Process and measurement errors of population size: their mutual effects on precision and bias of estimates for demographic parameters

2008 ◽  
Vol 17 (14) ◽  
pp. 3417-3429 ◽  
Author(s):  
Thomas Hovestadt ◽  
Piotr Nowicki
2017 ◽  
Vol 26 (9) ◽  
pp. 2449-2465 ◽  
Author(s):  
Marlene Waege Stubberud ◽  
Ane Marlene Myhre ◽  
Håkon Holand ◽  
Thomas Kvalnes ◽  
Thor Harald Ringsby ◽  
...  

2014 ◽  
Vol 61 (1) ◽  
pp. 129-133
Author(s):  
B. M. Levick

A quality not much considered here in the past, how often a work is likely be taken from the shelf, prompts me to put Saskia's Hin'sThe Demography of Roman Italyin first position. For that depends in turn on how reliable, clear, and broad of outlook the chapters are, and where they lead the reader. Though dry and plain it might seem (for all the developing technologies), the subject moves directly towards a hot, polarized topic – ‘the Roman economy’ and its development – with oscillation between extreme positions. It is a particular merit, then, to put forward a fresh view (though previously adumbrated elsewhere) that is not extreme and must be taken seriously. That is where Hin will take historians. But the book is structured in three sections: economic and ecological parameters, demographic parameters (morality, fertility, and migration), and population size. The separate chapters are well supported from a variety of evidence, judiciously treated and well written up. That on climate, with a mildly positive conclusion, needed no apology. If I have a complaint is it about the index: dive into a passage involving ‘Brass modelling’ and you will have to rummage back in the text (111) for hope of identifying it.


2015 ◽  
Vol 50 (5) ◽  
pp. 355-362 ◽  
Author(s):  
Cleonor Cavalcante Alves Silva ◽  
Raul Alberto Laumann ◽  
Maria Carolina Blassioli Moraes ◽  
Michely Ferreira Santos de Aquino ◽  
Miguel Borges

The objective of this work was to compare the biology of Chinavia impicticornis and C. ubica (Hemiptera: Pentatomidae), two species of stinkbugs that occur as secondary pests in soybean. Life table procedures were used for evaluating nymphs, and fecundity tables for evaluating adults, in order to establish the demographics of the two species. The two species have similar demographic parameters, and the development of immature stages, from egg to adult, had similar duration periods of approximately 30 days. In both species, eggs and second-instar nymphs were the stages with higher mortality. Total egg production did not differ between females of both species. Fecundity and survival curves for adults showed similar trends in both species. However, C. ubica had greater potential to increase its populations, since its fecundity parameters were significantly higher than those of C. impicticornis. Moreover, the generational time and the time required to double the population size were shorter in C. ubica. Prolonged longevity, long oviposition period, high fecundity, and the ability to rapidly increase their populations indicate that both species can become potential pests in favorable environments.


Author(s):  
Г.П. Неверова ◽  
G.P. Neverova

The paper investigates the model of population dynamics with age structure and density dependence of birth rate. We consider two situations: 1) the population develops freely and 2) the population is exploited. It was shown that harvesting leads to the stabilization of the dynamics. There is multiregimism, i.e. different dynamic regimes are possible with the same values of demographic parameters. It is shown that even a single harvesting in the current population size could lead to a change of the observed dynamic regime.


2018 ◽  
Author(s):  
Katherine R McLaughlin ◽  
Lisa G Johnston ◽  
Laura J Gamble ◽  
Trdat Grigoryan ◽  
Arshak Papoyan ◽  
...  

BACKGROUND Estimates of the sizes of hidden populations, including female sex workers (FSW), men who have sex with men (MSM), and people who inject drugs (PWID), are essential for understanding the magnitude of vulnerabilities, health care needs, risk behaviors, and HIV and other infections. OBJECTIVE This article advances the successive sampling-population size estimation (SS-PSE) method by examining the performance of a modification allowing visibility to be jointly modeled with population size in the context of 15 datasets. Datasets are from respondent-driven sampling (RDS) surveys of FSW, MSM, and PWID from three cities in Armenia. We compare and evaluate the accuracy of our imputed visibility population size estimates to those found for the same populations through other unpublished methods. We then suggest questions that are useful for eliciting information needed to compute SS-PSE and provide guidelines and caveats to improve the implementation of SS-PSE for real data. METHODS SS-PSE approximates the RDS sampling mechanism via the successive sampling model and uses the order of selection of the sample to provide information on the distribution of network sizes over the population members. We incorporate visibility imputation, a measure of a person’s propensity to participate in the study, given that inclusion probabilities for RDS are unknown and social network sizes, often used as a proxy for inclusion probability, are subject to measurement errors from self-reported study data. RESULTS FSW in Yerevan (2012, 2016) and Vanadzor (2016) as well as PWID in Yerevan (2014), Gyumri (2016), and Vanadzor (2016) had great fits with prior estimations. The MSM populations in all three cities had inconsistencies with expert prior values. The maximum low prior value was larger than the minimum high prior value, making a great fit impossible. One possible explanation is the inclusion of transgender individuals in the MSM populations during these studies. There could be differences between what experts perceive as the size of the population, based on who is an eligible member of that population, and what members of the population perceive. There could also be inconsistencies among different study participants, as some may include transgender individuals in their accounting of personal network size, while others may not. Because of these difficulties, the transgender population was split apart from the MSM population for the 2018 study. CONCLUSIONS Prior estimations from expert opinions may not always be accurate. RDS surveys should be assessed to ensure that they have met all of the assumptions, that variables have reached convergence, and that the network structure of the population does not have bottlenecks. We recommend that SS-PSE be used in conjunction with other population size estimations commonly used in RDS, as well as results of other years of SS-PSE, to ensure generation of the most accurate size estimation.


Genetics ◽  
2001 ◽  
Vol 157 (2) ◽  
pp. 911-925
Author(s):  
Renaud Vitalis ◽  
Denis Couvet

Abstract Standard methods for inferring demographic parameters from genetic data are based mainly on one-locus theory. However, the association of genes at different loci (e.g., two-locus identity disequilibrium) may also contain some information about demographic parameters of populations. In this article, we define one- and two-locus parameters of population structure as functions of one- and two-locus probabilities for the identity in state of genes. Since these parameters are known functions of demographic parameters in an infinite island model, we develop moment-based estimators of effective population size and immigration rate from one- and two-locus parameters. We evaluate this method through simulation. Although variance and bias may be quite large, increasing the number of loci on which the estimates are derived improves the method. We simulate an infinite allele model and a K allele model of mutation. Bias and variance are smaller with increasing numbers of alleles per locus. This is, to our knowledge, the first attempt of a joint estimation of local effective population size and immigration rate.


2019 ◽  
pp. 13-22
Author(s):  
Julian Renet

The estimation of demographic parameters in wild populations is strengthened by individual identification. For amphibians, various techniques are used to either temporarily or permanently mark individuals for identification. Photo-identification of body patterns offers a non-invasive technique. However, the reliability of photo-recognition software is key to the reliable estimation of the true demographic parameters. In the current study, we assessed the effectiveness of fully-automated and semi-automated software: Wild-ID and APHIS. We used the cryptic salamander Hydromantes strinatii as our study species. We used the False Rejection Rate (FRR) of Top 1, Top 5 and Top 10 matches of chest and cloaca pictures. Finally, we assessed the bias induced by our FRR for the estimation of population size through simulation. Wild-ID FRRs ranged from 0.042 to 0.093 while APHIS’ ranged from 0.227 to 0.547. Wild-ID was equally efficient with pictures from the chest and from the cloaca, while APHIS was significantly more efficient with chest pictures than cloaca pictures. Cropping pictures did not significantly improve Wild-ID effectiveness. Our Wild-ID FRRs are among the lowest ever obtained from pictures of an amphibian with a complex chromatophore pattern. Simulation showed that the Top 10 FRR from selected software Wild-ID induced a low bias 2.7% on the estimation of population size. The effectiveness and plasticity of Wild-ID provides opportunities for reliably monitoring amphibian species with complex colour patterns.


2020 ◽  
Author(s):  
Alissa L. Severson ◽  
Shai Carmi ◽  
Noah A. Rosenberg

AbstractRecent modeling studies interested in runs of homozygosity (ROH) and identity by descent (IBD) have sought to connect these properties of genomic sharing to pairwise coalescence times. Here, we examine a variety of features of pairwise coalescence times in models that consider consanguinity. In particular, we extend a recent diploid analysis of mean coalescence times for lineage pairs within and between individuals in a consanguineous population to derive the variance of coalescence times, studying its dependence on the frequency of consanguinity and the kinship coefficient of consanguineous relationships. We also introduce a separation-of-time-scales approach that treats consanguinity models analogously to mathematically similar phenomena such as partial selfing, using this approach to obtain coalescence-time distributions. This approach shows that the consanguinity model behaves similarly to a standard coalescent, scaling population size by a factor 1 − 3c, where c represents the kinship coefficient of a randomly chosen mating pair. It provides the explanation for an earlier result describing mean coalescence time in the consanguinity model in terms of c. The results extend the potential to make predictions about ROH and IBD in relation to demographic parameters of diploid populations.


2009 ◽  
Vol 173 (6) ◽  
pp. 722-733 ◽  
Author(s):  
Giacomo Tavecchia ◽  
Panagiotis Besbeas ◽  
Tim Coulson ◽  
Byron J. T. Morgan ◽  
Tim H. Clutton‐Brock

Author(s):  
Delbert E. Philpott ◽  
W. Sapp ◽  
C. Williams ◽  
T. Fast ◽  
J. Stevenson ◽  
...  

Space Lab 3 (SL-3) was flown on Shuttle Challenger providing an opportunity to measure the effect of spaceflight on rat testes. Cannon developed the idea that organisms react to unfavorable conditions with highly integrated metabolic activities. Selye summarized the manifestations of physiological response to nonspecific stress and he pointed out that atrophy of the gonads always occurred. Many papers have been published showing the effects of social interaction, crowding, peck order and confinement. Flickinger showed delayed testicular development in subordinate roosters influenced by group numbers, social rank and social status. Christian reported increasing population size in mice resulted in adrenal hypertrophy, inhibition of reproductive maturation and loss of reproductive function in adults. Sex organ weights also declined. Two male dogs were flown on Cosmos 110 for 22 days. Fedorova reported an increase of 30 to 70% atypical spermatozoa consisting of tail curling and/or the absence of a tail.


Sign in / Sign up

Export Citation Format

Share Document