Home | Community | Message Board


This site includes paid links. Please support our sponsors.


Welcome to the Shroomery Message Board! You are experiencing a small sample of what the site has to offer. Please login or register to post messages and view our exclusive members-only content. You'll gain access to additional forums, file attachments, board customizations, encrypted private messages, and much more!

Shop: Sporeworks.EU Spores for European Microscopy   Myyco.com APE Liquid Culture For Sale   North Spore Bulk Substrate   Original Sensible Seeds Bulk Cannabis Seeds   Mushroom-Hut Substrate Bags

Jump to first unread post Pages: < First | | 1350 | 1351 | 1352 | 1353 | 1354 | 1355 | 1356 | 1357 | 1358 | 1359 | 1360 | 1361 | 1362 | 1363 | 1364 | 1365 | 1366 | 1367 | 1368 | 1369 | 1370 | | Last >
Re: Ask Quick Questions, Get Quick Answers [Re: AskingAlexis]
    #28528516 -

Yup no doubt!

Extras: Filter Print Post Top
Re: Ask Quick Questions, Get Quick Answers [Re: Bigworm]
    #28528517 -

Bigworm said:
Yup no doubt!



the devil knows his own

Extras: Filter Print Post Top
Re: Ask Quick Questions, Get Quick Answers [Re: BeefExtreme] * 1
    #28528555 -

Best>Worst  -->  Red > Pink > Yellow = Orange

I'd take reds and pinks all day.

Extras: Filter Print Post Top
Re: Ask Quick Questions, Get Quick Answers [Re: Kinoko314]
    #28528577 -

Kinoko314 said:
Best>Worst  -->  Red > Pink > Yellow = Orange

I'd take reds and pinks all day.




Pinks are definitely without a doubt the best.

Extras: Filter Print Post Top
Re: Ask Quick Questions, Get Quick Answers [Re: AskingAlexis]
    #28528611 -

Quick question..

I came around some EZfelt so want to try upgrade some of my lids. But the store sells 3,  5 and 7 mm thick.

(Now I found out with gluing wattman filters to my lids ,that you can have too little GE for grain jars)

So I don't want to overdo it. Do you guys have any idea if 3 mm is thick enough?

Even in this original post thickness never gets mentioned.

https://www.shroomery.org/forums/showflat.php/Number/14488446/fpart/all/vc/1


--------------------
Cum grege non gradior






Edited by TheOffice (11/04/23 07:41 AM)

Extras: Filter Print Post Top
Re: Ask Quick Questions, Get Quick Answers [Re: TheOffice]
    #28528644 -

Ok, firstly, don’t judge me!

First time doing agar, and these are my first two dishes.




One was done with a swab, and the other with a hook scrape. (Yes, I gouged tf out of it, but like I said, literally my first time…)
Both were done Oct 23, so it’s been 12 days.

Now, the question(s): I think it’s time to transfer to new plates to further isolate from germs. In the two photos below, I made red circles to show which areas I think are viable for harvest for transfer, but I made smaller, blue circles for where I think it would be BEST to harvest.




And if I am correct, and those are viable and/or good options, when I put them on a new dish, do I just put the sample on top of the agar hand maybe lightly press it down)?

Thanks for any advice.

Extras: Filter Print Post Top
Re: Ask Quick Questions, Get Quick Answers *DELETED* [Re: RisnDevil]
    #28528648 -

Post deleted by ButtFace

Reason for deletion:

Extras: Filter Print Post Top
Re: Ask Quick Questions, Get Quick Answers [Re: RisnDevil]
    #28528658 -

RisnDevil said:
Ok, firstly, don’t judge me!

First time doing agar, and these are my first two dishes.




One was done with a swab, and the other with a hook scrape. (Yes, I gouged tf out of it, but like I said, literally my first time…)
Both were done Oct 23, so it’s been 12 days.

Now, the question(s): I think it’s time to transfer to new plates to further isolate from germs. In the two photos below, I made red circles to show which areas I think are viable for harvest for transfer, but I made smaller, blue circles for where I think it would be BEST to harvest.




And if I am correct, and those are viable and/or good options, when I put them on a new dish, do I just put the sample on top of the agar hand maybe lightly press it down)?

Thanks for any advice.



Looking at your plates, i think it will be pretty hard to transfer away from the bacteria . Maybe it is possible but because your plates are so contaminated I doubt your sterile technique is good enough to manage that (not judging, I understand how hard it is at first)

IMO you probably would be better off starting with a new streak of spores and judge where you can be lacking in sterile technique.

If you do want to take a sample from these plates , don't take it from the blue circles but from the outer edge from the red circle. (As far away from the bacteria as possible)
Just gently put it on a new plate, don't need to press it down.

Good luck


--------------------
Cum grege non gradior






Extras: Filter Print Post Top
Re: Ask Quick Questions, Get Quick Answers [Re: ButtFace]
    #28528662 -

ButtFace said:
Will this work to fruit these three shoeboxes in a 66 qt Sterlite tub or should I remove one of them?






I think they will be fine..

Maybe surface conditions won't be optimal because of the placements of the holes. Maybe you could tape them up completely and just use it as an unmodified tub. But I would like to hear from someone with more experience with monotubs.

If you still got the lids from the shoeboxes they will fruit fine just on their own with their lids on.


--------------------
Cum grege non gradior






Extras: Filter Print Post Top
Re: Ask Quick Questions, Get Quick Answers [Re: TheOffice]
    #28528670 -

Oh, I absolutely know it will take multiple transfers (I attempted to sterilize a ghetto hook and used a clean swab, so while I made some effort, I’m in no rush and would rather do multiple transfers to isolate, which I will now do with proper flame-and-alcohol sterilized tools in a still air box), but having never done this I was more verifying if those areas would continue to grow. I don’t know fully what I’m looking for/at to determine that.

I was looking at the growth and since I see clear “hair”/“fibers”, I thought it would be good for transfer. Is that what I should continue to look for? Is it more important to transfer a specific or larger size sample (even if it may be contaminated and have to be isolated again), or is a clean sample (almost no matter how small) more important when transferring?

Extras: Filter Print Post Top
Re: Ask Quick Questions, Get Quick Answers [Re: RisnDevil]
    #28528679 -

Thanks to those who answered

Extras: Filter Print Post Top
Re: Ask Quick Questions, Get Quick Answers [Re: Zav3r]
    #28528687 -

After cleaning water heater i have a lot of limescale. Should be good for adding in casing? I can dry it in oven and crush it.
Or should not be used because of chlorine and other things in water? Not correct type of limescale?

Extras: Filter Print Post Top
Re: Ask Quick Questions, Get Quick Answers [Re: r0kovski] * 2
    #28528723 -

Just stop making things more difficult than they need to be 😜


--------------------
🅃 🄴 🄰 🄼    🄲 🄻 🄸 🄽 🄶 🅆 🅁 🄰 🄿


Help US help YOU TEK

2023 Dehydrator TEK

Extras: Filter Print Post Top
Re: Ask Quick Questions, Get Quick Answers [Re: Screwup]
    #28528741 -

Are these what I think they are? I mixed up this ape shoebox on the 13th and cut half of it out due to some trick back on Monday.


Extras: Filter Print Post Top
Re: Ask Quick Questions, Get Quick Answers [Re: shakology]
    #28528742 -

Yep yep


--------------------
CV+

Extras: Filter Print Post Top
Re: Ask Quick Questions, Get Quick Answers [Re: RisnDevil]
    #28528769 -

RisnDevil said:
Oh, I absolutely know it will take multiple transfers (I attempted to sterilize a ghetto hook and used a clean swab, so while I made some effort, I’m in no rush and would rather do multiple transfers to isolate, which I will now do with proper flame-and-alcohol sterilized tools in a still air box), but having never done this I was more verifying if those areas would continue to grow. I don’t know fully what I’m looking for/at to determine that.

I was looking at the growth and since I see clear “hair”/“fibers”, I thought it would be good for transfer. Is that what I should continue to look for? Is it more important to transfer a specific or larger size sample (even if it may be contaminated and have to be isolated again), or is a clean sample (almost no matter how small) more important when transferring?





The latter., you want a sample as small as possible (can't hardly be small enough, as long as you can handle it with your scalpel) (grain of rice size)

Do you have a scalpel?

And yes you are looking for white mycelium as far away as possible from the contaminated areas.

Good luck!


--------------------
Cum grege non gradior






Edited by TheOffice (11/04/23 11:14 AM)

Extras: Filter Print Post Top
Re: Ask Quick Questions, Get Quick Answers [Re: TheOffice]
    #28528785 -

QQ: How long can I leave plain nutrient broth sitting around after PCing?


--------------------
🅃 🄴 🄰 🄼    🄲 🄻 🄸 🄽 🄶 🅆 🅁 🄰 🄿

Extras: Filter Print Post Top
Re: Ask Quick Questions, Get Quick Answers [Re: TheOffice]
    #28528790 -

you got the right idea bud.  ill be impressed if you can pull this off.  you gonna need a scalpel.

Extras: Filter Print Post Top
Re: Ask Quick Questions, Get Quick Answers [Re: BeefExtreme] * 2
    #28528802 -

Pnin said:
QQ: How long can I leave plain nutrient broth sitting around after PCing?




Sealed up? Long ass time. Like it should have the shelf life of canned goods now.


--------------------
A Love Letter to New Growers
The 7 Edicts of Mushroom Cultivation as Decreed by Smellyhobbit

:kodama:


Anyone can get a canopy. But can you get what you want?

Extras: Filter Print Post Top
Re: Ask Quick Questions, Get Quick Answers [Re: RisnDevil]
    #28528963 -

RisnDevil said:
Oh, I absolutely know it will take multiple transfers (I attempted to sterilize a ghetto hook and used a clean swab, so while I made some effort, I’m in no rush and would rather do multiple transfers to isolate, which I will now do with proper flame-and-alcohol sterilized tools in a still air box), but having never done this I was more verifying if those areas would continue to grow. I don’t know fully what I’m looking for/at to determine that.

I was looking at the growth and since I see clear “hair”/“fibers”, I thought it would be good for transfer. Is that what I should continue to look for? Is it more important to transfer a specific or larger size sample (even if it may be contaminated and have to be isolated again), or is a clean sample (almost no matter how small) more important when transferring?



It's hard to say the mycelium there is definitely cube myc. Could very well be mold.


--------------------
"Remember, kids, the difference between science and screwing around is writing it down" -adam savage
Flowchart for Recommended plan of action.
Learn the tried and true way to grow mushrooms
Use the Damn search engine
After you know what you're doing, take a break 
Pick a book, Make some chips!
Josex said:Don't take the site seriously bro, ain't worth it.
 

Extras: Filter Print Post Top
Jump to top Pages: < First | | 1350 | 1351 | 1352 | 1353 | 1354 | 1355 | 1356 | 1357 | 1358 | 1359 | 1360 | 1361 | 1362 | 1363 | 1364 | 1365 | 1366 | 1367 | 1368 | 1369 | 1370 | | Last >

Shop: Sporeworks.EU Spores for European Microscopy   Myyco.com APE Liquid Culture For Sale   North Spore Bulk Substrate   Original Sensible Seeds Bulk Cannabis Seeds   Mushroom-Hut Substrate Bags


Similar ThreadsPosterViewsRepliesLast post
* quick question, finished colonizing? usefulidiot 1,863 1 04/06/03 06:31 PM
by kindkesey
* Quick Question grateful_head 1,242 2 08/18/01 03:40 PM
by Billyblastoff
* New to the boards, and a quick question to start ! Anonymous 1,848 4 03/11/02 03:18 AM
by 2shrewmen
* some quick questions about my treasure coasts alf 3,860 19 11/16/01 01:54 AM
by Anonymous
* Quick Question needs quick answer Wheedhead! 1,188 2 01/19/03 09:06 AM
by Wheedhead!
* quick question SuppaFly 1,046 1 09/18/02 04:41 PM
by mickey_rourke
* Re: Quick Question
( 1 2 all )
Anonymous 4,554 22 06/14/00 05:46 AM
by hitterg
* Quick Question LXTC 1,811 11 09/24/02 10:09 PM
by LXTC

Extra information
You cannot start new topics / You cannot reply to topics
HTML is disabled / BBCode is enabled
Moderator: DERRAYLD, Shroomism, george castanza, RogerRabbit, veggie, mushboy, fahtster, the_chosen_one, LogicaL Chaos, 13shrooms, hamloaf, cronicr, Stipe-n Cap, Pastywhyte, bodhisatta, Tormato, Land Trout, A.k.a
1,188,059 topic views. 11 members, 310 guests and 202 web crawlers are browsing this forum.
[ Show Images Only | Sort by Score | Print Topic ]
Search this thread:

Copyright 1997-2026 Mind Media. Some rights reserved.

Generated in 0.044 seconds spending 0.024 seconds on 16 queries.