These girls seem to love abuse.. on a side note, one plant is throwing dense little nugs on fan leaves (video). Loving the smell in the tent😁

(Have been thinking about it, decided to just do both runts under one diary and just using the Green Sensation on them both. Had only used growdots on the other one, but will be bringing the other runtz into this diary aswell) Beginning to add the Green Sensation nutrients this week. Really curious to see how she looks in the next 2 weeks now that its being added!. But these Runtz are growing well, looks great to me so far nothing crazy , bit different pheno then my other grow but I'm happy with both .. Can't wait to see how they flower fully. Not much else was done, I do regret not training but wanted to let it do its thing , didn't have the space for anything big (I never go for massive, one of these days I'll veg longer tho just for the experience of it) Had cut off a handful of leaves that were laying on each other. Did alil form of lollipoping but not extreme. And only plan besides Green Bay is the Recharge will also be used 1x weekly. Lights are currently around 32 DLI roughly 700/750ppfd off the top of my head. I'm thinking around 40 I may push to peak but we will see, no added CO2 besides environmental atleast its above 500 pretty steady raises to 8/900 amd alil higher when I'm in talkin shit to them. The water input is picking up in frequency aswell. Watering every other day still due to how cold it is they are drinking slow but their just about 3/4s of a gallon currently.. Temps have been way lower this run then I really wanted just last heater I had decides to quit on me.. big area so tough to replace that thing and of course it was just out of warranty lol by 2 months. The one is getting some purples on it this one's pretty light green , ec is in range after a quick lil media test, had been curious if she was hungry so decide to check did alil runoff when watered prior to feeding the plagron. Ec was fine and PH was alil low so bringing that up as I feed. Besides that tho , their smelling really sweet.. literally like a pack of runtz already ...anxious to get to smoke some of my first try at a runtz plant! As always I appreciate everyone's time checking these things out.. thanks for your support and encouragement. And another big thank you to Zamnesia and Plagron for throwing this together!! Been a fun contest so far.. Beans: https://www.zamnesia.com/uk/ https://www.zamnesia.com/us/

12/08/24 beautiful plant. buds are like mountainous structures. cant wait for harvest with this one. in the home stretch. 12/14 getting chunky. may need support

Fastbuds Frostbanger 75days from seed

67

No feed this week, due to the high nutrient level in runoff. Watered 2x this week with 5.8 ph water. Runoff was 6.9 ph and 1200ppm

Week 8 has gone well and she is chugging along. She is still putting out new pistils with some turning orange. Calyx's are growing longer and buds are still soft. I'm thinking a min of 10 weeks flowering for her. I removed some leaves on inner canopy to bring some air and light deeper. She is so bushy its hard to even defoliate maybe next time i will remove some more lateral branches... afterremoving the leaves I must have come incontact with a pollen sack as where I defoliated all seemed to be polinated over night and are making seeds :( I will cut my losses and harvest while seeds are still small.

This week my leaves have started yellowing and claw footing. Not sure what is gonna on... Any help?

She stopped growing up, but she's still producing new leaves and her flowers keep getting bigger. I think I'm probably gonna get about 10 grams. I'm really worried though, because her lowest leaves are turning yellow and shows burn signs. I thought it was because of the hot weather, but her leaves should have been all bent down (this is what I read on the internet). Since the plant is overall healthy, I guess it might be just normal. Anyway, I found out that it also might be caused by a potassium deficiency, so I'll try and give her some. All been said, I'm still really happy with the results and I love her

ANTHOCYANIN production is primarily controlled by the Cryptochrome (CR1) Photoreceptor ( !! UV and Blue Spectrums are primary drivers in the production of the pigment that replaces chlorophyll, isn't that awesome! 1. Diverse photoreceptors in plants Many civilizations, including the sun god of ancient Egypt, thought that the blessings of sunlight were the source of life. In fact, the survival of all life, including humans, is supported by the photosynthesis of plants that capture solar energy. Plants that perform photosynthesis have no means of transportation except for some algae. Therefore, it is necessary to monitor various changes in the external environment and respond appropriately to the place to survive. Among various environmental information, light is especially important information for plants that perform photosynthesis. In the process of evolution, plants acquired phytochrome, which mainly receives light in the red light region, and multiple blue light receptors, including his hytropin and phototropin, in order to sense the light environment. .. In addition to these, an ultraviolet light receptor named UVR8 was recently discovered. The latest image of the molecular structure and function of these various plant photoreceptors (Fig. 1), focusing on phytochrome and phototropin. Figure 1 Ultraviolet-visible absorption spectra of phytochrome, cryptochrome, phototropin, and UVR8. The dashed line represents each bioactive absorption spectrum. 2. Phytochrome; red-far red photoreversible molecular switch What is phytochrome? Phytochrome is a photochromic photoreceptor, and has two absorption types, a red light absorption type Pr (absorption maximum wavelength of about 665 nm) and a far-red light absorption type Pfr (730 nm). Reversible light conversion between the two by red light and far-red light, respectively(Fig. 1A, solid line and broken line). In general, Pfr is the active form that causes a physiological response. With some exceptions, phytochrome can be said to function as a photoreversible molecular switch. The background of the discovery is as follows. There are some types of plants that require light for germination (light seed germination). From that study, it was found that germination was induced by red light, the effect was inhibited by subsequent far-red light irradiation, and this could be repeated, and the existence of photoreceptors that reversibly photoconvert was predicted. In 1959, its existence was confirmed by the absorption spectrum measurement of the yellow sprout tissue, and it was named phytochrome. Why does the plant have a sensor to distinguish between such red light and far-red light? There is no big difference between the red and far-red light regions in the open-field spectrum of sunlight, but the proportion of red light is greatly reduced due to the absorption of chloroplasts in the shade of plants. Similar changes in light quality occur in the evening sunlight. Plants perceive this difference in light quality as the ratio of Pr and Pfr, recognize the light environment, and respond to it. Subsequent studies have revealed that it is responsible for various photomorphogenic reactions such as photoperiodic flowering induction, shade repellent, and deyellowing (greening). Furthermore, with the introduction of the model plant Arabidopsis thaliana (At) and the development of molecular biological analysis methods, research has progressed dramatically, and his five types of phytochromes (phyA-E) are present in Arabidopsis thaliana. all right. With the progress of the genome project, Fi’s tochrome-like photoreceptors were found in cyanobacteria, a photosynthetic prokaryotes other than plants. Furthermore, in non-photosynthetic bacteria, a homologue molecule called bacteriophytochrome photoreceptor (BphP) was found in Pseudomonas aeruginosa (Pa) and radiation-resistant bacteria (Deinococcus radiodurans, Dr). Domain structure of phytochrome molecule Phytochrome molecule can be roughly divided into N-terminal side and C-terminal side region. PAS (Per / Arndt / Sim: blue), GAF (cGMP phosphodiesterase / adenylyl cyclase / FhlA: green), PHY (phyto-chrome: purple) 3 in the N-terminal region of plant phytochrome (Fig. 2A) There are two domains and an N-terminal extension region (NTE: dark blue), and phytochromobilin (PΦB), which is one of the ring-opening tetrapyrroles, is thioether-bonded to the system stored in GAF as a chromophore. ing. PAS is a domain involved in the interaction between signal transduction-related proteins, and PHY is a phytochrome-specific domain. There are two PASs and her histidine kinase-related (HKR) domain (red) in the C-terminal region, but the histidine essential for kinase activity is not conserved. 3. Phototropin; photosynthetic efficiency optimized blue light receptor What is phototropin? Charles Darwin, who is famous for his theory of evolution, wrote in his book “The power of move-ment in plants” published in 1882 that plants bend toward blue light. Approximately 100 years later, the protein nph1 (nonphoto-tropic hypocotyl 1) encoded by one of the causative genes of Arabidopsis mutants causing phototropic abnormalities was identified as a blue photoreceptor. Later, another isotype npl1 was found and renamed phototropin 1 (phot1) and 2 (phot2), respectively. In addition to phototropism, phototropin is damaged by chloroplast photolocalization (chloroplasts move through the epidermal cells of the leaves and gather on the cell surface under appropriate light intensity for photosynthesis. As a photoreceptor for reactions such as escaping to the side of cells under dangerous strong light) and stomata (reactions that open stomata to optimize the uptake of carbon dioxide, which is the rate-determining process of photosynthetic reactions). It became clear that it worked. In this way, phototropin can be said to be a blue light receptor responsible for optimizing photosynthetic efficiency. Domain structure and LOV photoreaction of phototropin molecule Phototropin molecule has two photoreceptive domains (LOV1 and LOV2) called LOV (Light-Oxygen-Voltage sensing) on the N-terminal side, and serine / on the C-terminal side. It is a protein kinase that forms threonine kinase (STK) (Fig. 4Aa) and whose activity is regulated by light. LOV is one molecule as a chromophore, he binds FMN (flavin mononucleotide) non-covalently. The LOV forms an α/βfold, and the FMN is located on a β-sheet consisting of five antiparallel β-strands (Fig. 4B). The FMN in the ground state LOV shows the absorption spectrum of a typical oxidized flavin protein with a triplet oscillation structure and an absorption maximum wavelength of 450 nm, and is called D450 (Fig. 1C and Fig. 4E). After being excited to the singlet excited state by blue light, the FMN shifts to the triplet excited state (L660t *) due to intersystem crossing, and then the C4 (Fig. 4C) of the isoaroxazine ring of the FMN is conserved in the vicinity. It forms a transient accretionary prism with the tain (red part in Fig. 4B Eα) (S390I). When this cysteine is replaced with alanine (C / A substitution), the addition reaction does not occur. The effect of adduct formation propagates to the protein moiety, causing kinase activation (S390II). After that, the formed cysteine-flavin adduct spontaneously dissociates and returns to the original D450 (Fig. 4E, dark regression reaction). Phototropin kinase activity control mechanism by LOV2 Why does phototropin have two LOVs? Atphot1 was found as a protein that is rapidly autophosphorylated when irradiated with blue light. The effect of the above C / A substitution on this self-phosphorylation reaction and phototropism was investigated, and LOV2 is the main photomolecular switch in both self-phosphorylation and phototropism. It turns out that it functions as. After that, from experiments using artificial substrates, STK has a constitutive activity, LOV2 functions as an inhibitory domain of this activity, and the inhibition is eliminated by photoreaction, while LOV1 is kinase light. It was shown to modify the photosensitivity of the activation reaction. In addition to this, LOV1 was found to act as a dimerization site from the crystal structure and his SAXS. What kind of molecular mechanism does LOV2 use to photoregulate kinase activity? The following two modules play important roles in this intramolecular signal transduction. Figure 4 (A) Domain structure of LOV photoreceptors. a: Phototropin b: Neochrome c: FKF1 family protein d: Aureochrome (B) Crystal structure of auto barley phot1 LOV2. (C) Structure of FMN isoaroxazine ring. (D) Schematic diagram of the functional domain and module of Arabidopsis thaliana phot1. L, A’α, and Jα represent linker, A’α helix, and Jα helix, respectively. (E) LOV photoreaction. (F) Molecular structure model (mesh) of the LOV2-STK sample (black line) containing A’α of phot2 obtained based on SAXS under dark (top) and under bright (bottom). The yellow, red, and green space-filled models represent the crystal structures of LOV2-Jα, protein kinase A N-lobe, and C-robe, respectively, and black represents FMN. See the text for details. 1) Jα. LOV2 C of oat phot1-to α immediately after the terminus Rix (Jα) is present (Fig. 4D), which interacts with the β-sheet (Fig. 4B) that forms the FMN-bound scaffold of LOV2 in the dark, but unfolds and dissociates from the β-sheet with photoreaction. It was shown by NMR that it does. According to the crystal structure of LOV2-Jα, this Jα is located on the back surface of the β sheet and mainly has a hydrophobic interaction. The formation of S390II causes twisting of the isoaroxazine ring and protonation of N5 (Fig. 4C). As a result, the glutamine side chain present on his Iβ strand (Fig. 4B) in the β-sheet rotates to form a hydrogen bond with this protonated N5. Jα interacts with this his Iβ strand, and these changes are thought to cause the unfold-ing of Jα and dissociation from the β-sheet described above. Experiments such as amino acid substitution of Iβ strands revealed that kinases exhibit constitutive activity when this interaction is eliminated, and that Jα plays an important role in photoactivation of kinases. 2) A’α / Aβ gap. Recently, several results have been reported showing the involvement of amino acids near the A’α helix (Fig. 4D) located upstream of the N-terminal of LOV2 in kinase photoactivation. Therefore, he investigated the role of this A’α and its neighboring amino acids in kinase photoactivation, photoreaction, and Jα structural change for Atphot1. The LOV2-STK polypeptide (Fig. 4D, underlined in black) was used as a photocontrollable kinase for kinase activity analysis. As a result, it was found that the photoactivation of the kinase was abolished when amino acid substitution was introduced into the A’α / Aβ gap between A’α and Aβ of the LOV2 core. Interestingly, he had no effect on the structural changes in Jα examined on the peptide map due to the photoreaction of LOV2 or trypsin degradation. Therefore, the A’α / Aβ gap is considered to play an important role in intramolecular signal transduction after Jα. Structural changes detected by SAXS Structural changes of Jα have been detected by various biophysical methods other than NMR, but structural information on samples including up to STK is reported only by his results to his SAXS. Not. The SAXS measurement of the Atphot2 LOV2-STK polypeptide showed that the radius of inertia increased from 32.4 Å to 34.8 Å, and the molecular model (Fig. 4F) obtained by the ab initio modeling software GASBOR is that of LOV2 and STK. It was shown that the N lobes and C lobes lined up in tandem, and the relative position of LOV2 with respect to STK shifted by about 13 Å under light irradiation. The difference in the molecular model between the two is considered to reflect the structural changes that occur in the Jα and A’α / Aβ gaps mentioned above. Two phototropins with different photosensitivity In the phototropic reaction of Arabidopsis Arabidopsis, Arabidopsis responds to a very wide range of light intensities from 10–4 to 102 μmol photon / sec / m2. At that time, phot1 functions as an optical sensor in a wide range from low light to strong light, while phot2 reacts with light stronger than 1 μmol photon / sec / m2. What is the origin of these differences? As is well known, animal photoreceptors have a high photosensitivity due to the abundance of rhodopsin and the presence of biochemical amplification mechanisms. The exact abundance of phot1 and phot2 in vivo is unknown, but interesting results have been obtained in terms of amplification. The light intensity dependence of the photoactivation of the LOV2-STK polypeptide used in the above kinase analysis was investigated. It was found that phot1 was about 10 times more photosensitive than phot2. On the other hand, when the photochemical reactions of both were examined, it was found that the rate of the dark return reaction of phot1 was about 10 times slower than that of phot2. This result indicates that the longer the lifetime of S390II, which is in the kinase-activated state, the higher the photosensitivity of kinase activation. This correlation was further confirmed by extending the lifespan of her S390II with amino acid substitutions. This alone cannot explain the widespread differences in photosensitivity between phot1 and phot2, but it may explain some of them. Furthermore, it is necessary to investigate in detail protein modifications such as phosphorylation and the effects of phot interacting factors on photosensitivity. Other LOV photoreceptors Among fern plants and green algae, phytochrome ɾphotosensory module (PSM) on the N-terminal side and chimera photoreceptor with full-length phototropin on the C-terminal side, neochrome (Fig. There are types with 4Ab). It has been reported that some neochromes play a role in chloroplast photolocalization as a red light receiver. It is considered that fern plants have such a chimera photoreceptor in order to survive in a habitat such as undergrowth in a jungle where only red light reaches. In addition to this, plants have only one LOV domain, and three proteins involved in the degradation of photomorphogenesis-related proteins, FKF1 (Flavin-binding, Kelch repeat, F-box 1, ZTL (ZEITLUPE)), LKP2 ( There are LOV Kelch Protein2) (Fig. 4Ac) and aureochrome (Fig. 4Ad), which has a bZip domain on the N-terminal side of LOV and functions as a gene transcription factor. 4. Cryptochrome and UVR8 Cryptochrome is one of the blue photoreceptors and forms a superfamily with the DNA photoreceptor photolyase. It has FAD (flavin adenine dinucle-otide) as a chromophore and tetrahydrofolic acid, which is a condensing pigment. The ground state of FAD is considered to be the oxidized type, and the radical type (broken line in Fig. 1B) generated by blue light irradiation is considered to be the signaling state. The radical type also absorbs in the green to orange light region, and may widen the wavelength region of the plant morphogenesis reaction spectrum. Cryptochrome uses blue light to control physiological functions similar to phytochrome. It was identified as a photoreceptor from one of the causative genes of UVR8 Arabidopsis thaliana, and the chromophore is absorbed in the UVB region by a Trp triad consisting of three tryptophans (Fig. 1D). It is involved in the biosynthesis of flavonoids and anthocyanins that function as UV scavengers in plants. Conclusion It is thought that plants have acquired various photoreceptors necessary for their survival during a long evolutionary process. The photoreceptors that cover the existing far-red light to UVB mentioned here are considered to be some of them. More and more diverse photoreceptor genes are conserved in cyanobacteria and marine plankton. By examining these, it is thought that the understanding of plant photoreceptors will be further deepened.

Buds development seems to be going strong , trichomes are very present and sticky, smell is an hybrid between candy and skunk , those buds are really hard , I almost feel bad for touching them

Hey ,✋ good to be back again with another grow, i was not able to upload and keep up my diaries because i had my last exams for my degree on Bio farming. Now things are rolling good and i have some free time to work on my diaries. I will separate this grow into 2 or 3 diaries because i have a lot of different strains and i will add more strains soon. See you soon 👿 Specs Lighting : Samsung Spider Grow 800 W Climate Control : 150 mm exhaust fan connected to a carbon filter with 150 mm diameter. Nutrients : Advanced Nutrients , Guano kalong

Mein Problemkind zeigt langsam erste anzeichen von Stretch. Riesige Fächerblätter... teilweise auch Interessante Muster vom Stickstoff überschuss zu sehen. Um den unteren Trieben für den Stretch nochmal die Chance zu geben, habe ich die großen Fächerblätter entfernt. Präventiv Neemöl gesprüht, weil ich ein paar Freunde gesehen habe. Spraymix alle 2 Tage. Heute wird auch die Lampe auf 12/12 umgestellt.

1/11/2024 Vegetation Week 1 Day 1- I have a root almost in the water.. Yay!! Top feeding is almost done. she is looking a little sad as I work the transition Top feeding but once the roots are fully in the water she will start to take off. Ensured my PPFD is set between 250-300 it is set to: 258 1/12/2024 Vegetation Week 1 Day 2- I have a root in the water.... NO TOP FEED TODAY SIR!!! now that a root is touching the water and she looks stable, I am not going to topfeed, I will see how she looks tomorrow and as long as everything looks good I am going to go ahead and do a change and week 1 fill on Nutes.. I know it is a couple of days in but the same Nutes go through Week 2 and get changed at Week 3 So I should be good to go.. I will just ensure I fill to root touching the water when I change tomorrow. 1/13/2024 Vegetation Week 1 Day 3- Water Change Day!! I added 36 Gallons of Water to the system: Silica= .5mil/gal= 18mil CalMag= .75mil/gal = 27mil FloraMicro=3.0mil/gal = 108mil FloraGro=2.0mil/gal = 72mil FloraBloom= 2.0mil/gal = 72mil PH DOWN= 30mil Very important thing with this system is to now wait the 24 hours for the system to adjust.. Do not make any further adjustments to your PH up or Down for 24 hours to allow time for the system to balance. 1/14/2024 Vegetation Week 1 Day 4- Today I just adjusted the PH to ensure that it was right at 6.0 1/15/2024 Vegetation Week 1 Day 5- Today I Cleaned up the lower damaged leaves from the transition from top feeding to roots in the water. She looks good today. 1/16/2024 Vegetation Week 1 Day 6- Today I just took a picture of the beautiful lady for Log. Other than that just normal day to day operations, check the pH, check the Humidifiers and fill as necessary, check level of water in the Res. Everything looks great. onto Tomorrow!! 1/17/2024 Vegetation Week 1 Day 7- Today I filled the humidifers, checked the PH and just let her grow.. Grow baby Grow.....

Finally starting to look like she might be finishing, but every time I think that, a bunch of new pistils shoot out. Trichomes are getting more cloudy but still a lot of clear ones. Lots of stacked calyxes now packing on. Remember this plant has already had 5 zips of dried bud removed at 11 weeks! I have not changed the reservoir for 4 weeks, I topped it up with a little bit of extra nutrient after two weeks but there seemed no reason to do anything else, she has not been using much recently ppm is constant at about 800. Only now beginning to see some leaves dying. I'm going to let her go for as long as she wants.

These are doing great! FIM the larger of the two. Shooting for 12 nice colas. Larger started preflower yesterday so I laid her over with LST. Happy growing!

ZSKITTLES OG AUTO SHE FINISHED NOW BUT HEAR SHE IS

So I have decided to only note when changes are made, observations are warranted, or I feel something of note has happened. I'll still do daily progressions, but the rest has already been documented and no need to create a hundred new pics showing the same. Just understand that if I say "7.1ph," or something with tested amounts that I mean I first calibrated and tested my ph pens and all units are measured for accuracy. I am learning as I go, so it would be of no benefit to report inaccurate details. 112/42 VPD and PPFD are still the same this week. 73-76F in the day and 66-68 overnight with RH set to not exceed 55% but is mostly at 45 to 50% now that winter is here. The fan is set to auto and I have 2 de-humidifiers in the tent. The PH lockout issue is still in progress but I am starting to get the soil up to snuff now. I think using the knitting needles has the most beneficial effect on the soil as it both aerates and allows the nutes to get deeper. 113/43 Defoliated today. I removed the worst of the affected fan leaves and this unfortunately only leaves sugar leaves to run photosynthesis process. Im hoping she still gets enough of everything else to grow the buds, but only time will tell. I will take new control pics for new progression on 3 other sites now. Watering Days. All feeds with nutes use either a whole ratio, or combination, of "Veg Mix" and "Bloom Mix"concentrates. These are/will be DILUTED in water until a total ppm of add-in is reached using a (Total Dissolved Solids) TDS Meter measured in PPM (parts per million). The "Veg Mix" concentrate will eventually be added-in larger, then smaller, ratios while the "Bloom Mix" concentrate will eventually replace the "Veg Mix" concentrate entirely. The ppm and ratios will be listed when I feed. Veg mix recipe is on week 3. Bloom Mix recipe is on week 5. Last feed was day 110/40 (next will be +3) I expect to continue to use 7.1ph with 650ppm of bloom mix concentrate and feed 2.5 gallons every 3 to 4 days, so I expect about 8 to 11 cups of runoff at that time as well. I have decided that I will try to add 1 ml of CaliMagic (General Hydroponics 1-0-0) per gallon of feed on each feed for a week or two to see if this can help against ph lockout of calcium since it cant be N,P, or K. Cant be N because she uses WAY less N in flower, and it cant be P or K because I am getting nute burn with the feeds I am already using... so my conclusion is that she need more micro nutes from the lockout, and since I was thinking it was Calcium in the start, I am going to try a more detailed treatment to test results against from here. Day 113/43 (last feed was day 110/40) Tested and Calibrated my ph pens. Fed 2.5 gallons of purified water (starting with 16ppm) mixed with 658ppm of 100% Bloom Mix Concentrate. Due to this soil showing a possible calcium deficit, I am starting a 1ml per gallon add-in to test on all plants using this soil, so I added 2.5ml of CaliMagic (General Hydroponics 1-0-0) to the feed then I ph balanced before feeding. The ph on this feed was balanced to 7.1. I used knitting needles to help both aerate the soil and create new water pathways for the roots. (a practice I may consider a new feeding standard for all my plants) I got ~7 cups of runoff (~11 cups last feed). Higher runoff volume was expected with the feed volume but glad to see she's taking it better now since I started knitting needles. Runoff was tested at 6.12ph and 2250ppm (5.9ph with 1860ppm last feed). Top soil tested at 6.23,6.31,6.57,6.38 for an avg of 6.372 (6.327 avg after last feed) - next feed will be 7.1ph again as I'm still liking where the ph is finally going, but rather see it closer to 6.3 or 6.4 top and bottom. I dont see any issues with the feed's data other than the possible calcium deficit and I will continue to monitor runoff ppms as I expected this to be lower with less runoff but have to consider they maybe washing out salt with the knitting needles. Next Feed should be 3 gallons of de-chlorinated tap water ph balanced to 7.1 in +4 days (117/47). I will run 650ppm and 3ml of CaliMagic (General Hydroponics 1-0-0) again. Day 117/47 (last feed was day 113/43) Tested and Calibrated my ph pens. Fed 3 gallons of de-chlorinated tap water (starting with 299ppm) mixed with 671ppm of 100% Bloom Mix Concentrate. Due to this soil showing a possible calcium deficit, I am starting a 1ml per gallon add-in to test on all plants using this soil, so I added 3.0ml of CaliMagic (General Hydroponics 1-0-0) to the feed then I ph balanced before feeding. The ph on this feed was balanced to 7.4. I used knitting needles to help both aerate the soil and create new water pathways for the roots. (a practice I may consider a new feeding standard for all my plants) I got ~20 cups of runoff (~7 cups last feed). Higher runoff volume was expected with the feed volume increase might let her go to 4 days again and 2.5 next feed. It could be a result of the knitting needle treatment when feeding. Runoff was tested at 6.10ph and 2070ppm - again thinking it could be a result of the knitting needles (6.12ph and 2250ppm last feed). Top soil tested at 6.23,6.31,6.57,6.38 for an avg of 6.372 (6.372 avg after last feed)- next feed will be 7.1ph again as I'm still liking where the ph is finally going, but rather see it closer to 6.3 or 6.4 top and bottom. I dont see any issues with the feed's data other than the possible calcium deficit and I will continue to monitor runoff ppms as I expected this to be lower with less runoff but have to consider they maybe washing out salt with the knitting needles. Next Feed should be 2.5 gallons of de-chlorinated tap water ph balanced to 7.1 in +4 days (121/51). I will run 700ppm and 2.5ml of CaliMagic (General Hydroponics 1-0-0) again.

Aquí tenemos la quinta semana se nuestras plantitas PurpleKush de la familia de Kannabiaseeds. están creciendo muy bien, tienen buen color y espero que sigan así de sanas. Pronto nuevas noticias 😘

Vaso de 750ml, 12 dias de vida e 9º dia na iluminação! Está se desenvolvendo rápido. Raizes fortes e bem ramificadas . Adicionei 0,2 ml de top veg pra ajudar no vegetativo Temperatura elevada, durante o acender das luzes 30C°