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A quantitative narrative on movement, disease and patch exploitation in nesting agent groups
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Matrix Population Models
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Global properties of a class of HIV infection models with Beddington–DeAngelis functional response
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On the Dynamics of Predator–Prey Models with the Beddington–DeAngelis Functional Response
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A Formal Derivation of the “Beddington” Functional Response
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The Ecology of Pathogen Spillover and Disease Emergence at the Human-Wildlife-Environment Interface
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A review of techniques for parameter sensitivity analysis of environmental models
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Bimodal Epidemic Size Distributions for Near-Critical SIR with Vaccination
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The shape of the size distribution of an epidemic in a finite population
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Mesocosm Experiments as a Tool for Ecological Climate-Change Research
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Global properties for virus dynamics model with Beddington–DeAngelis functional response
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Global analysis for delay virus dynamics model with Beddington–DeAngelis functional response
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Appropriate complexity landscape modeling
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A standard protocol for describing individual-based and agent-based models
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The ODD protocol: A review and first update
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The role of agent-based models in wildlife ecology and management
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From the Lotka–Volterra model to a spatialised population-driven individual-based model
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Sensitivity analysis: A review of recent advances
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Describing human decisions in agent-based models – ODD + D, an extension of the ODD protocol
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Sensitivity analysis of environmental models: A systematic review with practical workflow
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Dynamics of a nonautonomous predator–prey system with the Beddington–DeAngelis functional response
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Dynamics of the density dependent predator–prey system with Beddington–DeAngelis functional response
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Spatiotemporal dynamics of epidemics: synchrony in metapopulation models
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The SIRC model and influenza A
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Qualitative analysis of predator-prey models with Beddington-DeAngelis functional response and diffusion
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Size matters: What have we learnt from microcosm studies of decomposer fungus–invertebrate interactions?
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Spatial epidemiology: an emerging (or re-emerging) discipline
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Should we expect population thresholds for wildlife disease?
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Infecting epidemiology with genetics: a new frontier in disease ecology
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Stochastic models of population extinction
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Global analysis of the predator–prey system with Beddington–DeAngelis functional response
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Epidemiology meets evolutionary ecology
inferredcites →https://doi.org/10.1017/s0950268813000708openalex-snapshot
A review of bovine tuberculosis at the wildlife–livestock–human interface in sub-Saharan Africa
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Travelling waves and spatial hierarchies in measles epidemics
inferredcites →https://doi.org/10.1038/nature04153openalex-snapshot
Superspreading and the effect of individual variation on disease emergence
inferredcites →https://doi.org/10.1038/nature06199openalex-snapshot
Revisiting Lévy flight search patterns of wandering albatrosses, bumblebees and deer
inferredcites →https://doi.org/10.1038/nrmicro1845openalex-snapshot
Mathematical models of infectious disease transmission
inferredcites →https://doi.org/10.1073/pnas.0407293101openalex-snapshot
Dynamical resonance can account for seasonality of influenza epidemics
inferredcites →https://doi.org/10.1073/pnas.1613616114openalex-snapshot
Unraveling the disease consequences and mechanisms of modular structure in animal social networks
inferredcites →https://doi.org/10.1073/pnas.1801383115openalex-snapshot
Disease outbreak thresholds emerge from interactions between movement behavior, landscape structure, and epidemiology
inferredcites →https://doi.org/10.1073/pnas.69.5.1109openalex-snapshot
Niche Overlap as a Function of Environmental Variability
inferredcites →https://doi.org/10.1073/pnas.71.5.2141openalex-snapshot
Niche Overlap and Diffuse Competition
inferredcites →https://doi.org/10.1080/15659801.2013.797676openalex-snapshot
Computational population biology: linking the inner and outer worlds of organisms
inferredcites →https://doi.org/10.1080/17513758.2017.1401677openalex-snapshot
Discrete stochastic analogs of Erlang epidemic models
inferredcites →https://doi.org/10.1080/23737867.2016.1217756openalex-snapshot
Bottom-up ecology: an agent-based model on the interactions between competition and predation
inferredcites →https://doi.org/10.1086/282676openalex-snapshot
Community Equilibria and Stability, and an Extension of the Competitive Exclusion Principle
inferredcites →https://doi.org/10.1086/284112openalex-snapshot
Epidemic Models: Thresholds and Population Regulation
inferredcites →https://doi.org/10.1090/dimacs/071/05openalex-snapshot
Basic methods for modeling the invasion and spread of contagious diseases
inferredcites →https://doi.org/10.1093/oso/9780198545996.001.0001openalex-snapshot
Infectious Diseases of Humans
inferredcites →https://doi.org/10.1097/01.ede.0000181633.80269.4copenalex-snapshot
Dynamically Modeling SARS and Other Newly Emerging Respiratory Illnesses
inferredcites →https://doi.org/10.1098/rspb.2003.2481openalex-snapshot
Curtailing transmission of severe acute respiratory syndrome within a community and its hospital
inferredcites →https://doi.org/10.1098/rstb.2018.0282openalex-snapshot
Adequacy of SEIR models when epidemics have spatial structure: Ebola in Sierra Leone
inferredcites →https://doi.org/10.1111/0272-4332.00039openalex-snapshot
Identification and Review of Sensitivity Analysis Methods
inferredcites →https://doi.org/10.1111/brv.12420openalex-snapshot
Spores and soil from six sides: interdisciplinarity and the environmental biology of anthrax ( Bacillus anthracis )
inferredcites →https://doi.org/10.1111/ele.12917openalex-snapshot
Going through the motions: incorporating movement analyses into disease research
inferredcites →https://doi.org/10.1111/j.1461-0248.2006.00885.xopenalex-snapshot
Effects of species diversity on disease risk
inferredcites →https://doi.org/10.1111/j.1461-0248.2010.01566.xopenalex-snapshot
Biomass transformation webs provide a unified approach to consumer–resource modelling
inferredcites →https://doi.org/10.1111/nrm.12120openalex-snapshot
A web app for population viability and harvesting analyses
inferredcites →https://doi.org/10.1126/science.1177345openalex-snapshot
Epidemic Dynamics at the Human-Animal Interface
inferredcites →https://doi.org/10.1126/science.1194694openalex-snapshot
Animal Migration and Infectious Disease Risk
inferredcites →https://doi.org/10.1126/science.1239401openalex-snapshot
Climate Change and Infectious Diseases: From Evidence to a Predictive Framework
inferredcites →https://doi.org/10.1126/science.1259504openalex-snapshot
Why infectious disease research needs community ecology
inferredcites →https://doi.org/10.1126/science.292.5521.1528openalex-snapshot
Age, Sex, Density, Winter Weather, and Population Crashes in Soay Sheep
inferredcites →https://doi.org/10.1128/jvi.01680-06openalex-snapshot
Influenza Seasonality: Underlying Causes and Modeling Theories
inferredcites →https://doi.org/10.1137/s0036144500371907openalex-snapshot
The Mathematics of Infectious Diseases
inferredcites →https://doi.org/10.1146/annurev.es.09.110178.001201openalex-snapshot
Lotka-Volterra Population Models
inferredcites →https://doi.org/10.1155/2015/736507openalex-snapshot
Tactics and Strategies for Managing Ebola Outbreaks and the Salience of Immunization
inferredcites →https://doi.org/10.1186/s12862-016-0617-0openalex-snapshot
Sympatric speciation in structureless environments
inferredcites →https://doi.org/10.1186/s40462-014-0020-7openalex-snapshot
Consequences of animal interactions on their dynamics: emergence of home ranges and territoriality
inferredcites →https://doi.org/10.1214/11-ps191openalex-snapshot
Quasi-stationary distributions and population processes
inferredcites →https://doi.org/10.1371/currents.outbreaks.4d41fe5d6c05e9df30ddce33c66d084copenalex-snapshot
Modeling the Impact of Interventions on an Epidemic of Ebola in Sierra Leone and Liberia
inferredcites →https://doi.org/10.1371/currents.outbreaks.91afb5e0f279e7f29e7056095255b288openalex-snapshot
Estimating the Reproduction Number of Ebola Virus (EBOV) During the 2014 Outbreak in West Africa
inferredcites →https://doi.org/10.1371/journal.pntd.0001865openalex-snapshot
Global Burden of Human Brucellosis: A Systematic Review of Disease Frequency
inferredcites →https://doi.org/10.1371/journal.pone.0014539openalex-snapshot
Consumer-Resource Dynamics: Quantity, Quality, and Allocation
inferredcites →https://doi.org/10.1371/journal.pone.0021128openalex-snapshot
Travelling Waves of a Delayed SIR Epidemic Model with Nonlinear Incidence Rate and Spatial Diffusion
inferredcites →https://doi.org/10.1371/journal.pone.0133732openalex-snapshot
Panmictic and Clonal Evolution on a Single Patchy Resource Produces Polymorphic Foraging Guilds
inferredcites →https://doi.org/10.1890/070086openalex-snapshot
Causal inference in disease ecology: investigating ecological drivers of disease emergence
inferredcites →https://doi.org/10.1890/1540-9295(2005)003[0029:etteid]2.0.co;2openalex-snapshot
Ecological theory to enhance infectious disease control and public health policy
inferredcites →https://doi.org/10.20506/rst.21.3.1356openalex-snapshot
The economics of foot and mouth disease
inferredcites →https://doi.org/10.2307/1938141openalex-snapshot
The Niche Concept Revisited: Mechanistic Models and Community Context
inferredcites →https://doi.org/10.2307/3866openalex-snapshot
Mutual Interference Between Parasites or Predators and its Effect on Searching Efficiency
inferredcites →https://doi.org/10.2307/j.ctvcm4gk0openalex-snapshot
Modeling Infectious Diseases in Humans and Animals
inferredcites →https://doi.org/10.3109/00365548.2012.693197openalex-snapshot
A review on human toxoplasmosis
inferredcites →https://doi.org/10.3390/ijerph16060954openalex-snapshot
Modeling R0 for Pathogens with Environmental Transmission: Animal Movements, Pathogen Populations, and Local Infectious Zones
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1101/819763openalex-snapshot
A hierarchical framework for segmenting movement paths
inferred← citeshttps://doi.org/10.20944/preprints202312.1000.v1openalex-snapshot
Assessing Eelgrass Wasting Disease Dynamics in California Estuaries in the Context of Climate Change
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