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Presents an overview of the complex biological systems used within a global public health setting and features a focus on malaria analysis Bridging the gap between agent-based modeling and simulation (ABMS) and geographic information systems (GIS), Spatial Agent-Based Simulation Modeling in Public Health: Design, Implementation, and Applications for Malaria Epidemiology provides a useful introduction to the development of agent-based models (ABMs) by following a conceptual and biological core model of Anopheles gambiae for malaria epidemiology. Using spatial ABMs, the book includes mosquito (vector) control interventions and GIS as two example applications of ABMs, as well as a brief description of epidemiology modeling. In addition, the authors discuss how to most effectively integrate spatial ABMs with a GIS. The book concludes with a combination of knowledge from entomological, epidemiological, simulation-based, and geo-spatial domains in order to identify and analyze relationships between various transmission variables of the disease. Spatial Agent-Based Simulation Modeling in Public Health: Design, Implementation, and Applications for Malaria Epidemiology also features: * Location-specific mosquito abundance maps that play an important role in malaria control activities by guiding future resource allocation for malaria control and identifying hotspots for further investigation * Discussions on the best modeling practices in an effort to achieve improved efficacy, cost-effectiveness, ecological soundness, and sustainability of vector control for malaria * An overview of the various ABMs, GIS, and spatial statistical methods used in entomological and epidemiological studies, as well as the model malaria study * A companion website with computer source code and flowcharts of the spatial ABM and a landscape generator tool that can simulate landscapes with varying spatial heterogeneity of different types of resources including aquatic habitats and houses Spatial Agent-Based Simulation Modeling in Public Health: Design, Implementation, and Applications for Malaria Epidemiology is an excellent reference for professionals such as modeling and simulation experts, GIS experts, spatial analysts, mathematicians, statisticians, epidemiologists, health policy makers, as well as researchers and scientists who use, manage, or analyze infectious disease data and/or infectious disease-related projects. The book is also ideal for graduate-level courses in modeling and simulation, bioinformatics, biostatistics, public health and policy, and epidemiology.
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Veröffentlichungsjahr: 2016
COVER
WILEY SERIES IN MODELING AND SIMULATION
Title Page
COPYRIGHT
DEDICATION
LIST OF CONTRIBUTORS
LIST OF FIGURES
LIST OF TABLES
PREFACE
OUTLINE OF CHAPTERS
INTENDED AUDIENCE
ACKNOWLEDGMENTS
LIST OF ABBREVIATIONS
CHAPTER 1: INTRODUCTION
1.1 OVERVIEW
1.2 MALARIA
1.3 AGENT-BASED MODELING OF MALARIA
1.4 CONTRIBUTIONS
1.5 ORGANIZATION
CHAPTER 2: MALARIA: A BRIEF HISTORY
2.1 OVERVIEW
2.2 MALARIA IN HUMAN HISTORY
2.3 MALARIA EPIDEMIOLOGY: A GLOBAL VIEW
2.4 MALARIA CONTROL
CHAPTER 3: AGENT-BASED MODELING AND MALARIA
3.1 OVERVIEW
3.2 AGENT-BASED MODELS (ABMs)
3.3 HISTORY AND APPLICATIONS
3.4 ADVANTAGES OF ABMs
3.5 MALARIA MODELS: A REVIEW
3.6 SUMMARY
CHAPTER 4: THE BIOLOGICAL CORE MODEL
4.1 OVERVIEW
4.2 THE AQUATIC PHASE
4.3 THE ADULT PHASE
4.4 AQUATIC HABITATS AND OVIPOSITION
4.5 SENESCENCE AND MORTALITY RATES
4.6 MORTALITY IN THE CORE MODEL
4.7 DISCUSSION
4.8 SUMMARY
CHAPTER 5: THE AGENT-BASED MODEL (ABM)
5.1 OVERVIEW
5.2 MODEL ARCHITECTURE
5.3 MOSQUITO POPULATION DYNAMICS
5.4 MODEL FEATURES
5.5 SUMMARY
CHAPTER 6: THE SPATIAL ABM
6.1 OVERVIEW
6.2 THE SPATIAL ABM
6.3 RESOURCE CLUSTERING
6.4 FLIGHT HEURISTICS FOR MOSQUITO AGENTS
6.5 SIMULATION RESULTS
6.6 SPATIAL HETEROGENEITY
6.7 SUMMARY
CHAPTER 7: VERIFICATION, VALIDATION, REPLICATION, AND REPRODUCIBILITY
7.1 OVERVIEW
7.2 VERIFICATION AND VALIDATION (V&V): A REVIEW
7.3 REPLICATION AND REPRODUCIBILITY (R&R): A REVIEW
7.4 SUMMARY
CHAPTER 8: VERIFICATION AND VALIDATION (V&V) OF ABMs
8.1 OVERVIEW
8.2 VERIFICATION AND VALIDATION (V&V) OF ABMs
8.3 PHASE-WISE DOCKING
8.4 COMPARTMENTAL DOCKING
8.5 SUMMARY
CHAPTER 9: REPLICATION AND REPRODUCIBILITY (R&R) OF ABMs
9.1 OVERVIEW
9.2 VECTOR CONTROL INTERVENTIONS
9.3 SIMULATION RESULTS
9.4 REPLICATION AND REPRODUCIBILITY (R&R) GUIDELINES
9.5 DISCUSSION
9.6 SUMMARY
CHAPTER 10: A LANDSCAPE EPIDEMIOLOGY MODELING FRAMEWORK
10.1 OVERVIEW
10.2 GIS IN PUBLIC HEALTH
10.3 THE STUDY AREA AND THE ABM
10.4 THE GEOGRAPHIC INFORMATION SYSTEM (GIS)
10.5 SIMULATIONS AND SPATIAL ANALYSES
10.6 RESULTS
10.7 DISCUSSION
10.8 CONCLUSIONS
CHAPTER 11: THE EMOD INDIVIDUAL-BASED MODEL
11.1 OVERVIEW
11.2 MODEL STRUCTURE
11.3 RESULTS
11.4 DISCUSSION
APPENDIX A: ENZYME KINETICS MODEL FOR VECTOR GROWTH AND DEVELOPMENT
A.1 OVERVIEW
A.2 STOCHASTIC THERMODYNAMIC MODELS
A.3 POIKILOTHERMIC DEVELOPMENT MODELS
A.4 THE SHARPE AND DEMICHELE MODEL
A.5 THE SCHOOLFIELD
ET AL.
MODEL
A.6 DEPINAY
ET AL.
MODEL
A.7 SUMMARY
APPENDIX B: FLOWCHART FOR THE ABM
B.1 FLOWCHART FOR THE AGENT-BASED MODEL (ABM)
APPENDIX C: ADDITIONAL FILES FOR CHAPTER 10
APPENDIX D: A POSTSIMULATION ANALYSIS MODULE FOR AGENT-BASED MODELS
D.1 OVERVIEW
D.2 SIMULATION OUTPUT ANALYSIS: A REVIEW
D.3 THE LINK MODEL
D.4 P-SAM ARCHITECTURE
D.5 POSTSIMULATION ANALYSIS AND VISUALIZATION
D.6 P-SAM PERFORMANCE
D.7 CONCLUSION
REFERENCES
INDEX
END USER LICENSE AGREEMENT
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Cover
Table of Contents
Preface
Begin Reading
CHAPTER 1: INTRODUCTION
Figure 1.1 Book components. Logical connections between the major components and the chapters are indicated. This book primarily concerns modeling & simulation (M&S), specifically agent-based modeling (ABM), in public health (malaria epidemiology). Chapters 2 and 3 present some general background of malaria and agent-based models (ABMs) and discuss the applicability of ABMs in malaria epidemiology research, which, in turn, broadly falls under the realm of computational biology. Chapters 4–6 describe the biological core model, the agent-based models (ABMs), and the spatial ABMs, and form the core of the book. Chapters 7–9 discuss the verification, validation, and replication issues of the ABMs. Chapter 10 presents a landscape epidemiology modeling framework, and Chapter 11 presents the
EMOD
individual-based model. Note that some chapters may overlap into multiple components. All components of the book share the global/public health implications.
CHAPTER 2: MALARIA: A BRIEF HISTORY
Figure 2.1 Life cycle of the malaria parasite.
CHAPTER 4: THE BIOLOGICAL CORE MODEL
Figure 4.1 Life cycle of mosquitoes in the models. The
An. gambiae
mosquito life cycle consists of
aquatic
and
adult
phases. The
aquatic
phase consists of three aquatic stages:
Egg (E)
,
Larva (L)
, and
Pupa (P)
. The
adult
phase consists of five adult stages:
Immature Adult (IA)
,
Mate Seeking (MS)
,
Blood Meal Seeking (BMS)
,
Blood Meal Digesting (BMD)
, and
Gravid (G)
. Each oval represents a stage in the model. Permissible time transition windows (from one stage to another) are shown next to the corresponding stage transition arrows as rounded rectangles. Note that adult males, once reaching the
Mate Seeking
stage, remain forever in that stage until they die; adult females cycle through obtaining blood meals (in
Blood Meal Seeking
stage), developing eggs (in
Blood Meal Digesting
stage), and ovipositing the eggs (in
Gravid
stage) until they die.
Figure 4.2 The egg hatching time distribution used in the core model. The
An. gambiae
egg hatching time distribution is strongly skewed to the right, with 89% of the eggs hatching during the second and third day after oviposition, 10% hatching during the next 4 days, and the remaining 1% hatching over the subsequent week [575]. The x-axis denotes hatching time (days), and the y-axis denotes the probability of hatching.
CHAPTER 5: THE AGENT-BASED MODEL (ABM)
Figure 5.1 A simplified class diagram of the model architecture in the ABM. Attributes and methods are omitted for simplicity.
Figure 5.2 A simplified class diagram for the agents in the ABM. Each
MosquitoAgent
class instance is inherited as a subclass of an
Agent
superclass instance. The
get
and
set
methods are used to access and modify the corresponding attributes, respectively. Attributes and methods that are added for the spatial extension are marked in gray.
Figure 5.3 A simplified class diagram for the environments in the ABM. A generic
Environment
class can be inherited as a
MosquitoEnvironment
class, which can be further specialized as either an
AquaticEnvironment
or a
HumanEnvironment
class. The
get
and
set
methods are used to access and modify the corresponding attributes, respectively. Attributes and methods that are added for the spatial extension are marked in gray.
Figure 5.4 A simplified class diagram for the agentlists in the ABM. Agentlists bind different sets of mosquito agents to their corresponding environments depending on their life-cycle phases. A generic
AgentList
class instance can be inherited as either an
AquaticAgentList
or an
AdultAgentList
class instance. An
AquaticAgentList
instance contains aquatic mosquito agents for a specific
AquaticEnvironment
instance and an
AdultAgentList
instance contains adult mosquito agents for a specific
MosquitoEnvironment
instance. The
get
and
set
methods are used to access and modify the corresponding attributes, respectively.
Figure 5.5 An event-action-list (EAL) diagram for the ABM. Each
squashed rectangle
represents an event-action pair, in which the
event
is denoted at the upper half, and the
action
is denoted at the lower half. Each
rectangle
represents the
list(s)
(data structures) of agents affected by the event-action pair.
Figure 5.6 The ordering of the key processing steps performed in a single time step of a simulation run. The
dependency relationships
between the processing steps are crucial to ensure the correctness of the model's output.
Figure 5.7 Dependency relationships in processing steps ordering can be viewed as a
directed acyclic graph (DAG)
. (a) The interdependent steps performed in a single time step of a simulation run are connected by directed dashed lines. (b) and (c) Two possible ordering that preserve the dependency relationships of all the major processing steps. By
topological sort
, (c) can be arranged so that all directed edges go from left to right, as in (b).
CHAPTER 6: THE SPATIAL ABM
Figure 6.1 Examples of three types of landscapes: (a) regular, (b) random, and (c) hybrid. Gray and white rectangles represent spatial resources and empty cells in the mosquito environment, respectively.
Figure 6.2 Screenshot of an early version of the landscape generator tool,
AnophGUI
.
Figure 6.3 Screenshot of the latest version of the landscape generator tool,
VectorLand
.
VectorLand
can generate landscapes with varying spatial heterogeneity of both types of resources: aquatic habitats and houses. Locations of resources can be controlled using the
Clustering
sliders across both axes. Additional statistics about the generated landscape and legends are also shown in separate panels.
Figure 6.4 Examples of landscapes with different clustering schemes of resources. Filled and open circles denote different types of resources. (a) Cluster around center. (b) Cluster around the first object. (c) Dynamic clustering. (d) Multiple clusters ().
Figure 6.5 Controlling the clusters along a specific axis. Twenty resources of both types are used. (a) Along
x
-axis. (b) Along both axes.
Figure 6.6 Foraging event for mosquito agents. (a) Agent movement in
Blood Meal Seeking
(
BMS
) stage. (b) Agent movement in
Gravid (G)
stage. (c) The
movement
event.
Figure 6.7 Flight heuristics for mosquito agents. Detailed activities by mosquito agents in host-seeking, oviposition, and foraging/search are shown.
Figure 6.8 Model verification results. Both the nonspatial and the spatial ABMs yield consistent results with identical parameter settings. Each graph represents the average of 40 simulation runs and shows only relevant portions of the 1-year simulation results.
Figure 6.9 Results of using different landscape patterns. In the spatial ABM, the use of
regular
and
random
landscape patterns does not significantly alter the population levels. Each graph represents the average of 40 simulation runs and shows only relevant portions of the 1-year simulation results.
Figure 6.10 Results for resource size variation with 1 and 16 aquatic habitats. For both the nonspatial and the spatial models, the numbers of aquatic habitats are increased as squares of the first 10 integers. This Figure shows
VA
with landscapes having 1 and 16 aquatic habitats.
Figure 6.11 Results for resource size variation with 49 and 100 aquatic habitats. For both the nonspatial and the spatial models, the numbers of aquatic habitats are increased as squares of the first 10 integers. This Figure shows with landscapes having 49 and 100 aquatic habitats.
Figure 6.12 Results for resource density variation. This Figure shows the effects of varying by increasing the number of
AH
s within the same hybrid landscape. Each graph represents the average of 40 simulation runs and shows only relevant portions of the 1-year simulation results.
Figure 6.13 Results for system capacity variation. Using hybrid landscapes, the system capacity is gradually increased from to . Each graph represents the average of 40 simulation runs and shows only relevant portions of the 1-year simulation results.
Figure 6.14 Sample landscapes. (a) A landscape with resource densities
below
the critical level. (b) A landscape with resource densities
above
the critical level.
Figure 6.15 Results for resource density
below
the critical level. in a landscape with and resource density
below
the critical level. Each graph represents the average of 40 simulation runs and shows only relevant portions of the 1-year simulation results.
Figure 6.16 Results for resource density
above
the critical level. in a landscape with and resource density
above
the critical level. Each graph represents the average of 40 simulation runs and shows only relevant portions of the 1-year simulation results.
CHAPTER 8: VERIFICATION AND VALIDATION (V&V) OF ABMs
Figure 8.1 The phase-wise docking workflow. The programming language-specific implementations and versions of the ABMs developed in Java and C++ are denoted as
J1
,
J2
,
J3
, and
CPP
. Unidirectional solid arrows indicate immediate successorship between the implementations. Bidirectional solid arrow indicates
verification
relationships between
J1
&
CPP
. Dashed arrows indicate
validation
relationships with the core model.
Figure 8.2 Phase-wise docking results for Phase 1. Mosquito abundance graphs from
J1
&
CPP
outputs are plotted for different populations. The -axis denotes simulation time (in days) and the -axis denotes abundances.
Figure 8.3 Phase-wise docking results for Phase 3. Mosquito abundance graphs from
J3
&
CPP
outputs are plotted for different populations. The -axis denotes simulation time (in days) and the -axis denotes abundances.
Figure 8.4 The compartmental docking workflow. The programming language-specific implementations and versions of the ABMs developed in Java and C++ are denoted as
J1
,
J2
,
CPP1
, and
CPP2
. Bidirectional arrows indicate
verification
relationships between the four implementations. The dashed arrow, between the re-factored implementations
J2
and
CPP2
, indicates
internal verification
, since these two are docked with respect to each other. Unidirectional dashed arrows indicate
validation
relationships between the core model and the four implementations. source© 2010 IEEE. Reprinted, with permission, from Arifin
et al.
[22].
Figure 8.5 Simplified life cycle of mosquitoes for compartmental docking. Two slightly different versions were used as follows: (a) A model with a single aquatic habitat and (b) A model with multiple aquatic habitats. The
aquatic
phase is unchanged, consisting of three aquatic stages:
Egg
,
Larva
, and
Pupa
. The
adult
phase, however, consists of four adult stages:
Immature Adult
,
Blood Meal Seeking
,
Blood Meal Digesting
, and
Gravid
. Each oval represents a stage in the model. Male agents are omitted. Adult female agents cycle through obtaining blood meals, developing eggs, and ovipositing the eggs until they die.
Figure 8.6 Compartmental docking results for
Phase 1
. Each subFigure depicts the fourfold outputs from the four ABMs:
CPP1
,
J1
, and
CPP2/Java2
(since
CPP2
and
J2
were verified with respect to each other, their outputs were merged as a single graph). Different mosquito populations are shown: (a) adult agents, (b) all agents (adults and aquatic), (c) the 1-day-old equivalent larval population (see Eq. 4.9), and (d) biomass (see Eq. 4.8). The legend at the bottom shows the corresponding ABMs. Within each subfigure, each color-coded plot represents outputs from a specific ABM, with color keys presented in the legend. The -axis denotes simulation time (days) and the -axis denotes abundance. The first 100 days of the simulations are shown.
Figure 8.7 Compartmental docking results for
Phase 2
. Each subFigure depicts the fourfold outputs from the four ABMs:
CPP1
,
J1
, and
CPP2/Java2
. Different mosquito populations are shown: (a) adult agents, (b) all agents (adults and aquatic), (c) the 1-day-old equivalent larval population (see Eq. 4.9), and (d) biomass (see Eq. 4.8). The legend at the bottom shows the corresponding ABMs. Within each subfigure, each color-coded plot represents outputs from a specific ABM, with color keys presented in the legend. The -axis denotes simulation time (days) and the -axis denotes abundance. The first 100 days of the simulations are shown.
Figure 8.8 Compartmental docking results for
Phase 3
. Each subFigure depicts the fourfold outputs from the four ABMs:
CPP1
,
J1
, and
CPP2/Java2
. Different mosquito populations are shown: (a) all agents (adults and aquatic) and (b) biomass (see Eq. (4.8)). The legend at the bottom shows the corresponding ABMs. The -axis denotes simulation time (days) and the -axis denotes abundance. The first 100 days of the simulations are shown.
CHAPTER 9: REPLICATION AND REPRODUCIBILITY (R&R) OF ABMs
Figure 9.1 Coverage schemes for ITNs. (a) Household-level partial coverage with single chance. (b) Household-level partial coverage with multiple chances. denotes the number of persons in the house. (c) Household-level complete coverage.
Figure 9.2 Landscapes for Applying LSM in Isolation. The grid-based landscapes are digitized and reproduced from the GN-LSM study [222]. Each landscape contains 70 aquatic habitats (circles) and 20 houses (house icons). Within each landscape, the houses are arranged either diagonally, horizontally, or vertically. For each arrangement, seven scenarios of LSM are shown; from left to right: NOCTRL means no LSM; T1, T2, and T3 refer to targeted removal of aquatic habitats within 100, 200, and of surrounding houses, accounting for 4, 17, and 28 of 70 habitats, respectively. C1, C2, and C3 refer to nontargeted, random removal of the same numbers of aquatic habitats as the corresponding targeted interventions.
Figure 9.3 Landscape for Applying ITNs in Isolation. The landscape is digitized and reproduced from the GN-ITNs study [221]. It contains 90 aquatic habitats (circles) that are randomly distributed and 50 houses (house icons) that are arranged diagonally.
Figure 9.4 Sample landscapes for applying LSM and ITNs in combination. Each landscape contains 200 aquatic habitats and different densities of houses (). (a) with human population of 100. (b) with human population of 350. (c) with human population of 1000. Aquatic habitats and houses are shown as circles and house-shaped icons, respectively. For 240 distinct parameter combinations (see Table 9.3), similar landscapes are generated and 50 replicated simulations are run for each.
Figure 9.5 Sufficient number of replicated simulation runs can smooth out the simulation stochasticity effects. The importance of performing multiple simulation runs (instead of a single run) can be seen by comparing abundances for
maximum
,
minimum
, and
average
cases. Four LSM scenarios are shown (see Figure 9.2): (a) and (b) refer to scenarios C1 and C2, respectively, and use absorbing boundaries with nontargeted, random removal of aquatic habitats. (c) and (d) refer to the same scenarios and use nonabsorbing boundaries. Within each scenario, the three time-series plots represent the maximum, the minimum, and the average mosquito abundances, respectively, obtained across all 50 replicated runs in each time step.
Figure 9.6 The Figure depicts the full 1-year results of applying LSM in isolation with absorbing boundaries as we replicate the results of GN-LSM [222]. Each subFigure represents a specific LSM scenario. The -axis denotes simulation time (days) and the -axis denotes mosquito abundance. The three targeted interventions T1, T2, and T3 refer to the removal of aquatic habitats within 100, 200, and of surrounding houses, accounting for 4, 17, and 28 of 70 habitats, respectively. C1, C2, and C3 refer to nontargeted, random removal of the same numbers of aquatic habitats as the corresponding targeted interventions. Within each subfigure, the
Diagonal
,
Horizontal
, and
Vertical
plots represent abundances (for the specified LSM scenario) for three different arrangements of houses in the landscapes (see Figure 9.2 for the landscapes). With an
absorbing boundary
, mosquitoes are killed when they hit an edge of the landscape's boundary. Each simulation is run 50 times and the average results are reported. This Figure represents averages of a total of 900 () simulations.
Figure 9.7 The Figure depicts the full 1-year results of applying LSM in isolation with nonabsorbing boundaries as we replicate the results of GN-LSM [222]. Each subFigure represents a specific LSM scenario. The -axis denotes simulation time (days) and the -axis denotes mosquito abundance. The three targeted interventions T1, T2, and T3 refer to the removal of aquatic habitats within , , and of surrounding houses, accounting for 4, 17, and 28 of 70 habitats, respectively. C1, C2, and C3 refer to nontargeted, random removal of the same numbers of aquatic habitats as the corresponding targeted interventions. Within each subfigure, the
Diagonal
,
Horizontal
, and
Vertical
plots represent abundances (for the specified LSM scenario) for three different arrangements of houses in the landscapes (see Figure 9.2 for the landscapes). With a
nonabsorbing boundary
, when mosquitoes hit an edge of the landscape's boundary, they enter the landscape from the edge directly opposite of the exiting edge and thus are not killed due to hitting the edge. Each simulation is run 50 times and the average results are reported. This Figure represents averages of a total of 900 () simulations.
Figure 9.8 The Figure depicts the full 1-year results of applying ITNs in isolation with household-level partial coverage and single chance for host-seeking as we replicate the results of GN-ITNs [221]. Each subFigure represents a specific combination for the three ITNs parameters of coverage, repellence, and mortality. The -axis denotes simulation time (days) and the -axis denotes mosquito abundance. Each row represents a specific coverage () for ITNs (e.g., ). Each column represents a specific repellence () for ITNs (e.g., ). Within each subfigure, each color-coded plot represents a specific mortality () value for ITNs (e.g., ), with mortality () color keys at the bottom of the Figure The Figure represents averages of a total of 3000 () simulations. Nonabsorbing boundaries are used. For the partial coverage schemes, see Section 9.2.4.
Figure 9.9 The Figure depicts the full 1-year results of applying ITNs in isolation with household-level complete coverage as we replicate the results of GN-ITNs [221]. Each subFigure represents a specific combination for the three ITNs parameters of coverage, repellence, and mortality. The -axis denotes simulation time (days) and the -axis denotes mosquito abundance. Each row represents a specific coverage () for ITNs (e.g., ). Each column represents a specific repellence () for ITNs (e.g., ). Within each subfigure, each color-coded plot represents a specific mortality () value for ITNs (e.g., ), with mortality () color keys at the bottom of the Figure The Figure represents averages of a total of 3000 () simulations. Nonabsorbing boundaries are used. For the complete coverage scheme, see Section 9.2.4.
Figure 9.10 The Figure depicts the full 1-year results of applying ITNs in isolation with household-level partial coverage and multiple chances for host-seeking as we replicate the results of GN-ITNs [221]. Each subFigure represents a specific combination for the three ITNs parameters of coverage, repellence, and mortality. The -axis denotes simulation time (days) and the -axis denotes mosquito abundance. Each row represents a specific coverage () for ITNs (e.g., ). Each column represents a specific repellence () for ITNs (e.g., ). Within each subfigure, each color-coded plot represents a specific mortality () value for ITNs (e.g., ), with mortality () color keys at the bottom of the Figure The Figure represents averages of a total of 3000 () simulations. Nonabsorbing boundaries are used. For the partial coverage schemes, see Section 9.2.4.
Figure 9.11 Percent reductions in mosquito abundance by ITNs, applied in isolation, comparing household-level partial coverage (with multiple chances for host-seeking) and complete coverage. Each subFigure represents a specific combination of coverage scheme (partial or complete) and repellence () for ITNs: (a) and (b) show the partial scheme with and , respectively. (c) and (d) show the complete scheme with and , respectively. The -axis denotes ITNs coverage and the -axis denotes ITNs mortality. The upper row represents household-level partial coverage and the lower row represents household-level complete coverage, as marked on the left. Each column represents a specific repellence () value, as marked on the top. ITNs are applied at day 100 in the grid-based landscape with 50 houses having a total human population of 185. The percent reduction (PR) values are represented as filled contour plots in each subFigure The color bar on the right quantifies the PR isolines. Results for the entire parameter space are depicted in Figure 9.12.
Figure 9.12 Percent reductions in mosquito abundance by ITNs, applied in isolation, comparing household-level partial coverage (with multiple chances for host-seeking) and complete coverage. This Figure shows results for the entire parameter space. For other details, see Figure 9.11.
Figure 9.13 Percent reductions in mosquito abundance as a function of LSM coverage and ITNs coverage when LSM and ITNs are applied in combination. The -axis denotes ITNs coverage and the -axis denotes LSM coverage. Each subFigure represents a filled contour plot where the isolines are labeled with specific percent reduction (PR) values, with specific combination of density of houses () and mortality () for ITNs: subFigure (a)–(c) represent with of
Low
,
Medium
, and
High
, respectively; subFigure (d)–(f) represent with of
Low
,
Medium
, and
High
, respectively. ITNs repellence () is fixed at 0.5. Each simulation is run for 1 year; both LSM and ITNs are applied at day 100 and continued up to the end of the simulation. The color bar on the right quantifies the PR isolines. The Figure represents average percent reduction values of a total of 6000 () simulations. For ITNs, household-level complete coverage scheme is used (see Figure 9.1c). Nonabsorbing boundaries are used. Sample landscapes with the three levels are shown in Figure 9.4. The Figure depicts selected results that involve a subset of the parameters from Table 9.3.
Figure 9.14 The Figure depicts percent reductions results that involve the entire parameter space from Table 9.3 as a function of LSM coverage and ITNs coverage when LSM and ITNs are applied in combination. This Figure shows results for the entire parameter space. For other details, see Figure 9.13.
CHAPTER 10: A LANDSCAPE EPIDEMIOLOGY MODELING FRAMEWORK
Figure 10.1 The study area. (a) Kenya boundary and administrative units (provinces). (b) Study area with selected data layers; the outlined polygon represents a subset of villages selected for the simulation runs in this study. (c) Village cluster in Asembo. (d) Legends.
Figure 10.2 Selected sets of GIS features for Kenya. (a) Villages. (b) Water sources.
Figure 10.3 Maps for the
mosquito abundances
index. (a) Abundance map for baseline. (b) Legends: for clarity, houses and pit latrines are not shown. (c) Abundance map for . (d) Abundance map for . (e) Abundance map for . (f) Abundance map for .
Figure 10.4 Kriged maps for the
mosquito abundances
index. (a) Kriged abundance map for baseline. (b) Legends. (c)–(f) The four intervention scenarios.
Figure 10.5 Maps for the
oviposition count per aquatic habitat
index. Oviposition counts are categorized using the same quantitative scale and are shown using graduated symbols. For clarity, houses and pit latrines are not shown. Hot spots and cold spots are spatially clustered. (a) Baseline. (b) Legends. (c)–(f) The four intervention scenarios.
Figure 10.6 Kriged maps for the
oviposition count per aquatic habitat
index. (a) Baseline. (b) Legends. (c)–(f) The four intervention scenarios.
Figure 10.7 Maps for the
blood meal count per house
index. Blood meal counts are categorized using the same quantitative scale. For clarity, houses and pit latrines are not shown. Hot spots and cold spots are spatially clustered using two confidence intervals (CIs) of 95 and . (a) Baseline. (b) Legends. (c)–(f) The four intervention scenarios.
Figure 10.8 Kriged maps for all scenarios for the
blood meal count per house
index. (a) Baseline. (b) Legends. (c)–(f) The four intervention scenarios.
CHAPTER 11: THE EMOD INDIVIDUAL-BASED MODEL
Figure 11.1 The EMOD model of the mosquito feeding cycle with outcomes.
Figure 11.2 Simulation of Namawala, Tanzania, as described in [160], shows changes in EIR due to seasonal variations at baseline (a), with IRS (b), and with IRS and a transmission-blocking vaccine (c). Adding interventions adds variability to the simulation, with the transmission-blocking vaccine providing an additional reduction in transmission of over a factor of 2, which would be difficult for further interventions targeting indoor feeding to achieve on top of IRS.
Figure 11.3 Outcomes of different intervention combinations in the Garki District [163]. The light gray is baseline, the dark gray adds in IRS, the dark line is with infrequent drug campaigns, and the dark dashed line with frequent drug campaigns. The dots are field data from the Project.
Figure 11.4 Modeled distribution of detected prevalence in Madagascar. This can be compared to estimates for prevalence from the Malaria Atlas Project [232].
Figure 11.5 Modeled vector population density distributions in Madagascar. (a) Adult vector distribution averaged daily over a simulated 3-year period. (b) Sporozoite rates for all local
Anopheles
averaged over the same period. Average rates are highest in tropical wet and dry climate zones due to the high rates at the end of the wet season, when the average age of the vector population increases without a large influx of emerging mosquitoes.
Figure 11.6 (a) Separatrix plots of the modeled probability of successful Eradication in Madagascar, showing the division of the high probability of success region separated from the low probability of success region. (b) The estimate variance. The two parameters shown here are ITN coverage and a linear scaling of migration rates. In these simulations, all vectors are indoor feeders and bed nets have perfect efficacy and do not decay. For realistic vector populations including outdoor biting, bed nets alone are insufficient for elimination and must be combined with other interventions. Increasing migration rates given broadly uniform high coverage spreads out the transition from low probability of success to high probability of success.
APPENDIX A: ENZYME KINETICS MODEL FOR VECTOR GROWTH AND DEVELOPMENT
Figure A.1 Energy states of the kinetic model (redrawn from [488]). The directed arrows indicate possible transitions.
Energy State 1
predominates at low temperatures.
Energy State 2
represents the active enzyme configuration and predominates over the mid-temperature range.
Energy State 3
predominates at high temperatures.
APPENDIX C: ADDITIONAL FILES FOR CHAPTER 10
Figure C.1 Clipped eater sources for Kenya. The Figure shows different water source features, including rivers, wetlands, and other types of water points, clipped within Kenya.
Figure C.2 Clipped village projections for Kenya.
Figure C.3 Polygon creation process. The polygon is created using the ArcGIS software release 10 [16]. A new shapefile is created for the desired polygon. The boundary for the polygon is created in the editing mode and the area of the polygon is calculated using the
Calculate Areas
tool. Finally, the polygon area is highlighted in the editing mode.
Figure C.4 Clipped habitats within the selected polygon. A new shapefile is created for the desired polygon. The boundary for the polygon is created in the editing mode and the area of the polygon is calculated using the
Calculate Areas
tool using the ArcGIS software release 10 [16]. Finally, the polygon area is highlighted in the editing mode.
Figure C.5 Data conversion to raster format, Part 1. The figure shows the values and counts of house features in the attribute table after the raster conversion. From these attributes, the counts of features per grid cell are generated.
Figure C.6 Data conversion to raster format, Part 2. The Figure shows all features converted into the raster format within the polygon area for the ABM. The interpretation of each (as supplied by the ABM) for each feature and count of features per grid cell are also linked.
APPENDIX D: A POSTSIMULATION ANALYSIS MODULE FOR AGENT-BASED MODELS
Figure D.1 The P-SAM architecture.
Figure D.2 P-SAM Infection Statistics tab.
Figure D.3 P-SAM Roaming Infection Statistics tab.
Figure D.4 P-SAM birth and death statistics tab.
Figure D.5 Example of a
pathogen transmission graph
. Nodes represent macaques and edges represent infection events. Loops represent autoinfection.
Figure D.6 P-SAM Summary Statistics tab.
Figure D.7 P-SAM performance. For each phase, the seven data points represent average values of output files, obtained by varying parameter settings of the LiNK model. The same seven sets of parameters are used for all phases.
Phase 1
bypasses the GUI.
Phase 2
eliminates unnecessary existence checks for
infection
hash used in the
Writer
, thus reducing search penalties for
macaque
nodes in the hash. Finally,
Phase 3
optimizes some hash operations using sets.
CHAPTER 3: AGENT-BASED MODELING AND MALARIA
Table 3.1 Applications of Agent-Based Models (ABMs)
Table 3.2 Malaria Models: A Comparison of Features
CHAPTER 4: THE BIOLOGICAL CORE MODEL
Table 4.1 Summary of Updated Features in the Core Model
Table 4.2 Symbols and parameters used in the core model and the ABMs. Parameters are listed in order of appearance in the text
Table 4.3 Larval development parameters for
An. gambiae
CHAPTER 7: VERIFICATION, VALIDATION, REPLICATION, AND REPRODUCIBILITY
Table 7.1 Methodologies and Techniques Commonly Used for V&V in M&S Research
CHAPTER 8: VERIFICATION AND VALIDATION (V&V) OF ABMs
Table 8.1 V&V Techniques Used for the ABMs
Table 8.2 Simplified Stage Transition Times for Phase-Wise Docking
Table 8.3 Compartmental Docking Issues in Phase 1
Table 8.4 Compartmental Docking Issues in Phases 2–3
CHAPTER 9: REPLICATION AND REPRODUCIBILITY (R&R) OF ABMs
Table 9.1 Population Profiles for Varying Levels of ITNs Coverage
Table 9.2 Parameter Space for ITNs
Table 9.3 Parameter Space for LSM and ITNs
Table 9.4 Percent Reductions in Abundance with LSM
CHAPTER 10: A LANDSCAPE EPIDEMIOLOGY MODELING FRAMEWORK
Table 10.1 Vector Control Intervention Scenarios
Table 10.2 GIS Feature Types and Counts for the ABM
CHAPTER 11: THE EMOD INDIVIDUAL-BASED MODEL
Table 11.1 Summary of Issues for Eradication Modeling
Table 11.2 Summary of Features Desired for Eradication Modeling
APPENDIX A: ENZYME KINETICS MODEL FOR VECTOR GROWTH AND DEVELOPMENT
Table A.1 Entropy and Enthalpy of Activation
Table A.2 Enzyme, Reaction, and Rate Constant
APPENDIX D: A POSTSIMULATION ANALYSIS MODULE FOR AGENT-BASED MODELS
Table D.1 Perl Extension Modules Used
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S. M. NIAZ ARIFIN
Department of Computer Science and EngineeringUniversity of Notre DameIN, USA
GREGORY R. MADEY
Department of Computer Science and EngineeringUniversity of Notre DameIN, USA
FRANK H. COLLINS
Department of Biological SciencesUniversity of Notre DameIN, USA
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Library of Congress Cataloging-in-Publication Data:
Arifin, S.M. Niaz, author.
Spatial agent-based simulation modeling in public health : design, implementation, and applications for malaria epidemiology / S.M. Niaz Arifin, Gregory R. Madey, Frank H. Collins.
p. ; cm.
Includes bibliographical references and index.
ISBN 978-1-118-96435-4 (hardback)
I. Madey, Gregory Richard, author. II. Collins, Frank H., author. III. Title.
[DNLM: 1. Malaria–epidemiology. 2. Computer Simulation. 3. Geographic Information Systems. 4. Models, Theoretical. 5. Spatial Analysis. WC 755.1]
RA644.M2
614.5′32090285–dc23
2015033121
To my parents:
Engineer S. M. Golam Mostofa
B.Sc. Engg. (Civil), FIE (B), PGD (CS)
My Father and Guide
Professor Parvin Akhter Jahan
M.A. (Economics), B.A. (Honors)
My Mother and Best Friend
and my wife:
Rumana Reaz Arifin
B.S., M.S.
My Soulmate
and my sister:
Mafruhatul Jannat
Ph.D., M.S., B.S.
We Grew up Together
- S. M. Niaz Arifin
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