2011), HGDP01029 and HGDP00456 (MEYER et al. 2012)). Please see Song et al. 2016 for more information. The following files are included: HG02799.fosmid.phased.vcf.gz, HG02799.mask.bed.gz, HG03108.fosmid.phased.vcf.gz, HG03108.mask.bed.gz, HG03428.fosmid.phased.vcf.gz, HG03428.mask.bed.gz, HGDP00456.fosmid.phased.vcf.gz, HGDP00456.mask.bed.gz, HGDP01029.fosmid.phased.vcf.gz, HGDP01029.mask.bed.gz, NA12878.fosmid.phased.vcf.gz, NA12878.mask.bed.gz, NA19240.fosmid.phased.vcf.gz, NA19240.mask.bed.gz, NA20847.fosmid.phased.vcf.gz, NA20847.mask.bed.gz, NA21302.fosmid.phased.vcf.gz, NA21302.mask.bed.gz.c...

In 1800, the region of Germany was not a single, unified nation, but a collection of decentralized, independent states, bound together as part of the Holy Roman Empire. This empire was dissolved, however, in 1806, during the Revolutionary and Napoleonic eras in Europe, and the German Confederation was established in 1815. Napoleonic reforms led to the abolition of serfdom, extension of voting rights to property-owners, and an overall increase in living standards. The population grew throughout the remainder of the century, as improvements in sanitation and medicine (namely, mandatory vaccination policies) saw child mortality rates fall in later decades. As Germany industrialized and the economy grew, so too did the argument for nationhood; calls for pan-Germanism (the unification of all German-speaking lands) grew more popular among the lower classes in the mid-1800s, especially following the revolutions of 1948-49. In contrast, industrialization and poor harvests also saw high unemployment in rural regions, which led to waves of mass migration, particularly to the U.S.. In 1886, the Austro-Prussian War united northern Germany under a new Confederation, while the remaining German states (excluding Austria and Switzerland) joined following the Franco-Prussian War in 1871; this established the German Empire, under the Prussian leadership of Emperor Wilhelm I and Chancellor Otto von Bismarck. 1871 to 1945 - Unification to the Second World War The first decades of unification saw Germany rise to become one of Europe's strongest and most advanced nations, and challenge other world powers on an international scale, establishing colonies in Africa and the Pacific. These endeavors were cut short, however, when the Austro-Hungarian heir apparent was assassinated in Sarajevo; Germany promised a "blank check" of support for Austria's retaliation, who subsequently declared war on Serbia and set the First World War in motion. Viewed as the strongest of the Central Powers, Germany mobilized over 11 million men throughout the war, and its army fought in all theaters. As the war progressed, both the military and civilian populations grew increasingly weakened due to malnutrition, as Germany's resources became stretched. By the war's end in 1918, Germany suffered over 2 million civilian and military deaths due to conflict, and several hundred thousand more during the accompanying influenza pandemic. Mass displacement and the restructuring of Europe's borders through the Treaty of Versailles saw the population drop by several million more.

Reparations and economic mismanagement also financially crippled Germany and led to bitter indignation among many Germans in the interwar period; something that was exploited by Adolf Hitler on his rise to power. Reckless printing of money caused hyperinflation in 1923, when the currency became so worthless that basic items were priced at trillions of Marks; the introduction of the Rentenmark then stabilized the economy before the Great Depression of 1929 sent it back into dramatic decline. When Hitler became Chancellor of Germany in 1933, the Nazi government disregarded the Treaty of Versailles' restrictions and Germany rose once more to become an emerging superpower. Hitler's desire for territorial expansion into eastern Europe and the creation of an ethnically-homogenous German empire then led to the invasion of Poland in 1939, which is considered the beginning of the Second World War in Europe. Again, almost every aspect of German life contributed to the war effort, and more than 13 million men were mobilized. After six years of war, and over seven million German deaths, the Axis powers were defeated and Germany was divided into four zones administered by France, the Soviet Union, the UK, and the U.S.. Mass displacement, shifting borders, and the relocation of peoples based on ethnicity also greatly affected the population during this time. 1945 to 2020 - Partition and Reunification In the late 1940s, cold war tensions led to two distinct states emerging in Germany; the Soviet-controlled east became the communist German Democratic Republic (DDR), and the three western zones merged to form the democratic Federal Republic of Germany. Additionally, Berlin was split in a similar fashion, although its location deep inside DDR territory created series of problems and opportunities for the those on either side. Life quickly changed depending on which side of the border one lived. Within a decade, rapid economic recovery saw West Germany become western Europe's strongest economy and a key international player. In the east, living standards were much lower, although unemployment was almost non-existent; internationally, East Germany was the strongest economy in the Eastern Bloc (after the USSR), though it eventually fell behind the West by the 1970s. The restriction of movement between the two states also led to labor shortages in t...