Toward a More “Useful” Model: Population Projection, 1920-1955
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Modeling Population Dynamics
Modeling Population Dynamics Gary C. White INTRODUCTION Population modeling is a tool used by wildlife managers. At its simplest, population modeling is a book keeping system to keep track of the four components of population change: births, deaths, immigration, and emigration. In mathematical symbolism, a population model can be expressed as Nt+1 = Nt + Bt - Dt + It - Et . Population size (N) at time t+1 is equal to the population size at time t plus births (B) minus deaths (D) plus immigrants (I) minus emigrants (E). The simplicity of the relationship belies its usefulness. If you were managing a business, you would be interested in knowing how much money was being paid out of the business, relative to how much money was coming in. The net difference represents your “profit”. The same is true for managing a wildlife population. By knowing the net change in the size of the wildlife population from one year to the next, you as a wildlife manager know whether the population is “profitable” (i.e., gaining in size), or headed towards bankruptcy (i.e., becoming smaller). Two examples will demonstrate typical uses of population models in big game management. In November 1995, voters in Colorado passed an amendment to the state’s constitution that outlawed hunting black bears during spring. Wildlife managers were asked if the bear population would increase because of no spring harvest. A population model can be used to answer this question. The second example of the use of a model is to determine which of two management schemes (e.g., no antlerless harvest versus significant antlerless harvest) will result in Modeling Population Dynamics – Draft May 6, 1998 2 the largest buck harvest in a mule deer population. -
Immigration and the Stable Population Model
IMMIGRATION AND THE STABLE POPULATION MODEL Thomas J. Espenshade The Urban Institute, 2100 M Street, N. W., Washington, D.C. 20037, USA Leon F. Bouvier Population Reference Bureau, 1337 Connecticut Avenue, N. W., Washington, D.C. 20036, USA W. Brian Arthur International Institute for Applied Systems Analysis, A-2361 Laxenburg, Austria RR-82-29 August 1982 Reprinted from Demography, volume 19(1) (1982) INTERNATIONAL INSTITUTE FOR APPLIED SYSTEMS ANALYSIS Laxenburg, Austria Research Reports, which record research conducted at IIASA, are independently reviewed before publication. However, the views and opinions they express are not necessarily those of the Institute or the National Member Organizations that support it. Reprinted with permission from Demography 19(1): 125-133, 1982. Copyright© 1982 Population Association of America. All rights reserved. No part of this publication may be reproduced or transmitted in any form or by any means, electronic or mechanical, including photocopy, recording, or any information storage or retrieval system, without permission in writing from the copyright holder. iii FOREWORD For some years, IIASA has had a keen interest in problems of population dynamics and migration policy. In this paper, reprinted from Demography, Thomas Espenshade, Leon Bouvier, and Brian Arthur extend the traditional methods of stable population theory to populations with below-replacement fertility and a constant annual quota of in-migrants. They show that such a situation results in a stationary population and examine how its size and ethnic structure depend on both the fertility level and the migration quota. DEMOGRAPHY© Volume 19, Number 1 Februory 1982 IMMIGRATION AND THE STABLE POPULATION MODEL Thomos J. -
Metabolic Theories of Aging
Metabolic Theories of Aging Chris Burley, Lisa K. Lashley, Charles J. Golden Nova Southeastern University Metabolic theories of aging postulate that aging is due to energy expenditure, which ultimately results in the breakdown and eventual death of cells. Historically, within the realm of metabolic theories of aging, there have been three models: The Rate-of-Living theory, The Oxidative Damage/Free Radical theory, and the Metabolic Stability theory. All three theories maintain that aging is directly related to metabolic rate, but the theories differ in how they arrive at that conclusion. The Rate-of Living theory of aging is the most antiquated of the metabolic aging theories. It proposes that two factors are responsible for determining longevity in all living organisms: 1) a genetically pre-determined capacity for overall metabolic potential, and 2) metabolic rate. The first empirical evidence for this theory dates back to 1908, when Max Rubner observed increasing metabolic rates as a function of increasing body mass in five mammalian species of varying longevities (guinea pig, cat, dog, cow, and horse). Rubner reported that the animals’ metabolic rates increased as a function of body mass, and that larger animals had longer lifespans. Based on these results, Rubner postulated that longevity could be determined by calculating the pre-determined capacity for organic energy use and the rate at which the energy was being expended. Rubner’s observation was supported by Raymond Pearl when he concluded that slower metabolism resulted in an increased lifespan among fruit flies and cantaloupe seeds. Despite the evidence for the Rate-of-Living theory, modern scientific developments have refuted the accuracy of the theory. -
Mathematical Analysis of Population Growth Subject to Environmental Change
SCIENTIA MANU E T MENTE MATHEMATICAL ANALYSIS OF POPULATION GROWTH SUBJECT TO ENVIRONMENTAL CHANGE A thesis submitted for the degree of Doctor of Philosophy By Hamizah Mohd Safuan M.Sc.(Mathematics) Applied and Industrial Mathematics Research Group, School of Physical, Environmental and Mathematical Sciences, The University of New South Wales, Canberra, Australian Defence Force Academy. November 2014 PLEASE TYPE THE UNIVERSITY OF NEW SOUTH WALES Thesis/Dissertation Sheet Surname or Family name: Mohd Safuan First name: Hamizah Other name/s: - Abbreviation for degree as given in the University calendar: Ph.D (Mathematics) School: Faculty: UNSW Canberra School of Physical, Environmental and Mathematical Sciences Tille: Mathematical analysis of population growth subject lo environmental change Abstract 350 words maximum: (PLEASE TYPE) Many ecosystems are pressured when the environment is perturbed, such as when resources are scarce, or even when they are over-abundant. Changes in the environment impact on its ability lo support a population of a given species. However, most current models do not lake the changing environment into consideration. The standard approach in modelling a population in its environment is lo assume that the carrying capacity, which is a proxy for the state of the environment, is unchanging. In effect, the assumption also posits that the population is negligible compared lo the environment and cannot alter the carrying capacity in any way. Thus, modelling the interplay of the population with its environments is important lo describe varying factors that exist in the system. This objective can be achieved by treating the carrying capacity as lime- and space-dependent variables in the governing equations of the model. -
Math 636 - Mathematical Modeling Discrete Modeling 1 Discrete Modeling – Population of the United States U
Discrete Modeling { Population of the United States Discrete Modeling { Population of the United States Variation in Growth Rate Variation in Growth Rate Autonomous Models Autonomous Models Outline Math 636 - Mathematical Modeling Discrete Modeling 1 Discrete Modeling { Population of the United States U. S. Population Malthusian Growth Model Programming Malthusian Growth Joseph M. Mahaffy, 2 Variation in Growth Rate [email protected] General Discrete Dynamical Population Model Linear Growth Rate U. S. Population Model Nonautonomous Malthusian Growth Model Department of Mathematics and Statistics Dynamical Systems Group Computational Sciences Research Center 3 Autonomous Models San Diego State University Logistic Growth Model San Diego, CA 92182-7720 Beverton-Holt Model http://jmahaffy.sdsu.edu Analysis of Autonomous Models Fall 2018 Discrete Modeling U. S. Population | Discrete Modeling U. S. Population | Joseph M. Mahaffy, [email protected] (1/34) Joseph M. Mahaffy, [email protected] (2/34) Discrete Modeling { Population of the United States Discrete Modeling { Population of the United States Malthusian Growth Model Malthusian Growth Model Variation in Growth Rate Variation in Growth Rate Programming Malthusian Growth Programming Malthusian Growth Autonomous Models Autonomous Models United States Census Census Data Census Data United States Census 1790 3,929,214 1870 39,818,449 1950 150,697,361 Constitution requires census every 10 years 1800 5,308,483 1880 50,189,209 1960 179,323,175 Census used for budgeting federal payments and representation -
Simulation of Working Population Exposures to Carbon Monoxide Using EXPOLIS-Milan Microenvironment Concentration and Time-Activity Data
Journal of Exposure Analysis and Environmental Epidemiology (2004) 14, 154–163 r 2004 Nature Publishing GroupAll rights reserved 1053-4245/04/$25.00 www.nature.com/jea Simulation of working population exposures to carbon monoxide using EXPOLIS-Milan microenvironment concentration and time-activity data YURI BRUINEN DE BRUIN,a,b,c OTTO HA¨ NNINEN,b PAOLO CARRER,a MARCO MARONI,a STYLIANOS KEPHALOPOULOS,c GRETA SCOTTO DI MARCOc AND MATTI JANTUNENb aDepartment of Occupational Health, University of Milan, Via San Barnaba 8, 20122 Milan, Italy bKTL, Department of Environmental Health, P.O. Box 95, FIN-70701, Kuopio, Finland cEC Joint Research Centre, Institute for Health and Consumer Protection, Via E. Fermi, 21020 (VA), Ispra, Italy Current air pollution levels have been shown to affect human health. Probabilistic modeling can be used to assess exposure distributions in selected target populations. Modeling can and should be used to compare exposures in alternative future scenarios to guide society development. Such models, however, must first be validated using existing data for a past situation. This study applied probabilistic modeling to carbon monoxide (CO) exposures using EXPOLIS-Milan data. In the current work, the model performance was evaluated by comparing modeled exposure distributions to observed ones. Model performance was studied in detail in two dimensions; (i) for different averaging times (1, 8 and 24 h) and (ii) using different detail in defining the microenvironments in the model (two, five and 11 microenvironments). (iii) The number of exposure events leading to 8-h guideline exceedance was estimated. Population time activity was modeled using a fractions-of-time approach assuming that some time is spent in each microenvironment used in the model. -
Harvesting in a Resource Dependent Age Structured Leslie Type
1 Final version Harvesting in a resource dependent age structured Leslie type population model Rui Dilão1, Tiago Domingos1 and Elman M. Shahverdiev1,2 1) Grupo de Dinâmica Não-Linear, Instituto Superior Técnico, Av. Rovisco Pais, 1049- 001 Lisboa, Portugal. 2) Institute of Physics, 33, H. Javid Avenue, 370143 Baku, Azerbaijan. Short Title: Harvesting in a resource dependent model. Corresponding author: Rui Dilão Grupo de Dinâmica Não-Linear, Instituto Superior Técnico Av. Rovisco Pais, 1049-001 Lisbon, Portugal [email protected] Phone (351)218417617; Fax (351)218419123. 2 Abstract We analyse the effect of harvesting in a resource dependent age structured population model, deriving the conditions for the existence of a stable steady state as a function of fertility coefficients, harvesting mortality and carrying capacity of the resources. Under the effect of proportional harvest, we give a sufficient condition for a population to extinguish, and we show that the magnitude of proportional harvest depends on the resources available to the population. We show that the harvesting yield can be periodic, quasi-periodic or chaotic, depending on the dynamics of the harvested population. For populations with large fertility numbers, small harvesting mortality leads to abrupt extinction, but larger harvesting mortality leads to controlled population numbers by avoiding over consumption of resources. Harvesting can be a strategy in order to stabilise periodic or quasi-periodic oscillations in the number of individuals of a population. Key words: harvesting, age structured population models, population extinction. 3 1. Introduction In natural environments and in the laboratory the number of individuals of a population change in time in different ways. -
2 the Biology of Ageing
The biology of ageing 2 Aprimer JOAO˜ PEDRO DE MAGALHAES˜ OVERVIEW .......................................................... This chapter introduces key biological concepts of ageing. First, it defines ageing and presents the main features of human ageing, followed by a consideration of evolutionary models of ageing. Causes of variation in ageing (genetic and dietary) are reviewed, before examining biological theories of the causes of ageing. .......................................................... Introduction Thanks to technological progress in different areas, including biomed- ical breakthroughs in preventing and treating infectious diseases, longevity has been increasing dramatically for decades. The life expectancy at birth in the UK for boys and girls rose, respectively, from 45 and 49 years in 1901 to 75 and 80 in 1999 with similar fig- ures reported for other industrialized nations (see Chapter 1 for further discussion). A direct consequence is a steady increase in the propor- tion of people living to an age where their health and well-being are restricted by ageing. By the year 2050, it is estimated that the per- centage of people in the UK over the age of 65 will rise to over 25 per cent, compared to 14 per cent in 2004 (Smith, 2004). The greying of the population, discussed elsewhere (see Chapter 1), implies major medical and societal changes. Although ageing is no longer considered by health professionals as a direct cause of death (Hayflick, 1994), the major killers in industrialized nations are now age-related diseases like cancer, diseases of the heart and 22 Joao˜ Pedro de Magalhaes˜ neurodegenerative diseases. The study of the biological mechanisms of ageing is thus not merely a topic of scientific curiosity, but a crucial area of research throughout the twenty-first century. -
Doctorates Awarded in America in Botany and Zoology More Than Doubled
DIVISION OF THE HUMANITIES AND SOCIAL SCIENCES CALIFORNIA INSTITUTE OF TECHNOLOGY PASADENA, CALIFORNIA 91125 GENETICS IN THE UNITED STATES AND GREAT BRITAIN 1890 to 1930: QUERIES AND SPECULATIONS Daniel J. Kev1es HUMANITIES WORKING PAPER 15 December 1978 According to recent scholarship in the early history of genetics, by the l890s many younger biologists were growing restless with phylogenetic morphology and embryology, the traditional descriptive approaches to the much-debated problems of evolutionary theory. Eager to break away from these approaches, a number of these biologists -- and some older ones such as Alfred R. Wallace called for programs of experimental research in evolution addressed in particular to the problems of heredity and variation. "No problems in the whole range of biology," Charles O. Whitman of Woods Hole typically said, were of 1 "higher scientific interest or deeper practical import to humanity." In England Francis Galton inspired one of the more important experimental research programs -- W. F. R. Weldon's statistical analyses, developed in collaboration with Karl Pearson, of variations in large populations. Another important departure was the program of hybridization experiments exemplified in the research of William Bateson. Pearson and Weldon helped establish the field of heredity studies known as biometry. The research of Bateson and others paved the way for the rediscovery in 2 1900 and then vigorous advocacy of the Mendelian paradigm. Mendel's ideas did not gain rapid acceptance in all biological quarters in either the United States or Great Britain, In England, the biometricians Weldon and Pearson hotly disputed the validity of Mendel's results, the merits of his conceptual scheme, and even the integrity of his British advocates, especially Bateson. -
Peak Oil and the Everyday Complexity of Human Progress Narratives
Peak Oil and the Everyday Complexity of Human Progress Narratives John C. Pruit University of Missouri The “big” story of human progress has polarizing tendencies featuring the binary options of progress or decline. I consider human progress narratives in the context of everyday life. Analysis of the “little” stories from two narrative environments focusing on peak oil offers a more complex picture of the meaning and contours of the narrative. I consider the impact of differential blog site commitments to peak oil perspectives and identify five narrative types culled from two narrative dimensions. I argue that the lived experience complicates human progress narratives, which is no longer an either/or proposition This is going to be an environmental disaster of unprecedented proportions and the only thing that people seem to really care about is keeping the Mississippi open to shipping traffic so that BAU [business as usual] can continue. I weep for the wetlands and what their loss will mean. “FMagyar” April 30, 2010 What's the worst the doomers can moan about now? An oil spill (not even a big one by historical standards) and a bit of toxic mess in Canada. Woo, I'm so scared! Come on doomers, you can do better than this! :) “Mr Potato Head” July 9, 2010 Oil and oil-related events such as the 2010 BP spill in the Gulf of Mexico are part of the story of human progress and important to how people story their own lives. Oil powers lifestyles and plays a role in everything from transportation to food production. -
Interconnections Accelerate Collapse in a Socio-Ecological
bioRxiv preprint doi: https://doi.org/10.1101/195412; this version posted September 28, 2017. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. Interconnections accelerate collapse in a socio-ecological metapopulation Zachary Dockstader1, Chris T. Bauch1, and Madhur Anand2* 1University of Waterloo, Department of Applied Mathematics, Waterloo, N2L 3G1, Canada 2University of Guelph, School of Environmental Sciences, Guelph, N1G 2W1, Canada *[email protected] ABSTRACT Resource over-exploitation can have profound effects on both ecosystems and the human populations residing in them. Models of population growth based on a depletable resources have been studied previously, but relatively few consider metapopulation effects. Here we analyze a socio-ecological metapopulation model where resources grow logistically on each patch. Each population harvests resources on its own patch to support population growth, but can also harvest resources from other patches when their own patch resources become scarce. We find that allowing populations to harvest from other patches significantly accelerates collapse and also increases the parameter regime for which collapse occurs, compared to a model where populations are not able to harvest resources from other patches. As the number of patches in the metapopulation increases, collapse is more sudden, more severe, and occurs sooner. These effects also persist under scenarios of asymmetry and inequality between patches. We conclude that metapopulation effects in socio-ecological systems can be both helpful and harmful and therefore require urgent study. -
Footprints to Singularity: a Global Population Model Explains Late 20Th Century Slow
bioRxiv preprint doi: https://doi.org/10.1101/2021.02.04.429734; this version posted February 5, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. 1 title: 2 Footprints to Singularity: A global population model explains late 20th century slow- 3 down and predicts peak within ten years. 4 5 short title: 6 Systems dynamics models for global human population 7 8 Christopher Bystroff 9 Dept of Biological Sciences, Dept of Computer Science, Rensselaer Polytechnic Institute, Troy NY 12180 10 11 1 bioRxiv preprint doi: https://doi.org/10.1101/2021.02.04.429734; this version posted February 5, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. 12 Abstract 13 14 Projections of future global human population are traditionally made using birth/death trend 15 extrapolations, but these methods ignore limits. Expressing humanity as a K-selected species whose 16 numbers are limited by the global carrying capacity produces a different outlook. Population data 17 for the second millennium up to the year 1970 was fit to a hyper-exponential growth equation, 18 where the rate constant for growth itself grows exponentially due to growth of life-saving 19 technology. The discrepancies between the projected growth and the actual population data since 20 1970 are accounted for by a decrease in the global carrying capacity due to ecosystem degradation. 21 A system dynamics model that best fits recent population numbers suggests that the global 22 biocapacity may already have been reduced to one-half of its historical value and global carrying 23 capacity may be at its 1965 level and falling.