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.

Lost some footage sadly but they are done :)

Smell Increased a lot this week and got that real sticky-icky-ickyness to the touch now it’s like glue :) and smells fire… So fruity and sweet took a few more fans off possibly almost all apart from a few lol got a bit aggressive with her so she paid me back by giving me hives or whatever the bumps on my arms I always get are haha 😂 but yeah to allow the lighter green lower bits to get a little More light for the last few weeks 💚🔥💪

I still found a few places with bud rot and I keep removing every spot I see. The plants have been doing fine beside that, they are looking and smelling great, they are super dense and I can't wait for them to be ready. Most trichomes are still clear so I am awaiting for the first ambers to show up, aiming for around 5% amber and 95% milky.

Über die letzten Tage habe ich die einzelnen Nährstoffe aus der NL gerechnet und in 3 Schritten "ausgeschlichen". 1: Tag 56 Zuerst habe ich den Phosphor rausgenommen, indem ich das PK13/14 gegen Mono-Kalium getauscht habe. EC von 3,3 auf 3,0 gesenkt. 2: Tag 66 Etwa 10 Tage später habe ich das Kalium weggelassen und bin auf das normale Schema ohne PK13/14 zurück gewechselt. Zusätzlich habe ich das Magnesium rausgenommen, indem ich den Calmag-Agent durch Mono-Calcium getauscht habe. EC von 3,0 auf 2,8 gesenkt. 3: Tag 70 4 Tage später habe ich dann den Stickstoff rausgenommen und das Calcium minimal reduziert, um die Verhältnisse aufeinander abzustimmen. Ec von 2,8 auf 2,0 gesenkt. Außerdem trinkt die OG Kush den Tank ja in einem Tag leer, also gebe ich ihr am Morgen kein zusätzliches Wasser mehr. Sie leidet also am Abend ein wenig an Trockenstress, bevor sie neue NL bekommt. Die Chemdawg schafft das nicht, also lasse ich sie "normal" laufen als kleinen Vergleich. Sie bekommt alle 3 Tage neue NL, da sie höchstens 1 Liter am Tag trinkt. Für den anfallenden Trim hab ich mich schonmal mit einer Waschmaschine vorbereitet, da mir die letzten Male von Hand rühren oder in der Box schütteln zu anstrengend und zeitaufwändig war. Ich werde nur 2 Siebungen machen und zwar 160er micron und 45er micron, da mein Anspruch da nicht übertrieben hoch ist, was die einzelnen Stufen angeht. Alles von 45 bis 120 war immer ok für mich. Die ersten Übungen mach ich mit den Resten aus dem Outdoor-Run, das ist eh nicht gerade der Hit und kann deshalb für sowas gut herhalten.

Inizio 2 settiman...anche loro stanno venendo su benissimo.da questa 2°settimana inizierò anche dandogli poco Ph perfect ,......... Oggi 17/10/2024 .queste papaya cookies auto Che mi ha regalato la cara Molly di fastbuds, stanno esplodendo di vita😉💪🙏🤣😂.... Forza belle piantine mie ... Oggi 18/10/24 sto pensando di toppare una di ogni varietà...tipo 3 le toppo e 3 no e vediamo qual'è che viene meglio Toppata...,....

Gracias al equipo de Zamnesia, Marshydro, XpertNutrients y Trolmaster sin ellos esto no sería posible. 💐🍁 Frosted Guava: La Frosted Guava es una cepa índica dominante y súper resinosa, que es un cruce de la Guava y la Frosted Skywalker. Con unas características de cultivo muy versátiles, un aroma exótico y afrutado, y un subidón relajante y lúcido, la Frosted Guava es ideal para cualquier plantación de marihuana. 🌻🚀 Consigue aqui tus semillas: Código Descuento 20%: ZAMMIGD2023 💡TS-3000 + TS-1000: se usaran dos de las lámparas de la serie TS de Marshydro, para cubrir todas las necesidades de las plantas durante el ciclo de cultivo, uso las dos lámparas en floracion para llegar a toda la carpa de 1.50 x 1.50 x 1.80. https://marshydro.eu/products/mars-hydro-ts-3000-led-grow-light/ 🏠 : Marshydro 1.50 x 1.50 x 1.80, carpa 100% estanca con ventanas laterales para llegar a todos los lugares durante el grow https://marshydro.eu/products/diy-150x150x200cm-grow-tent-kit 🌬️💨 Marshydro 6inch + filtro carbon para evitar olores indeseables. https://marshydro.eu/products/ifresh-smart-6inch-filter-kits/ 🍣🍦🌴 Xpert Nutrients es una empresa especializada en la producción y comercialización de fertilizantes líquidos y tierras, que garantizan excelentes cosechas y un crecimiento activo para sus plantas durante todas las fases de cultivo. Consigue aqui tus Nutrientes: https://xpertnutrients.com/es/shop/ 💻 Trolmaster Tent-X TCS-1 como controlador de luz, optimiza tu cultivo con la última tecnología del mercado, desde donde puedes controlar todos los parametros. https://www.trolmaster.com/Products/Details/TCS-1 📆 Semana 4: Aparecieron un monton de erizos esta semana, el temporal ha hecho algo de mella en la carpa al bajar las temperaturas aunque todo sigue correcto. Continuamos con las dosis de nutrientes recomendadas por el fabricante.

Started Week 9 Day 57 Very proud of being a Canna Grower Very proud of planting the first seeds Now look what we have after almost 60 days, full of buds, crystal en resin coming deep in each flower! Day 58 Time to feed them nutes Going hard 1900ppm This is my top and then going down Then flushing so they get what they need and clean the extra for last 2 weeks Day 59 Not bad after all, no nutrient burnt All leaves looking good All plants doing great And getting closer to the harvest season! Day 60 Probably gonna give them some tap water 143 ppm TDS reads Ph 6 sounds good to me! More pictures coming up soon... Day 61.62.63 She's doing great didn't have the time to go crazy on pics lately so I owe you that guys Sorry but for next week will have tons Quick update They're doing good but it was hot lately like 28/30 at night and 32 at day inside AC Humidity lvl was 60/70% Was Rainy outside some days Not anymore tho

12/8 - Here we are at the beginning of week 10. Her buds are starting to frost up and she is definitely bulking up more than her sister, but her sister has a longer projected flowering time-frame (Heavy Sativa vs Indica). Anyways, did some minor pruning for airflow optimization and to remove some unhappy leaves from her undergrowth. They weren't yellow, but they weren't getting enough light and it was showing. Haven't done much to her this week other than top her off with Tap every other day. Seems like her feed from last week was on point as her pH and EC were solid as the water level lowered. After her first top-off, her EC started to fall as she ate more (reflected in the lower ec in the res after topping off with tap). Tapered her down to 80% strength as she is moving further along in flower and should hopefully finish sooner than her sister. If she needs a bump in her EC, I may top off with full strength nutes, but I'm going to just wait and see how she responds. Breeder's timeline reflects a ~65 day seed-to-harvest, but I can assure anyone out there growing this strain in DWC that she will not be ready in that time-frame. Currently she is sitting on day 67 and still looks like she has another 2 weeks or more. I grew her in soil before and she was ready pretty darn close to her expected time-frame (~70 days), but this strain responds to DWC differently. She didn't have slow growth or anything; just seems like she will veg longer in hydro than in soil. Not sure why. Thanks for stopping by the garden, and, as always, Happy Growing!

Great growth this week despite a pretty scary heat wave that rose my tent temp from 78-84/85...but she survived!

All good, buds are packing on weight. Feeding will be 3 times this week, afterwards it should be enough nutrients in the soil till finish. Smell is getting stronger, i like the scent! It’s not skunky more fruity and minty. I removed the lower fanleaves. Maybe I will cut the Upper fanleaves at the end of the week. We will see. I will update over the week. Humidity over nights is constantly above 80% currently. I have no idea how to get the Lady in a more dry environment… so this is a real test concerning her mold resistance… And the hours of direct sunlight are going down towards 4h soon… it is a race against time… Wednesday: today it’s windy. Added a video. Friday: a lot of pollen from the trees around in my buds… maybe I will try to pick the shit out of my beautiful flowers… The buds getting bigger… maybe i will harvest end of next week to reduce the risk of mold….

Start of week 7 and they looking great I think 🙃 had a problem with spiders but it's controlled now. That product "Anti-Sniper X" did worked very well. What you guys think? Out of 10?

Começamos na semana 5, não tenho registos das semanas anteriores, espero quer gostem deste diário em português. A Planta do meio é a NLA e as em volta as GGA. Atualização com fotos todos os Sábados. Resumo DIario: - Dia 37 - 04/10 : Misturei 50g de guano de morcego (1-15-1) na superfície de cada vaso, reguei cada um deles com 1.5L de agua com Ph ajustado em 6.3, o desenvolvimento está bom, sem nada mais a apontar. - Dia 38 - 05/10 : Notei um aumento significativo na intensidade do cheiro, estão a crescer bastante bem, não apresentam nenhum problema de nutrição, a NLA, naturalmente, está com a floração mais atrasada. - Dia 39 - 6/10 : Fiz mais uma rega de 1.5L em cada vaso, o solo estava seco, como já havia fertilizado o solo á 2 dia com guano de morcego, coloquei apenas 3ml/L de CANNA Terra Flores e ajustei o Ph para 6.3. Elas estão a exigir muita agua, é bom sinal. - Dia 40 - 7/10 : As meninas deram uma boa secada no solo, a intensidade do cheiro está realmente mais forte, estão a florir bem. - Dia 41 - 8/10 : A terra estava praticamente seca, reparei que uma das GGA está a apresentar a ponta das folhas amarelada/queimada, principalmente nas folhas inferiores, poderá ser possível carência de Nitrogénio, pois é um nutriente móvel que a planta pode levar para as folhas superiores na falta do mesmo, adicionei 2ml/L de CANNA Terra Vega, que é um nutriente baseado em Nitrogénio e Ferro, á solução habitual, ajustei o Ph para 6.3 e reguei cada vaso com 1.5L, vou deixar a terra secar bem em 3/4 dias e acompanhar como reagem.

Día de cosecha y la verdad estoy muy contento con lo que veo, son hermosas estas flores y su fragancia exquisita. La planta tuvo una deficiencia de Cal/Mag, la que se corrigió a tiempo pero de igual manera afectó en su crecimiento y rendimiento, más allá de eso estoy feliz por las flores de calidad que tendré para degustar más adelante.

Die Bedingungen sind in der letzten Blütewoche sehr gut! Die Entwicklung der Blüten sind sehr gut und es geht dem Ende zu. Ich denke in 2-3 Tagen sind Sie bereit zur Fällung. Tage der Keimung = 4 Tage. Tage in Wachstum = 28 Tage Tage Blüte = 42 Tage Wachstum h Woche 9 = 0 cm 2 mal in dieser Woche mit Purolyt Mischung 1:25 besprüht Lichtstärke: 75 % PPFD: ca. 630 umol Lichtabstand: 35 cm Std Tag/Nacht: 18/6 Temperatur Tag: ca. 26,0 Grad RLF Tag: 50% Temperatur Nacht: 22 Grad RLF Nacht: ca. 50 % VPD Wert: ca. 1,0-1,2 PH Wert Wasser/Düngelösung: 6,3 EC Wert: 0,4 Ventilator Oszillation: Stufe 1 Befeuchter: an Entfeuchter: aus Zusätzlicher Entfeuchter: 0 Stk. außerhalb vom Zelt im Raum Bewässerung: 2* bewässert mit Dünger mit den o.g. Mengen, Purolyt Besprühung: 2 mal Fast Plant Spray: 0 mal Controlling: Grow Control Dünger: Greenbuzz Nutrients Licht: Pro Emit Vollspektrum Abluft: EC Carbon Active 750 m3 gesteuert Danke an James von Royal Queen Seeds für die F1 Seeds. https://www.royalqueenseeds.de/56-f1-hybrid-cannabissamen Danke an Greenbuzz https://greenbuzznutrients.com/de/ Ihr bekommt 25 % Rabatt bei der Nutzung des Codes auf der GB Homepage https://greenbuzzliquids.com/de/shop/ Code: GD42025 (Mindestbestellwert 75€)

Salute comrade ! According to the passport, it would be time to harvest, and they look very appetizing. Not all trichomes are still amber, it will stand for 1 week in a solution with honey and molasses. 5 days of flush, 2 days of the night👌

Really love the smell, one plant yielded about 5oz the other about 3. As far as I can tell the herb from either is as good. Yeah an award winner for sure. Wow what a taste✌️🏻🤤✌️🏻 Update. 2 plants grown, 1 was better but both very good. From the better plant, 5 people to date who I have let sample excellent quality dried and cured buds of Zombie Kush have all reported to me that it’s the best herb they’ve ever tried😉😂😍😍😍😍😍😍 I was smoking it outside a Wailers concert this week also and about 3 people there couldn’t help but compliment on the smell. This stuff really is top quality and I could truly smoke it 24/7