Designing my new gardens

calliandra

Well-Known Member
yeah she's still 1.60m tall, which is kind of a pain, me being 1.63 haha
Also, to my chagrin I just realized I need to regard this plant more like a landscape - I had been looking more at the parts near the door, but just now I saw something very disagreeable-looking spreading out from the left corner :shock: - small white spots spread out quite evenly across the leaf surfaces, making me think of sucky critters... I'm too tired today, so will look into that tomorrow. It's so frustrating, to know exactly what to do to remediate, but not have the means at hand to get it done!!
May brew up a compost tea anyway. On my last one, I managed to actually grow the fungi more than the bacteria for the very first time, leaving me with an end F:B mass ratio of 6:1, which is amazing, from a compost that was at 0.5 :mrgreen:
But I still have a ways to go, I wasn't happy with the overall populations and diversity - and that probably comes from the compost still being weak too. ACTs can only be as good as the compost they're made of, they can get populations to multiply and become very active, they can wake up some that were dormant, but it can't magick sets of microbes in that weren't there to begin with..
Better than nothing? Going to try and find out who the culprit is first ;)
Cheers!
 

ShLUbY

Well-Known Member
yeah she's still 1.60m tall, which is kind of a pain, me being 1.63 haha
Also, to my chagrin I just realized I need to regard this plant more like a landscape - I had been looking more at the parts near the door, but just now I saw something very disagreeable-looking spreading out from the left corner :shock: - small white spots spread out quite evenly across the leaf surfaces, making me think of sucky critters... I'm too tired today, so will look into that tomorrow. It's so frustrating, to know exactly what to do to remediate, but not have the means at hand to get it done!!
May brew up a compost tea anyway. On my last one, I managed to actually grow the fungi more than the bacteria for the very first time, leaving me with an end F:B mass ratio of 6:1, which is amazing, from a compost that was at 0.5 :mrgreen: But I still have a ways to go, I wasn't happy with the overall populations and diversity - and that probably comes from the compost still being weak too. ACTs can only be as good as the compost they're made of, they can get populations to multiply and become very active, they can wake up some that were dormant, but it can magick sets of microbes in that weren't there to begin with..
Better than nothing? Going to try and find out who the culprit is first ;)
Cheers!
what was your tea recipe? i been using inghams recipe on her site to brew fungal dom tea... but i dont have a scope so i never really know how effective the result of the brew is lol.
 

calliandra

Well-Known Member
Well in the course she only gives us recommendations to start experimenting with, there are so many factors that play into it she's making a point of NOT calling them recipes hehe
It was my first try with just kelp and humic acid - of questionable nature, it's actually called potassium humate in the ingredients part of the packaging (which I only saw post delivery), and has a pH of 9-11?! WTF? I asked Elaine about it, but that webinar had to be postponed (= the pine needle one haha), so still mystified :dunce:

In any case, I added 1 teaspoon of that humic whatever powder and one of kelp meal to 5L of water bubbled by a 400L airpump, and a bit later a cup of compost. I ended up adding another tsp of kelp later on as things were slow, that got things going, very lowlevel, but very fungal. oh and it was a very long brew too44 hrs or so haha
what have you been using?

I'm looking to change my brewer build, which is taking its time as I need to hunt out the parts.
But I already know I want to change a few things right away: add those 2 tsp klp from the get-go, maybe bubble the foods a bit longer first, and have the compost in a bag, to reduce the amounts that settle in the bucket corners, where I know anaerobic pockets must be, it's the spotty way ciliate-friendly colonies start appearing in samples, or finding them in surroundings that aren't anaerobic-looking at all. the actual solution will be having something without corners, in which the upstreaming air bubbles will create a torus-shaped current in the container. I'm thinking of those bell-shaped chicken feeders/waterers, drill a hole in top of dome, attach a valve, through which air can be blown in, as well as the tea let out of :bigjoint:
because, did you know that anaerobic bacteria can decimate fungal strands within 20 minutes? :oI'm pretty sure my past woes with my ACTs were due to microfilms accumulating, and allowing ever new waves of anaerobic assaults when given the chance haha

I also really feel like trying fish hydrolysate as a food - but want to look into how fermentation modifies the fresh stuff first, i have some doubts there and making fresh every time seems to be a tad overkill, especially in the amounts needed? 1 small sardine, please? lol

Haven't you dealt with fish hydrolysate too? any thoughts? :D
Cheers!
 

ShLUbY

Well-Known Member
Well in the course she only gives us recommendations to start experimenting with, there are so many factors that play into it she's making a point of NOT calling them recipes hehe
It was my first try with just kelp and humic acid - of questionable nature, it's actually called potassium humate in the ingredients part of the packaging (which I only saw post delivery), and has a pH of 9-11?! WTF? I asked Elaine about it, but that webinar had to be postponed (= the pine needle one haha), so still mystified :dunce:

In any case, I added 1 teaspoon of that humic whatever powder and one of kelp meal to 5L of water bubbled by a 400L airpump, and a bit later a cup of compost. I ended up adding another tsp of kelp later on as things were slow, that got things going, very lowlevel, but very fungal. oh and it was a very long brew too44 hrs or so haha
what have you been using?

I'm looking to change my brewer build, which is taking its time as I need to hunt out the parts.
But I already know I want to change a few things right away: add those 2 tsp klp from the get-go, maybe bubble the foods a bit longer first, and have the compost in a bag, to reduce the amounts that settle in the bucket corners, where I know anaerobic pockets must be, it's the spotty way ciliate-friendly colonies start appearing in samples, or finding them in surroundings that aren't anaerobic-looking at all. the actual solution will be having something without corners, in which the upstreaming air bubbles will create a torus-shaped current in the container. I'm thinking of those bell-shaped chicken feeders/waterers, drill a hole in top of dome, attach a valve, through which air can be blown in, as well as the tea let out of :bigjoint:
because, did you know that anaerobic bacteria can decimate fungal strands within 20 minutes? :oI'm pretty sure my past woes with my ACTs were due to microfilms accumulating, and allowing ever new waves of anaerobic assaults when given the chance haha

I also really feel like trying fish hydrolysate as a food - but want to look into how fermentation modifies the fresh stuff first, i have some doubts there and making fresh every time seems to be a tad overkill, especially in the amounts needed? 1 small sardine, please? lol

Haven't you dealt with fish hydrolysate too? any thoughts? :D
Cheers!
well my thoughts are worthless because i don't have a scope to look at anything lol. but yeah, the "instructions" on elaine's site suggest using humic acid, fish hydrolysate, kelp meal (or cannabis meal or both lol), and compost (which hopefully contains some fungus lol). I have brewed up said tea a few times... usually for 36-48ish hours. but have no ability to quantify the tea yet... i'm working on my lab tech at school to maybe get a microscope to "fall off the shelf" so to speak lol.

what magnification do you desire to be looking at the samples? will 400x suffice?
 

calliandra

Well-Known Member
No your thoughts aren't worthless, ever! Sometimes a tad chemical at the moment but that's logical, you're immersed! - and I know you'll survive it too :mrgreen:
MY issues begin on the ground floor, by not understanding what fermentation actually means - I think I need to stop jobseeking, which seems to be pointless anyway, and get myself back to Khan Academy lol :P

Yess 400x total magnification is enough, though sometimes I wish I had a bit more for detail, but as I understand it higher magnifications then require using the oil technique, and that is quite daunting if all I want is to get a better look... :mrgreen:
What is crucial is that the microscope have am iris diaphragm so you can shadow - otherwise you can't see most of the microbes.
I'm sure you'd have an easier time with the statistical assessment method though, I still really struggle to understand standard deviation and how to handle situations where the sample is unevenly spread out, and am becoming very aware of the potential fallacies! Yet another Khan lesson awaiting me haha

I just hooked up my digiscope and yup, I got da mites.:evil:
I'm so retarded! I just remembered I uppotted the NLH into a tomato pot that had been out on the deck, where all the tomatoes had gotten mites over the summer - what was I thinking! - though the particular plant was clean when I brought her inside...
But actually, it's kind of funny, last week I had this intuition to give her (and what turned out to be a pepper plant, no less inclined to generate aphids lol - removed from closet now preventatively) a foliar of neem juice, but then, not really seeing the point, changed my mind and watered it into my banana plant instead lmao
Gonna be a fun showering day here :rolleyes:
cheers :bigjoint:
 
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