Two species when occupy in same habitat accumulating same resource in same manner then competition is inevitable. The normal logistic growth is not expected. Lotka and Volterra proposed equation to describe the interspecific competition among the species. Either one of the species wins other is excluded or they co-exist in unstable or stable manner.
Life tables concept was first formulated by Raymond Pearl (1924)
Life tables is the systematic tabulation of births and deaths of an organism. It is summary statement on the life of a typical individual of population or a cohort of individuals. .
It is an especially useful approach in entomology where developmental stages are discrete and mortality rates may vary widely from one life stage to another.
From a pest management standpoint, it is very useful to know when (and why) a pest population suffers high mortality.
Iczn(The International Commission on Zoological Nomenclature )Al Nahian Avro
The International Commission on Zoological Nomenclature (ICZN) acts as adviser and arbiter for the zoological community by generating and disseminating information on the correct use of the scientific names of animals. The ICZN is responsible for producing the International Code of Zoological Nomenclature - a set of rules for the naming of animals and the resolution of nomenclatural problems.
Two species when occupy in same habitat accumulating same resource in same manner then competition is inevitable. The normal logistic growth is not expected. Lotka and Volterra proposed equation to describe the interspecific competition among the species. Either one of the species wins other is excluded or they co-exist in unstable or stable manner.
Life tables concept was first formulated by Raymond Pearl (1924)
Life tables is the systematic tabulation of births and deaths of an organism. It is summary statement on the life of a typical individual of population or a cohort of individuals. .
It is an especially useful approach in entomology where developmental stages are discrete and mortality rates may vary widely from one life stage to another.
From a pest management standpoint, it is very useful to know when (and why) a pest population suffers high mortality.
Iczn(The International Commission on Zoological Nomenclature )Al Nahian Avro
The International Commission on Zoological Nomenclature (ICZN) acts as adviser and arbiter for the zoological community by generating and disseminating information on the correct use of the scientific names of animals. The ICZN is responsible for producing the International Code of Zoological Nomenclature - a set of rules for the naming of animals and the resolution of nomenclatural problems.
When a perfectly harmless animal resembles in its colour and shape, with a well protected species, the phenomenon is called mimicry.
The concept of mimicry was first given by H. W. Bates in 1862.
Mimicry is an important feature of organism which protect the animals against enemies. Mimicry often used as self defense which increases the survival value of organisms.
Social organization and social behaviour in insectsPoojaVishnoi7
Introduction
Properties of a society
Advantages of a society
Disadvantages of a society
Social organisation and social behaviour in insects:-
1. Termites
2.Honeybees
3.Ants
4.Yellow wasp
Two broad categories of behaviors are Proximate and Ultimate behaviour. The presentation gives a brief introduction on Proximate and Ultimate causes of behaviour
When a perfectly harmless animal resembles in its colour and shape, with a well protected species, the phenomenon is called mimicry.
The concept of mimicry was first given by H. W. Bates in 1862.
Mimicry is an important feature of organism which protect the animals against enemies. Mimicry often used as self defense which increases the survival value of organisms.
Social organization and social behaviour in insectsPoojaVishnoi7
Introduction
Properties of a society
Advantages of a society
Disadvantages of a society
Social organisation and social behaviour in insects:-
1. Termites
2.Honeybees
3.Ants
4.Yellow wasp
Two broad categories of behaviors are Proximate and Ultimate behaviour. The presentation gives a brief introduction on Proximate and Ultimate causes of behaviour
predator prey interactions are of great importance in the agro ecosystems. insects being the largest group of arthropods have a major role in designing various management strategies against different crop pests. these interactions influence the structure and dynamics of an agro ecosystem.
presentation contain different type of interactions, competition-intra and inter-specific, mechanism of competition-Exploitation and Interference, Mathematical models of Competition i.e. Hutchinson Ratio, Exponential Growth, Logistic Model, Lotka-Volterra Competition Model, Tilman's Resource Model, Results of Competition i.e. Range restriction, Competitive Displacement, Competitive Exclusion , Competitive Displacement Hypothesis, Ecological Niche, Evolution of new species, Factors Affecting Competition, Case studies
This presentation covers the basic terminology and key parameters of Population Genetics. Presentation is helpful for the students of Life Sciences and Evolutionary biology.
ECOL203403 – Ecology Populations to Ecosystems Assignment .docxbudabrooks46239
ECOL203/403 – Ecology: Populations to Ecosystems
Assignment 2: Predator-Prey Interactions
T1 2020
Figure 0. Tarantula Theraphosa blondi pulling a captured giant earthworm (presumably
Rhinodrilus sp.) into its burrow in rainforest in French Guiana. Photo by C.E. Timothy Paine. Find
more information about earthworm-eating tarantulas in Nyffler et. al. 2017. Journal of
Arachnology 45:242–247.
Objective
The purpose of this assignment is for you to run a manipulative experiment using
a realistic predator-prey model. In so doing, you will
1. explore how predators affect prey populations and vice versa
2. explore the linkages between ecological processes and their
representations in models
3. design and execute an ecological experiment
Introduction
This assignment demonstrates how the actions of individuals compound to
generate population dynamics. We know that all populations can grow
exponentially, and we also know that never occurs for long, as the resources
available to populations eventually restrict their growth. In this practical, you will
explore how and when this occurs. You will further explore conditions under
which more complicated – and even interesting – population dynamics occur.
In simple models, one could assume that all predators had access to all prey at
all times. In reality, however, populations have spatial structure, because
individuals are located at specific locations in space. This has several effects on
their ecology. First, an individual’s spatial location restricts the set of individuals
that it can interact with to be those in its local neighborhood. Second, space
(together with the sensory organs of the organism in question) affects the
detectability of predators and prey. Third, heterogeneity in the spatial distribution
of resource availability, refuges, mates, and abiotic conditions (etc) can strongly
influence ecological processes. Finally, the viscosity (or ‘thickness’) of the
environment, together with the dispersal abilities of the organism, affects how
quickly they can move through space. All of these factors influence ecological
interactions among organisms. A final consideration is the dimensionality of
space. For terrestrial organisms, the world is (to a first approximation) flat,
whereas for aquatic, marine or airborne organisms it is three-dimensional. In the
sky, a predator may be above you. In water, predators may lurk above or below
you. In this model, we assume that the predators and prey exist in a flat (two-
dimensional) homogeneous field.
Modeling platform
You will use a modeling platform, NetLogo, in which the spatially explicit two-
species model has been developed. NetLogo is a multi-agent programmable
modeling environment used by tens of thousands of students, teachers and
researchers worldwide. Models are written in the NetLogo language, which
provides a graphical user interface for users.
Description of model
ARENA: You will si.
ECOL203403 – Ecology Populations to Ecosystems Assignment .docxtidwellveronique
ECOL203/403 – Ecology: Populations to Ecosystems
Assignment 2: Predator-Prey Interactions
T1 2020
Figure 0. Tarantula Theraphosa blondi pulling a captured giant earthworm (presumably
Rhinodrilus sp.) into its burrow in rainforest in French Guiana. Photo by C.E. Timothy Paine. Find
more information about earthworm-eating tarantulas in Nyffler et. al. 2017. Journal of
Arachnology 45:242–247.
Objective
The purpose of this assignment is for you to run a manipulative experiment using
a realistic predator-prey model. In so doing, you will
1. explore how predators affect prey populations and vice versa
2. explore the linkages between ecological processes and their
representations in models
3. design and execute an ecological experiment
Introduction
This assignment demonstrates how the actions of individuals compound to
generate population dynamics. We know that all populations can grow
exponentially, and we also know that never occurs for long, as the resources
available to populations eventually restrict their growth. In this practical, you will
explore how and when this occurs. You will further explore conditions under
which more complicated – and even interesting – population dynamics occur.
In simple models, one could assume that all predators had access to all prey at
all times. In reality, however, populations have spatial structure, because
individuals are located at specific locations in space. This has several effects on
their ecology. First, an individual’s spatial location restricts the set of individuals
that it can interact with to be those in its local neighborhood. Second, space
(together with the sensory organs of the organism in question) affects the
detectability of predators and prey. Third, heterogeneity in the spatial distribution
of resource availability, refuges, mates, and abiotic conditions (etc) can strongly
influence ecological processes. Finally, the viscosity (or ‘thickness’) of the
environment, together with the dispersal abilities of the organism, affects how
quickly they can move through space. All of these factors influence ecological
interactions among organisms. A final consideration is the dimensionality of
space. For terrestrial organisms, the world is (to a first approximation) flat,
whereas for aquatic, marine or airborne organisms it is three-dimensional. In the
sky, a predator may be above you. In water, predators may lurk above or below
you. In this model, we assume that the predators and prey exist in a flat (two-
dimensional) homogeneous field.
Modeling platform
You will use a modeling platform, NetLogo, in which the spatially explicit two-
species model has been developed. NetLogo is a multi-agent programmable
modeling environment used by tens of thousands of students, teachers and
researchers worldwide. Models are written in the NetLogo language, which
provides a graphical user interface for users.
Description of model
ARENA: You will si.
The increased availability of biomedical data, particularly in the public domain, offers the opportunity to better understand human health and to develop effective therapeutics for a wide range of unmet medical needs. However, data scientists remain stymied by the fact that data remain hard to find and to productively reuse because data and their metadata i) are wholly inaccessible, ii) are in non-standard or incompatible representations, iii) do not conform to community standards, and iv) have unclear or highly restricted terms and conditions that preclude legitimate reuse. These limitations require a rethink on data can be made machine and AI-ready - the key motivation behind the FAIR Guiding Principles. Concurrently, while recent efforts have explored the use of deep learning to fuse disparate data into predictive models for a wide range of biomedical applications, these models often fail even when the correct answer is already known, and fail to explain individual predictions in terms that data scientists can appreciate. These limitations suggest that new methods to produce practical artificial intelligence are still needed.
In this talk, I will discuss our work in (1) building an integrative knowledge infrastructure to prepare FAIR and "AI-ready" data and services along with (2) neurosymbolic AI methods to improve the quality of predictions and to generate plausible explanations. Attention is given to standards, platforms, and methods to wrangle knowledge into simple, but effective semantic and latent representations, and to make these available into standards-compliant and discoverable interfaces that can be used in model building, validation, and explanation. Our work, and those of others in the field, creates a baseline for building trustworthy and easy to deploy AI models in biomedicine.
Bio
Dr. Michel Dumontier is the Distinguished Professor of Data Science at Maastricht University, founder and executive director of the Institute of Data Science, and co-founder of the FAIR (Findable, Accessible, Interoperable and Reusable) data principles. His research explores socio-technological approaches for responsible discovery science, which includes collaborative multi-modal knowledge graphs, privacy-preserving distributed data mining, and AI methods for drug discovery and personalized medicine. His work is supported through the Dutch National Research Agenda, the Netherlands Organisation for Scientific Research, Horizon Europe, the European Open Science Cloud, the US National Institutes of Health, and a Marie-Curie Innovative Training Network. He is the editor-in-chief for the journal Data Science and is internationally recognized for his contributions in bioinformatics, biomedical informatics, and semantic technologies including ontologies and linked data.
(May 29th, 2024) Advancements in Intravital Microscopy- Insights for Preclini...Scintica Instrumentation
Intravital microscopy (IVM) is a powerful tool utilized to study cellular behavior over time and space in vivo. Much of our understanding of cell biology has been accomplished using various in vitro and ex vivo methods; however, these studies do not necessarily reflect the natural dynamics of biological processes. Unlike traditional cell culture or fixed tissue imaging, IVM allows for the ultra-fast high-resolution imaging of cellular processes over time and space and were studied in its natural environment. Real-time visualization of biological processes in the context of an intact organism helps maintain physiological relevance and provide insights into the progression of disease, response to treatments or developmental processes.
In this webinar we give an overview of advanced applications of the IVM system in preclinical research. IVIM technology is a provider of all-in-one intravital microscopy systems and solutions optimized for in vivo imaging of live animal models at sub-micron resolution. The system’s unique features and user-friendly software enables researchers to probe fast dynamic biological processes such as immune cell tracking, cell-cell interaction as well as vascularization and tumor metastasis with exceptional detail. This webinar will also give an overview of IVM being utilized in drug development, offering a view into the intricate interaction between drugs/nanoparticles and tissues in vivo and allows for the evaluation of therapeutic intervention in a variety of tissues and organs. This interdisciplinary collaboration continues to drive the advancements of novel therapeutic strategies.
Multi-source connectivity as the driver of solar wind variability in the heli...Sérgio Sacani
The ambient solar wind that flls the heliosphere originates from multiple
sources in the solar corona and is highly structured. It is often described
as high-speed, relatively homogeneous, plasma streams from coronal
holes and slow-speed, highly variable, streams whose source regions are
under debate. A key goal of ESA/NASA’s Solar Orbiter mission is to identify
solar wind sources and understand what drives the complexity seen in the
heliosphere. By combining magnetic feld modelling and spectroscopic
techniques with high-resolution observations and measurements, we show
that the solar wind variability detected in situ by Solar Orbiter in March
2022 is driven by spatio-temporal changes in the magnetic connectivity to
multiple sources in the solar atmosphere. The magnetic feld footpoints
connected to the spacecraft moved from the boundaries of a coronal hole
to one active region (12961) and then across to another region (12957). This
is refected in the in situ measurements, which show the transition from fast
to highly Alfvénic then to slow solar wind that is disrupted by the arrival of
a coronal mass ejection. Our results describe solar wind variability at 0.5 au
but are applicable to near-Earth observatories.
Seminar of U.V. Spectroscopy by SAMIR PANDASAMIR PANDA
Spectroscopy is a branch of science dealing the study of interaction of electromagnetic radiation with matter.
Ultraviolet-visible spectroscopy refers to absorption spectroscopy or reflect spectroscopy in the UV-VIS spectral region.
Ultraviolet-visible spectroscopy is an analytical method that can measure the amount of light received by the analyte.
Observation of Io’s Resurfacing via Plume Deposition Using Ground-based Adapt...Sérgio Sacani
Since volcanic activity was first discovered on Io from Voyager images in 1979, changes
on Io’s surface have been monitored from both spacecraft and ground-based telescopes.
Here, we present the highest spatial resolution images of Io ever obtained from a groundbased telescope. These images, acquired by the SHARK-VIS instrument on the Large
Binocular Telescope, show evidence of a major resurfacing event on Io’s trailing hemisphere. When compared to the most recent spacecraft images, the SHARK-VIS images
show that a plume deposit from a powerful eruption at Pillan Patera has covered part
of the long-lived Pele plume deposit. Although this type of resurfacing event may be common on Io, few have been detected due to the rarity of spacecraft visits and the previously low spatial resolution available from Earth-based telescopes. The SHARK-VIS instrument ushers in a new era of high resolution imaging of Io’s surface using adaptive
optics at visible wavelengths.
A brief information about the SCOP protein database used in bioinformatics.
The Structural Classification of Proteins (SCOP) database is a comprehensive and authoritative resource for the structural and evolutionary relationships of proteins. It provides a detailed and curated classification of protein structures, grouping them into families, superfamilies, and folds based on their structural and sequence similarities.
2. Introduction
• These models in regards their relation to classical biological control,
which is the practice of introducing a natural enemy of an insect pest with
the goal of reducing the insect pest's population to a level that is no longer
dangerous to the local region.
• Predator-prey models are
arguably the building blocks of
the bio and ecosystems as
biomasses are grown out of their
resource masses.
3. Basic Framework of Models
• Models have been favoured due to the following three assumptions
that can be made:
1. Closed system:
2. Equivalent generation times
3. Ignore/simplify age structure
4. ØThere are two major categories for host-parasitoid
models which depends on how generations are
measured in time.
These two categories are
Discrete generations
Continuous
generations
5. TYPES OF MODEL
Basically models are categorised in two broad categories-
• Early models
• Refinements of early models
6. Early models Refinements of the Models
vLotka-Volterra Model
vThompson Model
vNicholson-Bailey Model
vHolling Model
ØDensity-Dependent Self-Limitation
ØTemporal Limitations:Age-Structure
7. Lotka-Volterra Model
What is lotka volterra model?
• Lotka volterra model provide information about
competion between two species living in same
ecosystem.
• Lotka volterra model help us predicting the outcome
of a competition based on impact of one species on
another.
8. History
• Initially proposed by Alfred J. Lotka in
the theory of autocatalytic chemical
reactions in 1910.
• In 1925 he used the equations to analyse
predator– prey interactions in his book
on biomathematics.
• The same set of equations was published
in 1926 by Vito Volterra, a
mathematician and physicist, who had
become interested in mathematical
biology.
Alfred J. Lotka
Vito Volterra
9. Assumptions of lotka- velterra
equation
• Animals move at random.
• Every encounter with a prey results in a capture and every prey that
is captured is eaten. This is independent of densities of population of
predation and prey.
• The population of both predator and prey have all the qualities
necessary for them to conform logistic theory –growth rate
accelerates until alimiting factor causes deceleration.
10. Lotka–Volterra equations
• The Lotka–V
olterra equations, also known as the predator–prey
equations, are a pair of first order nonlinear differential equations.
• Frequently used to describe the dynamics of biological systems in
which two species interact, one as a predator and the other as prey.
11. Prey equation
• 𝜹𝒙/ 𝜹𝒕 = 𝜶𝒙 – 𝜷𝒙
• 𝒙 is the number ofprey
• 𝒚 is the number of somepredator
• 𝜹𝒙/ 𝜹𝒕 and 𝜹𝒚/ 𝜹𝒕 represent the instantaneous growth rates of the two
populations.
• t represents time
• α, β, γ, δ are positive real parameters describing the interaction of the two
species.
12. About prey equation
• The prey are assumed to have an unlimited food supply and to
reproduce exponentially, unless subject to predation.
• This exponential growth is represented in the equation above by the
term 𝜶𝒙.
• The rate of predation upon the prey is assumed to be proportional to
the rate at which the predators and the prey meet, this is represented
above by 𝜷𝒙𝒚.
• If either 𝒙 or 𝒚 is zero, then there can be no predation.
13. P r e d a t o r equation
• 𝜹𝒚 /𝜹𝒕 = 𝜹𝒙𝒚 – 𝜸𝒚
• • 𝒙 is the number ofprey
• • 𝒚 is the number of somepredator
• • 𝜹𝒙/ 𝜹𝒕 and 𝜹𝒚/ 𝜹𝒕 represent the instantaneous growth rates of the two
populations.
• t represents time;
• α, β, γ, δ are positive real parameters describing the interaction of the two
species.
14. About p r e d a t o r equation
• In this equation, 𝜹𝒙𝒚 represents the growth of the predator population.
• Note the similarity to the predation rate; however, a different constant is
used, as the rate at which the predator population grows is not
necessarily equal to the rate at which it consumes the prey.
• 𝜸𝒚 represents the loss rate of the predators due to either natural death
or
emigration, it leads to an exponential decay in the absence of prey.
15. Predator prey model’s assumptions
1.The prey population finds ample food at all times.
2.In the absence of a predator, the prey grows at a rate
proportional to the current population.
3.The food supply of the predator population depends entirely
on the prey populations.
4. In the absence of the prey, the predator dies out.
5.The number of encounters between predator and prey is
proportional to the product of their populations. Encounters
between predator and prey tends to promote the growth of the
predator and inhibit the growth of the prey.
6.During the process, the environment does not change in favor
of one species and the genetic adaptation is sufficiently slow.
16. Nicholson and Bailey model
• This model is also known as host-parasitoid model.
• The Nicholson–Bailey model was developed in the 1930s to describe
the population dynamics of a coupled host-parasitoid system.
• It is named after Alexander John Nicholson and Victor Albert Bailey.
• Host-parasite and prey-predator systems can also be represented with the
Nicholson-Bailey model.
• The model is closely related to the Lotka–Volterra model, which
describes the dynamics of antagonistic populations (preys and predators)
using differential equations.
17. Alexander John Nicholson Victor Albert Bailey
History
The classic model was discribed by Nicholson and Bailey in
1935.
18. Derivation
• The model is defined indiscrete time.It is usually expressed as-
Nt+1 = λNt e-aP
t
Pt+1 = cNt[1 -e-aP
t]
Where,
Nt = density of host species in generationt
Pt = density of parasitoid in generation t
a = searching efficiency of parasitoids
λ = host reproductive rate
c = average number of viable eggs laid by a parasitoid on a single host.
19. Case Studies
Winter moth
• In the 1950s, winter moths were harming
hardwood trees in eastern Canada, so a parasitoid
was introduced from the moths' native Europe,
which greatly reduced the abundance of winter
moths. This reduction was most easily modeled at
the time with the Nicholson-Bailey model and
aggregrated parasitoid attack rates, but upon
review of the data, the winter moth case study
appeared to be more a matter of predation that
parasitism because of the decline in unparasitized
pupae in the soil.
20. Cassava mealy bug & California red
scale
• More recent application of host-parasitoid interactions include the cassava
mealybug, an insect pest found in Africa, and the California red scale, which
is found in California.
• The interactions of these populations with their respective parasitoid
models, and some
populations were modeled using Lotka-Volterra
interesting conclusions were reached for both systems:
• Very little evidence of aggregrated parasitoid attack.
21. • Age structure, in some form, is
essential in order to correctly model
host-parasitoid interactions.
• Local dynamics of the interactions
are strongly influenced by parasitism
refuges, in the form of physical
refuges or host quality effects.
• Temporal refuges (i.e. syncroization
issues) were not apparent, and host
feeding did not significantly change
overall dynamics.
22. A TWO-PATCH PREY-PREDATOR MODEL WITH
PREDATOR DISPERSAL DRIVEN BY THE PREDATION
STRENGTH
• Foraging movements of predator play an important role in population dynamics
of prey-predator systems, which have been considered as mechanisms that
contribute to spatial self-organization of prey and predator.
• In nature, there are many examples of prey-predator interactions where prey is
immobile while predator disperses between patches non-randomly through
different factors such as stimuli following the encounter of a prey.
• In the work, formulated a prey-predator two patch model with mobility only in
predator and the assumption that predators move towards patches with more
concentrated prey-predator interactions.
• It provide completed local and global analysis of model.
23. • Analytical results combined with bifurcation diagrams suggest that:
ü Dispersal may stabilize or destabilize the coupled system
ü Dispersal may generate multiple interior equilibria that lead to rich
bistable dynamics or may destroy interior equilibria that lead to the
extinction of predator in one patch or both patches
ü Under certain conditions, the large dispersal can promote the permanence
of the system. In addition, we compare the dynamics of our model to the
classic two patch model to obtain a better understanding how different
dispersal strategies may have different impacts on the dynamics and
spatial patterns.
24. Epidemics in predator–prey models:
disease in the predators
• The investigated models for the study of interacting species subject to an
additional factor, a disease spreading among one of them, that somehow
affects the other one. The inadequacy of such a model comes from the
basic assumption on the interacting species. It is well known that the
cycles found in the Lotka–Volterra system exhibit a neutral stability, and
this phenomenon is carried over to the proposed model. Here we would
like to extend the study to account for population dynamics leading to
carrying capacities, i.e. logistic behaviour.
• This corresponds to the so-called quadratic predator–prey models found in
the literature.
25. Mean free-path length theory of
predator–prey interactions: Application
to juvenile salmon migration
• Ecological theory traditionally describes predator–prey interactions in terms
of a law of mass action in which the prey mortality rate depends on the
density of predators and prey.
• This simplifying assumption makes population-based models more tractable
but ignores potentially important behaviors that characterize predator–prey
dynamics.
• Here this model expand traditional predator–prey models by incorporating
directed and random movements of both predators and prey. The model is
based on theory originally developed to predict collision rates of molecules.
26. Importance of Crop Modeling in
Agriculture with reference to Pest
Management
27. An agricultural system, or agro-ecosystem, is a collection of
components that has as its overall purpose the production of
crops and raising livestock to produce food, fiber, and energy
from the Earth's natural resources and such systems may
also cause undesired effects on the environment. (Jones et al.,
2016).
Introduction
28. What is a model?
ØA physical, mathematical, or otherwise logical
representation of a system, entity, phenomenon,
or process (DoD 1998).
ØA representation of one or more concepts that may be
realized in the physical world (Friedenthal, Moore, and
Steiner 2009).
ØA simplified representation of a system at some particular
point in time or space intended to promote understanding of
the real system (Bellinger 2004).
29. vMathematical Model - Physical relationship of natural phenomenon by
Means of a mathematical equation are called mathematical Model .
vGrowth Model - If the phenomenon is expressed in the growth define it
is define as growth model
vCrop Weather Model - Crop weather model is based on the principle
that govern the development of crop and its growing period based on
temperature and day length .
Types of Models
30. Ø Crop modeling helps in yield predicting and forecasting
Ø Helps in evaluation of weather change, thus helps in weather forecasting
Ø Helps in formation of stocks, making of agricultural policies and zoning
Ø Optimum seed rate can be calibrated from these models
Ø Useful in cropping management system by predicting cultural practices
Ø Helps to quantify optimum amount of fertilizer and decide optimum time
of application
Ø Helps to predict pests outbreak through crop weather model
Application of Crop Modeling in Agriculture
31. Some Crop Models Reported in Recent Literature
Software Details
SLAM II Forage harvesting operation
SPICE Whole plant water flow
IRRIGATE Irrigation scheduling model
COTTAM Cotton
CropSyst Wheat & other crops
TUBERPRO Potato & disease
WOFOST Wheat & maize, Water and nutrient
WAVE Water and agrochemicals
ORYZA1 Rice, water
SIMCOY Corn
APSIM-Sugarcane
Sugarcane, potential growth, water and
nitrogen stress
32. Model uses
Simulation modelling is increasingly being applied in
research, teaching, farm and resource management, policy
analysis and production forecasts.
These model can be applied into three areas, namely;
ØResearch tools,
ØCrop system management tools, and
ØPolicy analysis tools.
33. As research tools
Ø Research understanding
Ø Integration of knowledge across disciplines
Ø Improvement in experiment documentation and
data organization
Ø Genetic improvement
Ø Yield analysis
34. As crop system management tools
Ø Cultural and input management,
Ø Risks assessment and investment support
Ø Site-specific farming
35. As Policy Analysis Tools
Ø Best management practices
Ø Yield forecasting
Ø Introduction of a new crop
Ø Global climate change and crop production
36. Agricultural systems are characterized by high levels of interaction
between the components that are not completely understood.
Lack of knowledge and data can give rise to simplified
representation of a rather intensive system.
The need for model verification in a new situation arises because
all processes are not fully understood and even the best
mechanistic model still contains some empiricism making
parameter adjustments vital in a new situation.
Model performance is limited to the quality of input data.
Limitations: