Al 09/02/24 se pueden ver a las plantas bastante sanas, no han mostrado ningún síntoma de stress por el transplante. Esta semana he aumentado la dosis de agua a 3. Litros, El drenaje del riego me tiro un ph de 5.7 y una ec de 2000.

This two were part of another diary and got moved out due to space reasons at VW8 and moved back indoors at VW20 https://growdiaries.com/diaries/218151-auto-god-s-glue-grow-journal-by-yan402 13.09.25 VW21 Both are looking good and are developing tighter nodes than when they were outside, I'm going to have to keep cutting them back every once and a while I also applied nematodes against thrips and fungus gnats. 20.09.25 VW22 some spots and some yellow leafs, I think it's a root problem, probably root bound, but both seem healthy and are getting thicker so maybe just top up with Coco coir and give a slight different nutrient schedule less Tri Part Bloom could do the trick MAYBE lol. 27.09.25 VW23 Topped up the pots with extra coco coir and trimmed the side roots a bit, both plants were root bound 📹 03.10.25 VW23 did a HST/LST session 📹 12.10.25 VW25 Done a major HST session to try and keep them in line with the Sunset Sherbet GF I have going in the same tent, rest in the video 📹 17.10.25 VW25 ffj/fpj/fish 30 → 60 ml 19.10.25 VW26 it just became a one plant diary, keeping #5, #6 gets it's own diary for testing nutrients. 20.10.25 VW26(?) Feed tweak: added 3 g Calcium Nitrate/ 30 L (≈ 15 ppm N + 10 ppm Ca) 24.10.25 VW26 did a defoliation and trimming session 📹 25.10.25 VW26 I'll be repoting tomorrow, 26.10.25 VW27 rest in the video📹 27.10.25 VW27 Epsom Salt 0 → 2.5, Calcium Nitrate 3 → 9 g 01.11.25 VW28 CalMag 60 → 30ml, TriPartBloom 20 → 30ml, Magnesium 2.5 → 3.5g 04.11.25 VW28 no more yellowing between the veins and no new spots, the changes to the schedule worked, rest in the video 📸 🌱💦🌱💦🌱💦🌱💦🌱💦🌱 Day to day tasks & actions 🌿 🌱💦🌱💦🌱💦🌱💦🌱💦🌱 01.11.25 VW27 -- no feed no water 02.11.25 VW28 – Fed 5l of #1 → 2l runoff 03.11.25 VW28 – Fed 5l of #1 → 2l runoff 04.11.25 VW28– Fed 5l of #1 → 2l runoff 05.11.25 VW28 – Fed 5l of #1 → 2l runoff 06.11.25 VW28 – Fed 5l of #1 → 2l runoff 07.11.25 VW28 – no feed no water 08.11.25 VW28 – no feed no water (*RUNOFF reused for indoor house plants) 🍶💧🍶💧🍶💧🍶💧🍶 💧 Nutrients in 30 L #1 🍶💧🍶💧🍶💧🍶💧🍶 💧 TriPart Micro: 10 → 30 → 40 ml = 0.33 → 1.00 → 1.33 ml/L 🍶 TriPart Grow: 0 ml = 0.00 ml/L 💧 TriPart Bloom: 10 → 30 → 20 ml = 0.33 → 1.00 → 0.67 ml/L 💧 Cal-Mag: 60 ml = 2.00 ml/L 🍶 Home-made FFJ/FPJ (new batch): 30 → 60 ml = 1.00 → 2.00 ml/L 🍶 Calcium Nitrate (Calcinit): 3 g ≈ 15 ppm N + 10 ppm Ca 💧 pH Down: Citric acid (BuxXtrade) — adjust to ~pH 6.0 📦 TOTAL: ≈ 160 ml liquids + 3 g solids per 30 L = ~6.0 ml/L active mix 🍶💧🍶💧🍶💧🍶💧🍶 ⚙️✂️⚙️✂️⚙️✂️⚙️✂️⚙️ ✂️ Tools & equipment ✂️ ⚙️✂️⚙️✂️⚙️✂️⚙️✂️⚙️ ✂️ 2× MarsHydro SP3000 ⚙️ MarsHydro 150mm ACF Ventilator ✂️ Trotec dehumidifier (big unit) ⚙️ Mini no-name dehumidifier ✂️ Kebab skewers (LST – stainless) ⚙️ Wire + roast skewers (LST assist) ✂️ Scissors (HST) ⚙️ Vacuum (for spills & cleanup) ✂️⚙️✂️⚙️✂️⚙️⚙️✂️⚙️✂️⚙️✂️⚙️ 🍒🍭🍬🌈🍒🍭🍬🌈🍒🍭🍬🌈🍒 🦄Fantasy Feast ( Seeds)🦄 🌈🍒🍭🍬🌈🍒🍭🍬🌈🍒🍭🍬🌈🍒 Species: Hybrid (Regular) Genetics: The mother is Unicorn Whip by Dirty Bird Genetics. The father is Charcuterie by Cannarado Genetics. Effect: Unknown Mixed effect body and head high Flavor: Some phenos are Skunky gassy fruity, some are fruity sour citrus with a chemical touch and a touch of skunk Flowering: Estimated 8–10 weeks Resistance: Strong — Testing phase done YouTube Link: https://youtube.com/-m8h?si=A7x4Zlr2kj-_ga31

Ufffff😍😍

📆 Semana 7 El cultivo continúa avanzando en el engorde, con los cogollos aumentando de tamaño y los cálices apilando cada vez con más fuerza a lo largo de las puntas. La resina sigue ganando presencia y las flores empiezan a verse más compactas, mientras la canopia mantiene un trabajo uniforme aprovechando bien la luz. Los aromas del armario se vuelven más intensos y complejos a medida que la planta centra su energía en densidad y producción de terpenos. Seguimos creciendo fuerte 💪!

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.

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Harvested Girl Scout cookies auto from Fast Buds! Very satisfied with result: 200gr. dry buds!. Thank You Fast Buds for consistently such a strong genetics!

dear beautiful old Lady... ... your time has come...

Day 79 - Another week passes, not much to post, normal feeding, 1000 ppm 6.2 PH, normal lights, the girls are fattening up nicely...... 😎 Day 84 - some pics/vids.... pics of a Test Bud (ready for curing)......doing some experimentation..... read up about drying and curing, but i don't have a set method, so test abit..... never grown bud before..... 👍 my tent is really small, i think 50x120x160 or something... and it's tight in there, i have no other source of herb, so i'm going to start getting into the smaller one, and focus the light on the larger one..... i've been trimming and drying all during the grow.... there's really only enough room for the big one, and it's really squishy in the tent........ 😎

Bueno, para no perder a nadie, el sistema que manejo es con dos indoors en paralelo. Uno en flora y otro creciendo la madre. A la madre la hago crecer hasta sacarle esquejes. Luego pasan al otro indoor, la madre y los esquejes, y ahí comienza la floración. Y ahí mismo comienza la nueva madre en el indoor pequeño. La variedad es de un banco argentino que no sé si sigue existiendo. Se llama "kali seeds" y la variedad es superhaze. Que en teoría tiene unas 10 semanas de floración. Día 01. Puse la planta para obligarme a terminar el prototipo. En este caso decidí usar madera de palets y algunas otras cosas que encontré en la calle. Ya casi termino todo, pero me falta armar los cierres. No voy a hacer puertas, dado que no está centrado, así que uso una tela de microfibra que ayuda a opacar mucho y era mas barata que el blackout. Ademas es impermeable y me sirve para un nuevo mecanismo de seguridad para fugas que quiero implementar. Es bastante simple, pero me soluciona mucho. Hoy no hay mucho más que mostrar. Cuando lo haya terminado voy a ir mostrando como va quedando. No me voy a enroscar con los tsp. Voy a poner lo que use aca. Ahora puse un litro de agua con un poco menos de 1g. de Feeding Grow de Greenhouse. Al menos por ahora, ya que tengo que comprar medidores porque los míos ya no dan confianza. Día 4. Ya estoy terminando de acomodar el indoor. Lo forré con refractario e instalé las "puertas" que en realidad son telas tipo blackout, pero mucho más finitas. Me falta terminar de ordenar la electricidad para que cada sector tenga su timer. Van a ser 3 timer diferentes. Por un lado van a ir luces y ventilaciones de flora (12hs). Por otro lado bombas de aire, bomba de agua y probablemente vientos de floración (15 min/hr). Y por último luz y ventilación del modulo de madres (18hs). Hice el cambio del depósito, a uno de 5 litros, ya que los próximos 10 dias pienso intentar mantener la misma solución (mantuve la proporción 1g/L de feeding grow). La planta tuvo un ataque de una plaga que fue a sus primeras hojas. Por suerte en el momento puse tierra de diatomeas y parece haberse detenido. Pero se pueden ver los amarillos en las puntas. No me preocupa, dado que en hidroponia esos problemas se resuelven y la planta se recobra enseguida. Ahora igual habrá que ir monitoreando, dado que me había olvidado de desinfectar el indoor, cosa que hice luego de este ataque. Tengo fé que llegando al mes y medio de crecimiento, ya esté en condiciones de cortar unos esquejes. Día 07. Por el momento el crecimiento viene rápido cómo suele ser en hidroponia. En unos días le voy a estar haciendo el corte apical. La ansiedad me viene ganando, pero sigo con fé. Esta semana tengo que comprar un par de aditivos y medidores que me están faltando. Pero ya está todo encaminado.

Hey Growmies, So week one and my Blackberries has twisted growth for some reason, i may move the light further away and see if that helps. Apart from that shes grown nicely from her initial popping and just pushing out her 2nd set of leaves. Thats all from me this week, thanks for stopping by 😊✌️

Hey! At last the day of the harvest arrived. Before that, I stopped watering the plant 4 days ago, and turned off the lights 2 days ago. As for questionable techniques, I adhere to the principle - if it doesn’t get worse, why not try?😄 So, I put the harvested crop in a dark ventilated box, for about 10 days, I will observe. p.s. I invite everyone to the next update of the diary - I will sum up, remember the interesting moments of the cycle, and of course I will try the finished product, see you! 😍 Glory to Ukraine! 🇺🇦

Switched from acti-vera to bio-grow to trigger flowering. The autoflower is already showing pistils.

Great strain, would recommend. Nice smoke/vapor, friends love it, stupefying and euphoric, no heavy couch lock like heavy indicas. Taste great in The Mighty vaporizer, citrus with a hint of pine.

Vamos familia que ya actualizamos la cosecha de estas Candy Rain de Zamnesia, para el concurso POWER BUDS Plagron x Zamnesia CONTEST. Ya era hora de cosechar, estoy bastante contento con los resultados. Vaya flores que se han marcado repletas de tricomas, y las flores se marcan aromas dulces y afrutados. Es una variedad bastante fácil de cultivar y muy resistente, crecieron desde el principio bien vigorosas, sin problemas y al final de todo recompensó. Las condiciones ambiéntales han sido máximas en 25 y mínimas en 20 y una humedad estable en torno al 36% al final de floración y en el secado. Os comento que tengo un descuento y para que compréis en la web de Zamnesia de un 20%, el código es ZAMMIGD2023 The discount 20% and the code is ZAMMIGD2023 https://www.zamnesia.com/ Espero que disfruteis este diario, buenos humos 💨💨

14 days on the auto watering system and the girls are looking happy. Everything survived well and my reservoir size was just right. They are looking a little hungry, but nothing s fresh mix of nutes shouldn't fix. Things are starting to look frosty. I'll Be pulling all the Larfy bits this week to optimize my tops.

Hello Diary. At the end of the story, I am very happy with the whole cycle and finally the outcome. 😍 More or less all the information is in the diary, there are really a lot of photos that speak more than words. What I would point out at the end of this story, the Hulkberries were different. One was more developed in width and that eventually had a higher yield as well. He reached a height of 105cm, while the other was more developed in height and grew to 117cm. But the Hulkberry is a great sativa strain, I didn’t have any problems throughout the cycle, I didn’t do any training I just did a little defoliation twice. 👌 The branches were dried for 12 days after which they were finished in jars for another three weeks. In the end I would like to thank the Royal Queen Seeds for making this wonderful strain, Grow Diaries where I can learn, and share something I really love. Thanks to everyone who stopped by and looked at the diary, squeezed the like button or commend the diary. See you soon with new journey.

Nothing really Changed. Did a topping today. She's A little taller. Love to See her growing ❤️