The Grow Awards 2026 🏆

Clone race

7
2
47
5d ago
Mix
TERRÔ SUPER SOIL
Indoor
Room Type
Transplantation
weeks 1
ScrOG
weeks 1-3
LST
weeks 1, 3
12-12
weeks 3
Defoliation
weeks 3
7 liters
Pot Size
0.7 liters
Watering
Start at 3 Week
1
Week 1. Vegetation
14d ago
18 hrs
Light Schedule
27 °C
Day Air Temp
6.9
pH
Weak
Smell
65 %
Air Humidity
20 °C
Night Air Temp
7 liters
Pot Size
55 cm
Lamp Distance
THEFROZEN710 Happy to finish one cycle and start a new one, that's the good news. The bad news is that I didn't write down any of the clones I took, but I've already seen that most are Bakers, maybe there's a Pure Glitter one, hopefully! The reason for not identifying them is that they were in a place not conducive to rooting because the humidifier broke and on very hot days, an improvised lamp was used. I actually doubted that any would survive, but here we are. I will notify you if I manage to determine if any others are different genetics, but I remember the smell of the veg of this Bakers as if it were yesterday. Transplanted into 7-liter pots and I added 15g of bokashi to each soil level, watering with about 1L in order to leach some microorganisms that I inserted and some beneficial bacteria for roots and prevention of gnat proliferation, Trichoderma Harzianum for roots and Bacillus Turingensis Israelis for mosquito larvae.
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Used techniques
LST
Technique
ScrOG
Technique
Transplantation
Technique
2
Week 2. Vegetation
14d ago
18 hrs
Light Schedule
27 °C
Day Air Temp
6.9
pH
Weak
Smell
65 %
Air Humidity
20 °C
Night Air Temp
7 liters
Pot Size
55 cm
Lamp Distance
THEFROZEN710 End of the second week and everything seems to be going very well, the plants have started to smell good, most of the ones that had strange leaves have already started to show new leaves with a healthy green color, in addition to the weekly application of Harzianum and daily application of BTi, I added 100ppm of NitCal and 40ppm of Mg via Epsom salt, I added more biostimulants for veg and flor, I believe I will flip these plants by next week, all in a very good flowering rhythm, only one is a little behind, maybe I will remove it to avoid the risk of hermaphroditism.
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2 comments
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Used techniques
ScrOG
Technique
3
Week 3. Flowering
5d ago
30 cm
Height
18 hrs
Light Schedule
29 °C
Day Air Temp
6.3
pH
Normal
Smell
55 %
Air Humidity
22 °C
Night Air Temp
7 liters
Pot Size
0.7 liters
Watering Volume
55 cm
Lamp Distance
Nutrients 5
Bokashi
15 mll
NitCal Prime
0.026 mll
MKP
0.1 mll
THEFROZEN710 I performed a runoff test on the pots to check the nutrient release from the soil; all showed an average of 500 ppm and a pH of 6.3, understandable given the organomineral growing method. All plants appear very healthy and fragrant. I defoliated them on the third day of flowering to allow more light to reach the buds I want to penetrate the SCROG screen. On day 6, I did a light lollipoping to remove some clones and a few leaves to continue stretching branches upwards over the screen. I don't like to be invasive and try to remove only a few branches from those that aren't developing and only a few leaves from a single plant to avoid hindering the stretch. All plants responded positively to the management, with no apparent stress. They received a concentrated dose of BTi and Trichoderma, BTi for the gnat larvae and Trichoderma to preserve the roots, and this week a higher dose to aid in phosphorus absorption in the roots, 60ppm of NitCal and 0.5g in 5L of MKP totaling 120ppm. With all this addition, the water pH dropped to 5.7. I mixed 25g in 5L of a veg biostimulant, which is rich in fermented fish, algae, and amino acids, to raise the water pH, which rose to 6.6. The biostimulant will aid in stretching. Some plants showed slight chlorosis due to a possible lack of nitrogen, understandable since they are drawing all the nutrients from the leaves to grow upwards while the soil is releasing them more slowly than they consume, hence the conservative doses. See you next week.
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Used techniques
12-12
Technique
Defoliation
Technique
ScrOG
Technique
LST
Technique

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