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Re: AGAR ENVY! (Anything and All things agar!) [Re: footpath]
    #26508125 -

footpath said:
Yeah. And to keep them away from cats and hamsters.



:congrats:

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Re: AGAR ENVY! (Anything and All things agar!) [Re: footpath]
    #26508129 -

footpath said:
Yeah. And to keep them away from cats and hamsters.



So footpath, I think I put myself in a bad spot recently. I suspected that the strain I was using had a hidden intermeshed contam, so I started over with a few spore prints.

I grabbed a chunk of spores off of a print... and put them on agar plates that I now realize had a 3 to one sugar to agar recipe (pre-made MEA) The growth hit the top of the petri plates.

Its the same agar I've been using for years. I'm concerned that too high of nutes in agar might actually have caused problems.

Mixing my own agar now, just trying to understand my past mistakes.


--------------------
--------------------
Deep pour soft agar plates-->bags of WBS-->Low Profile Monos
Clean spawn thread | Put a thermometer on your PC

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Re: AGAR ENVY! (Anything and All things agar!) [Re: tedoro]
    #26508141 -

As I understand it and have experienced:

Higher nutrient contents encourage tomentose (fluffy) growth.
Lower nutrient contents encourage rhizomorphic (ropy) growth.

I usually shoot for no more than 50/50 - 20g agar / 20g LME / 1L H2O.
My normal recipe is 20g agar / 14g LME / 1L H2O. It usually gets me rhizomorphic growth that doesn't race to the edge of the plate before I can catch it (I'll have a couple days sometimes where I don't get the chance to look at my cultivation stuff)

There are other factors that will cause different styles of growth, too - contaminants, environment, etc. But, in normal conditions, I've noticed the nutrient content to be the most impactful.

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Re: AGAR ENVY! (Anything and All things agar!) [Re: footpath]
    #26508168 -

footpath said:
As I understand it and have experienced:

Higher nutrient contents encourage tomentose (fluffy) growth.
Lower nutrient contents encourage rhizomorphic (ropy) growth.

I usually shoot for no more than 50/50 - 20g agar / 20g LME / 1L H2O.
My normal recipe is 20g agar / 14g LME / 1L H2O. It usually gets me rhizomorphic growth that doesn't race to the edge of the plate before I can catch it (I'll have a couple days sometimes where I don't get the chance to look at my cultivation stuff)

There are other factors that will cause different styles of growth, too - contaminants, environment, etc. But, in normal conditions, I've noticed the nutrient content to be the most impactful.



I'm putting all of this into my pipe and smoking it.

I've come to believe (only from reading) that, in order of priority:

ropey fast growth stimulated by:

1) low nute agar plates
2) shallow poured plates
3) stiffer pucks (less water)

But my ponderings currently are... I wonder if my huge initial spore drop, and way too much sugar creates a perfect situation for contams to intermesh with the mycelia.


--------------------
--------------------
Deep pour soft agar plates-->bags of WBS-->Low Profile Monos
Clean spawn thread | Put a thermometer on your PC

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Re: AGAR ENVY! (Anything and All things agar!) [Re: tedoro]
    #26508169 -

like if you put too many dogs and cats and hamsters in too small of a room they start intermating.


--------------------
--------------------
Deep pour soft agar plates-->bags of WBS-->Low Profile Monos
Clean spawn thread | Put a thermometer on your PC

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Re: AGAR ENVY! (Anything and All things agar!) [Re: tedoro]
    #26508180 -

It's definitely possible. They won't mate, of course. But they will latch on to your culture and cause problems any time they get their opportunity.
I used to just put one drop on the middle of the plate and that worked totally fine for me until recently. Had to separate my cultures from some obvious contamination, but it was fairly easy to pick it out.
It's not terribly efficient to try to isolate from spores - agar anyhow. Unless you do what's known as a serial dilution - essentially just putting a small amount of spores into a lot of sterile water and swabbing a small amount onto a plate.
I'd put more effort into just finding a good clone.

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Re: AGAR ENVY! (Anything and All things agar!) [Re: footpath]
    #26508191 -

Yah... seems that cloning is them move.

I was wrong headed thinking I could get some fruits from some MS that had been transferred 3 times on agar.... put to grains (18 tubs) and the damn things didn't fruit... didn't mold either... just sat there. They are finally molding.... 5 weeks in.

Many thanks for these explanations... I ignored good agar, isolation technique cause I made a clone I liked years ago... but it started to not work.


--------------------
--------------------
Deep pour soft agar plates-->bags of WBS-->Low Profile Monos
Clean spawn thread | Put a thermometer on your PC

Extras: Filter Print Post Top
Re: AGAR ENVY! (Anything and All things agar!) [Re: tedoro]
    #26508197 -

tedoro said:
footpath said:
As I understand it and have experienced:

Higher nutrient contents encourage tomentose (fluffy) growth.
Lower nutrient contents encourage rhizomorphic (ropy) growth.

I usually shoot for no more than 50/50 - 20g agar / 20g LME / 1L H2O.
My normal recipe is 20g agar / 14g LME / 1L H2O. It usually gets me rhizomorphic growth that doesn't race to the edge of the plate before I can catch it (I'll have a couple days sometimes where I don't get the chance to look at my cultivation stuff)

There are other factors that will cause different styles of growth, too - contaminants, environment, etc. But, in normal conditions, I've noticed the nutrient content to be the most impactful.



I'm putting all of this into my pipe and smoking it.

I've come to believe (only from reading) that, in order of priority:

ropey fast growth stimulated by:

1) low nute agar plates
2) shallow poured plates
3) stiffer pucks (less water)

But my ponderings currently are... I wonder if my huge initial spore drop, and way too much sugar creates a perfect situation for contams to intermesh with the mycelia.



interesting , haven't heard of the depth of the poured agar being influential ; nor the stiffer gel ,

might just have to try it ;  my last batch was 20 gs agaras , 8 gs LME , 1 liter h2o , aiming for the ropey growth ,


--------------------
...and when you loose control ; you'll reap the harvest you have sown.

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Re: AGAR ENVY! (Anything and All things agar!) [Re: footpath]
    #26508315 -

footpath said:
It's definitely possible. They won't mate, of course. But they will latch on to your culture and cause problems any time they get their opportunity.
I used to just put one drop on the middle of the plate and that worked totally fine for me until recently. Had to separate my cultures from some obvious contamination, but it was fairly easy to pick it out.
It's not terribly efficient to try to isolate from spores - agar anyhow. Unless you do what's known as a serial dilution - essentially just putting a small amount of spores into a lot of sterile water and swabbing a small amount onto a plate.
I'd put more effort into just finding a good clone.



Ok so many vectors here. Just a noob here trying to prioritize different approaches.
So:
1. Serial dilution, c10 mentioned that and his streaking pattern seems to get there.
2. But what I find contradicting
Quote:
Clone the best fruit from each jar, and then test all of these against each other, separately, under the environment you will be growing them under. This will solve all of the PROBLEMS associated with false matings between partially compatible, but non fruiting, matings!!! -RR




So, it just seems like, just grow something, clone from a nice medium-sized cluster, eat it, and then you know if it's worthy. :hatsoff:


--------------------
:sporedrop: GLOSSARY  :sporedrop: ACROMYMS!   :sporedrop: GETTING STARTED :sporedrop:

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Re: AGAR ENVY! (Anything and All things agar!) [Re: Inthepit]
    #26508321 -

I'm also finding the standard 2% is too nutritious for my current strains... I'm about 200 plates in on 5 different varieties and so far have only had a handful of good looking rhizo growth... everything else still grows -tomentose and slow- but they all fruit and function.

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Re: AGAR ENVY! (Anything and All things agar!) [Re: Inthepit]
    #26508346 -

I like the 20g agar 14g ME 1l h2o recipe too

Inthepit said:
footpath said:
It's definitely possible. They won't mate, of course. But they will latch on to your culture and cause problems any time they get their opportunity.
I used to just put one drop on the middle of the plate and that worked totally fine for me until recently. Had to separate my cultures from some obvious contamination, but it was fairly easy to pick it out.
It's not terribly efficient to try to isolate from spores - agar anyhow. Unless you do what's known as a serial dilution - essentially just putting a small amount of spores into a lot of sterile water and swabbing a small amount onto a plate.
I'd put more effort into just finding a good clone.



Ok so many vectors here. Just a noob here trying to prioritize different approaches.
So:
1. Serial dilution, c10 mentioned that and his streaking pattern seems to get there.
2. But what I find contradicting
Quote:
Clone the best fruit from each jar, and then test all of these against each other, separately, under the environment you will be growing them under. This will solve all of the PROBLEMS associated with false matings between partially compatible, but non fruiting, matings!!! -RR




So, it just seems like, just grow something, clone from a nice medium-sized cluster, eat it, and then you know if it's worthy. :hatsoff:



Where is the contradiction?

Growing from clones is usually the best route for newbies

I wouldnt worry about isolates at this point. But still, if you start from spores, streaking gives you lots of benefits. Gives you more to choose from and more organized growth

You could start with spores,  streak a plate, transfer a few colonies, grow out the t1 plates , transfer a healthy sector from as many as you like, repeat this process as many times as you want, till you get organized growth. Then make a LI or a2g to make some jars (or a grain master to g2g) , grow those out and fruit them, then clone the best looking fruits/clusters, and keep notes on potency


--------------------

C10's Agar Guide + Tips and Tricks | c10's Flow Hood Build Guide


"Partial knowledge is more triumphant than complete knowledge; it takes things to be simpler than they are, and so makes its theory more popular and convincing."

"Convictions are more dangerous enemies of truth than lies"
― Friedrich Nietzsche

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Re: AGAR ENVY! (Anything and All things agar!) [Re: c10h12n2o]
    #26508525 -

Quote:
I wouldnt worry about isolates at this point. But still, if you start from spores, streaking gives you lots of benefits. Gives you more to choose from and more organized growth

You could start with spores,  streak a plate, transfer a few colonies, grow out the t1 plates , transfer a healthy sector from as many as you like, repeat this process as many times as you want, till you get organized growth. Then make a LI or a2g to make some jars (or a grain master to g2g) , grow those out and fruit them, then clone the best looking fruits/clusters, and keep notes on potency



Woof what he said...

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Re: AGAR ENVY! (Anything and All things agar!) [Re: Inthepit]
    #26509300 -

What about using diluted coffee and agar for plates? I want to experiment with a higher nutrient source for plates to get some old spores to germinate. I'm sure someone has used 250ml coffee 250ml water to 14grams agar. Any thoughts? Should I use a pH buffer as well?

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Re: AGAR ENVY! (Anything and All things agar!) [Re: Sockadin]
    #26509959 -

There's ready made plates on the market. Agar kimmig. It holds a lot of nutes. I think like 14 percent

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Re: AGAR ENVY! (Anything and All things agar!) [Re: Tweeq]
    #26510067 -

Is this bacterial?


transferred from this last night

Edited by ichugwindex (02/29/20 05:10 PM)

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Re: AGAR ENVY! (Anything and All things agar!) [Re: ichugwindex]
    #26510089 -

ichugwindex said:
Is this bacterial?


transferred from this last night



It looks nice to this noob, but which mushroom culture are we looking at?

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Re: AGAR ENVY! (Anything and All things agar!) [Re: ichugwindex]
    #26510093 -

lol idk but that’s one of the more interesting plates I’ve seen, instead of rings it has spokes.

Doesn’t look very healthy but I’m curious how the transfer does.


--------------------
LAGM2020

Edited by A.k.a (02/29/20 05:23 PM)

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Re: AGAR ENVY! (Anything and All things agar!) [Re: A.k.a]
    #26510157 -

I vote bacterial


--------------------

C10's Agar Guide + Tips and Tricks | c10's Flow Hood Build Guide


"Partial knowledge is more triumphant than complete knowledge; it takes things to be simpler than they are, and so makes its theory more popular and convincing."

"Convictions are more dangerous enemies of truth than lies"
― Friedrich Nietzsche

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Re: AGAR ENVY! (Anything and All things agar!) [Re: c10h12n2o]
    #26510205 -

It's supposed to be PE6. Hopefully transfers look better... trying to clean up these spores has been hard this will be my 4th attempt at taking the spores to agar and trying to get something clean


--------------------
Only hope can give rise to the emotion we call despair. But it is nearly impossible for a man to try to live without hope, so I guess that leaves Man no choice but to walk around with despair as his companion.

Edited by ichugwindex (02/29/20 06:47 PM)

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Re: AGAR ENVY! (Anything and All things agar!) [Re: ichugwindex]
    #26510260 -

Well don't know about the plate, but I went ahead and made some coffee Agar plates. They thickened nicely. Will post pictures once I get germination.

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Shop: Mushroom-Hut Substrate Bags   Sporeworks.EU Spores for European Microscopy   Myyco.com Isolated Cubensis Liquid Culture For Sale   Original Sensible Seeds Bulk Cannabis Seeds   North Spore Injection Grain Bag   MagicBag.co All-In-One Bags That Don't Suck   Unfolding Nature Unfolding Nature: Being in the Implicate Order


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