day 1 - shes getting her sugar on the leafs now clearly and you can start to really notice her smell after just a few minutes of the tent being open. not too strong of a smell yet but there is still much time to improve, really happy with the bud developement so far!!! day 4 - trichome producktion is just kickin off since 1-2 days, love to smell her sweetness. stretch has come to a stop a few days also. day 6 - when i opened the tent today she was showing me her flowers big. there was a big diffrence visible for my eye from last open yesterday to today and i like it! the pistils on the main bud start to get orange color and the others also seem to get a few pistols with color totay!

I didn't really finish this diary. I took them back outdoors to finish for the last week. It finished kinda scraggly and the buds were fluffy. As soon as the bud was dry, I pressed it for the rosin...and forgot to do the diary. Decent for a freebie, but I won't be growing it again. Potency: 6/10 Yield: 4/10 Aroma: 7/10 Flavor: 5/10 Bag-appeal: 3/10

Week one of flush.

Good Grow

She's almost there and going strong , buds got a little thicker during this week, I did some trimming of shadowleaves. It's just the waiting game now 😅

These 3 Gelato auto are part of a 30 plant SOG project, in this diary we will only focus on this fantastic strain as you can see, this is Gelato auto by fast buds grown with nothing but FLO (living soil blend) mixed up with the soil and water 💦, let's see what type of flavors we are going to find! Stay tuned for this one! 👨‍🌾❤️💚

Harvest Part One, Day 93: First harvest of the Main colas, as a lot of the trichomes turned brown. An awful lot of work to trim wet, but wanted to get rid of all the dryed leaves. A comment on another diary said leaves turned yellow because of possible lockout. Well, i cant deny it, but i have no experience at all with it. In hindsight i should have used a lot more fertilizer during the vegi phase, i guess, because this monster turned out to be super hungry (if that makes sense). Density after removing the leaves is ok i think. Expected a bit more to be honest. Massive headbuds still though. However, kinda „raw“ on the inside as you can see by the color and general appearance. So wondering if it was to early still. Alright, half of the plant cut down, and placed in dryferm bags (compare to dryaging but tailored to Cannabis), as i have mentioned before. Still in the process, after like 7 days half of the weight gone already. A Bit more to go i think. I think i will post another update with the bottom part of the plant and for sure one with the finished product. So far very surprising strain in a positive way, still very delicate smell (i get the „doughy“ and in a sense creamy part of dutch Passions Description, its very subtile though and not much else, almost citrusy tea like), great yield, grows somewhat easy but probably isnt easy to maintain and doesnt like errors in handling. All in all im very happy and cant wait to try the First Buds. So far 7.5/10 — very decent. Let‘s see how it performs. Might change the evaluation then. And sorry, might totally be wrong about everything. Let me know your opinion, criticism, etc., please!

Starting to see where the buds will grow

19.1.25: I have watered all plants with 300ml of dechlorinated water PH'd to 6.3, with 1/3 jar of black strap molasses with Ecothrive Biosys-1g. I am looking to increase the sugars for microbial life and plant processes. It'll also add some extra Calcium, Magnesium and trace elements. I also, watered all plants with Bloom nutrients. Using dechlorinated water PH'd to 6.3 with the following nutrients: (ml/l) ;- ♡ 2ml Cal-Mag ♡ 2ml Ecothrive Flourish ♡ 2ml Xpert Nutrients Bloom Booster ♡ 2ml Biobizz Bloom ♡ 2ml Biobizz Top Max ♡ 1g of Ecothrive Biosys I watered around 1-3 litres per plant. Depending on size and requirements. I'm still spilling water containing the nutrient solution. 🙄 I am using this to rub into the leaves. I think a nice foliar massage won't do any harm, make the most of the situation. The plants have become very hungry and thirsty. Increased the water by double. I ran out of my TNC cal-mag. I decided to order the Xpert Nutrients brand, as I like their products. It isn't organic as far as I can tell, but I don't think it matters too much to me, to be honest. I also want to top dress this week, so I bought some Green Leaf PK bud Booster dry amendment from Amazon, too. I'll mix it with canna coco, perlite, worm castings, and Ecothrive Life Cycle. 24.1.25: I went ahead and top dressed all the plants with 4.5 gallons of my supersoil custom mix. This consists of the following substrate and dry amendments: ♡ 60% Canna coco ♡ 20% Worm castings ♡ 15 % Perlite The remaining 5% consists of the following dry amendments;- ♡ 10g Ecothrive Biosys ♡ 1 Tsp RHS Mycorrhizal Fungi granules ♡ 3 Tsp Vitalink Bat guano ♡ 4 Tsp Diatomaceous earth ♡ 8 Tsp Ground Cinnamon ♡ 10g Green Leaf Bud Booster PK booster. ♡ 3 Tsp Ecothrive Life Cycle. •Worm castings for some all round nutrition. •Cinnamon for mildew and bug repellent. •Canna coco base substrate. •Perlite for adding oxygen to the root and soil system. •Green Leaf Bud Booster PK Booster for blooming. Building strong big buds. •Vitalink bat guano again for Bloom. •RHS Mycorrhizal Fungi granules, to boost beneficial microbes. •Ecothrive Life Cycle for lots of great benefits. •Diatomaceous earth for Silica. •Ecothrive Biosys, for an extra microbial boost. I have removed all LST equipment from both PPP1 and PPP2. I'm going to let them grow up now, and I plant to implement a Scrog net, if they get any taller, which I hope they will. However they are most likely finished with their final stretch. My mistake, I went too hard on the LST. Thanks for checking out my diary 🍃 ✌️

All good this week too. The strawberry lemonade turning purple!:)) gg#4 it’s a hermy… the other plants are good! White widow xxl it’s the first to harvest…In 3 weeks…. Fxxk

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.

The cherry bomb has done well in expanding her growth after topping. I am having a ph problem again, and had to move the tent due to really cold weather. She is starting to show signs of nute burn. I have cleaned out the DWC bucket, and I am flusing her for a few days. I have put this plant through a lot of stress, and she continues to bounce back. I am very pleased with this plants Resilience.

420FASTBUDS ORT2109 WEEK 7 The pair of these beautiful girls continue to surprise me every week. I give them a once over and look and the leafs for a weekly inspection to make sure all's well. The both have many flower sites showing up and I decided to do a mild defoliation to allow the plants energy to be focused on the upper sites. Over all I'll continue feeding them they way I have been with 2liters of water/nutes every 2-3days. Happy Growing

Week 8 and growth continues to be muted. Due to the poor soil, I'm only slightly scratching the strain's potential. I've attached a video of the insects that were in the soil, along with the fungus gnats. Today, the ladies were trimmed a bit at the bottom. ----------------------------------------------------------------------------------------------------------------------------------------------- woche 8 und weiterhin verhaltener wuchs. aufgrund der schlechten erde kratze ich natürlich nur leicht am potential des strains. ich habe mal ein video der insekten beigefügt die neben trauermücken in der erde inklusive waren. heute wurden die damen untenrum etwas freigeschnitten.

Wow going into the 3. Week of Flower. The plants have exploded since switching to 12/12 . #7 have close to doubled in size and are easily filling the second Trellis layer. #6 has also gotten bigger but it seems to have filled in more then shot up in height.. Will do a big defoiliate next Saturday. Will take everything below the first trellis including branches on #7  that do not reach the second trellis Turned IR to 75% 9-25-22 Feed the plants , they are looking great, but are ready for some trimming. Evening update: really don't know why but checked my soil this evening before lights turned off for the day and discovered it was bone dry. Watered the plants . Sure hope it starts cooling down soon. Temp in tent was upper 80's today, a tad warmer then wanted. 9-26-22 Plants seemed to have plenty of water left this morning, but might need checked on tonight. I am surprised that the plants are still stretching. Cheezy Puff & Cookies &Stash are much taller then the POG. The POG is more of a compact flower compared to the other two. The Flowers on all 3 are developing beautifully. 9-27-22 Day 17 It is amazing how much taller the Cheezy Puff as well as the Grandpa's Stash are compared to the POG All 3 look extremely happy and healthy and are developing plenty of bud sites. Feed plants this morning 9-28-22 Day 18 Is it only me that gets excited everyday when it's time to open the tent and feed the girls? Flowers are looking great but are ready for a trim! The incoming weather has me a little concerned, woke up to tent having RH of 70% closed the window and hope that helps 9-30-2022 day 20 The last two days have been tough on me and the geow. We got smashed by hurricane Ian and have been without electricity for the last 48 h with no end in sight. Opened the tent the last 2 days hoping the plants will get at least some daylight. With all the humidity in the air, the tent was at rh 98% when I opened it first this morning. Even after hours being opened the RH is still hovering around 75% Hope we get electricity back in the next 24h

4-5-18 FASTBUDS CA popped. Can’t wait to see what this strain can do.

She's maturing and getting more ripe and ripe by the day! Top nugs are still growing/foxtailing so their progress is never ending it seems! Gonna check trichomes within the next week. She's getting a super nice fade although not my intention, still very pretty. Very nice frosty, green with purple edges/tips. The sunlight shots of this are gonna be mind boggling! Took the pics on my actual camera phone so the quality was better! The Terps are amazing, and done developing I believe; it's a deep red Fruit Punch + Superboof + sum Pure Michigan hashiness. To die for. Absolutely smells up the entire grow area and most of the house when the doors open! Absolutely gonna be growing Homegrown again; excited for Apple Junky and Garlic Applez grows! Coming soon along with sum In House genetics & Dirty Bird grows aswell!

Week 3 D2 increased RH to ~70% D3 Height 14cm 1 / 13cm 2 Plants looking good. I'm full satisfied D4 3cm growth over night ***May the fourth be with you ;-)*** D5 1/19 cm 2/18 cm D7 No incidents, good week for the plants

Petite taille effectué, j’ai coupé l’apex et j’ai laisser seulement le noeud juste en dessous de celui qui étais le plus développé, pour vois si les deux repousse de l’apex et celle du noeud en dessous arrive à la même taille/croissance , afin d’être le plus symétrique possible. Car avant tous je suis passionné par l’art végétal et le bonsaï, j’ai commencé à cultiver du cannabis il y a maintenant 3ans, un été j’ai planté une petite graines dans un bête terreaux vide de nutriments, et là tout a commencé. Mais comme dis précédemment j’aimais l’art, et ce plant en question je l’ai transformé en bonsaï, un magnifique bonsaï, un chef d’œuvre, au quel j’ai perdu toutes photos. L’année d’après j’ai recommencé le même scénario, une graine et on recommence, la se fut un échec, plant trop gourmand et trop sensible au stress, il m’a lâché à 3/4semaine de floraison, puis maintenant 1ans que je cultive en intérieur a rechercher une bonne recette de living soil, toujours à la recherche de perfection jusqu’à couper avant même la fin de floraison car j’étais pas satisfait du résultat. (C’est pour ça aussi que j’ai supprimé tous mes journaux) J’ai coupé deux cultures comme ça et j’ai fais qu’une récoltes sur la troisième. Maintenant celle qui m’excite le plus est la petite graine d’extérieur, oui comme on dit jamais deux sans trois, plus de 1ans que j’attends cette variété, la Frosty purple freak. Le mutant violet de chez Khalifa Genetic. Que je vais bien évidemment travailler comme un bonsaï, mais symétrique , je vais éviter de trop le stresser comme j’ai eu du retard sur la croissance du a certain imprévu de type limace et temps catastrophique. (2 graines bien planté dans mon derrière.) je vais essayer de bien le diriger tous en essayant d’avoir une certaine récolte, en faire un bonsaï crée d’énormes stress au plant et ralenti considérablement la croissance, pour essayer de récolter 50/100 grammes sur le plant en extérieur faudrais approcher les 3/4 mois de végétation si tu implique des haut stress training et de la coupe a gogo. Et j’avoue que j’ai pas payer plus de 50litre de living soil juste pour 15/20 grammes de récoltes sur le plant, même si la satisfaction d’avoir fait une œuvre d’art, ça ne vaut pas le coup, je ferais mieux l’année prochaines, je dois accepter cette défaite. J’ai mis des vidéo de mon deuxième bonsaï, il étais en début de floraison et il avait environ 4mois, sans nutriments ,je lui estimais 30/50 grammes en fin de Flo, mais il m’a lâcher. Dans les deux dernières vidéo, il y en a une où on voit bien le dépôt bactérien et nutritifs du thé de compost oxygéné. Recette du thé pour la semaine 15litre d’eau de pluie 30 gr guano guali 15 gr Meal wormcastings 15 gr nettle 7 gr spirulina 7 gr Hydrosolat Kelp 225 gr wormcastings 15 gr hydrolysât de poisson 15 gr Comfrey 10 gr levure saccharomyces cerevisiae souches lycc 6420 60 gr Zeolit of chabasit 15 gr Azomite 45 ml de mélasse 15ml d’acide Humic et fluvic J’ai arroser 6 litre pour la purple freak et le reste a d’autre plantes Et un autre arrosage avec 500ml d’eau neutre avec 1gr bacilllus amyloliquefaciens x5 qui a été effectué le lendemain du thé La culture se passe bien, du côté de la purple freak Aucun problème à déplorer, plant très résistant, au changement de température et condition climatique supporte très bien les orages et les temps pluvieux et chaud, pas de signe de maladie, j’ai actuellement des ravageur depuis le début de la culture, pas un signe de problème. Réagit très bien au coupe, j’en suis plus que ravie, elle fait partis de mon top1. Seul truc qui m’inquiète, c’est ce mauvais temps. Un mélange de chaleur et de pluie, qui a amené de l’oidium sur certaine de mes plantes extérieur, j’ai peur que cela se propage sur la purple freak. Je vais devoir traiter tous cas, sans traitement agressif bien sûr.