-
Notifications
You must be signed in to change notification settings - Fork 0
New issue
Have a question about this project? Sign up for a free GitHub account to open an issue and contact its maintainers and the community.
By clicking “Sign up for GitHub”, you agree to our terms of service and privacy statement. We’ll occasionally send you account related emails.
Already on GitHub? Sign in to your account
primary_infection_intensity
function is misleading
#71
Comments
The model assumes there is no inoculum source other than the existing lesions on chickpea plants. That is to say, it is ignorant of the fact inoculum could be produced on stubble. Correct me if I am wrong, but I think the original purpose of this model was to simulate from infected seed. The statement To respond to the point the number of lesions ( Given the above consideration, I don't think this issue is a "bug" but an "enhancement" request for a new feature. |
I am closing this as an issue as this is a request for a new feature to the model. |
NO. The purpose of the model was to simulate spread from infested stubble, as 100% control of seed borne infections can be achieved via chemical treatment. Disease spread from stubble under natural conditions. Art used two infected seedlings (artificially inoculated) as primary inoculum source and studied spread from those two seedlings. If you read the Art paper, he has then compared his simulation against spread from INFECTED SEEDLINGS via heatmaps and disease curves etc. Originally, we wanted to use seedlings too, but then Jenny Davidson and Kevin suggested to use stubble as there is no need of doing the hard work of artificially inoculating seedling when simply infested stubble could be used.
Currently, it's telling the model that the model can't have more lesions than SEEDING RATE, which is incorrect. They have no association what so over. If you want to change that, you could say there can't be more lesions than
Exactly. The difinition is saying conidia splash from primary foci (stubble), then cause primary infection. Intensity refers to how many lesions resulting from that primary spread.......that's what YOUR definition says (
Of course, growing points multiply when they're infected. When we're sick, we don't grow/age? Growing points multiplication stop multiplying when plant is dead-same as humans. This is basic plant pathology
Infested stubble mainly provides initial inoculum. For example, if there are 10 pycnidia containing 20 conidia. It will provide those 20 conidia over time (can't be specified exactly) until those 10 pycnidia/20 conidia are depleted. So the inoculum on stubble is not growing over time, it is depleting over time |
Firstly I just want to say, what the model understands and knows is not a precise reflection of reality. It is merely a construct that we are using to simulate the dynamics of the epidemic over a field. Let me clarify. If as you describe the stubble was supposed to simulate plants with infected growing points, there is no reason to change the model to add stubble as a parameter to do your simulation. We built the model based on this aim, that the primary foci were infected plant lesions, which you have substituted for standing stubble at the center foci, a replacement for hand infected plants. Feel free to update the description for the As I mentioned earlier if you wish to change the parameter name If you are saying the premise that sporulating growing points don't produce new growing points I suggest you open a new issue so this can be addressed separately. I was told when building the model, and the model has been written this way, infected growing points die at the point they become lesions ( |
Sorry, I meant the model needs to inform growers how many |
If it helps with the model development, please keep in mind that growers aren't going to be using this model in this format. It may be the basis for an app like PowderyMildewMBM or YellowSpotWM. Those interfaces are quite different. I would frame these functions as what would another scientist using this model need to see to easily understand them. |
Well, I switched to the And |
Just for reference, as you think about naming this function, the initial value of infective sites is referred to |
|
The value of This issue has been an ongoing debate for a while and perhaps it should be resolved by defining primary inoculum intensity with two parameters.
|
The only mandate of the project is to develop a model of the spatio-temporal spread of AB in a paddock. My suggestion here is to work with what we have and deliver that. We can add more complexity later. But if we can demonstrate the spread in space and time in the paddock, then we've met the project's milestone. So I don't see any good reason to incorporate more complexity at this point with stubble inoculum, etc. That's largely irrelevant as I see it. Infection happens on day "x" when you start running the model, it spreads from there in a pattern. That's what this model needs to do for us to consider it to be complete. The source of the initial inoculum is not considered here. That's fine. That's an assumption to be documented. We can always add more detail later if it is absolutely needed (i.e., funding supports it). |
Inoculum source is stubble already. No modification is required for this
From: "Adam H. Sparks" ***@***.***>
Reply to: IhsanKhaliq/ascotraceR ***@***.***>
Date: Monday, 8 November 2021 at 2:30 pm
To: IhsanKhaliq/ascotraceR ***@***.***>
Cc: Ihsan Khaliq ***@***.***>, State change ***@***.***>
Subject: Re: [IhsanKhaliq/ascotraceR] `primary_infection_intensity` function is misleading (#71)
The only mandate of the project is to develop a model of the spatio-temporal spread of AB in a paddock. My suggestion here is to work with what we have and deliver that. We can add more complexity later. But if we can demonstrate the spread in space and time in the paddock, then we've met the project's milestone.
So I don't see any good reason to incorporate more complexity at this point with stubble inoculum, etc. That's largely irrelevant as I see it. Infection happens on day "x" when you start running the model, it spreads from there in a pattern. That's what this model needs to do for us to consider it to be complete. The source of the initial inoculum is not considered here. That's fine. That's an assumption to be documented.
We can always add more detail later if it is absolutely needed (i.e., funding supports it).
—
You are receiving this because you modified the open/close state.
Reply to this email directly, view it on GitHub<#71 (comment)>, or unsubscribe<https://github.com/notifications/unsubscribe-auth/ANBRP5LED7WUQYEMXIDULALUK5G6NANCNFSM5AZAHKUQ>.
…__________________________________________________________________
This email (including any attached files) is confidential and is
for the intended recipient(s) only. If you received this email by
mistake, please, as a courtesy, tell the sender, then delete this
email.
The views and opinions are the originator's and do not necessarily
reflect those of the University of Southern Queensland. Although
all reasonable precautions were taken to ensure that this email
contained no viruses at the time it was sent we accept no
liability for any losses arising from its receipt.
The University of Southern Queensland is a registered provider
of education with the Australian Government.
(CRICOS Institution Code QLD 00244B / NSW 02225M, TEQSA PRV12081)
|
OK. I was going through my dashboard of open issues after lunch and responding to the open issues as I saw them... |
This has been changed to |
Ok time to address this can of worms. Because this model should simulate from infested stubble as discussed in #117 and #104, I will then add a new feature describing Stubble inoculum presumably behaves differently to plant inoculum and I will assume it decays over time, so I will also introduce another new parameter This will also make this model more distinct from Arts model which only assumes inoculum occurs from plant-based inoculum. |
Feel free to change others, but please don't do this. This is a pathological sin and will lead to straight rejection. Everything decays over time, not just stubble Stubble inoculum presumably behaves differently to plant inoculum and I will assume it decays over time, so I will also introduce another new parameter stubble_innoculum_decay which defines the rate at which the inoculum decays over time (note: this should probably be based on decay against time and rainfall, but that can be a future feature). |
Both are stubble and seedlings are the sources of infection, and are exactly the same. Primary Infection can only occur on the seedling we have grown in the field. But feel free to change the names if that makes you happy |
The name clearly is confusing and I don’t see an issue with what Paul proposed about stubble inoculum. We have other models that provide decay functions for sporulation. So there are no “sins” here. However, this is rather simple, IMO. The name needs to change and be clearly defined. |
Agreed. There will be no changes to how plants become infected, only how we are defining the source of inoculum ( |
HOW WOULD YOU INTRODUCE SPORE DECAY IN THIS MODEL, IF IT'S NOT A SIN? I'M CONFUSED BUT HAPPY TO BE GUIDED BY YOUR WISDOM |
@IhsanKhaliq, I stated it was possible but it would take more time and research. Not that we should do it for this model. There are other models that implement these sorts of factors but this one does not need it. Since it’s Saturday and I’m having ☕️, my wisdom for the day is take some time off and enjoy your weekend. |
What you're referring to is possible when you do disease forecasting for the next season. That is, when you put infested stubble out there and quantify spore dispersal at different times. Initially, more spore would disperse and decline towards the end of growing season because of the depletion of inoculum source. This is mainly done to identify possible sowing dates, as already done by DPIRD for some pathosystems. Here we're tying to determine the spatial and temporal spread patterns within season, so it's not applicable, as disease would increased with time due to increase in the number of infected seedlings, not decrease. I'm just that if the reviewer saw that seedling and inoculum have been treated differently and saw |
No. You clearly don’t know what I’m referring to or thinking of here. We do have models that predict decay in-season it is possible, but it is out of scope for this model as it sits right now.
Cheers!
… On 11 Dec 2021, at 09:11, IhsanKhaliq ***@***.***> wrote:
@IhsanKhaliq, I stated it was possible but it would take more time and research. Not that we should do it for this model. There are other models that implement these sorts of factors but this one does not need it.
Since it’s Saturday and I’m having ☕️, my wisdom for the day is take some time off and enjoy your weekend.
What you're referring to is possible when you do disease forecasting for the next season. That is, when you put infested stubble out there and quantify spore dispersal at different times. Initially, more spore would disperse and decline towards the end of growing season because of the depletion of inoculum source. This is mainly done to identify possible sowing dates, as already done by DPIRD for some pathosystems. Here we're tying to determine the spatial and temporal spread patterns within season, so it's not applicable, as disease would increased with time due to increase in the number of infected seedlings, not decrease. I'm just that if the reviewer saw that seedling and inoculum have been treated differently and saw stubble_inoculum_decay, he would reject the paper straight away
—
You are receiving this because you commented.
Reply to this email directly, view it on GitHub, or unsubscribe.
|
Was busy cleaning the house so did not get to this till now. The decay parameter is optional to use. So don't be too concerned. You don't have to use it but perhaps some people may want to define some sort of stubble decay as is common in other models. |
HOW DO YOU MEASURE THIS? 1 would indicate no stubble inoculum decay, 0.6 = 40% decay, 0.2 = 80% decay |
Available inoculum is measured in wind tunnels and/or microscopically by inspecting pycnidia / perithecia. The decay scale is a proportion, so you could postulate that each rainfall event 5% of the inoculum decays (or does not replenish conidia). Therefore you would use a value of |
I believe this issue has now been addressed with the addition of stubble inoculum variables created in #129 |
It's not applicable for this model. Since the value is 1, I am not bothered by it and closing the issue Lines 59 to 63 in e6092a4
|
This is the description of the function
The intensity of the starting epidemic as described by the number of number of sporulating growing points
.This is the function
if (primary_infection_intensity > seeding_rate) {
stop(
"primary_infection_intensity exceeds the number of starting growing points - 'seeding_rate': ",
seeding_rate
)
}
Reasons why it's invalid
The function is saying conidia splash from primary foci (stubble), then cause primary infection. Intensity refers to how many lesions resulting from that primary spread, so lesions can be greater than seeding rate
If I increase or decrease the value, it doesn't have much effect on the disease spread
The major problem is the way the model is interpreting it. It the value is 100, then the model can produce a total of 100 lesions over the duration of the experiment
It the value is 1000, then the model can produce a total of 1000 lesions over the duration of the experiment
The text was updated successfully, but these errors were encountered: