Asma Azizi’s research while affiliated with Kennesaw State University and other places

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Publications (22)


Dynamics of Information Flow and Task Allocation of Social Insect Colonies: Impacts of Spatial Interactions and Task Switching
  • Article

April 2024

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57 Reads

Bulletin of Mathematical Biology

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Daniel Charbonneau

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Yun Kang

Models of social interaction dynamics have been powerful tools for understanding the efficiency of information spread and the robustness of task allocation in social insect colonies. How workers spatially distribute within the colony, or spatial heterogeneity degree (SHD), plays a vital role in contact dynamics, influencing information spread and task allocation. We used agent-based models to explore factors affecting spatial heterogeneity and information flow, including the number of task groups, variation in spatial arrangements, and levels of task switching, to study: (1) the impact of multiple task groups on SHD, contact dynamics, and information spread, and (2) the impact of task switching on SHD and contact dynamics. Both models show a strong linear relationship between the dynamics of SHD and contact dynamics, which exists for different initial conditions. The multiple-task-group model without task switching reveals the impacts of the number and spatial arrangements of task locations on information transmission. The task-switching model allows task-switching with a probability through contact between individuals. The model indicates that the task-switching mechanism enables a dynamical state of task-related spatial fidelity at the individual level. This spatial fidelity can assist the colony in redistributing their workforce, with consequent effects on the dynamics of spatial heterogeneity degree. The spatial fidelity of a task group is the proportion of workers who perform that task and have preferential walking styles toward their task location. Our analysis shows that the task switching rate between two tasks is an exponentially decreasing function of the spatial fidelity and contact rate. Higher spatial fidelity leads to more agents aggregating to task location, reducing contact between groups, thus making task switching more difficult. Our results provide important insights into the mechanisms that generate spatial heterogeneity and deepen our understanding of how spatial heterogeneity impacts task allocation, social interaction, and information spread.


Figure 1. A schematic illustrating the process of updating the characteristic parameters of an individual ant at a specific time-step. The turning angle ∆θ p t+1 is selected from a Laplace distribution with a location parameter of 0 and a scale parameter of 1 ω as described in Eq (2.1). Additionally, the speed s p t+1 is chosen from an exponential distribution with an average of λ p t according to Eq (2.3), and the speed jump Λ p is selected from a truncated exponential distribution with an average of a −1 as outlined in Eq (2.2).
Initialization, movement, and contact parameters: The baseline values provided were applied consistently across all replicates and figures, unless specified otherwise.
Mechanistic modeling of alarm signaling in seed-harvester ants
  • Article
  • Full-text available

March 2024

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18 Reads

Mathematical Biosciences & Engineering

Ant colonies demonstrate a finely tuned alarm response to potential threats, offering a uniquely manageable empirical setting for exploring adaptive information diffusion within groups. To effectively address potential dangers, a social group must swiftly communicate the threat throughout the collective while conserving energy in the event that the threat is unfounded. Through a combination of modeling, simulation, and empirical observations of alarm spread and damping patterns, we identified the behavioral rules governing this adaptive response. Experimental trials involving alarmed ant workers (Pogonomyrmex californicus) released into a tranquil group of nestmates revealed a consistent pattern of rapid alarm propagation followed by a comparatively extended decay period [1]. The experiments in [1] showed that individual ants exhibiting alarm behavior increased their movement speed, with variations in response to alarm stimuli, particularly during the peak of the reaction. We used the data in [1] to investigate whether these observed characteristics alone could account for the swift mobility increase and gradual decay of alarm excitement. Our self-propelled particle model incorporated a switch-like mechanism for ants' response to alarm signals and individual variations in the intensity of speed increased after encountering these signals. This study aligned with the established hypothesis that individual ants possess cognitive abilities to process and disseminate information, contributing to collective cognition within the colony (see [2] and the references therein). The elements examined in this research support this hypothesis by reproducing statistical features of the empirical speed distribution across various parameter values.

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Effect of Human Behavior on the Evolution of Viral Strains During an Epidemic

November 2022

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19 Reads

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6 Citations

Bulletin of Mathematical Biology

It is well known in the literature that human behavior can change as a reaction to disease observed in others, and that such behavioral changes can be an important factor in the spread of an epidemic. It has been noted that human behavioral traits in disease avoidance are under selection in the presence of infectious diseases. Here, we explore a complementary trend: the pathogen itself might experience a force of selection to become less “visible,” or less “symptomatic,” in the presence of such human behavioral trends. Using a stochastic SIR agent-based model, we investigated the co-evolution of two viral strains with cross-immunity, where the resident strain is symptomatic while the mutant strain is asymptomatic. We assumed that individuals exercised self-regulated social distancing (SD) behavior if one of their neighbors was infected with a symptomatic strain. We observed that the proportion of asymptomatic carriers increased over time with a stronger effect corresponding to higher levels of self-regulated SD. Adding mandated SD made the effect more significant, while the existence of a time-delay between the onset of infection and the change of behavior reduced the advantage of the asymptomatic strain. These results were consistent under random geometric networks, scale-free networks, and a synthetic network that represented the social behavior of the residents of New Orleans.


Figure 4. The average b AS per second estimated by RFML model (grey line) and the average velocity per second obtained by ABCTracker from experiments (black line) (1 pixel/frame = 4.1 mm s −1 ).
Figure 5. Spatial characteristics of alarm recruitment. Variation in unalarmed ants b AS during the time of approaching their alarmed neighbours. Each point indicates one unalarmed ant. The y-axis shows the variation in b AS during the time the two ants were near each other, and the x-axis shows the minimum distance between the two ants during that time. Unalarmed ants which came closer to alarmed neighbours varied more in their b AS (7.3 pixel = 1 mm). Circles represent observations; curve represents expectations in exponential decay model equation (3.1).
Figure 7. A right-skewed distribution of individual alarm responsiveness. The Lilliefors-corrected K-S test on the alarm responsiveness, indicates observed frequencies are not significantly different from expectations in a geometric distribution (D = 0.33, d.f. = 46, p = 0.12). Bars represent the proportion of observations; curve represents expectations in a geometric distribution.
Decoding alarm signal propagation of seed-harvester ants using automated movement tracking and supervised machine learning

January 2022

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146 Reads

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11 Citations

Alarm signal propagation through ant colonies provides an empirically tractable context for analysing information flow through a natural system, with useful insights for network dynamics in other social animals. Here, we develop a methodological approach to track alarm spread within a group of harvester ants, Pogonomyrmex californicus. We initially alarmed three ants and tracked subsequent signal transmission through the colony. Because there was no actual standing threat, the false alarm allowed us to assess amplification and adaptive damping of the collective alarm response. We trained a random forest regression model to quantify alarm behaviour of individual workers from multiple movement features. Our approach translates subjective categorical alarm scores into a reliable, continuous variable. We combined these assessments with automatically tracked proximity data to construct an alarm propagation network. This method enables analyses of spatio-temporal patterns in alarm signal propagation in a group of ants and provides an opportunity to integrate individual and collective alarm response. Using this system, alarm propagation can be manipulated and assessed to ask and answer a wide range of questions related to information and misinformation flow in social networks.


Effect of human behavior on the evolution of viral strains during an epidemic

September 2021

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40 Reads

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4 Citations

It is well known in the literature that human behavior can change as a reaction to disease observed in others, and that such behavioral changes can be an important factor in the spread of an epidemic. It has been noted that human behavioral traits in disease avoidance are under selection in the presence of infectious diseases. Here we explore a complimentary trend: the pathogen itself might experience a force of selection to become less "visible", or less "symptomatic", in the presence of such human behavioral trends. Using a stochastic SIR agent-based model, we investigated the co-evolution of two viral strains with cross-immunity, where the resident strain is symptomatic while the mutant strain is asymptomatic. We assumed that individuals exercised self-regulated social distancing (SD) behavior if one of their neighbors was infected with a symptomatic strain. We observed that the proportion of asymptomatic carriers increased over time with a stronger effect corresponding to higher levels of self-regulated SD. Adding mandated SD made the effect more significant, while the existence of a time-delay between the onset of infection and the change of behavior reduced the advantage of the asymptomatic strain. These results were consistent under random geometric networks, scale-free networks, and a synthetic network that represented the social behavior of the residents of New Orleans.


Social Ecological Contexts and Alcohol Drinking Dynamics: An Application of the Survey Data-Driven Agent-Based Model for University Students

August 2021

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25 Reads

Journal of the Indian Institute of Science

College-aged students are one of the most vulnerable populations to high-risk alcohol drinking behaviors that could cause them consequences such as injury or sexual assault. An important factor that may influence college students’ decision on alcohol drinking behavior is socializing in certain contexts across the university environment. In the present study, we aim to identify and better understand the ecological conditions driving the dynamics of distribution of alcohol use among college-aged students. To this end, a pilot survey study is conducted to evaluate students’ movement patterns in different contexts across the Arizona State University (ASU) campus, and the results are used to develop an agent-based simulation model designed for examining the role of environmental factors on development and maintenance of alcohol drinking behavior by a representative sample of ASU students. The proposed model, which resembles an approximate reaction–diffusion model, accounts for movement of agents (i.e., diffusion) in various contexts and alcohol drinking influences within those contexts (i.e., reaction) via a Susceptible-Infected-Recovered type individual-based model. Of the four most visited contexts at ASU Tempe campus—Library, Memorial Union, Fitness Center, and Dorm—the context with the highest visiting probability, Memorial Union, is the most influential and most sensitive context (around sixteen times higher an impact of alcohol-related influences than the other contexts) in terms of spreading alcohol drinking behavior. Our findings highlight the crucial role of socialization in local environments on the dynamics of students’ alcohol use as well as on the long-term prediction of the college drinking prevalence.


Fig. 1. (a) Different patterns of COVID19 spread during social distancing across different states in the USA. Group 0 states show a relatively sharp decline of infections. Group 1 states show an initial decline, followed by convergence to a plateau. Group 2 states show a plateau without a significant decline during social distancing. Group 3 states show a rise, followed by a plateau. Group 4 states show a rise without convergence to a plateau. See Supplementary Materials for grouping methodology. (b) Correlation between the COVID19 spread pattern during social distancing with the relative timing of the epidemic rise (see Supplement Section 3 for details). A later rise of the epidemic is associated with a relatively early implementation of social distancing, which happens before the infection has spread significantly through the population. Thus earlier initiation of distancing correlates with the occurrence of a plateau or even a "rise" (which is thought to correspond to pre-plateau dynamics). Initiation of distancing after significant virus spread tends to correlate with a "hump"-shaped epidemic: a significant infection spread followed by a decline and lack of a plateau. (c) The same trend is seen when considering deaths as an indicator of the severity of infection when distancing is initiated. Less death correlates with the appearance of a plateau or a rise. More death correlates with a sharp rise of infection followed by a decline in the absence of a plateau.
Fig. 2. Different network types considered in this paper and their properties (See Section 2.1 of the Supplement for details of construction). In (A-C), a typical degree histogram and a graphical representation of a typical network are presented. (A) A random spatial network, where nodes are connected largely to their neighbors, i.e. connections are short-range. (B) Scale-free Barabasi-Albert network, where no spatial correlations are found and there is a power law like tail in the degree distribution. (C) A hybrid network, in which a scale-free component is superimposed onto a spatial component. (D) Growth curves showing the infection spread in the three different networks. Standard errors are shown as dashed lines, which in some cases are too small to see. Parameters were chosen as follows. P inf = 0.0001 min 1 per edge; P rec = 0.0001 min 1 ; P death = 0.00005 min 1 .
Fig. 3. Social distancing dynamics in the spatial network. (A) Growth in the uncut spatial network occurs until 100 infected individuals are present, at which point half of the network connections are randomly removed. The average trajectory over 900 runs is plotted, and standard errors are indicated by dashed lines. A plateau is observed, eventually followed by a decline phase. (B) Same simulation, but cumulative infection numbers are plotted. (C) Schematic illustration of a typical (uncut) spatial network. (D) Schematic illustration of the cut network, which results in the existence of onedimensional infection corridors. (E) The cut network (red) superimposed onto the uncut network. (F) Same type of simulation as in part (A), but social distancing is initiated when different numbers of infected individuals are reached: 100 (as in part A), 200, 300, 400, 500, 500, 700. These are again averages over 900 simulations, and standard errors are indicated by dashed lines. (G) Same, but cumulative number of infections are plotted. Parameters were as follows. P inf = 0.0001 min 1 per edge; P rec = 0.0001 min 1 ; P death = 0.00005 min 1 . (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article).
Fig. 4. Infection spread dynamics when social distancing is relaxed in the spatial network model. (A) The number of infected individuals is plotted against time. Simulations start with the uncut network. When the infected population reaches size 100, ½ of randomly chosen edges are removed. At different times following the cut, the simulation reverts back to the original network. This results in a renewed wave of spread, and we let the infection spread in the simulation without further network cutting. Generally, a later return to the uncut network leads to a lower peak of the renewed growth. This reduction, however, is very minor, unless the return to the uncut network occurs when the infection levels are already in the decline phase during social distancing. The average over 900 simulations is shown. Standard errors are shown by dashed lines. (B) Same, but cumulative infections over time are shown. (C) Dynamics of the second wave after return to the uncut network, comparing different degrees of social distancing. The blue curve assumes that 50 % of the connections are cut during social distancing. The orange curve assumes that 65 % of the connections are cut during social distancing, i.e. distancing is stricter. Panels (i) -(iv) show return to the uncut network after longer durations of social distancing. Generally, stricter social distancing leads to a lower peak of the second wave of infections. For final epidemic size, see Fig. S10. Each curve represents the average over 900 simulations. Standard errors are shown by dashed lines, which in some cases are too small to see. P inf = 0.0001 min 1 per edge; P rec = 0.0001 min 1 ; P death = 0.00005 min 1 . (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article).
Network models and the interpretation of prolonged infection plateaus in the COVID19 pandemic

May 2021

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57 Reads

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15 Citations

Epidemics

Non-pharmaceutical intervention measures, such as social distancing, have so far been the only means to slow the spread of SARS-CoV-2. In the United States, strict social distancing during the first wave of virus spread has resulted in different types of infection dynamics. In some states, such as New York, extensive infection spread was followed by a pronounced decline of infection levels. In other states, such as California, less infection spread occurred before strict social distancing, and a different pattern was observed. Instead of a pronounced infection decline, a long-lasting plateau is evident, characterized by similar daily new infection levels. Here we show that network models, in which individuals and their social contacts are explicitly tracked, can reproduce the plateau if network connections are cut due to social distancing measures. The reason is that in networks characterized by a 2D spatial structure, infection tends to spread quadratically with time, but as edges are randomly removed, the infection spreads along nearly one-dimensional infection “corridors”, resulting in plateau dynamics. Further, we show that plateau dynamics are observed only if interventions start sufficiently early; late intervention leads to a “peak and decay” pattern. Interestingly, the plateau dynamics are predicted to eventually transition into an infection decline phase without any further increase in social distancing measures. Additionally, the models suggest that a second wave becomes significantly less pronounced if social distancing is only relaxed once the dynamics have transitioned to the decline phase. The network models analyzed here allow us to interpret and reconcile different infection dynamics during social distancing observed in various US states.


Suppose the persons i and j are not currently social contacts in SocNetbut have three different common social contacts k0,k1, and k2 through different activities. They might be connected in the extended social network, ESocNet, when at least one of their common social contacts meet them within the same activity location. Suppose Aik0=Ajk0=Aik1=Ajk1=A≠Aik2≠Aik2\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$A_{ik_0}=A_{jk_0}=A_{ik_1}=A_{jk_1}=A\ne A_{ik_2}\ne A_{ik_2}$$\end{document}, that is, k0 meets i and j at the same location, similarly k1 meets i and j at the same location to k0’s, however, k2 meets them in different places. To compute piA\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$p^A_i$$\end{document} and pjA\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$p^A_j$$\end{document} we only count the social contacts who meet them at the same location A, therefore, piA=(Tik0A+Tik1A)/2\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$p^A_i=(T^A_{ik_0}+T^A_{ik_1})/{2}$$\end{document}, and pjA=(Tjk0A+Tjk1A)/2\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$p^A_j=(T^A_{jk_0}+T^A_{jk_1})/{2}$$\end{document}. Finally, the probability that i and j make an edge- are connected in the extended social network- is 1-(1-piApjA)2\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$1-(1-p^A_ip^A_j)^{2}$$\end{document}
Schematic of steps 1 and 2 of Rewiring approach to correct BJD
Box plot representing the size of the giant component and bi-component for each group of networks: x-axis are the level of the subgraph of SocNet. For example the value 20%\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$20\%$$\end{document} refers to the SexNets which 20% of their edges comes from SocNet. The stars are the average values for each box and the orange line are their median values. The size of the giant component becomes bigger when the portion of the subgraph becomes stronger, however, the social network does not have much impact on the size of the giant bi-component
Box plot representing the number of connected components, Nc, for each group of networks: x-axis are the level of the subgraph of SocNet, for example the value 20%\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$20\%$$\end{document} refers to the SexNets which 20%\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$20\%$$\end{document} of their edges comes from SocNet. The stars are the average values for each box and the orange line are their median values. A significant difference is observed in Nc between each group, Nc is lower in larger subgraph of social networks
Scatter plot of Redundancy Coefficient Rc versus degree for five different networks: Rc for SexNet which is strong subgraph of BSocNet (higher percentage of subgraph p) is higher, because clustering coefficient for BSocNet is high and therefore, SexNet inherits this property by having higher Rc than the ones which are weak subgraph of BSocNet
Generating a heterosexual bipartite network embedded in social network

April 2021

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91 Reads

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2 Citations

Applied Network Science

We describe an approach to generate a heterosexual network with a prescribed joint-degree distribution embedded in a prescribed large-scale social contact network. The structure of a sexual network plays an important role in how all sexually transmitted infections (STIs) spread. Generating an ensemble of networks that mimics the real-world is crucial to evaluating robust mitigation strategies for controlling STIs. Most of the current algorithms to generate sexual networks only use sexual activity data, such as the number of partners per month, to generate the sexual network. Real-world sexual networks also depend on biased mixing based on age, location, and social and work activities. We describe an approach to use a broad range of social activity data to generate possible heterosexual networks. We start with a large-scale simulation of thousands of people in a city as they go through their daily activities, including work, school, shopping, and activities at home. We extract a social network from these activities where the nodes are the people, and the edges indicate a social interaction, such as working in the same location. This social network captures the correlations between people of different ages, living in different locations, their economic status, and other demographic factors. We use the social contact network to define a bipartite heterosexual network that is embedded within an extended social network. The resulting sexual network captures the biased mixing inherent in the social network, and models based on this pairing of networks can be used to investigate novel intervention strategies based on the social contacts among infected people. We illustrate the approach in a model for the spread of chlamydia in the heterosexual network representing the young sexually active community in New Orleans.


Using an agent-based sexual-network model to analyze the impact of mitigation efforts for controlling chlamydia

March 2021

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54 Reads

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9 Citations

Epidemics

Chlamydia trachomatis (Ct) is the most reported sexually transmitted infection in the United States, with a major cause of infertility, pelvic inflammatory disease, and ectopic pregnancy among women. Despite decades of screening women for Ct, rates increase among young African Americans (AA). We create and analyze a heterosexual agent-based network model to help understand the spread of Ct. We calibrate the model parameters to agree with survey data showing Ct prevalence of 12% of the women and 10% of the men in the 15−25 year-old AA in New Orleans, Louisiana. Our model accounts for both long-term and casual partnerships. The network captures the assortative mixing of individuals by preserving the joint-degree distributions observed in the data. We compare the effectiveness of intervention strategies based on randomly screening men, notifying partners of infected people, which includes partner treatment, partner screening, and rescreening for infection. We compare the difference between treating partners of an infected person both with and without testing them. We observe that although increased Ct screening, rescreening, and treating most of the partners of infected people will reduce the prevalence, these mitigations alone are not sufficient to control the epidemic. The current practice is to treat the partners of an infected individual without first testing them for infection. The model predicts that if a sufficient number of the partners of all infected people are tested and treated, then there is a threshold condition where the epidemic can be mitigated. This threshold results from the expanded treatment network created by treating an individual’s infected partners’ partners. Although these conclusions can help design future Ct mitigation studies, we caution the reader that these conclusions are for the mathematical model, not the real world, and are contingent on the validity of the model assumptions.


Citations (13)


... Based on the geospatial database, we established an ecological resiliency index system with reference to relevant literature (Kazanci et al., 2023), including LUCC, DEM, NDVI, RB and LPI factors indexes and sub-indexes . LPI factors can quantify the current state of the landscape pattern and make the evaluation of ecological restoration in the study area more scientific . ...

Reference:

The seeds of ecological recovery in urbanization – Spatiotemporal evolution of ecological resiliency of Dianchi Lake Basin, China
Resilience, indirect effects and cycling in ecological networks
  • Citing Article
  • July 2023

Ecological Modelling

... Epidemics and pandemics have always been a major threat to humanity throughout history and have seriously endangered public health, social and economic development, such as the COVID-19 pandemic that emerged in late 2019 and spread rapidly around the world, causing more than 6.9 million deaths and disruption to normal functioning of society. The outbreaks and recurrences of infectious diseases have reminded the world of the importance of uncovering the underlying mechanisms that influence disease transmission and have sparked a sustained interest in the dynamic modelling (Azizi, Kazanci, Komarova, & Wodarz, 2022;Hethcote, 2000;Panicker & Sasidevan, 2024). Mathematical modelling of viral epidemics, basically including deterministic modelling and stochastic modelling, allows for an understanding of the transmission dynamics in order to assist in controlling and preventing the spread of diseases (Laarabi, Rachik, Kahlaoui, & Labriji, 2013;Wang & Zhang, 2024;Yerlanov, Agarwal, Colijn, & Stockdale, 2023). ...

Effect of Human Behavior on the Evolution of Viral Strains During an Epidemic

Bulletin of Mathematical Biology

... For instance, ants have been shown to exhibit lower levels of aggression when alone versus in a group owing to the need for colony defence [62] or the presence of social cues [60,63]. In a colony setting, the social environment can amplify individual defence based on the social information individuals perceive (e.g. via alarm pheromones [64,65] or non-nestmate cues [66]). Additionally, past work on social insects involved colonies containing individuals of varying ages, genetic backgrounds and/or morphology. ...

Decoding alarm signal propagation of seed-harvester ants using automated movement tracking and supervised machine learning

... The evolution of resistance of SARS-COV2 against vaccination or existing treatments as well as enhanced transmissibility or lethality is a major concern, which has given rise to an impressive number of studies [12][13][14][15][16][17][18][19][20][21][22][23][24][25][26][27] that have been founded on a long history of modelling the emergence of resistance against treatment in other viruses 28-36 and epidemiological models for disease spread 18,19,37,38 . ...

Effect of human behavior on the evolution of viral strains during an epidemic

... Interventions such as mask-wearing and social distancing played a critical role in significantly reducing the transmission of respiratory viruses (10,13,14). Although the presence of a dominant virus like SARS-CoV-2 may have influenced the spread of other viruses through competition for ecological niches, these patterns were likely driven by changes in human behavior, such as improved personal hygiene and altered healthcare-seeking practices (12, [15][16][17][18]. ...

Network models and the interpretation of prolonged infection plateaus in the COVID19 pandemic

Epidemics

... Similar to the approach in Azizi et al. 9 , we constructed a closed 5000-member synthetic population, where the heterosexual partnerships were represented by bipartite sexual networks. The heterosexual networks reflected the assortative mixing pattern among our targeted population by matching the population-level quantities from two surveys in New Orleans: the ongoing Check It study 7 and the "You Geaux Girl!" (YGG) study 8 , which enrolled 1318 AA men (as of April 2019, age-range 15-24) and 649 AA women (age range [18][19], respectively. ...

Generating a heterosexual bipartite network embedded in social network

Applied Network Science

... Inhibitory or exploitative competition typically drive these outcomes, and the parallels, in terms of population dynamics we observed, raise the intriguing possibility that mutualists and parasites exhibit similar patterns of host occupancy. Agent based models have also been used to examine several parasite-caused diseases (e.g., malaria (Amadi et al., 2021;reviewed in Smith et al., 2018); leishmaniasis (Tabasi et al., 2011); chlamydia (Azizi et al., 2021)). The approach we offer represents a novel application of ABMs to intracellular symbioses that involve reciprocal mutual benefits between interacting partners. ...

Using an agent-based sexual-network model to analyze the impact of mitigation efforts for controlling chlamydia

Epidemics

... Screening programmes should also consider targeting. Previous research has shown that screening men for sexually transmitted infections can be a cost-effective strategy for reducing PID in women [23]. Further efforts should be made to screen for chlamydia in men and encourage partner notification, which can prevent adverse health outcomes in women. ...

Effect of screening young men for Chlamydia trachomatis on the rates among women: a network modelling study for high-prevalence communities

... In particular, Pastor et al. revealed the fact that epidemic threshold of an SIS model tends to be 0 in scale-free (SF) networks, which is quite different from the traditional epidemic threshold theory and leading to a large volume of relevant studies [11,12]. Zhang et al. confirmed the existence of a unique global periodic solution if the basic reproduction number is greater than one while a scale-free SIS epidemic model is employed [13]. Bacear et al. developed a mathematical model that considers seasonality of the vector-borne population to estimate the basic reproduction number [14]. ...

Dynamics of an SIS model on network with a periodic infection rate
  • Citing Article
  • August 2020

Applied Mathematical Modelling

... The potential flow of spreading elements, such as viruses, in the communication networks of social insects, has some general similarities with that in human populations. Although they have different spreading dynamics, some features that are typical of human systems (e.g., bursty interaction patterns with heavy-tailed delay distributions in models) were observed in the ants Temnothorax rugatulusants and the honeybee Apis mellifera (Blonder and Dornhaus 2011;Gernat et al. 2018;Guo et al. 2020). ...

Dynamics of Social Interactions, in the Flow of Information and Disease Spreading in Social Insects Colonies: Effects of Environmental Events and Spatial Heterogeneity

Journal of Theoretical Biology