harvested her 6/21/25 after 8 weeks flowering indoors and then 1 week in the outdoor sunshine. will update more with drying and curing and smoke report

Der Stretch ist bei allen Pflanzen abgeschlossen. Bin diese Woche bei den Photos auf Terra Flores umgestiegen. Hab leider keine Fotos vom Ende der Woche weil ich nicht zuhause war. Die Cookies Kush ist einfach am Purpeln, womit hab ich das verdient 😂 Die Zkittly fängt schon kräftig an Harz zu produzieren. Der Geruch in der Box ist langsam unglaublich. Die Skywalker OG sieht schon so weit aus aber es sind noch sehr viele Trichome durchsichtig und keine Bernsteinfarbenen in sicht. Hab ihr diese Wochr nochmal Dünger gegeben. Mal schauen wies aussieht wenn ich wieder zuhause bin.

Bonjour à tous, ces derniers jours ce sont bien passé pour mes petit bébés elles grandissent doucement mais sûrement.C’est la première fois que je travail avec cette gamme de produits (je vous est mis des photos des produits 😉) pour l’instant j’en suis satisfait après, il faut voir le résultat final ce qui est moins facile 😂. Mes petit bébés commence leurs 5ème semaine (je me suis trompé d’une semaine 😕 désolé 😉) trop pressé!!! 😂 de mettre de nouvelles photos 😜. Je vous dis à là semaine prochaine vivement 😉 bonne journée à tous. Je vous remercie 😉.

Día 71 (24/03) La planta lo ha pasado mal tras 2 días sin riego (casi 3 ciclos completos de 12 horas de luz sin riego...) A lo que se suma altas temperaturas en mi zona, han tenido 28 ºC durante las horas de luz... Las hojas inferiores se encuentran caidas y alguna quebradiza... Le hago un riego con 750 ml H2O EC 0,45 a ver si se recuperan.... Día 72 (25/03) Riego con 250 ml H2O EC 0,45 Elimino las hojas quebradizas que no se van a recuperar después de la "sequia" que han pasado Se encuentra en buen estado general y formando nuevos pistilos! 😍💥 Día 73 (26/03) Riego con 250 ml H2O EC 0,45 Día 74 (27/03) Riego con 500 ml H2O EC 0,45 con BIO PK 5-8 a 10 ml / L (solo Limon Blanco) Riego con 100 ml H2O EC 0,45 (el resto) Reviso los tricomas, y GG4 Sherbet FF y Blueberry Pie F1 solo les faltan unos días! 😍💥 Día 75 (28/03) Riego con 400 ml H2O EC 0,45 Día 76 (29/03) Riego con 500 ml H2O EC 0,45 Día 77 (30/03) Fiesta de la Cosecha! Reviso los tricomas y están un 10% ambar, 85% nublados y 5% transparentes 🚀 FastBuds 15% DISCOUNT code "NONICK" 2fast4buds.com @fastbuds.official 🚀 Khalifa Genetics - https://khalifagenetics.com/product/lemon-blanco-v3/ @khalifa.genetics 💦 BioTabs 15% DISCOUNT code "GDBT420" biotabs.nl/en/shop/ @biotabs_official 🌱Substrate PRO-MIX HP BACILLUS + MYCORRHIZAE @promixmitch @promixgrowers_unfiltered 💡2 x Mars Hydro FC1500 EVO Led Grow Light (2024 NEW FC 1500-EVO Samsung LM301H 150W LED) - https://marshydro.eu/products/fc1500-evo-led-grow-lights/ - https://www.amazon.de/dp/B0CSSGN5D8?ref=myi_title_dp

Starting week 6 Tent is being slowly full A little bit too hot for the next days as the weather outside will climb to 36-38°C, I thnk I will bring them some CO2. I will check with the growshop. Any idea is welcome. The stretch is really impressive, 1 of them get 20cm in 7 days Waiting for the buds 😁 Day 39 I have now added CO2 with an organic boost, it is linked it to the fan. Should be a little bit better with that temperature

There is very little to do with the plants, they are getting fatter by the day and frostier by the day. I found out I was giving them way too much nutrient so I started giving them 0.4 EC less (its still a work in progress). The lights are still on 85%. It is starting to smell more and more sour and there is also a fresh lemon smell coming from it now.

I don't understand why my kickass auto is budding so early.! Have to figure something for her. Otherwise all my girls are doing well especially california orange crush and my favorite black domain, both those are photos. Until next week GD peeps 👊🏿👊🏿

harvest soon day 83 - turned off the light

Final week! I am starting the flush process at week 8 so going to do quarter nuts for 2days then half then 1/3 and then finish with 2-3 days water Tricombs where about 75% milk rest where clear maybe a few random turning amber She really must have put on weigh this last week because she is sagging hard now!

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.

Switched to bloom nutes. The lowered screen has already filled up to the second level and filled in very nicely. About ready for autopilot.

Just keep watering as it drys. Supporting buds along the way that are getting too heavy. Smells like skunk and gas. Little fruit but not much. Trics still getting thick. Look forward to it finishing. Tricomes still cloudy. Little amber on sugar leaves but it's still going strong. Some leave fading finally to fall colors.

Siamo entrati ufficialmente in fioritura con le piante più vecchie,sono tutte molto grandi a parte una che é rimasta più piccola,questo indica una genetica stabile,abbiamo ancora un mese di tempo,continuiamo questo viaggio

Harvested after 3 days flush and two days night after recommended 9 weeks. Got 2 phenos. One better and more representative of the strain description which i kept a clone of to S1 and stabilize. As usual uploading here is a pita it didnt upload my videos again really annoying, but pics show the better strain is stronger bramches, stretchier, and better buds. I cut them in the video so no one cries i didnt harvest lol. Smell is from sourish sweet to sweet and mossy like a green slurpy or something. 6 week testers were potent and frosty already so i cant imagine after proper harvest and cure.

This week was good..the ladies are in better health overall. Did some defoliating throughout the week and also did a flush 3 days ago with florakleen.gave em a light feeding today.Just finished setting the timer. Will be flipping them into flower tomorrow at 8 am ..will keep yall updated in my next upload..Happy growing 😎

✨ Fairytale Leaves & Phenotype Magic Welcome to flowering, where potential meets reality. Both Gelonade phenos are stepping into this new phase with vigor, balance, and beauty — but one of them is telling a very special story. 🍃 Pheno #2: The Leaf Dancer This pheno has leaves that defy convention — opening in a structure that resembles a human hand folding out from the palm, each finger unfurling in elegant rhythm. Imagine: • Three central “fingers” • Each outer one splitting into three more • Forming a seven-pointed star, nested within a trinity of growth It’s not a mutation that hinders — it’s a genetic flourish. A dance of symmetry, expression, and vitality. 🌿 These aren’t just leaves. They’re art. 🖼️ We’ve captured this in photos and video — no filter needed. Just nature doing its finest work. Plant Stats – Week 1 Flower / Week 5 from Seed: • Height: approximately 40 cm • Light Intensity (PPFD): 766 µmol/m²/s • Temperature: 31°C • Humidity: 50% • VPD: 2.23 kPa • EC: 0.6 • pH: 6.1 Despite slightly high temps and VPD, the girls are loving it. They’re adapting, stretching slightly, and showing excellent turgor and coloration. ⸻ 💧 Nutrition & Soil Strategy This run is driven by a super soil base, and it’s doing the heavy lifting. That’s why we’re keeping the water feed light and strategic. 💦 Current Feed (per liter): • Aptus Regulator – 0.15 ml → Strengthens cell walls, improves nutrient flow • Aptus CalMag Boost – 0.25 ml → Supports structure and photosynthesis • Aptus Top Booster – 0.25 ml (new this week) → Prepares for flower, encourages early bloom structure ⚠️ No All-In-One Liquid now → The slow-release pellets in the soil cover the macro-nutrient demands. → This keeps EC low (~0.6) and prevents salt buildup. We’re letting the soil biome + amendments guide the bulk of nutrition. Water is a carrier, not a crutch. ⸻ Why Switch from Start Booster to Top Booster? Start Booster = roots & early leaf Top Booster = flower signal + potassium focus This switch marks the turning point: Roots are now established, and it’s time to nudge the girls toward blooming, gently and with precision. Top Booster also enhances: • Early bud site formation • Transition metabolism • Potassium availability for cell expansion ⸻ Gear Check Everything is tuned in and working in harmony: • Lights: Future of Grow LED + ThinkGrow Model One • Controllers: TrolMaster Tent-X + Spider Farmer GGS • Airflow: • Two 6” carbon-filtered exhaust fans • One 6” filtered intake • Controlled by both ecosystems All this tech = manual precision + automated consistency ⸻ 🔮 What to Expect Next We’re not seeing pistils yet, but the structure is shifting. Nodes are spacing. Branches are reaching. Energy is focusing upward. Here’s what we might expect in Week 2 Flower: • First signs of pistils • Shift in leaf texture • Possible terpene expression (early scent) • Stretch phase (up to 2x height) ⸻ The Fairytale of Pheno #2 Sometimes, a single plant will speak louder than others. Pheno #2 is doing just that, not with speed or size, but with shape, rhythm, and elegance. The leaves whisper a story: Of lineage, light, and mystery. Of something old reborn in a new form. Of a garden that listens, and a grower who sees. ⸻ 💚 Final Thoughts This isn’t just a grow. It’s a living exploration of genetics, care, and love. As the Gelonades move toward flower, we’re watching not just for yield, but for expression. For surprises. For beauty in all forms. Week 1 of flower is quiet, but underneath, everything is shifting. Let’s walk slowly. Observe closely. Love fully. And let’s see what Week 2 has to say 🌸 With love and green respect, DD (Dogdoctor) & The Gelonade Girls 📲 Don’t forget to Subscribe and follow me on Instagram and YouTube @DogDoctorOfficial for exclusive content, real-time updates, and behind-the-scenes magic. We’ve got so much more coming, including transplanting and all the amazing techniques that go along with it. You won’t want to miss it. • GrowDiaries Journal: https://growdiaries.com/grower/dogdoctorofficial • Instagram: https://www.instagram.com/dogdoctorofficial/ • YouTube: https://www.youtube.com/@dogdoctorofficial ⸻ Explore the Gear that Powers My Grow If you’re curious about the tech I’m using, check out these links: • Genetics, gear, nutrients, and more – Zamnesia: https://www.zamnesia.com/ • Environmental control & automation – TrolMaster: https://www.trolmaster.eu/ • Advanced LED lighting – Future of Grow: https://www.futureofgrow.com/ • Root and growth nutrition – Aptus Holland: https://aptus-holland.com/ • Nutrient systems & boosters – Plagron: https://plagron.com/en/ • Soil & substrate excellence – PRO-MIX BX: https://www.pthorticulture.com/en-us/products/pro-mix-bx-mycorrhizae • Curing and storage – Grove Bags: https://grovebags.com/ ⸻ We’ve got much more coming as we move through the grow cycles. Trust me, you won’t want to miss the next steps, let’s push the boundaries of indoor horticulture together! As always, this is shared for educational purposes, aiming to spread understanding and appreciation for this plant. Let’s celebrate it responsibly and continue to learn and grow together. With true love comes happiness. Always believe in yourself, and always do things expecting nothing and with an open heart. Be a giver, and the universe will give back in ways you could never imagine. 💚 Growers love to all 💚

I have problems with her. I think it's because of the local water. the earth is not fertilized with any product. only earthworm humis.

The plant is in his last phase of flowering and after this week I'm stopping giving nutrients to it, The plants looks good, the older leaves are turning yellow and the pistils are 40% brown,