935 research outputs found
Race and Education in New Orleans: Creating the Segregated City, 1764-1960
Race and Education in New Orleans considers an important question for American historians: What forces created racial segregation? Using schooling as a focal point, Walter Stern skillfully unpacks the complex factors underlying white supremacy and the city’s social and racial order. Although New Orleans is critical for students of urban America, it possessed distinctive features that, over time, became transformed into a pattern resembling the rest the country
Schooling In The Antebellum South: The Rise Of Public And Private Education In Louisiana, Mississippi, And Alabama
Antebellum Education Revised In nineteenth-century southern education, the lines distinguishing public and private were thin, and wisely Sarah L. Hyde casts a wide net in her new study, Schooling in the Antebellum South. Hyde writes against the common misconception that portrays inhabitants...
Probit models for capture-recapture data subject to imperfect detection, individual heterogeneity and misidentification
As noninvasive sampling techniques for animal populations have become more
popular, there has been increasing interest in the development of
capture-recapture models that can accommodate both imperfect detection and
misidentification of individuals (e.g., due to genotyping error). However,
current methods do not allow for individual variation in parameters, such as
detection or survival probability. Here we develop misidentification models for
capture-recapture data that can simultaneously account for temporal variation,
behavioral effects and individual heterogeneity in parameters. To facilitate
Bayesian inference using our approach, we extend standard probit regression
techniques to latent multinomial models where the dimension and zeros of the
response cannot be observed. We also present a novel Metropolis-Hastings within
Gibbs algorithm for fitting these models using Markov chain Monte Carlo. Using
closed population abundance models for illustration, we re-visit a DNA
capture-recapture population study of black bears in Michigan, USA and find
evidence of misidentification due to genotyping error, as well as temporal,
behavioral and individual variation in detection probability. We also estimate
a salamander population of known size from laboratory experiments evaluating
the effectiveness of a marking technique commonly used for amphibians and fish.
Our model was able to reliably estimate the size of this population and
provided evidence of individual heterogeneity in misidentification probability
that is attributable to variable mark quality. Our approach is more
computationally demanding than previously proposed methods, but it provides the
flexibility necessary for a much broader suite of models to be explored while
properly accounting for uncertainty introduced by misidentification and
imperfect detection. In the absence of misidentification, our probit
formulation also provides a convenient and efficient Gibbs sampler for Bayesian
analysis of traditional closed population capture-recapture data.Comment: Published in at http://dx.doi.org/10.1214/14-AOAS783 the Annals of
Applied Statistics (http://www.imstat.org/aoas/) by the Institute of
Mathematical Statistics (http://www.imstat.org
Estimating age from recapture data: integrating incremental growth measures with ancillary data to infer age-at-length
Estimating the age of individuals in wild populations can be of fundamental importance for answering ecological questions, modeling population demographics, and managing exploited or threatened species. Significant effort has been devoted to determining age through the use of growth annuli, secondary physical characteristics related to age, and growth models. Many species, however, either do not exhibit physical characteristics useful for independent age validation or are too rare to justify sacrificing a large number of individuals to establish the relationship between size and age. Length-at-age models are well represented in the fisheries and other wildlife management literature. Many of these models overlook variation in growth rates of individuals and consider growth parameters as population parameters. More recent models have taken advantage of hierarchical structuring of parameters and Bayesian inference methods to allow for variation among individuals as functions of environmental covariates or individual-specific random effects. Here, we describe hierarchical models in which growth curves vary as individual-specific stochastic processes, and we show how these models can be fit using capture–recapture data for animals of unknown age along with data for animals of known age. We combine these independent data sources in a Bayesian analysis, distinguishing natural variation (among and within individuals) from measurement error. We illustrate using data for African dwarf crocodiles, comparing von Bertalanffy and logistic growth models. The analysis provides the means of predicting crocodile age, given a single measurement of head length. The von Bertalanffy was much better supported than the logistic growth model and predicted that dwarf crocodiles grow from 19.4 cm total length at birth to 32.9 cm in the first year and 45.3 cm by the end of their second year. Based on the minimum size of females observed with hatchlings, reproductive maturity was estimated to be at nine years. These size benchmarks are believed to represent thresholds for important demographic parameters; improved estimates of age, therefore, will increase the precision of population projection models. The modeling approach that we present can be applied to other species and offers significant advantages when multiple sources of data are available and traditional aging techniques are not practical
On thinning of chains in MCMC
1. Markov chain Monte Carlo (MCMC) is a simulation technique that has revolutionised the analysis of ecological data, allowing the fitting of complex models in a Bayesian framework. Since 2001, there have been nearly 200 papers using MCMC in publications of the Ecological Society of America and the British Ecological Society, including more than 75 in the journal Ecology and 35 in the Journal of Applied Ecology.
2. We have noted that many authors routinely ‘thin’ their simulations, discarding all but every kth sampled value; of the studies we surveyed with details on MCMC implementation, 40% reported thinning.
3. Thinning is often unnecessary and always inefficient, reducing the precision with which features of the Markov chain are summarised. The inefficiency of thinning MCMC output has been known since the early 1990’s, long before MCMC appeared in ecological publications.
4. We discuss the background and prevalence of thinning, illustrate its consequences, discuss circumstances when it might be regarded as a reasonable option and recommend against routine thinning of chains unless necessitated by computer memory limitations
Population dynamics and harvest management of eastern mallards
Managing sustainable harvest of wildlife populations requires regular collection of demographic data and robust estimates of demographic parameters. Estimates can then be used to develop a harvest strategy to guide decision‐making. Mallards (Anas platyrhynchos) are an important species in the Atlantic Flyway for many users and they exhibited exponential growth in the eastern United States between the 1970s and 1990s. Since then, estimates of mallard abundance have declined 16%, prompting the Atlantic Flyway Council and United States Fish and Wildlife Service to implement more restrictive hunting regulations and develop a new harvest strategy predicated on an updated population model. Our primary objective was to develop an integrated population model (IPM) for use in an eastern mallard harvest management strategy. We developed an IPM using annual estimates of breeding abundance, 2‐season banding and recovery data, and hunterharvest data from 1998 to 2018.When developing the model, we used novel model selection methods to test various forms of a submodel for survival including estimating the degree of harvest additivity and any age‐specific trends. The top survival sub‐model included a negative annual trend on juvenile survival. The IPM posterior estimates for population abundance tracked closely with the observed estimates and estimates of mean annual population growth rate ranged from 0.88 to 1.08. Our population model provided increased precision in abundance estimates compared to survey methods for use in an updated harvest strategy. The IPM
posterior estimates of survival rates were relatively stable for adult cohorts, and annual growth rate was positively correlated with the female age ratio, a measure of reproduction. Either or both of those demographic parameters, juvenile survival or reproduction, could be a target for management efforts to address the population decline. The resulting demographic parameters provided information on the equilibrium population size and can be used in an adaptive harvest strategy for mallards in eastern North America
Population dynamics and harvest management of eastern mallards
Managing sustainable harvest of wildlife populations requires regular collection of demographic data and robust estimates of demographic parameters. Estimates can then be used to develop a harvest strategy to guide decision‐making. Mallards (Anas platyrhynchos) are an important species in the Atlantic Flyway for many users and they exhibited exponential growth in the eastern United States between the 1970s and 1990s. Since then, estimates of mallard abundance have declined 16%, prompting the Atlantic Flyway Council and United States Fish and Wildlife Service to implement more restrictive hunting regulations and develop a new harvest strategy predicated on an updated population model. Our primary objective was to develop an integrated population model (IPM) for use in an eastern mallard harvest management strategy. We developed an IPM using annual estimates of breeding abundance, 2‐season banding and recovery data, and hunterharvest data from 1998 to 2018.When developing the model, we used novel model selection methods to test various forms of a submodel for survival including estimating the degree of harvest additivity and any age‐specific trends. The top survival sub‐model included a negative annual trend on juvenile survival. The IPM posterior estimates for population abundance tracked closely with the observed estimates and estimates of mean annual population growth rate ranged from 0.88 to 1.08. Our population model provided increased precision in abundance estimates compared to survey methods for use in an updated harvest strategy. The IPM posterior estimates of survival rates were relatively stable for adult cohorts, and annual growth rate was positively correlated with the female age ratio, a measure of reproduction. Either or both of those demographic parameters, juvenile survival or reproduction, could be a target for management efforts to address the population decline. The resulting demographic parameters provided information on the equilibrium population size and can be used in an adaptive harvest strategy for mallards in eastern North America
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