24 datasets found
  1. d

    Data from: Identifying Critical Life Stage Transitions for Biological...

    • catalog.data.gov
    • cloud.csiss.gmu.edu
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    Updated Apr 21, 2025
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    Agricultural Research Service (2025). Data from: Identifying Critical Life Stage Transitions for Biological Control of Long-lived Perennial Vincetoxicum Species [Dataset]. https://catalog.data.gov/dataset/data-from-identifying-critical-life-stage-transitions-for-biological-control-of-long-lived-41b5d
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    Dataset updated
    Apr 21, 2025
    Dataset provided by
    Agricultural Research Service
    Description

    This dataset includes data on 25 transitions of a matrix demographic model of the invasive species Vincetoxicum nigrum (L.) Moench (black swallow-wort or black dog-strangling vine) and Vincetoxicum rossicum (Kleopow) Barb. (pale swallow-wort or dog-strangling vine) (Apocynaceae, subfamily Asclepiadoideae), two invasive perennial vines in the northeastern U.S.A. and southeastern Canada. The matrix model was developed for projecting population growth rates as a result of changes to lower-level vital rates from biological control although the model is generalizable to any control tactic. Transitions occurred among the five life stages of seeds, seedlings, vegetative juveniles (defined as being in at least their second season of growth), small flowering plants (having 1–2 stems), and large flowering plants (having 3 or more stems). Transition values were calculated using deterministic equations and data from 20 lower-level vital rates collected from 2009-2012 from two open field and two forest understory populations of V. rossicum (43°51’N, 76°17’W; 42°48'N, 76°40'W) and two open field populations of V. nigrum (41°46’N, 73°44’W; 41°18’N, 73°58’W) in New York State. Sites varied in plant densities, soil depth, and light levels (forest populations). Detailed descriptions of vital rate data collection may be found in: Milbrath et al. 2017. Northeastern Naturalist 24(1):37-53. Five replicate sets of transition data obtained from five separate spatial regions of a particular infestation were produced for each of the six populations. Note: Added new excel file of vital rate data on 12/7/2018. Resources in this dataset:Resource Title: Matrix model transition data for Vincetoxicum species. File Name: Matrix_model_transition_data.csvResource Description: This data set includes data on 25 transitions of a matrix demographic model of two invasive Vincetoxicum species from six field and forest populations in New York State.Resource Title: Variable definitions. File Name: Matrix_model_metadata.csvResource Description: Definitions of variables including equations for each transition and definitions of the lower-level vital rates in the equationsResource Title: Vital Rate definitions. File Name: Vital_Rate.csvResource Description: Vital Rate definitions of lower-level vital rates used in transition equations - to be substituted into the Data Dictionary for full definition of each transition equation.Resource Title: Data Dictionary. File Name: Matrix_Model_transition_data_DD.csvResource Description: See Vital Rate resource for definitions of lower-level vital rates used in transition equations where noted.Resource Title: Matrix model vital rate data for Vincetoxicum species. File Name: Matrix_model_vital rate_data.csvResource Description: This data set includes data on 20 lower-level vital rates used in the calculation of transitions of a matrix demographic model of two invasive Vincetoxicum species in New York State as well as definitions of the vital rates. (File added on 12/7/2018)Resource Software Recommended: Microsoft Excel,url: https://office.microsoft.com/excel/

  2. i

    Demographic and Health Survey 1987 - Thailand

    • catalog.ihsn.org
    • datacatalog.ihsn.org
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    Updated Mar 29, 2019
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    Institute of Population Studies (IPS) (2019). Demographic and Health Survey 1987 - Thailand [Dataset]. https://catalog.ihsn.org/catalog/2489
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    Dataset updated
    Mar 29, 2019
    Dataset authored and provided by
    Institute of Population Studies (IPS)
    Time period covered
    1987
    Area covered
    Thailand
    Description

    Abstract

    The Thai Demographic and Health Survey (TDHS) was a nationally representative sample survey conducted from March through June 1988 to collect data on fertility, family planning, and child and maternal health. A total of 9,045 households and 6,775 ever-married women aged 15 to 49 were interviewed. Thai Demographic and Health Survey (TDHS) is carried out by the Institute of Population Studies (IPS) of Chulalongkorn University with the financial support from USAID through the Institute for Resource Development (IRD) at Westinghouse. The Institute of Population Studies was responsible for the overall implementation of the survey including sample design, preparation of field work, data collection and processing, and analysis of data. IPS has made available its personnel and office facilities to the project throughout the project duration. It serves as the headquarters for the survey.

    The Thai Demographic and Health Survey (TDHS) was undertaken for the main purpose of providing data concerning fertility, family planning and maternal and child health to program managers and policy makers to facilitate their evaluation and planning of programs, and to population and health researchers to assist in their efforts to document and analyze the demographic and health situation. It is intended to provide information both on topics for which comparable data is not available from previous nationally representative surveys as well as to update trends with respect to a number of indicators available from previous surveys, in particular the Longitudinal Study of Social Economic and Demographic Change in 1969-73, the Survey of Fertility in Thailand in 1975, the National Survey of Family Planning Practices, Fertility and Mortality in 1979, and the three Contraceptive Prevalence Surveys in 1978/79, 1981 and 1984.

    Geographic coverage

    National

    Analysis unit

    • Household
    • Women age 15-49

    Universe

    The population covered by the 1987 THADHS is defined as the universe of all women Ever-married women in the reproductive ages (i.e., women 15-49). This covered women in private households on the basis of a de facto coverage definition. Visitors and usual residents who were in the household the night before the first visit or before any subsequent visit during the few days the interviewing team was in the area were eligible. Excluded were the small number of married women aged under 15 and women not present in private households.

    Kind of data

    Sample survey data

    Sampling procedure

    SAMPLE SIZE AND ALLOCATION

    The objective of the survey was to provide reliable estimates for major domains of the country. This consisted of two overlapping sets of reporting domains: (a) Five regions of the country namely Bangkok, north, northeast, central region (excluding Bangkok), and south; (b) Bangkok versus all provincial urban and all rural areas of the country. These requirements could be met by defining six non-overlapping sampling domains (Bangkok, provincial urban, and rural areas of each of the remaining 4 regions), and allocating approximately equal sample sizes to them. On the basis of past experience, available budget and overall reporting requirement, the target sample size was fixed at 7,000 interviews of ever-married women aged 15-49, expected to be found in around 9,000 households. Table A.I shows the actual number of households as well as eligible women selected and interviewed, by sampling domain (see Table i.I for reporting domains).

    THE FRAME AND SAMPLE SELECTION

    The frame for selecting the sample for urban areas, was provided by the National Statistical Office of Thailand and by the Ministry of the Interior for rural areas. It consisted of information on population size of various levels of administrative and census units, down to blocks in urban areas and villages in rural areas. The frame also included adequate maps and descriptions to identify these units. The extent to which the data were up-to-date as well as the quality of the data varied somewhat in different parts of the frame. Basically, the multi-stage stratified sampling design involved the following procedure. A specified number of sample areas were selected systematically from geographically/administratively ordered lists with probabilities proportional to the best available measure of size (PPS). Within selected areas (blocks or villages) new lists of households were prepared and systematic samples of households were selected. In principle, the sampling interval for the selection of households from lists was determined so as to yield a self weighting sample of households within each domain. However, in the absence of good measures of population size for all areas, these sampling intervals often required adjustments in the interest of controlling the size of the resulting sample. Variations in selection probabilities introduced due to such adjustment, where required, were compensated for by appropriate weighting of sample cases at the tabulation stage.

    SAMPLE OUTCOME

    The final sample of households was selected from lists prepared in the sample areas. The time interval between household listing and enumeration was generally very short, except to some extent in Bangkok where the listing itself took more time. In principle, the units of listing were the same as the ultimate units of sampling, namely households. However in a small proportion of cases, the former differed from the latter in several respects, identified at the stage of final enumeration: a) Some units listed actually contained more than one household each b) Some units were "blanks", that is, were demolished or not found to contain any eligible households at the time of enumeration. c) Some units were doubtful cases in as much as the household was reported as "not found" by the interviewer, but may in fact have existed.

    Mode of data collection

    Face-to-face

    Research instrument

    The DHS core questionnaires (Household, Eligible Women Respondent, and Community) were translated into Thai. A number of modifications were made largely to adapt them for use with an ever- married woman sample and to add a number of questions in areas that are of special interest to the Thai investigators but which were not covered in the standard core. Examples of such modifications included adding marital status and educational attainment to the household schedule, elaboration on questions in the individual questionnaire on educational attainment to take account of changes in the educational system during recent years, elaboration on questions on postnuptial residence, and adaptation of the questionnaire to take into account that only ever-married women are being interviewed rather than all women. More generally, attention was given to the wording of questions in Thai to ensure that the intent of the original English-language version was preserved.

    a) Household questionnaire

    The household questionnaire was used to list every member of the household who usually lives in the household and as well as visitors who slept in the household the night before the interviewer's visit. Information contained in the household questionnaire are age, sex, marital status, and education for each member (the last two items were asked only to members aged 13 and over). The head of the household or the spouse of the head of the household was the preferred respondent for the household questionnaire. However, if neither was available for interview, any adult member of the household was accepted as the respondent. Information from the household questionnaire was used to identify eligible women for the individual interview. To be eligible, a respondent had to be an ever-married woman aged 15-49 years old who had slept in the household 'the previous night'.

    Prior evidence has indicated that when asked about current age, Thais are as likely to report age at next birthday as age at last birthday (the usual demographic definition of age). Since the birth date of each household number was not asked in the household questionnaire, it was not possible to calculate age at last birthday from the birthdate. Therefore a special procedure was followed to ensure that eligible women just under the higher boundary for eligible ages (i.e. 49 years old) were not mistakenly excluded from the eligible woman sample because of an overstated age. Ever-married women whose reported age was between 50-52 years old and who slept in the household the night before birthdate of the woman, it was discovered that these women (or any others being interviewed) were not actually within the eligible age range of 15-49, the interview was terminated and the case disqualified. This attempt recovered 69 eligible women who otherwise would have been missed because their reported age was over 50 years old or over.

    b) Individual questionnaire

    The questionnaire administered to eligible women was based on the DHS Model A Questionnaire for high contraceptive prevalence countries. The individual questionnaire has 8 sections: - Respondent's background - Reproduction - Contraception - Health and breastfeeding - Marriage - Fertility preference - Husband's background and woman's work - Heights and weights of children and mothers

    The questionnaire was modified to suit the Thai context. As noted above, several questions were added to the standard DHS core questionnaire not only to meet the interest of IPS researchers hut also because of their relevance to the current demographic situation in Thailand. The supplemental questions are marked with an asterisk in the individual questionnaire. Questions concerning the following items were added in the individual questionnaire: - Did the respondent ever

  3. f

    The Evolving Demographic and Health Transition in Four Low- and...

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    Updated Jun 1, 2023
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    Ayaga Bawah; Brian Houle; Nurul Alam; Abdur Razzaque; Peter Kim Streatfield; Cornelius Debpuur; Paul Welaga; Abraham Oduro; Abraham Hodgson; Stephen Tollman; Mark Collinson; Kathleen Kahn; Tran Khan Toan; Ho Dang Phuc; Nguyen Thi Kim Chuc; Osman Sankoh; Samuel J. Clark (2023). The Evolving Demographic and Health Transition in Four Low- and Middle-Income Countries: Evidence from Four Sites in the INDEPTH Network of Longitudinal Health and Demographic Surveillance Systems [Dataset]. http://doi.org/10.1371/journal.pone.0157281
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    docxAvailable download formats
    Dataset updated
    Jun 1, 2023
    Dataset provided by
    PLOS ONE
    Authors
    Ayaga Bawah; Brian Houle; Nurul Alam; Abdur Razzaque; Peter Kim Streatfield; Cornelius Debpuur; Paul Welaga; Abraham Oduro; Abraham Hodgson; Stephen Tollman; Mark Collinson; Kathleen Kahn; Tran Khan Toan; Ho Dang Phuc; Nguyen Thi Kim Chuc; Osman Sankoh; Samuel J. Clark
    License

    Attribution 4.0 (CC BY 4.0)https://creativecommons.org/licenses/by/4.0/
    License information was derived automatically

    Description

    This paper contributes evidence documenting the continued decline in all-cause mortality and changes in the cause of death distribution over time in four developing country populations in Africa and Asia. We present levels and trends in age-specific mortality (all-cause and cause-specific) from four demographic surveillance sites: Agincourt (South Africa), Navrongo (Ghana) in Africa; Filabavi (Vietnam), Matlab (Bangladesh) in Asia. We model mortality using discrete time event history analysis. This study illustrates how data from INDEPTH Network centers can provide a comparative, longitudinal examination of mortality patterns and the epidemiological transition. Health care systems need to be reconfigured to deal simultaneously with continuing challenges of communicable disease and increasing incidence of non-communicable diseases that require long-term care. In populations with endemic HIV, long-term care of HIV patients on ART will add to the chronic care needs of the community.

  4. z

    Population dynamics and Population Migration

    • zenodo.org
    Updated Apr 8, 2025
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    Rutuja Sonar Riya Patil; Rutuja Sonar Riya Patil (2025). Population dynamics and Population Migration [Dataset]. http://doi.org/10.5281/zenodo.15175736
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    Dataset updated
    Apr 8, 2025
    Dataset provided by
    Zenodo
    Authors
    Rutuja Sonar Riya Patil; Rutuja Sonar Riya Patil
    Description

    Population dynamics, its types. Population migration (external, internal), factors determining it, main trends. Impact of migration on population health.

    Under the guidance of Moldoev M.I. Sir By Riya Patil and Rutuja Sonar

    Abstract

    Population dynamics influence development and vice versa, at various scale levels: global, continental/world-regional, national, regional, and local. Debates on how population growth affects development and how development affects population growth have already been subject of intensive debate and controversy since the late 18th century, and this debate is still ongoing. While these two debates initially focused mainly on natural population growth, the impact of migration on both population dynamics and development is also increasingly recognized. While world population will continue growing throughout the 21st century, there are substantial and growing contrasts between and within world-regions in the pace and nature of that growth, including some countries where population is stagnating or even shrinking. Because of these growing contrasts, population dynamics and their interrelationships with development have quite different governance implications in different parts of the world.

    1. Population Dynamics

    Population dynamics refers to the changes in population size, structure, and distribution over time. These changes are influenced by four main processes:

    Birth rate (natality)

    Death rate (mortality)

    Immigration (inflow of people)

    Emigration (outflow of people)

    Types of Population Dynamics

    Natural population change: Based on birth and death rates.

    Migration-based change: Caused by people moving in or out of a region.

    Demographic transition: A model that explains changes in population growth as societies industrialize.

    Population distribution: Changes in where people live (urban vs rural).

    2. Population Migration

    Migration refers to the movement of people from one location to another, often across political or geographical boundaries.

    Types of Migration

    External migration (international):

    Movement between countries.

    Examples: Refugee relocation, labor migration, education.

    Internal migration:

    Movement within the same country or region.

    Examples: Rural-to-urban migration, inter-state migration.

    3. Factors Determining Migration

    Migration is influenced by push and pull factors:

    Push factors (reasons to leave a place):

    Unemployment

    Conflict or war

    Natural disasters

    Poverty

    Lack of services or opportunities

    Pull factors (reasons to move to a place):

    Better job prospects

    Safety and security

    Higher standard of living

    Education and healthcare access

    Family reunification

    4. Main Trends in Migration

    Urbanization: Mass movement to cities for work and better services.

    Global labor migration: Movement from developing to developed countries.

    Refugee and asylum seeker flows: Due to conflict or persecution.

    Circular migration: Repeated movement between two or more locations.

    Brain drain/gain: Movement of skilled labor away from (or toward) a country.

    5. Impact of Migration on Population Health

    Positive Impacts:

    Access to better healthcare (for migrants moving to better systems).

    Skills and knowledge exchange among health professionals.

    Remittances improving healthcare affordability in home countries.

    Negative Impacts:

    Migrants’ health risks: Increased exposure to stress, poor living conditions, and occupational hazards.

    Spread of infectious diseases: Especially when health screening is lacking.

    Strain on health services: In receiving areas, especially with sudden or large influxes.

    Mental health challenges: Due to cultural dislocation, discrimination, or trauma.

    Population dynamics is one of the fundamental areas of ecology, forming both the basis for the study of more complex communities and of many applied questions. Understanding population dynamics is the key to understanding the relative importance of competition for resources and predation in structuring ecological communities, which is a central question in ecology.

    Population dynamics plays a central role in many approaches to preserving biodiversity, which until now have been primarily focused on a single species approach. The calculation of the intrinsic growth rate of a species from a life table is often the central piece of conservation plans. Similarly, management of natural resources, such as fisheries, depends on population dynamics as a way to determine appropriate management actions.

    Population dynamics can be characterized by a nonlinear system of difference or differential equations between the birth sizes of consecutive periods. In such a nonlinear system, when the feedback elasticity of previous events on current birth size is larger, the more likely the dynamics will be volatile. Depending on the classification criteria of the population, the revealed cyclical behavior has various interpretations. Under different contextual scenarios, Malthusian cycles, Easterlin cycles, predator–prey cycles, dynastic cycles, and capitalist–laborer cycles have been introduced and analyzed

    Generally, population dynamics is a nonlinear stochastic process. Nonlinearities tend to be complicated to deal with, both when we want to do analytic stochastic modelling and when analysing data. The way around the problem is to approximate the nonlinear model with a linear one, for which the mathematical and statistical theories are more developed and tractable. Let us assume that the population process is described as:

    (1)Nt=f(Nt−1,εt)

    where Nt is population density at time t and εt is a series of random variables with identical distributions (mean and variance). Function f specifies how the population density one time step back, plus the stochastic environment εt, is mapped into the current time step. Let us assume that the (deterministic) stationary (equilibrium) value of the population is N* and that ε has mean ε*. The linear approximation of Eq. (1) close to N* is then:

    (2)xt=axt−1+bϕt

    where xt=Nt−N*, a=f

    f(N*,ε*)/f

    N, b=ff(N*,ε*)/fε, and ϕt=εt−ε*

    The term population refers to the members of a single species that can interact with each other. Thus, the fish in a lake, or the moose on an island, are clear examples of a population. In other cases, such as trees in a forest, it may not be nearly so clear what a population is, but the concept of population is still very useful.

    Population dynamics is essentially the study of the changes in the numbers through time of a single species. This is clearly a case where a quantitative description is essential, since the numbers of individuals in the population will be counted. One could begin by looking at a series of measurements of the numbers of particular species through time. However, it would still be necessary to decide which changes in numbers through time are significant, and how to determine what causes the changes in numbers. Thus, it is more sensible to begin with models that relate changes in population numbers through time to underlying assumptions. The models will provide indications of what features of changes in numbers are important and what measurements are critical to make, and they will help determine what the cause of changes in population levels might be.

    To understand the dynamics of biological populations, the study starts with the simplest possibility and determines what the dynamics of the population would be in that case. Then, deviations in observed populations from the predictions of that simplest case would provide information about the kinds of forces shaping the dynamics of populations. Therefore, in describing the dynamics in this simplest case it is essential to be explicit and clear about the assumptions made. It would not be argued that the idealized population described here would ever be found, but that focusing on the idealized population would provide insight into real populations, just as the study of Newtonian mechanics provides understanding of more realistic situations in physics.

    Population migration

    The vast majority of people continue to live in the countries where they were born —only one in 30 are migrants.

    In most discussions on migration, the starting point is usually numbers. Understanding changes in scale, emerging trends, and shifting demographics related to global social and economic transformations, such as migration, help us make sense of the changing world we live in and plan for the future. The current global estimate is that there were around 281 million international migrants in the world in 2020, which equates to 3.6 percent of the global population.

    Overall, the estimated number of international migrants has increased over the past five decades. The total estimated 281 million people living in a country other than their countries of birth in 2020 was 128 million more than in 1990 and over three times the estimated number in 1970.

    There is currently a larger number of male than female international migrants worldwide and the growing gender gap has increased over the past 20 years. In 2000, the male to female split was 50.6 to 49.4 per cent (or 88 million male migrants and 86 million female migrants). In 2020 the split was 51.9 to 48.1 per cent, with 146 million male migrants and 135 million female migrants. The share of

  5. f

    Appendix B. Correlation between the sensitivities (respectively...

    • wiley.figshare.com
    html
    Updated May 31, 2023
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    Curtis A. Smith; Itamar Giladi; Young-Seon Lee (2023). Appendix B. Correlation between the sensitivities (respectively elasticities) of spread rate and population growth rate λ to changes in the demographic transitions found in matrix B (Eq. 4). [Dataset]. http://doi.org/10.6084/m9.figshare.3531812.v1
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    htmlAvailable download formats
    Dataset updated
    May 31, 2023
    Dataset provided by
    Wiley
    Authors
    Curtis A. Smith; Itamar Giladi; Young-Seon Lee
    License

    CC0 1.0 Universal Public Domain Dedicationhttps://creativecommons.org/publicdomain/zero/1.0/
    License information was derived automatically

    Description

    Correlation between the sensitivities (respectively elasticities) of spread rate and population growth rate λ to changes in the demographic transitions found in matrix B (Eq. 4).

  6. d

    Data from: Accounting for uncertainty in dormant life stages in stochastic...

    • datadryad.org
    • data.niaid.nih.gov
    zip
    Updated Oct 11, 2016
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    Maria Paniw; Pedro F. Quintana-Ascencio; Fernando Ojeda; Roberto Salguero-Gómez (2016). Accounting for uncertainty in dormant life stages in stochastic demographic models [Dataset]. http://doi.org/10.5061/dryad.rq7t3
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    zipAvailable download formats
    Dataset updated
    Oct 11, 2016
    Dataset provided by
    Dryad
    Authors
    Maria Paniw; Pedro F. Quintana-Ascencio; Fernando Ojeda; Roberto Salguero-Gómez
    Time period covered
    2016
    Description

    dataDroso - census dataDemographic transitions of Drosophyllum lusitanicum populations recorded in annual censuses (from 2011 to 2015) in five populations. These data are used to quantify vital rates of above-ground individuals.dataDroso.csvdataDrosoSB - seed bankSeed fates (in a binary format) inferred from two experiments. These data are used to quantify the transitions related to the seed bank and associated parameter uncertainties.dataDrosoSB.csvBayModel - Bayesian vital rate GLMMsExecutes and saves the results of a Bayesian model quantifying all vital rates; illustrates basic diagnostics that can be run on the results of an MCMC run (i.e., the posterior parameter distribution) to check for model convergence and autocorrelation of the posterior samples.BayModel.RmcmcOUT - parameter samplesIn case the reader wishes to forego the step of fitting the Bayesian models, we provided a mcmcOUT.csv file with 1000 posterior parameter values for each of the parameters estimated with Bayesian m...

  7. f

    Demographic transition and factors associated with remaining in place after...

    • plos.figshare.com
    docx
    Updated May 31, 2023
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    Tomohiro Morita; Shuhei Nomura; Tomoyuki Furutani; Claire Leppold; Masaharu Tsubokura; Akihiko Ozaki; Sae Ochi; Masahiro Kami; Shigeaki Kato; Tomoyoshi Oikawa (2023). Demographic transition and factors associated with remaining in place after the 2011 Fukushima nuclear disaster and related evacuation orders [Dataset]. http://doi.org/10.1371/journal.pone.0194134
    Explore at:
    docxAvailable download formats
    Dataset updated
    May 31, 2023
    Dataset provided by
    PLOS ONE
    Authors
    Tomohiro Morita; Shuhei Nomura; Tomoyuki Furutani; Claire Leppold; Masaharu Tsubokura; Akihiko Ozaki; Sae Ochi; Masahiro Kami; Shigeaki Kato; Tomoyoshi Oikawa
    License

    Attribution 4.0 (CC BY 4.0)https://creativecommons.org/licenses/by/4.0/
    License information was derived automatically

    Area covered
    Fukushima
    Description

    IntroductionDemographic changes as a result of evacuation in the acute phase of the 2011 Fukushima nuclear disaster are not well evaluated. We estimated post-disaster demographic transitions in Minamisoma City—located 14–38 km north of the nuclear plant—in the first month of the disaster; and identified demographic factors associated with the population remaining in the affected areas.Materials and methodsWe extracted data from the evacuation behavior survey administered to participants in the city between July 11, 2011 and April 30, 2013. Using mathematical models, we estimated the total population in the city after the disaster according to sex, age group, and administrative divisions of the city. To investigate factors associated with the population remaining in place after the disaster, a probit regression model was employed, taking into account sex, age, pre-disaster dwelling area, and household composition.ResultsThe overall population decline in Minamisoma City peaked 11 days after the disaster, when the population reached 7,107 people—11% of the pre-disaster level. The remaining population levels differed by area: 1.1% for mandatory evacuation zone, 12.5% for indoor sheltering zone, and 12.6% for other areas of the city. Based on multiple regression analyses, higher odds for remaining in place were observed among men (odds ratio 1.72 [95% confidence intervals 1.64–1.85]) than women; among people aged 40–64 years (1.40 [1.24–1.58]) than those aged 75 years or older; and among those living with the elderly, aged 70 years or older (1.18 [1.09–1.27]) or those living alone (1.71 [1.50–1.94]) than among those who were not.DiscussionDespite the evacuation order, some residents of mandatory evacuation zones remained in place, signaling the need for preparation to respond to their post-disaster needs. Indoor sheltering instructions may have accelerated voluntary evacuation, and this demonstrates the need for preventing potentially disorganized evacuation in future nuclear events.

  8. d

    Demography of American black bears (Ursus americanus) in a semiarid...

    • search.dataone.org
    • data.niaid.nih.gov
    • +1more
    Updated Jan 3, 2025
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    Brenden M. Orocu; Cambria Armstrong; Janene Auger; Hal L. Black; Randy T. Larsen; Brock R. McMillan; Mark C. Belk (2025). Demography of American black bears (Ursus americanus) in a semiarid environment [Dataset]. http://doi.org/10.5061/dryad.98sf7m0t8
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    Dataset updated
    Jan 3, 2025
    Dataset provided by
    Dryad Digital Repository
    Authors
    Brenden M. Orocu; Cambria Armstrong; Janene Auger; Hal L. Black; Randy T. Larsen; Brock R. McMillan; Mark C. Belk
    Area covered
    United States
    Description

    The American black bear (Ursus americanus) has one of the broadest geographic distributions of any mammalian carnivore in North America. Populations occur from high to low elevations and from mesic to arid environments, and their demographic traits have been documented in a wide variety of environments. However, the demography of American black bears in semiarid environments, which comprise a significant portion of the geographic range, is poorly documented. To fill this gap in understanding, we used data from a long-term mark-recapture study of black bears in the semiarid environment of eastern Utah, USA. Cub and yearling survival were low and adult survival was high relative to other populations. Adult life stages had the highest reproductive value, comprised the largest proportion of the population, and exhibited the highest elasticity contribution to the population growth rate (i.e., λ). Vital rates of black bears in this semiarid environment are skewed toward higher survival of adu..., Mark-Recapture study We estimated survival rates from long-term mark-recapture data gathered as part of a 27-year study on American black bears of the East Tavaputs Plateau. During the first 12 years of the study (June to August 1991-2003) female bears were captured and radio-collared, and all bears were tagged in the ear, except for cubs and yearlings. For the entire study (1992 – 2019), collared females were visited in their dens annually during their winter hibernation to count newborn cubs and surviving yearlings. Age of individual bears was determined by 2 methods: (1) direct observation of cubs or yearlings (i.e., year of birth was known) or (2) cementum annuli analysis of a cross-section of the root of an extracted premolar (Palochak, 2004; Willey, 1974). The data we used to derive survival and fecundity rates consisted of the ID_number, cohort (cub, yearling, subadult, prime-aged adult, and old adult), age in years, sex (female, male, unknown), number of cubs, number of yearling..., , # Demography of American black bears (Ursus americanus) in a semiarid environment

    https://doi.org/10.5061/dryad.98sf7m0t8

    Description of the data and file structure

    Files and variables

    File: Age-Specific_Survivorship.csv

    Description:Â

    This CSV file contains data collected from a mark-recapture study during 1991 - 2019. We calculated the age-specific average survival rate for each cohort. The average survival rate of each cohort was later used in the matrix transition model as matrix elements to retrieve important demographic information about this population of North American black bears (Ursus americanus) found in a semiarid environment.Â

    Variables
    • Cohort:Â Yearling = 1 year to 2 years;Â Subadult = 2 years to 4 years;Â Prime-aged Adult = 4 years to 14 years;Â Old Adult = 15 years and older.
    • Sex:Â M = male; F = female; U = unknown
    • Cubs and Yearlings:Â NV = not visited; number = number of cubs or yearlings presen...
  9. Data from: Spatial-temporal change of climate in relation to urban fringe...

    • search.dataone.org
    • portal.edirepository.org
    Updated Oct 4, 2013
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    Anthony Brazel; Brent Hedquist (2013). Spatial-temporal change of climate in relation to urban fringe development in central Arizona-Phoenix [Dataset]. https://search.dataone.org/view/knb-lter-cap.34.9
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    Dataset updated
    Oct 4, 2013
    Dataset provided by
    Long Term Ecological Research Networkhttp://www.lternet.edu/
    Authors
    Anthony Brazel; Brent Hedquist
    Time period covered
    Aug 18, 2001 - May 1, 2002
    Area covered
    Variables measured
    RH, id, MAX, MIN, STD, SUM, AREA, Date, MEAN, time, and 8 more
    Description

    Not many studies have documented climate and air quality changes of settlements at early stages of development. This is because high quality climate and air quality records are deficient for the periods of the early 18th century to mid 20th century when many U.S. cities were formed and grew. Dramatic landscape change induces substantial local climate change during the incipient stage of development. Rapid growth along the urban fringe in Phoenix, coupled with a fine-grained climate monitoring system, provide a unique opportunity to study the climate impacts of urban development as it unfolds. Generally, heat islands form, particularly at night, in proportion to city population size and morphological characteristics. Drier air is produced by replacement of the countryside's moist landscapes with dry, hot urbanized surfaces. Wind is increased due to turbulence induced by the built-up urban fabric and its morphology; although, depending on spatial densities of buildings on the land, wind may also decrease. Air quality conditions are worsened due to increased city emissions and surface disturbances. Depending on the diversity of microclimates in pre-existing rural landscapes and the land-use mosaic in cities, the introduction of settlements over time and space can increase or decrease the variety of microclimates within and near urban regions. These differences in microclimatic conditions can influence variations in health, ecological, architectural, economic, energy and water resources, and quality-of-life conditions in the city. Therefore, studying microclimatic conditions which change in the urban fringe over time and space is at the core of urban ecological goals as part of LTER aims. In analyzing Phoenix and Baltimore long-term rural/urban weather and climate stations, Brazel et al. (In progress) have discovered that long-term (i.e., 100 years) temperature changes do not correlate with populations changes in a linear manner, but rather in a third-order nonlinear response fashion. This nonlinear temporal change is consistent with the theories in boundary layer climatology that describe and explain the leading edge transition and energy balance theory. This pattern of urban vs. rural temperature response has been demonstrated in relation to spatial range of city sizes (using population data) for 305 rural vs. urban climate stations in the U.S. Our recent work on the two urban LTER sites has shown that a similar climate response pattern also occurs over time for climate stations that were initially located in rural locations have been overrun bu the urban fringe and subsequent urbanization (e.g., stations in Baltimore, Mesa, Phoenix, and Tempe). Lack of substantial numbers of weather and climate stations in cities has previously precluded small-scale analyses of geographic variations of urban climate, and the links to land-use change processes. With the advent of automated weather and climate station networks, remote-sensing technology, land-use history, and the focus on urban ecology, researchers can now analyze local climate responses as a function of the details of land-use change. Therefore, the basic research question of this study is: How does urban climate change over time and space at the place of maximum disturbance on the urban fringe? Hypotheses 1. Based on the leading edge theory of boundary layer climate change, largest changes should occur during the period of peak development of the land when land is being rapidly transformed from open desert and agriculture to residential, commercial, and industrial uses. 2. One would expect to observe, on average and on a temporal basis (several years), nonlinear temperature and humidity alterations across the station network at varying levels of urban development. 3. Based on past research on urban climate, one would expect to see in areas of the urban fringe, rapid changes in temperature (increases at night particularly), humidity (decreases in areas from agriculture to urban; increases from desert to urban), and wind speed (increases due to urban heating). 4. Changes of the surface climate on the urban fringe are expected to be altered as a function of various energy, moisture, and momentum control parameters, such as albedo, surface moisture, aerodynamic surface roughness, and thermal admittance. These parameters relate directly to population and land-use change (Lougeay et al. 1996).

  10. f

    Description of parameters.

    • plos.figshare.com
    xls
    Updated Jan 24, 2025
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    Dejen Ketema Mamo; Mathew N. Kinyanjui; Nourridine Siewe (2025). Description of parameters. [Dataset]. http://doi.org/10.1371/journal.pone.0317040.t002
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    xlsAvailable download formats
    Dataset updated
    Jan 24, 2025
    Dataset provided by
    PLOS ONE
    Authors
    Dejen Ketema Mamo; Mathew N. Kinyanjui; Nourridine Siewe
    License

    Attribution 4.0 (CC BY 4.0)https://creativecommons.org/licenses/by/4.0/
    License information was derived automatically

    Description

    This study presents a novel non-autonomous mathematical model to explore the intricate relationship between temperature and desert locust population dynamics, considering the influence of both solitarious and gregarious phases across all life stages. The model incorporates temperature-dependent parameters for key biological processes, including egg development, hopper growth, adult maturation, and reproduction. Theoretical analysis reveals the model’s capacity for complex dynamical behaviors, such as multiple stable states and backward bifurcations, suggesting the potential for sudden and unpredictable population shifts. Sensitivity analysis identifies temperature-related parameters as critical drivers of population fluctuations, highlighting the importance of accurate temperature predictions for effective management. Numerical simulations demonstrate the significant impact of temperature on population growth, with optimal conditions promoting rapid development and increased survival, while extreme temperatures can hinder population growth and trigger phase transitions. By providing a deeper understanding of temperature-driven population shifts, this model enhances the ability to predict locust outbreaks, optimize control strategies, and reduce the socio-economic and ecological impacts of locust invasions.

  11. g

    Data from: Identifying Critical Life Stage Transitions for Biological...

    • gimi9.com
    Updated Dec 7, 2018
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    (2018). Data from: Identifying Critical Life Stage Transitions for Biological Control of Long-lived Perennial Vincetoxicum Species | gimi9.com [Dataset]. https://gimi9.com/dataset/data-gov_6aff8c47e997fc0830fb604cf7cbee12625d73df
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    Dataset updated
    Dec 7, 2018
    License

    U.S. Government Workshttps://www.usa.gov/government-works
    License information was derived automatically

    Description

    File Name: Matrix_model_transition_data.csvResource Description: This data set includes data on 25 transitions of a matrix demographic model of two invasive Vincetoxicum species from six field and forest populations in New York State.Resource Title: Variable definitions. File Name: Matrix_model_metadata.csvResource Description: Definitions of variables including equations for each transition and definitions of the lower-level vital rates in the equationsResource Title: Vital Rate definitions. File Name: Vital_Rate.csvResource Description: Vital Rate definitions of lower-level vital rates used in transition equations - to be substituted into the Data Dictionary for full definition of each transition equation.Resource Title: Data Dictionary. File Name: Matrix_Model_transition_data_DD.csvResource Description: See Vital Rate resource for definitions of lower-level vital rates used in transition equations where noted.Resource Title: Matrix model vital rate data for Vincetoxicum species. File Name: Matrix_model_vital rate_data.csvResource Description: This data set includes data on 20 lower-level vital rates used in the calculation of transitions of a matrix demographic model of two invasive Vincetoxicum species in New York State as well as definitions of the vital rates. (File added on 12/7/2018)Resource Software Recommended: Microsoft Excel,url: https://office.microsoft.com/excel/

  12. f

    A Life-Cycle Model of Human Social Groups Produces a U-Shaped Distribution...

    • plos.figshare.com
    • data.niaid.nih.gov
    • +2more
    docx
    Updated Jun 1, 2023
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    Gul Deniz Salali; Harvey Whitehouse; Michael E. Hochberg (2023). A Life-Cycle Model of Human Social Groups Produces a U-Shaped Distribution in Group Size [Dataset]. http://doi.org/10.1371/journal.pone.0138496
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    docxAvailable download formats
    Dataset updated
    Jun 1, 2023
    Dataset provided by
    PLOS ONE
    Authors
    Gul Deniz Salali; Harvey Whitehouse; Michael E. Hochberg
    License

    Attribution 4.0 (CC BY 4.0)https://creativecommons.org/licenses/by/4.0/
    License information was derived automatically

    Description

    One of the central puzzles in the study of sociocultural evolution is how and why transitions from small-scale human groups to large-scale, hierarchically more complex ones occurred. Here we develop a spatially explicit agent-based model as a first step towards understanding the ecological dynamics of small and large-scale human groups. By analogy with the interactions between single-celled and multicellular organisms, we build a theory of group lifecycles as an emergent property of single cell demographic and expansion behaviours. We find that once the transition from small-scale to large-scale groups occurs, a few large-scale groups continue expanding while small-scale groups gradually become scarcer, and large-scale groups become larger in size and fewer in number over time. Demographic and expansion behaviours of groups are largely influenced by the distribution and availability of resources. Our results conform to a pattern of human political change in which religions and nation states come to be represented by a few large units and many smaller ones. Future enhancements of the model should include decision-making rules and probabilities of fragmentation for large-scale societies. We suggest that the synthesis of population ecology and social evolution will generate increasingly plausible models of human group dynamics.

  13. Data from: Habitat suitability and the distribution of species: Polygonatum...

    • search.dataone.org
    • portal.edirepository.org
    Updated Mar 11, 2015
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    Coweeta Long Term Ecological Research Program; Ron Pulliam (2015). Habitat suitability and the distribution of species: Polygonatum biflorum demography data from the Coweeta Hydrologic Laboratory from 1998 to 2006 [Dataset]. https://search.dataone.org/view/https%3A%2F%2Fpasta.lternet.edu%2Fpackage%2Fmetadata%2Feml%2Fknb-lter-cwt%2F1002%2F14
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    Dataset updated
    Mar 11, 2015
    Dataset provided by
    Long Term Ecological Research Networkhttp://www.lternet.edu/
    Authors
    Coweeta Long Term Ecological Research Program; Ron Pulliam
    Time period covered
    Jun 1, 1998 - Jul 30, 2006
    Variables measured
    Day, Year, Month, Plant_ID, Grid_code, Grid_number, Time_grid_7, Time_grid_A, Time_grid_B, Time_grid_C, and 106 more
    Description

    Metapopulation theory posits that suitable habitat may frequently be unoccupied because it is isolated and has never been colonized or has been colonized followed by local extinction and has not yet been recolonized. This research addresses the question of how to identify suitable, unoccupied habitat and distinguish it from unsuitable habitat. We are studying a group of six species of forest understory herbs chosen to represent a broad range of habitat distribution and dispersal characteristics. Our aim is to quantify the fundamental niche of these species (sensu Hutchinson 1957), in terms of variables such as soil moisture and temperature, by developing a set of habitat specific demographic stage transition models (i.e. conditional on such environmental variables) for these species. These models, in combination with data from field surveys of the local distribution of the species, will be used to develop testable predictive maps of the distribution of suitable habitat which can be compared to the observed distribution of the plants. We hypothesize that both dispersal ability and the distribution of suitable habitat are important determinants of the actual distribution of species. The goal of this research is both to further our conceptual understanding of the relationships between habitat requirements and species distributions, and to provide a practical approach to operationalizing the concept of "suitable habitat."

  14. d

    Data from: A spatially explicit hierarchical model to characterize...

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    • datadryad.org
    Updated Apr 1, 2025
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    Steven P. Campbell; Erin R. Zylstra; Catherine R. Darst; Roy C. Averill-Murray; Robert J. Steidl (2025). A spatially explicit hierarchical model to characterize population viability [Dataset]. http://doi.org/10.5061/dryad.v0q5035
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    Dataset updated
    Apr 1, 2025
    Dataset provided by
    Dryad Digital Repository
    Authors
    Steven P. Campbell; Erin R. Zylstra; Catherine R. Darst; Roy C. Averill-Murray; Robert J. Steidl
    Time period covered
    Aug 10, 2018
    Description

    Many of the processes that govern the viability of animal populations vary spatially, yet population viability analyses (PVAs) that account explicitly for spatial variation are rare. We develop a PVA model that incorporates autocorrelation into the analysis of local demographic information to produce spatially explicit estimates of demography and viability at relatively fine spatial scales across a large spatial extent. We use a hierarchical, spatial autoregressive model for capture-recapture data from multiple locations to obtain spatially explicit estimates of adult survival (Φad), juvenile survival (Φjuv), and juvenile-to-adult transition rates (ψ), and a spatial autoregressive model for recruitment data from multiple locations to obtain spatially explicit estimates of recruitment (R). We combine local estimates of demographic rates in stage-structured population models to estimate the rate of population change (λ), then use estimates of λ (and its uncertainty) to forecast changes in...

  15. f

    Estimated parameters of the Wang model fitted to the temperature-dependent...

    • figshare.com
    • plos.figshare.com
    xls
    Updated Jun 2, 2023
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    Babasaheb B. Fand; Nitin T. Sul; Santanu K. Bal; P. S. Minhas (2023). Estimated parameters of the Wang model fitted to the temperature-dependent mortality rate for immature life stages of S. litura. [Dataset]. http://doi.org/10.1371/journal.pone.0124682.t004
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    xlsAvailable download formats
    Dataset updated
    Jun 2, 2023
    Dataset provided by
    PLOS ONE
    Authors
    Babasaheb B. Fand; Nitin T. Sul; Santanu K. Bal; P. S. Minhas
    License

    Attribution 4.0 (CC BY 4.0)https://creativecommons.org/licenses/by/4.0/
    License information was derived automatically

    Description

    Estimated parameters of the Wang model fitted to the temperature-dependent mortality rate for immature life stages of S. litura.

  16. Data from: Demographic stimulation of the obligate understorey herb, Panax...

    • zenodo.org
    • data.niaid.nih.gov
    • +2more
    bin
    Updated May 30, 2022
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    Jennifer L. Chandler; James B. McGraw; Jennifer L. Chandler; James B. McGraw (2022). Data from: Demographic stimulation of the obligate understorey herb, Panax quinquefolius L., in response to natural forest canopy disturbances [Dataset]. http://doi.org/10.5061/dryad.562bg
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    binAvailable download formats
    Dataset updated
    May 30, 2022
    Dataset provided by
    Zenodohttp://zenodo.org/
    Authors
    Jennifer L. Chandler; James B. McGraw; Jennifer L. Chandler; James B. McGraw
    License

    CC0 1.0 Universal Public Domain Dedicationhttps://creativecommons.org/publicdomain/zero/1.0/
    License information was derived automatically

    Description

    1.Natural and anthropogenic forest canopy disturbances significantly alter forest dynamics and lead to multi-dimensional shifts in the forest understorey. An understorey plant's ability to exploit alterations to the light environment caused by canopy disturbance leads to changes in population dynamics. The purpose of this work was to determine if population growth of a species adapted to low light increases in response to additional light inputs caused by canopy disturbance, or alternatively, declines due to long-term selection under low light conditions. 2.To address this question, we quantified the demographic response of an understorey herb to three contrasting forest canopy disturbances (ice storms, tent caterpillar defoliation and lightning strikes) that encompass a broad range of disturbance severity. We used a model shade-adapted understorey species, Panax quinquefolius, to parameterize stage-based matrix models. Asymptotic growth rates, stochastic growth rates and simulations of transient dynamics were used to quantify the population-level response to canopy disturbance. Life table response experiments were used to partition the underlying controls over differences in population growth rates. 3.Population growth rates at all three disturbed sites increased in the transition period immediately after the canopy disturbance relative to the transition period prior to disturbance. Stochastic population models revealed that growth rates increased significantly in simulations that included disturbance matrices relative to those simulations that excluded disturbance. Additionally, transient models indicated that population size (n) was larger for all three populations when the respective disturbance matrix was included in the model. 4.Synthesis Obligate shade species are most likely to be pre-adapted to take advantage of canopy gaps and light influx to a degree, and this pre-adaptation may be due to long-term selection under dynamic old growth forest canopies. We propose a model whereby population performance is represented by a parabolic curve where performance is maximized under intermediate levels of canopy disturbance. This study provides new evidence to aid our understanding of the population-level response of understorey herbs to disturbances whose frequency and intensity are predicted to increase as global climates continue to shift.

  17. w

    IDPH Population Projections 2014 Edition

    • data.wu.ac.at
    csv, json, rdf, xml
    Updated Aug 15, 2016
    + more versions
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    State of Illinois (2016). IDPH Population Projections 2014 Edition [Dataset]. https://data.wu.ac.at/schema/data_gov/YTE0MmIwNjktYzFjNC00YmIzLTllYzYtYWM4YTU1ZGI3NTM4
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    xml, rdf, csv, jsonAvailable download formats
    Dataset updated
    Aug 15, 2016
    Dataset provided by
    State of Illinois
    Description

    Introduction

    This report presents projections of population from 2015 to 2025 by age and sex for Illinois, Chicago and Illinois counties produced for the Certificate of Need (CON) Program. As actual future population trends are unknown, the projected numbers should not be considered a precise prediction of the future population; rather, these projections, calculated under a specific set of assumptions, indicate the levels of population that would result if our assumptions about each population component (births, deaths and net migration) hold true. The assumptions used in this report, and the details presented below, generally assume a continuation of current trends.

    Methodology These projections were produced using a demographic cohort-component projection model. In this model, each component of population change – birth, death and net migration – is projected separately for each five-year birth cohort and sex. The cohort – component method employs the following basic demographic balancing equation: P1 = P0 + B – D + NM Where: P1 = Population at the end of the period; P0 = Population at the beginning of the period; B = Resident births during the period; D = Resident deaths during the period; and NM = Net migration (Inmigration – Outmigration) during the period. The model roughly works as follows: for every five-year projection period, the base population, disaggregated by five-year age groups and sex, is “survived” to the next five-year period by applying the appropriate survival rates for each age and sex group; next, net migrants by age and sex are added to the survived population. The population under 5 years of age is generated by applying age specific birth rates to the survived females in childbearing age (15 to 49 years).

    Base Population These projections began with the July 1, 2010 population estimates by age and sex produced by the U.S. Census Bureau. The most recent census population of April 1, 2010 was the base for July 1, 2010 population estimates.

    Special Populations In 19 counties, the college dormitory population or adult inmates in correctional facilities accounted for 5 percent or more of the total population of the county; these counties were considered as special counties. There were six college dorm counties (Champaign, Coles, DeKalb, Jackson, McDonough and McLean) and 13 correctional facilities counties (Bond, Brown, Crawford, Fayette, Fulton, Jefferson, Johnson, Lawrence, Lee, Logan, Montgomery, Perry and Randolph) that qualified as special counties. When projecting the population, these special populations were first subtracted from the base populations for each special county; then they were added back to the projected population to produce the total population projections by age and sex. The base special population by age and sex from the 2010 population census was used for this purpose with the assumption that this population will remain the same throughout each projection period.

    Mortality Future deaths were projected by applying age and sex specific survival rates to each age and sex specific base population. The assumptions on survival rates were developed on the basis of trends of mortality rates in the individual life tables constructed for each level of geography for 1989-1991, 1999-2001 and 2009-2011. The application of five-year survival rates provides a projection of the number of persons from the initial population expected to be alive in five years. Resident deaths data by age and sex from 1989 to 2011 were provided by the Illinois Center for Health Statistics (ICHS), Illinois Department of Public Health.

    Fertility Total fertility rates (TFRs) were first computed for each county. For most counties, the projected 2015 TFRs were computed as the average of the 2000 and 2010 TFRs. 2010 or 2015 rates were retained for 2020 projections, depending on the birth trend of each county. The age-specific birth rates (ASBR) were next computed for each county by multiplying the 2010 ASBR by each projected TFR. Total births were then projected for each county by applying age-specific birth rates to the projected female population of reproductive ages (15 to 49 years). The total births were broken down by sex, using an assumed sex-ratio at birth. These births were survived five years applying assumed survival ratios to get the projected population for the age group 0-4. For the special counties, special populations by age and sex were taken out before computing age-specific birth rates. The resident birth data used to compute age-specific birth rates for 1989-1991, 1999-2001 and 2009-2011 came from ICHS. Births to females younger than 15 years of age were added to those of the 15-19 age group and births to women older than 49 years of age were added to the 45-49 age group.

    Net Migration Migration is the major component of population change in Illinois, Chicago and Illinois counties. The state is experiencing a significant loss of population through internal (domestic migration within the U.S.) net migration. Unlike data on births and deaths, migration data based on administrative records are not available on a regular basis. Most data on migration are collected through surveys or indirectly from administrative records (IRS individual tax returns). For this report, net migration trends have been reviewed using data from different sources and methods (such as residual method) from the University of Wisconsin, Madison, Illinois Department of Public Health, individual exemptions data from the Internal Revenue Service, and survey data from the U.S. Census Bureau. On the basis of knowledge gained through this review and of levels of net migration from different sources, assumptions have been made that Illinois will have annual net migrants of -40, 000, -35,000 and -30,000 during 2010-2015, 2015-2020 and 2020-2025, respectively. These figures have been distributed among the counties, using age and sex distribution of net migrants during 1995-2000. The 2000 population census was the last decennial census, which included the question “Where did you live five years ago?” The age and sex distribution of the net migrants was derived, using answers to this question. The net migration for Chicago has been derived independently, using census survival method for 1990-2000 and 2000-2010 under the assumption that the annual net migration for Chicago will be -40,000, -30,000 and -25,000 for 2010-2015, 2015-2020 and 2020-2025, respectively. The age and sex distribution from the 2000-2010 net migration was used to distribute the net migrants for the projection periods.

    Conclusion These projections were prepared for use by the Certificate of Need (CON) Program; they are produced using evidence-based techniques, reasonable assumptions and the best available input data. However, as assumptions of future demographic trends may contain errors, the resulting projections are unlikely to be free of errors. In general, projections of small areas are less reliable than those for larger areas, and the farther in the future projections are made, the less reliable they may become. When possible, these projections should be regularly reviewed and updated, using more recent birth, death and migration data.

  18. e

    IPCC Climate Change Data: CSIRO B1a Model: 2050 Radiation

    • knb.ecoinformatics.org
    • search.dataone.org
    Updated Aug 14, 2015
    + more versions
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    Intergovernmental Panel on Climate Change (IPCC) (2015). IPCC Climate Change Data: CSIRO B1a Model: 2050 Radiation [Dataset]. http://doi.org/10.5063/AA/dpennington.107.4
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    Dataset updated
    Aug 14, 2015
    Dataset provided by
    Knowledge Network for Biocomplexity
    Authors
    Intergovernmental Panel on Climate Change (IPCC)
    Time period covered
    Jan 1, 2050 - Dec 31, 2050
    Area covered
    Earth
    Description

    The CSIRO Atmospheric Research Mark 2b climate model (Hirst et al., 1996, 1999) has recently been used for a number of more sophisticated climate change simulations. These start from 1880 to avoid the "cold start problem". This version of the CSIRO model includes the Gent-McWilliams mixing scheme in the ocean and shows greatly reduced climate drift relative to earlier versions (e.g. Dix and Hunt, 1998). The drift in global mean surface temperature in the new control run is about -0.02 degrees C/century. Note that the model uses flux correction. The model atmosphere has 9 levels in the vertical and horizontal resolution of spectral R21 (approximately 5.6 by 3.2 degrees). The ocean model has the same horizontal resolution with 21 levels. The equilibrium sensitivity to doubled CO2 of a mixed layer ocean version of the model is 4.3 degrees. This is at the high end of the range of model sensitivities (e.g. IPCC 1995, Table 6.3). In the basic greenhouse gas experiment the model combines the effect of all radiatively active trace gases into an "equivalent" CO2 concentration. Observed concentrations are used from 1880 to 1990 and the IS92a projections into the future. This gives close to a 1%/year compounding increase of equivalent CO2. Another model experiment includes the negative radiative forcing from atmospheric sulphate aerosol. The direct aerosol forcing is included via a perturbation of the surface albedo, similarly to the Hadley Centre experiments described by Mitchell et al (1995) and Mitchell and Johns (1997) . The sulphate concentrations are the same as used in the Hadley Centre experiments. However the chosen aerosol optical properties are different, giving a present day forcing due to anthropogenic sulphate of about -0.4 W/m^2. This can be compared to the 1880-1990 greenhouse gas forcing of about 2 W/m^2. The magnitude of the 20th century warming in the model including aerosol matches the observed reasonably well. However there are a number of forcings missing from the model, including solar variability, sulphate indirect effect and the effect of soot. The climate sensitivity of CSIRO-Mk2 is about 4.3 degrees C (Watterson et al.,1997). The central elements of the B1 future are a high level of environmental and social consciousness combined with a globally coherent approach to sustainable development. A strong welfare net prevents social exclusion on the basis of poverty. However, counter-currents may develop and in some places people may not conform to the main social and environmental intentions of the mainstream in this scenario family. Particular effort is devoted to increasing resource efficiency. Comprehensive incentive systems, combined with advances in international institutions, permit the rapid diffusion of cleaner technology. R and D to this end is also enhanced together with education and capacity building for clean and equitable development. Organizational measures are adopted to reduce material wastage, maximizing reuse and recycling. The combination of technical and organizational change yields high levels of material and energy saving as well as reductions in pollution. Labor productivity also improves as a byproduct of these efforts. Variants considered within the B1 family of scenarios include different rates of GDP growth and dematerialization (e.g., energy intensity declines). The demographic transition to low mortality and fertility occurs at the same rate as in A1 but for slightly different reasons, motivated partly by social and environmental concerns. Global population reaches nine billion by 2050 and declines to about seven billion by 2100. This is a world with high levels of economic activity and significant and deliberate progress toward international and national income equality. Global income per capita in 2050 averages US$13,000; somewhat lower than in A1. A higher proportion of this income is spent on services rather than on material goods, and on quality rather than quantity, because of less emphasis on material goods and also higher resource prices. The B1 storyline sees a relatively smooth transition to alternative energy systems as conventional oil resources decline. There is extensive use of conventional and unconventional gas as the cleanest fossil resource during the transition, but the major push is ... Visit https://dataone.org/datasets/doi%3A10.5063%2FAA%2Fdpennington.107.4 for complete metadata about this dataset.

  19. e

    IPCC Climate Change Data: CSIRO B1a Model: 2050 Radiance

    • knb.ecoinformatics.org
    • dataone.org
    Updated Aug 14, 2015
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    Intergovernmental Panel on Climate Change (IPCC) (2015). IPCC Climate Change Data: CSIRO B1a Model: 2050 Radiance [Dataset]. http://doi.org/10.5063/AA/dpennington.107.2
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    Dataset updated
    Aug 14, 2015
    Dataset provided by
    Knowledge Network for Biocomplexity
    Authors
    Intergovernmental Panel on Climate Change (IPCC)
    Time period covered
    Jan 1, 2050 - Dec 31, 2050
    Area covered
    Earth
    Description

    The CSIRO Atmospheric Research Mark 2b climate model (Hirst et al., 1996, 1999) has recently been used for a number of more sophisticated climate change simulations. These start from 1880 to avoid the "cold start problem". This version of the CSIRO model includes the Gent-McWilliams mixing scheme in the ocean and shows greatly reduced climate drift relative to earlier versions (e.g. Dix and Hunt, 1998). The drift in global mean surface temperature in the new control run is about -0.02 degrees C/century. Note that the model uses flux correction. The model atmosphere has 9 levels in the vertical and horizontal resolution of spectral R21 (approximately 5.6 by 3.2 degrees). The ocean model has the same horizontal resolution with 21 levels. The equilibrium sensitivity to doubled CO2 of a mixed layer ocean version of the model is 4.3 degrees. This is at the high end of the range of model sensitivities (e.g. IPCC 1995, Table 6.3). In the basic greenhouse gas experiment the model combines the effect of all radiatively active trace gases into an "equivalent" CO2 concentration. Observed concentrations are used from 1880 to 1990 and the IS92a projections into the future. This gives close to a 1%/year compounding increase of equivalent CO2. Another model experiment includes the negative radiative forcing from atmospheric sulphate aerosol. The direct aerosol forcing is included via a perturbation of the surface albedo, similarly to the Hadley Centre experiments described by Mitchell et al (1995) and Mitchell and Johns (1997) . The sulphate concentrations are the same as used in the Hadley Centre experiments. However the chosen aerosol optical properties are different, giving a present day forcing due to anthropogenic sulphate of about -0.4 W/m^2. This can be compared to the 1880-1990 greenhouse gas forcing of about 2 W/m^2. The magnitude of the 20th century warming in the model including aerosol matches the observed reasonably well. However there are a number of forcings missing from the model, including solar variability, sulphate indirect effect and the effect of soot. The climate sensitivity of CSIRO-Mk2 is about 4.3 degrees C (Watterson et al.,1997). The central elements of the B1 future are a high level of environmental and social consciousness combined with a globally coherent approach to sustainable development. A strong welfare net prevents social exclusion on the basis of poverty. However, counter-currents may develop and in some places people may not conform to the main social and environmental intentions of the mainstream in this scenario family. Particular effort is devoted to increasing resource efficiency. Comprehensive incentive systems, combined with advances in international institutions, permit the rapid diffusion of cleaner technology. R and D to this end is also enhanced together with education and capacity building for clean and equitable development. Organizational measures are adopted to reduce material wastage, maximizing reuse and recycling. The combination of technical and organizational change yields high levels of material and energy saving as well as reductions in pollution. Labor productivity also improves as a byproduct of these efforts. Variants considered within the B1 family of scenarios include different rates of GDP growth and dematerialization (e.g., energy intensity declines). The demographic transition to low mortality and fertility occurs at the same rate as in A1 but for slightly different reasons, motivated partly by social and environmental concerns. Global population reaches nine billion by 2050 and declines to about seven billion by 2100. This is a world with high levels of economic activity and significant and deliberate progress toward international and national income equality. Global income per capita in 2050 averages US$13,000; somewhat lower than in A1. A higher proportion of this income is spent on services rather than on material goods, and on quality rather than quantity, because of less emphasis on material goods and also higher resource prices. The B1 storyline sees a relatively smooth transition to alternative energy systems as conventional oil resources decline. There is extensive use of conventional and unconventional gas as the cleanest fossil resource during the transition, but the major push is towards post fossil technologies driven in large part by environmental concerns. Given the high environmental consciousness and institutional effectiveness in the B1 storyline, environmental quality is high, as most potentially negative environmental aspects of rapid development are anticipated and dealt with effectively locally, nationally, and internationally. For example, transboundary air pollution (acid rain) is basically eliminated in the long-term. Land-use is carefully managed to counteract the impacts of activities potentially damagi... Visit https://dataone.org/datasets/doi%3A10.5063%2FAA%2Fdpennington.107.2 for complete metadata about this dataset.

  20. f

    Towards a novel model for studying the nutritional stage dynamics of the...

    • figshare.com
    docx
    Updated Jun 3, 2023
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    Jose D. Meisel; Olga L. Sarmiento; Camilo Olaya; Pablo D. Lemoine; Juan A. Valdivia; Roberto Zarama (2023). Towards a novel model for studying the nutritional stage dynamics of the Colombian population by age and socioeconomic status [Dataset]. http://doi.org/10.1371/journal.pone.0191929
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    docxAvailable download formats
    Dataset updated
    Jun 3, 2023
    Dataset provided by
    PLOS ONE
    Authors
    Jose D. Meisel; Olga L. Sarmiento; Camilo Olaya; Pablo D. Lemoine; Juan A. Valdivia; Roberto Zarama
    License

    Attribution 4.0 (CC BY 4.0)https://creativecommons.org/licenses/by/4.0/
    License information was derived automatically

    Description

    Low-and middle-income countries (LMICs) are experiencing a nutritional transition in which the burden of obesity tends to shift towards the lower-socioeconomic status (SES) group. We propose a system dynamics (SD) model for assessing the nutritional stage dynamics of the Colombian urban population by age and SES projected to 2030. This SD model captures the ageing population according to body mass index (BMI) categories and SES. In this model, the transference rates (TRs) between BMI categories by age and SES are estimated using a heuristic based on data obtained from national surveys. The simulation results show that the Colombian population, particularly those aged 20 to 39 years with a lower SES, is moving towards the overweight and obese categories. The TRs for overweight and obese categories in the lower SES group (the mean TR from not overweight to overweight = 0.0215 (per year) and mean TR from overweight to obese = 0.0098 (per year)) are increasing more rapidly than the those in the middle (the mean TR from not overweight to overweight = 0.0162 (per year) and mean TR from overweight to obese = 0.0065 (per year)) and higher SES groups (the mean TR from not overweight to overweight = 0.0166 and mean TR from overweight to obese = 0.0054 (per year)). Additionally, from 2005 to 2010, individuals aged 20 to 39 years had the highest TRs towards the overweight and obese categories (from 0.026 to 0.036 per year and from 0.0064 to 0.012 per year, respectively). The TRs also indicated that children aged 0 to 14 years are moving from the obese to overweight and from the overweight to not overweight categories. These TRs show that the Colombian population is experiencing an SES-related nutritional transition that is affecting the lower SES population. The proposed model could be implemented to assess the nutritional transitions experienced in other LMICs.

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Agricultural Research Service (2025). Data from: Identifying Critical Life Stage Transitions for Biological Control of Long-lived Perennial Vincetoxicum Species [Dataset]. https://catalog.data.gov/dataset/data-from-identifying-critical-life-stage-transitions-for-biological-control-of-long-lived-41b5d

Data from: Identifying Critical Life Stage Transitions for Biological Control of Long-lived Perennial Vincetoxicum Species

Related Article
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Dataset updated
Apr 21, 2025
Dataset provided by
Agricultural Research Service
Description

This dataset includes data on 25 transitions of a matrix demographic model of the invasive species Vincetoxicum nigrum (L.) Moench (black swallow-wort or black dog-strangling vine) and Vincetoxicum rossicum (Kleopow) Barb. (pale swallow-wort or dog-strangling vine) (Apocynaceae, subfamily Asclepiadoideae), two invasive perennial vines in the northeastern U.S.A. and southeastern Canada. The matrix model was developed for projecting population growth rates as a result of changes to lower-level vital rates from biological control although the model is generalizable to any control tactic. Transitions occurred among the five life stages of seeds, seedlings, vegetative juveniles (defined as being in at least their second season of growth), small flowering plants (having 1–2 stems), and large flowering plants (having 3 or more stems). Transition values were calculated using deterministic equations and data from 20 lower-level vital rates collected from 2009-2012 from two open field and two forest understory populations of V. rossicum (43°51’N, 76°17’W; 42°48'N, 76°40'W) and two open field populations of V. nigrum (41°46’N, 73°44’W; 41°18’N, 73°58’W) in New York State. Sites varied in plant densities, soil depth, and light levels (forest populations). Detailed descriptions of vital rate data collection may be found in: Milbrath et al. 2017. Northeastern Naturalist 24(1):37-53. Five replicate sets of transition data obtained from five separate spatial regions of a particular infestation were produced for each of the six populations. Note: Added new excel file of vital rate data on 12/7/2018. Resources in this dataset:Resource Title: Matrix model transition data for Vincetoxicum species. File Name: Matrix_model_transition_data.csvResource Description: This data set includes data on 25 transitions of a matrix demographic model of two invasive Vincetoxicum species from six field and forest populations in New York State.Resource Title: Variable definitions. File Name: Matrix_model_metadata.csvResource Description: Definitions of variables including equations for each transition and definitions of the lower-level vital rates in the equationsResource Title: Vital Rate definitions. File Name: Vital_Rate.csvResource Description: Vital Rate definitions of lower-level vital rates used in transition equations - to be substituted into the Data Dictionary for full definition of each transition equation.Resource Title: Data Dictionary. File Name: Matrix_Model_transition_data_DD.csvResource Description: See Vital Rate resource for definitions of lower-level vital rates used in transition equations where noted.Resource Title: Matrix model vital rate data for Vincetoxicum species. File Name: Matrix_model_vital rate_data.csvResource Description: This data set includes data on 20 lower-level vital rates used in the calculation of transitions of a matrix demographic model of two invasive Vincetoxicum species in New York State as well as definitions of the vital rates. (File added on 12/7/2018)Resource Software Recommended: Microsoft Excel,url: https://office.microsoft.com/excel/

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