scholarly journals Planktic foraminiferal diversity: logistic growth overprinted by a varying environment

2016 ◽  
Vol 21 (3) ◽  
pp. 501
Author(s):  
Andrés L. Cárdenas-Rozo ◽  
Peter J. Harries

Este estudio evalúa estadísticamente la relación entre el patrón de diversidad global de los foraminíferos planctónicos en el largo plazo (~170 Ma al Reciente) y los cuatro modelos de diversificación propuestos desde la rama de la paleobiología: (i) “Reina Roja” (Van Valen, 1973; Raup et al., 1973), (ii) remplazo pausado (Vrba, 1985; Brett y Baird, 1995), (iii) diversidad en equilibrio (Sepkoski, 1978; Rosenzweig, 1995), y (iv) el “crecimiento logístico complicado” (Alroy, 2010a). Nuestros resultados sugieren que la forma de este patrón global de diversidad y la inter-relación entre las tasas de extinción y originación de este grupo no corresponden con los primeros tres modelos anteriormente citados. Sin embargo, estos pueden ser explicados bajo el cuarto escenario. Consecuentemente, las dinámicas de diversidad (i.e. patrón de diversidad y tasas de extinción y originación) de este grupo posiblemente son controladas por la combinación de la competencia interespecífica de los foraminíferos planctónicos y varios cambios ambientales tales como temperaturas globales marinas que pudieron impactar el número de nichos dentro de la capa superior de los océanos.  Además, otros patrones globales de diversidad en el largo plazo han sido interpretados como el reflejo del modelo de crecimiento logístico complicado, lo que sugiere que la relación entre factores abióticos y bióticos tiene un carácter fundamental en los procesos evolutivos que han sucedido a lo largo de la historia de la vida.

2016 ◽  
Vol 21 (3) ◽  
Author(s):  
Andrés L. Cárdenas Rozo ◽  
Peter J. Harries

Cárdenas Rozo AL, Harries PJ. Planktic foraminiferal diversity: logistic growth overprinted by a varying environment. Acta biol. Colomb. 2016;21(3):501-508. The statistical analyses, were done using R (The R Project for Statistical Computing, www.r-project.org). This appendix includes: Supplementary data Supplementary methods Tables 1 to 11 Figures 1 to 4 Supplementary references


Genetics ◽  
1997 ◽  
Vol 146 (2) ◽  
pp. 723-733 ◽  
Author(s):  
Sarah P Otto ◽  
Michael C Whitlock

The rate of adaptive evolution of a population ultimately depends on the rate of incorporation of beneficial mutations. Even beneficial mutations may, however, be lost from a population since mutant individuals may, by chance, fail to reproduce. In this paper, we calculate the probability of fixation of beneficial mutations that occur in populations of changing size. We examine a number of demographic models, including a population whose size changes once, a population experiencing exponential growth or decline, one that is experiencing logistic growth or decline, and a population that fluctuates in size. The results are based on a branching process model but are shown to be approximate solutions to the diffusion equation describing changes in the probability of fixation over time. Using the diffusion equation, the probability of fixation of deleterious alleles can also be determined for populations that are changing in size. The results developed in this paper can be used to estimate the fixation flux, defined as the rate at which beneficial alleles fix within a population. The fixation flux measures the rate of adaptive evolution of a population and, as we shall see, depends strongly on changes that occur in population size.


2021 ◽  
Vol 29 (1) ◽  
Author(s):  
Kamrun Nahar Keya ◽  
Md. Kamrujjaman ◽  
Md. Shafiqul Islam

AbstractIn this paper, we consider a reaction–diffusion model in population dynamics and study the impact of different types of Allee effects with logistic growth in the heterogeneous closed region. For strong Allee effects, usually, species unconditionally die out and an extinction-survival situation occurs when the effect is weak according to the resource and sparse functions. In particular, we study the impact of the multiplicative Allee effect in classical diffusion when the sparsity is either positive or negative. Negative sparsity implies a weak Allee effect, and the population survives in some domain and diverges otherwise. Positive sparsity gives a strong Allee effect, and the population extinct without any condition. The influence of Allee effects on the existence and persistence of positive steady states as well as global bifurcation diagrams is presented. The method of sub-super solutions is used for analyzing equations. The stability conditions and the region of positive solutions (multiple solutions may exist) are presented. When the diffusion is absent, we consider the model with and without harvesting, which are initial value problems (IVPs) and study the local stability analysis and present bifurcation analysis. We present a number of numerical examples to verify analytical results.


2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Dipankar Ghosh ◽  
Prasun K. Santra ◽  
Abdelalim A. Elsadany ◽  
Ghanshaym S. Mahapatra

Abstract This paper focusses on developing two species, where only prey species suffers by a contagious disease. We consider the logistic growth rate of the prey population. The interaction between susceptible prey and infected prey with predator is presumed to be ruled by Holling type II and I functional response, respectively. A healthy prey is infected when it comes in direct contact with infected prey, and we also assume that predator-dependent disease spreads within the system. This research reveals that the transmission of this predator-dependent disease can have critical repercussions for the shaping of prey–predator interactions. The solution of the model is examined in relation to survival, uniqueness and boundedness. The positivity, feasibility and the stability conditions of the fixed points of the system are analysed by applying the linearization method and the Jacobian matrix method.


2013 ◽  
Vol 2013 ◽  
pp. 1-11 ◽  
Author(s):  
Yakui Xue ◽  
Tiantian Li

We study a delayed SIR epidemic model and get the threshold value which determines the global dynamics and outcome of the disease. First of all, for anyτ, we show that the disease-free equilibrium is globally asymptotically stable; whenR0<1, the disease will die out. Directly afterwards, we prove that the endemic equilibrium is locally asymptotically stable for anyτ=0; whenR0>1, the disease will persist. However, for anyτ≠0, the existence conditions for Hopf bifurcations at the endemic equilibrium are obtained. Besides, we compare the delayed SIR epidemic model with nonlinear incidence rate to the one with bilinear incidence rate. At last, numerical simulations are performed to illustrate and verify the conclusions.


2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Gerardo Chowell ◽  
Ruiyan Luo

AbstractBackgroundEnsemble modeling aims to boost the forecasting performance by systematically integrating the predictive accuracy across individual models. Here we introduce a simple-yet-powerful ensemble methodology for forecasting the trajectory of dynamic growth processes that are defined by a system of non-linear differential equations with applications to infectious disease spread.MethodsWe propose and assess the performance of two ensemble modeling schemes with different parametric bootstrapping procedures for trajectory forecasting and uncertainty quantification. Specifically, we conduct sequential probabilistic forecasts to evaluate their forecasting performance using simple dynamical growth models with good track records including the Richards model, the generalized-logistic growth model, and the Gompertz model. We first test and verify the functionality of the method using simulated data from phenomenological models and a mechanistic transmission model. Next, the performance of the method is demonstrated using a diversity of epidemic datasets including scenario outbreak data of theEbola Forecasting Challengeand real-world epidemic data outbreaks of including influenza, plague, Zika, and COVID-19.ResultsWe found that the ensemble method that randomly selects a model from the set of individual models for each time point of the trajectory of the epidemic frequently outcompeted the individual models as well as an alternative ensemble method based on the weighted combination of the individual models and yields broader and more realistic uncertainty bounds for the trajectory envelope, achieving not only better coverage rate of the 95% prediction interval but also improved mean interval scores across a diversity of epidemic datasets.ConclusionOur new methodology for ensemble forecasting outcompete component models and an alternative ensemble model that differ in how the variance is evaluated for the generation of the prediction intervals of the forecasts.


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