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TwitterThe 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.
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This list ranks the 1 cities in the Long County, GA by Asian population, as estimated by the United States Census Bureau. It also highlights population changes in each cities over the past five years.
When available, the data consists of estimates from the U.S. Census Bureau American Community Survey (ACS) 5-Year Estimates, including:
Variables / Data Columns
Good to know
Margin of Error
Data in the dataset are based on the estimates and are subject to sampling variability and thus a margin of error. Neilsberg Research recommends using caution when presening these estimates in your research.
Custom data
If you do need custom data for any of your research project, report or presentation, you can contact our research staff at research@neilsberg.com for a feasibility of a custom tabulation on a fee-for-service basis.
Neilsberg Research Team curates, analyze and publishes demographics and economic data from a variety of public and proprietary sources, each of which often includes multiple surveys and programs. The large majority of Neilsberg Research aggregated datasets and insights is made available for free download at https://www.neilsberg.com/research/.
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TwitterAccording to latest figures, the Chinese population decreased by 1.39 million to around 1.408 billion people in 2024. After decades of rapid growth, China arrived at the turning point of its demographic development in 2022, which was earlier than expected. The annual population decrease is estimated to remain at moderate levels until around 2030 but to accelerate thereafter. Population development in China China had for a long time been the country with the largest population worldwide, but according to UN estimates, it has been overtaken by India in 2023. As the population in India is still growing, the country is very likely to remain being home of the largest population on earth in the near future. Due to several mechanisms put into place by the Chinese government as well as changing circumstances in the working and social environment of the Chinese people, population growth has subsided over the past decades, displaying an annual population growth rate of -0.1 percent in 2024. Nevertheless, compared to the world population in total, China held a share of about 17 percent of the overall global population in 2024. China's aging population In terms of demographic developments, the birth control efforts of the Chinese government had considerable effects on the demographic pyramid in China. Upon closer examination of the age distribution, a clear trend of an aging population becomes visible. In order to curb the negative effects of an aging population, the Chinese government abolished the one-child policy in 2015, which had been in effect since 1979, and introduced a three-child policy in May 2021. However, many Chinese parents nowadays are reluctant to have a second or third child, as is the case in most of the developed countries in the world. The number of births in China varied in the years following the abolishment of the one-child policy, but did not increase considerably. Among the reasons most prominent for parents not having more children are the rising living costs and costs for child care, growing work pressure, a growing trend towards self-realization and individualism, and changing social behaviors.
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TwitterIn 2024, white Americans remained the largest racial group in the United States, numbering just over 254 million. Black Americans followed at nearly 47 million, with Asians totaling around 23 million. Hispanic residents, of any race, constituted the nation’s largest ethnic minority. Despite falling fertility, the U.S. population continues to edge upward and is expected to reach 342 million in 2025. International migrations driving population growth The United States’s population growth now hinges on immigration. Fertility rates have long been in decline, falling well below the replacement rate of 2.1. On the other hand, international migration stepped in to add some 2.8 million new arrivals to the national total that year. Changing demographics and migration patterns Looking ahead, the U.S. population is projected to grow increasingly diverse. By 2060, the Hispanic population is expected to grow to 27 percent of the total population. Likewise, African Americans will remain the largest racial minority at just under 15 percent.
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TwitterIndia's total population reached nearly **** billion people as of 2023, making the country by far the most populous throughout the Asia-Pacific region. Contrastingly, Micronesia had a total population of around *** thousand people in the same year. The demographics of APAC Asia-Pacific, made up of many different countries and regions, is the most populated region across the globe. Being home to a significant number of megacities, and with the population ever-increasing, the region is unsurprisingly expected to have the largest urban population by 2050. However, as of 2021, the majority of Asia-Pacific countries had rural populations greater than ** percent. Population densities Despite China being the most populated country across the region, it fell in the middle of Asia-Pacific regions in terms of population density. On the other hand, Macao, Singapore, and Hong Kong all had the highest population densities across the Asia-Pacific region. These three Asia-Pacific regions also ranked among the top four densest populations worldwide.
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TwitterThis layer shows Asian alone or in any combination by selected groups. This is shown by tract, county, and state boundaries. This service is updated annually to contain the most currently released American Community Survey (ACS) 5-year data, and contains estimates and margins of error. There are also additional calculated attributes related to this topic, which can be mapped or used within analysis. The numbers by detailed Asian groups do not add to the total population. This is because the detailed Asian groups are tallies of the number of Asian responses rather than the number of Asian respondents. Responses that include more than one race and/or Asian group are counted several times. To see the full list of attributes available in this service, go to the "Data" tab, and choose "Fields" at the top right. Current Vintage: 2019-2023ACS Table(s): B02001, B02011, B02018 (Not all lines of ACS table B02001 are available in this layer.)Data downloaded from: Census Bureau's API for American Community Survey Date of API call: December 12, 2024National Figures: data.census.govThe United States Census Bureau's American Community Survey (ACS):About the SurveyGeography & ACSTechnical DocumentationNews & UpdatesThis ready-to-use layer can be used within ArcGIS Pro, ArcGIS Online, its configurable apps, dashboards, Story Maps, custom apps, and mobile apps. Data can also be exported for offline workflows. For more information about ACS layers, visit the FAQ. Please cite the Census and ACS when using this data.Data Note from the Census:Data are based on a sample and are subject to sampling variability. The degree of uncertainty for an estimate arising from sampling variability is represented through the use of a margin of error. The value shown here is the 90 percent margin of error. The margin of error can be interpreted as providing a 90 percent probability that the interval defined by the estimate minus the margin of error and the estimate plus the margin of error (the lower and upper confidence bounds) contains the true value. In addition to sampling variability, the ACS estimates are subject to nonsampling error (for a discussion of nonsampling variability, see Accuracy of the Data). The effect of nonsampling error is not represented in these tables.Data Processing Notes:This layer is updated automatically when the most current vintage of ACS data is released each year, usually in December. The layer always contains the latest available ACS 5-year estimates. It is updated annually within days of the Census Bureau's release schedule. Click here to learn more about ACS data releases.Boundaries come from the US Census TIGER geodatabases, specifically, the National Sub-State Geography Database (named tlgdb_(year)_a_us_substategeo.gdb). Boundaries are updated at the same time as the data updates (annually), and the boundary vintage appropriately matches the data vintage as specified by the Census. These are Census boundaries with water and/or coastlines erased for cartographic and mapping purposes. For census tracts, the water cutouts are derived from a subset of the 2020 Areal Hydrography boundaries offered by TIGER. Water bodies and rivers which are 50 million square meters or larger (mid to large sized water bodies) are erased from the tract level boundaries, as well as additional important features. For state and county boundaries, the water and coastlines are derived from the coastlines of the 2023 500k TIGER Cartographic Boundary Shapefiles. These are erased to more accurately portray the coastlines and Great Lakes. The original AWATER and ALAND fields are still available as attributes within the data table (units are square meters).The States layer contains 52 records - all US states, Washington D.C., and Puerto RicoCensus tracts with no population that occur in areas of water, such as oceans, are removed from this data service (Census Tracts beginning with 99).Percentages and derived counts, and associated margins of error, are calculated values (that can be identified by the "_calc_" stub in the field name), and abide by the specifications defined by the American Community Survey.Field alias names were created based on the Table Shells file available from the American Community Survey Summary File Documentation page.Negative values (e.g., -4444...) have been set to null, with the exception of -5555... which has been set to zero. These negative values exist in the raw API data to indicate the following situations:The margin of error column indicates that either no sample observations or too few sample observations were available to compute a standard error and thus the margin of error. A statistical test is not appropriate.Either no sample observations or too few sample observations were available to compute an estimate, or a ratio of medians cannot be calculated because one or both of the median estimates falls in the lowest interval or upper interval of an open-ended distribution.The median falls in the lowest interval of an open-ended distribution, or in the upper interval of an open-ended distribution. A statistical test is not appropriate.The estimate is controlled. A statistical test for sampling variability is not appropriate.The data for this geographic area cannot be displayed because the number of sample cases is too small.
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TwitterThis layer shows Asian alone or in any combination by selected groups. This is shown by tract, county, and state centroids. This service is updated annually to contain the most currently released American Community Survey (ACS) 5-year data, and contains estimates and margins of error. There are also additional calculated attributes related to this topic, which can be mapped or used within analysis. The numbers by detailed Asian groups do not add to the total population. This is because the detailed Asian groups are tallies of the number of Asian responses rather than the number of Asian respondents. Responses that include more than one race and/or Asian group are counted several times. To see the full list of attributes available in this service, go to the "Data" tab, and choose "Fields" at the top right. Current Vintage: 2019-2023ACS Table(s): B02001, B02011, B02018 (Not all lines of ACS table B02001 are available in this layer.)Data downloaded from: Census Bureau's API for American Community Survey Date of API call: December 12, 2024National Figures: data.census.govThe United States Census Bureau's American Community Survey (ACS):About the SurveyGeography & ACSTechnical DocumentationNews & UpdatesThis ready-to-use layer can be used within ArcGIS Pro, ArcGIS Online, its configurable apps, dashboards, Story Maps, custom apps, and mobile apps. Data can also be exported for offline workflows. For more information about ACS layers, visit the FAQ. Please cite the Census and ACS when using this data.Data Note from the Census:Data are based on a sample and are subject to sampling variability. The degree of uncertainty for an estimate arising from sampling variability is represented through the use of a margin of error. The value shown here is the 90 percent margin of error. The margin of error can be interpreted as providing a 90 percent probability that the interval defined by the estimate minus the margin of error and the estimate plus the margin of error (the lower and upper confidence bounds) contains the true value. In addition to sampling variability, the ACS estimates are subject to nonsampling error (for a discussion of nonsampling variability, see Accuracy of the Data). The effect of nonsampling error is not represented in these tables.Data Processing Notes:This layer is updated automatically when the most current vintage of ACS data is released each year, usually in December. The layer always contains the latest available ACS 5-year estimates. It is updated annually within days of the Census Bureau's release schedule. Click here to learn more about ACS data releases.Boundaries come from the US Census TIGER geodatabases, specifically, the National Sub-State Geography Database (named tlgdb_(year)_a_us_substategeo.gdb). Boundaries are updated at the same time as the data updates (annually), and the boundary vintage appropriately matches the data vintage as specified by the Census. These are Census boundaries with water and/or coastlines erased for cartographic and mapping purposes. For census tracts, the water cutouts are derived from a subset of the 2020 Areal Hydrography boundaries offered by TIGER. Water bodies and rivers which are 50 million square meters or larger (mid to large sized water bodies) are erased from the tract level boundaries, as well as additional important features. For state and county boundaries, the water and coastlines are derived from the coastlines of the 2023 500k TIGER Cartographic Boundary Shapefiles. These are erased to more accurately portray the coastlines and Great Lakes. The original AWATER and ALAND fields are still available as attributes within the data table (units are square meters).The States layer contains 52 records - all US states, Washington D.C., and Puerto RicoCensus tracts with no population that occur in areas of water, such as oceans, are removed from this data service (Census Tracts beginning with 99).Percentages and derived counts, and associated margins of error, are calculated values (that can be identified by the "_calc_" stub in the field name), and abide by the specifications defined by the American Community Survey.Field alias names were created based on the Table Shells file available from the American Community Survey Summary File Documentation page.Negative values (e.g., -4444...) have been set to null, with the exception of -5555... which has been set to zero. These negative values exist in the raw API data to indicate the following situations:The margin of error column indicates that either no sample observations or too few sample observations were available to compute a standard error and thus the margin of error. A statistical test is not appropriate.Either no sample observations or too few sample observations were available to compute an estimate, or a ratio of medians cannot be calculated because one or both of the median estimates falls in the lowest interval or upper interval of an open-ended distribution.The median falls in the lowest interval of an open-ended distribution, or in the upper interval of an open-ended distribution. A statistical test is not appropriate.The estimate is controlled. A statistical test for sampling variability is not appropriate.The data for this geographic area cannot be displayed because the number of sample cases is too small.
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TwitterBetween 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.
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A changing environment directly influences birth and mortality rates, and thus population growth rates. However, population growth rates in the short-term are also influenced by population age-structure. Despite its importance, the contribution of age-structure to population growth rates has rarely been explored empirically in wildlife populations with long-term demographic data.
Here, we assessed how changes in age-structure influenced short-term population dynamics in a semi-captive population of Asian elephants (Elephas maximus).
We addressed this question using a demographic dataset of female Asian elephants from timber camps in Myanmar spanning 45 years (1970-2014). First, we explored temporal variation in age-structure. Then, using annual matrix population models, we used a retrospective approach to assess the contributions of age-structure and vital rates to short-term population growth rates with respect to the average environment.
Age-structure was highly variable over the study period, with large proportions of juveniles in the years 1970 and 1985, and made a substantial contribution to annual population growth rate deviations. High adult birth rates between 1970-1980 would have resulted in large positive population growth rates, but these were prevented by a low proportion of reproductive-aged females.
We highlight that an understanding of both age-specific vital rates and age-structure is needed to assess short-term population dynamics. Furthermore, this example from a human-managed system suggests that the importance of age-structure may be accentuated in populations experiencing human disturbance where age-structure is unstable, such as those in captivity or for endangered species. Ultimately, changes to the environment drive population dynamics by influencing birth and mortality rates, but understanding demographic structure is crucial for assessing population growth.
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The limited availability of resources is predicted to impose trade-offs between growth, reproduction and self-maintenance in animals. However, although some studies have shown that early reproduction suppresses growth, reproduction positively correlates with size in others. We use detailed records from a large population of semi-captive elephants in Myanmar to assess the relationships between size (height and weight), reproduction and survival in female Asian elephants, a species characterized by slow, costly life history. Although female height gain during the growth period overlapped little with reproductive onset in the population, there was large variation in age at first reproduction and only 81% of final weight had been reached by peak age of reproduction at the population level (19 years). Those females beginning reproduction early tended to be taller and lighter later in life, although these trends were not significant. We found that taller females were more likely to have reproduced by a given age, but such effects diminished with age, suggesting there may be a size threshold to reproduction which is especially important in young females. Because size was not linked with female survival during reproductive ages, the diminishing effect of height on reproduction with age is unlikely to be due to biased survival of larger females. We conclude that although reproduction may not always impose significant costs on growth, height may be a limiting factor to reproduction in young female Asian elephants, which could have important implications considering their birth rates are low and peak reproduction is young – 19 years in this population.
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TwitterIn 2025, India overtook China as the world's most populous country and now has almost 1.46 billion people. China now has the second-largest population in the world, still with just over 1.4 billion inhabitants, however, its population went into decline in 2023. Global population As of 2025, the world's population stands at almost 8.2 billion people and is expected to reach around 10.3 billion people in the 2080s, when it will then go into decline. Due to improved healthcare, sanitation, and general living conditions, the global population continues to increase; mortality rates (particularly among infants and children) are decreasing and the median age of the world population has steadily increased for decades. As for the average life expectancy in industrial and developing countries, the gap has narrowed significantly since the mid-20th century. Asia is the most populous continent on Earth; 11 of the 20 largest countries are located there. It leads the ranking of the global population by continent by far, reporting four times as many inhabitants as Africa. The Demographic Transition The population explosion over the past two centuries is part of a phenomenon known as the demographic transition. Simply put, this transition results from a drastic reduction in mortality, which then leads to a reduction in fertility, and increase in life expectancy; this interim period where death rates are low and birth rates are high is where this population explosion occurs, and population growth can remain high as the population ages. In today's most-developed countries, the transition generally began with industrialization in the 1800s, and growth has now stabilized as birth and mortality rates have re-balanced. Across less-developed countries, the stage of this transition varies; for example, China is at a later stage than India, which accounts for the change in which country is more populous - understanding the demographic transition can help understand the reason why China's population is now going into decline. The least-developed region is Sub-Saharan Africa, where fertility rates remain close to pre-industrial levels in some countries. As these countries transition, they will undergo significant rates of population growth.
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TwitterThis layer shows Asian alone or in any combination by selected groups. This is shown by tract, county, and state centroids. This service is updated annually to contain the most currently released American Community Survey (ACS) 5-year data, and contains estimates and margins of error. There are also additional calculated attributes related to this topic, which can be mapped or used within analysis. The numbers by detailed Asian groups do not add to the total population. This is because the detailed Asian groups are tallies of the number of Asian responses rather than the number of Asian respondents. Responses that include more than one race and/or Asian group are counted several times. To see the full list of attributes available in this service, go to the "Data" tab, and choose "Fields" at the top right. Current Vintage: 2019-2023ACS Table(s): B02001, B02011, B02018 (Not all lines of ACS table B02001 are available in this layer.)Data downloaded from: Census Bureau's API for American Community Survey Date of API call: December 12, 2024National Figures: data.census.govThe United States Census Bureau's American Community Survey (ACS):About the SurveyGeography & ACSTechnical DocumentationNews & UpdatesThis ready-to-use layer can be used within ArcGIS Pro, ArcGIS Online, its configurable apps, dashboards, Story Maps, custom apps, and mobile apps. Data can also be exported for offline workflows. For more information about ACS layers, visit the FAQ. Please cite the Census and ACS when using this data.Data Note from the Census:Data are based on a sample and are subject to sampling variability. The degree of uncertainty for an estimate arising from sampling variability is represented through the use of a margin of error. The value shown here is the 90 percent margin of error. The margin of error can be interpreted as providing a 90 percent probability that the interval defined by the estimate minus the margin of error and the estimate plus the margin of error (the lower and upper confidence bounds) contains the true value. In addition to sampling variability, the ACS estimates are subject to nonsampling error (for a discussion of nonsampling variability, see Accuracy of the Data). The effect of nonsampling error is not represented in these tables.Data Processing Notes:This layer is updated automatically when the most current vintage of ACS data is released each year, usually in December. The layer always contains the latest available ACS 5-year estimates. It is updated annually within days of the Census Bureau's release schedule. Click here to learn more about ACS data releases.Boundaries come from the US Census TIGER geodatabases, specifically, the National Sub-State Geography Database (named tlgdb_(year)_a_us_substategeo.gdb). Boundaries are updated at the same time as the data updates (annually), and the boundary vintage appropriately matches the data vintage as specified by the Census. These are Census boundaries with water and/or coastlines erased for cartographic and mapping purposes. For census tracts, the water cutouts are derived from a subset of the 2020 Areal Hydrography boundaries offered by TIGER. Water bodies and rivers which are 50 million square meters or larger (mid to large sized water bodies) are erased from the tract level boundaries, as well as additional important features. For state and county boundaries, the water and coastlines are derived from the coastlines of the 2023 500k TIGER Cartographic Boundary Shapefiles. These are erased to more accurately portray the coastlines and Great Lakes. The original AWATER and ALAND fields are still available as attributes within the data table (units are square meters).The States layer contains 52 records - all US states, Washington D.C., and Puerto RicoCensus tracts with no population that occur in areas of water, such as oceans, are removed from this data service (Census Tracts beginning with 99).Percentages and derived counts, and associated margins of error, are calculated values (that can be identified by the "_calc_" stub in the field name), and abide by the specifications defined by the American Community Survey.Field alias names were created based on the Table Shells file available from the American Community Survey Summary File Documentation page.Negative values (e.g., -4444...) have been set to null, with the exception of -5555... which has been set to zero. These negative values exist in the raw API data to indicate the following situations:The margin of error column indicates that either no sample observations or too few sample observations were available to compute a standard error and thus the margin of error. A statistical test is not appropriate.Either no sample observations or too few sample observations were available to compute an estimate, or a ratio of medians cannot be calculated because one or both of the median estimates falls in the lowest interval or upper interval of an open-ended distribution.The median falls in the lowest interval of an open-ended distribution, or in the upper interval of an open-ended distribution. A statistical test is not appropriate.The estimate is controlled. A statistical test for sampling variability is not appropriate.The data for this geographic area cannot be displayed because the number of sample cases is too small.
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Detailed demographic data on wild Asian elephants have been difficult to collect due to habitat characteristics of much of the species’ remaining range. Such data, however, are critical for understanding and modeling population processes in this endangered species. We present data from six years of an ongoing study of Asian elephants (Elephas maximus) in Uda Walawe National Park, Sri Lanka. This relatively undisturbed population numbering over one thousand elephants is individually monitored, providing cohort-based information on mortality and reproduction. Reproduction was seasonal, such that most births occurred during the long inter-monsoon dry season and peaked in May. During the study, the average age at first reproduction was 13.4 years and the 50th percentile inter-birth interval was approximately 6 years. Birth sex ratios did not deviate significantly from parity. Fecundity was relatively stable throughout the observed reproductive life of an individual (ages 11–60), averaging between 0.13–0.17 female offspring per individual per year. Mortalities and injuries based on carcasses and disappearances showed that males were significantly more likely than females to be killed or injured through anthropogenic activity. Overall, however, most observed injuries did not appear to be fatal. This population exhibits higher fecundity and density relative to published estimates on other Asian elephant populations, possibly enhanced by present range constriction. Understanding the factors responsible for these demographic dynamics can shed insight on the future needs of this elephant population, with probable parallels to other populations in similar settings.
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Asian elephants occurring in northern Borneo form a geographically isolated and genetically distinct population. Of this, the subpopulation of Central Sabah holds the greatest opportunity for long-term survival, due to a relatively large population size and occurrence over a vast, contiguous, and protected habitat. We surveyed this subpopulation in 2015 using advanced methods to obtain a population size estimate. We used the distance-sampling framework and laid out transects following a stratified random design for counting elephant dung piles; measured dung decay following the ‘retrospective’ method; and used Bayesian analysis to estimate dung decay rate and dung pile density. Thus, we estimated a posterior mean dung decay rate of 212 days (95% BCI: 133–319), an overall elephant density of 0.07 per km2 (95% BCI: 0.03–0.11), and a population size of 387 elephants (95% BCI: 169–621). These estimates were far lower than the population size of 1132 individuals and density of 1.18 per km2 estimated in 2008. It is unlikely that there has been a steep population decline, as there were no drastic land-use changes between 2008 and 2015, nor were there other identifiable causes for a population decline. Therefore, it appears that the methodological and analytical flaws in the previous estimate are the most plausible reason for this observed difference. Given that the new estimate suggests a much smaller population, it is prudent and precautionary to use the new estimate as the basis for all policy decisions and conservation actions for elephants in Sabah.
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TwitterAmong countries with the highest number of overseas Chinese on each continent, the largest Chinese diaspora community is living in Indonesia, numbering more than ten million people. Most of these people are descendants from migrants born in China, who have moved to Indonesia a long time ago. On the contrary, a large part of overseas Chinese living in Canada and Australia have arrived in these countries only during the last two decades. China as an emigration country Many Chinese people have emigrated from their home country in search of better living conditions and educational chances. The increasing number of Chinese emigrants has benefited from loosened migration policies. On the one hand, the attitude of the Chinese government towards emigration has changed significantly. Overseas Chinese are considered to be strong supporters for the overall strength of Chinese culture and international influence. On the other hand, migration policies in the United States and Canada are changing with time, expanding migration opportunities for non-European immigrants. As a result, China has become one of the world’s largest emigration countries as well as the country with the highest outflows of high net worth individuals. However, the mass emigration is causing a severe loss of homegrown talents and assets. The problem of talent and wealth outflow has raised pressing questions to the Chinese government, and a solution to this issue is yet to be determined. Popular destinations among Chinese emigrants Over the last decades, English speaking developed countries have been popular destinations for Chinese emigrants. In 2022 alone, the number of people from China naturalized as U.S. citizens had amounted to over 27,000 people, while nearly 68,000 had obtained legal permanent resident status as “green card” recipients. Among other popular immigration destinations for Chinese riches are Canada, Australia, Europe, and Singapore.
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Objectives: We aimed to conduct a comprehensive evaluation of the population impact of methadone maintenance treatment (MMT) for its future program planning.Methods: We conducted a literature review of the effects of MMT in China on HIV and HCV disease burden, injecting, and sexual behaviors and drug-related harm during 2004–2015. Data synthesis and analysis were conducted to obtain the pooled estimates of parameters for a mathematical model which was constructed to evaluate the effectiveness and cost-effectiveness of the program.Results: Based on a review of 134 articles, this study demonstrated that MMT is highly effective in reducing crime-related, high risk sexual, and injecting behaviors. The model estimated US$1,037 m which was invested in MMT from 2004 to 2015 has prevented 29,463 (15,325–43,600) new HIV infections, 130,563 (91,580–169,546) new HCV infections, 10,783 (10,380–11,187) deaths related to HIV, HCV and drug-related harm, and 338,920.0 (334,596.2–343,243.7) disability-adjusted life years (DALYs). The costs for each prevented HIV infection, HCV infection, death, and DALY were $35,206.8 (33,594.8–36,981.4), $7,944.7 ($7,714.4–8,189.2), $96,193.4 (92,726.0–99,930.2), and $3,060.6 ($3,022.0–3,100.1) respectively.Conclusion: The Chinese MMT program has been effective and cost-effective in reducing injecting, injecting-related risk behaviors and adversities due to HIV/HCV infection and drug-related harm among drug users.
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In vertebrate population estimation, converting faecal density into animal density requires information on faecal production rate, decay rate, and faecal density. Differences in the above factors for long-lived species across age classes were not evaluated. We have evaluated these factors associated with the dung count of Asian elephants (Elephas maximus) in the tropical forest of Southern India.
The defecation rate of elephants was determined in semi-wild elephants at the Mudumalai elephant camp. The relationship between dung bolus diameter and age was determined to estimate the age of the elephant. Total and age-specific elephant density based on dung bolus diameter were estimated. A total of 24 transect lines of 2-4 km (125 km) were sampled in the study area. An experiment was conducted to assess detection probability across the age classes of dung piles. The dung decay rates across age classes and seasons were determined by marking fresh dung piles (n=1551). The dung-based age structure assessment and its limitations were evaluated.
The mean defecation rate was 13.51±0.51 per day. The defecation rate was significantly lower for the younger age class and increased with the age of elephants. Defecation rates were significantly lower in the wet season than in the dry. The dung-boli diameter positively increased with the age of elephants, and the growth curve can be used to predict the age and age structure of the elephant population.
The disparity in the dung production rate results in the lower availability of younger age class (Juvenile and calf) dung in the transect for counting, that results in lower dung abundance. The detection probability of dung piles of younger age classes was low (0.58). The survival rates of dung piles of younger age classes were lower and increased with the age of elephants in the wet season. Hence, demography assessment of the population based on dung needs to consider age-specific differences in dung production, decay, and detection probability. Through demography assessment using dung provides insight into population age structure, it has limitations in predicting age structure for young elephants.
Methods
i. Defecation rate
The defecation rate of semi-wild Asian elephants was gathered for different age-sex classes at the forest elephant camp at Mudumalai. A total of 14 elephants in the dry season (Dec-Mar 2002) and 17 elephants in the wet season (Jun-Oct 2007) of different age-sex classes were observed for 42 days and 51 days, respectively (Table-1). Each elephant was followed for three consecutive days to quantify the defecation rate, thus resulting in a sampling effort of 504 and 612 hours of observation in the dry and wet seasons, respectively. Elephants were observed by the focal animal sampling method (Altmann, 1974) during the daytime for twelve hours, from 6:00 hours to 18:00 hours. All the activities were recorded with ten minutes of observation and a five-minute interval. But the defecation occurring in the observer’s interval time was noted, but other activities were not recorded. To determine the defecation rate, the interval between two defecations was averaged, i.e., If a total of 10 defecations were observed over 10 hours (observation duration from first defecation to last defecation), then an average of 9 intervals (n-1) was calculated (10hr/9 intervals = average defecation interval, x). The daily defecation rate was calculated by 24/x. Thus, the defecation rates were calculated based on daytime (12 hour) observations.
ii. Dung bolus size and age relationship
Measurements of dung bolus circumference were collected while observing elephants for estimation of defecation rate in the above-mentioned methods. A total of 17 males and 10 female elephants’ dung-boli measurements were used. At each defecation, the largest intact boli circumference was measured. The mean dung-boli diameter is calculated from the dung-boli circumference with the equation dung-boli diameter (d)=circumference (c)/p.
The Von Bertalanffy growth equation (VBGM) is useful for fitting vertebrate growth data (Ebert, 1999) and has been used in modelling elephant growth (Lee and Moss, 1995; Reilly, 2002; Morrison et al. 2005). The VBGM was used to construct the growth models and is defined by the growth parameters L, K and t0 and the length measurement L (Von Bertalanffy 1938; Eqn. 2) in this study was the mean dung-boli diameter to interpolate the growth of elephant.
iii. Age structure
Dung size has been correlated to the size (height) of elephants and consequently, to estimate age class (Reilly, 2002, Morrions et al., 2005). To determine the age from dung bolus diameter (calculated from circumference measured in the large end of dung bolus), the growth parameters were rearranged in the VBGE equation (Eqn. 3) to predict the mean age (t) from dung bolus diameter (L) measured in the dung transect.
As the asymptotic size is reached, the sensitivity of the growth model to changes in diameter increases greatly, such that a small increase in the diameter could indicate a large increase in age. Therefore, the dung bolus diameters greater than 15 cm, which was an asymptotic size were grouped together and denoted as 20+ years.
iv. Detection of dung piles
Detection of various age-class and size classes of dung at a different perpendicular distance was measured using an experimental two belt transect in tropical dry deciduous forest with a length of two kilometers and a width of 25m on either side of the transect. The age class of dung piles was determined based on dung (intact boli circumference measured at the large end) measurements. Initially, dung piles that were visible from the transect were counted and marked with calcium carbonate powder to identify them as detected dung piles.
After completion of the transect count, the dung piles that were present within a width of 25m on either side of transects that were not detected from the transect were recorded as missed dung piles. A 100m rope was kept in the middle of the transect, and then the entire area was searched by four observers walking at a five-meter interval on one side of the transect. All missed dung piles in the transect were recorded with details of perpendicular distance, the extent of dung spread, i.e. length and width of dung spread, the presence of boli, and dung boli circumference were measured. Then the other side of the transect was surveyed using the same method. The proportion of dung piles detected at different perpendicular distances was calculated by dividing the number of dung piles detected by the sum of the number of detected and non-detected dung piles at a particular distance.
Dung pile status i.e., observed or missed were coded as 1 and 0, respectively. Differences in detection were tested against independent predictors, i.e., perpendicular distance, age class (adult, sub-adult, juvenile and calf) of dung were tested using binary logistic regression using ‘glm’ function in R Software.
v. Dung survival rate
The elephant herds were located, tracked and fresh dung piles (less than six hours old) were marked in all three habitat types. Every month, an average of 125±77 fresh dung piles/month were marked using numbered bamboo stakes from Jan 2007 to Feb 2008. The variables such as geographic location, age class estimated based on dung circumference, grass composition, canopy cover and total length and width of dung spread were noted. Every month, dung piles were marked in different habitats and revisited every 15 days to assess the status of dung piles (Fig.1). To estimate the survival rate of dung piles, based on retrospective method dung piles were examined one day before the survey during dry and wet seasons (Laing et al., 2003; Hedges and Lawson, 2006).
vi. Age-specific elephant density
Dung density was determined using the indirect dung count method. A total of 24 transects of two to four kilometres resulting in a total of 125km (56.5km in dry season and 68.5 km in wet season) distance were walked (Fig.1). Transects were placed randomly in the study area to get adequate spatial coverage and proportional representation of three habitat types, similar to an earlier study (Baskaran, Udhayan and Desai, 2010). Dung piles that are visible from the transect were counted, and the perpendicular distance was measured using a measuring tape. The dungs were categorized into 'S-system’ based on the stage of decay of dung piles (S1-all boli intact; S2- one or more boli intact; S3-No boli intact with coherent fragments remain; S4-only traces of dung fragments remain) of the Mike dung pile classification system (Hedges and Lawson, 2006). All the dung piles encountered (S1 to S3) in the transects used to estimate dung density were measured. The largest circumference of an intact bolus in a dung pile was measured. If all the dung boli were not intact, the corresponding age class was denoted as unknown. The survey were completed within a month (July-2007-wet and March 2008 – dry).
The Distance 7.2 software was used to estimate overall and age-specific elephant densities (Buckland et al., 2001; Thomas et al., 2010). The age of elephant was determined based on the dung bolus diameter encountered in the transect using Eq. 3. The number of detections of dung piles across specific age was less, and hence they were grouped into 1-3, 4-7, 8-11, 12-15, 16-19, and 20+ age categories to estimate densities. The defecation rate estimated using prediction equation 1 and the mean decay rates for specific age classes were entered separately as multipliers to obtain density for specific age class.
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TwitterThis statistic shows the 20 countries with the highest population growth rate in 2024. In SouthSudan, the population grew by about 4.65 percent compared to the previous year, making it the country with the highest population growth rate in 2024. The global population Today, the global population amounts to around 7 billion people, i.e. the total number of living humans on Earth. More than half of the global population is living in Asia, while one quarter of the global population resides in Africa. High fertility rates in Africa and Asia, a decline in the mortality rates and an increase in the median age of the world population all contribute to the global population growth. Statistics show that the global population is subject to increase by almost 4 billion people by 2100. The global population growth is a direct result of people living longer because of better living conditions and a healthier nutrition. Three out of five of the most populous countries in the world are located in Asia. Ultimately the highest population growth rate is also found there, the country with the highest population growth rate is Syria. This could be due to a low infant mortality rate in Syria or the ever -expanding tourism sector.
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TwitterThe 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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TwitterNew York was the most populous state in the union in the year 1900. It had the largest white population, for both native born and foreign born persons, and together these groups made up over 7.1 million of New York's 7.2 million inhabitants at this time. The United States' industrial centers to the north and northeast were one of the most important economic draws during this period, and states in these regions had the largest foreign born white populations. Ethnic minorities Immigration into the agricultural southern states was much lower than the north, and these states had the largest Black populations due to the legacy of slavery - this balance would begin to shift in the following decades as a large share of the Black population migrated to urban centers to the north during the Great Migration. The Japanese and Chinese populations at this time were more concentrated in the West, as these states were the most common point of entry for Asians into the country. The states with the largest Native American populations were to the west and southwest, due to the legacy of forced displacement - this included the Indian Territory, an unorganized and independent territory assigned to the Native American population in the early 1800s, although this was incorporated into Oklahoma when it was admitted into the union in 1907. Additionally, non-taxpaying Native Americans were historically omitted from the U.S. Census, as they usually lived in separate communities and could not vote or hold office - more of an effort was made to count all Native Americans from 1890 onward, although there are likely inaccuracies in the figures given here. Changing distribution Internal migration in the 20th century greatly changed population distribution across the country, with California and Florida now ranking among the three most populous states in the U.S. today, while they were outside the top 20 in 1900. The growth of Western states' populations was largely due to the wave of internal migration during the Great Depression, where unemployment in the east saw many emigrate to "newer" states in search of opportunity, as well as significant immigration from Latin America (especially Mexico) and Asia since the mid-1900s.
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TwitterThe 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.