~ WEDDING CHEESECAKE FAST FLOWER by FastBuds ~ Well fam, here we go again with another epic strain from FastBuds Fast Flowering stable. After having such tremendous success growing their Gorilla Cookies Fast Flower outdoors last year, I've decided to run another of their fast flowering strains outdoors this year... Wedding Cheesecake Fast Flower! The best description of this awesome cultivar comes directly from my friends at FastBuds which is as follows: "A delight for the mind and body: Wedding Cheesecake FF (Fast-Flowering) is a delicious strain that offers XXL yields in a 7-8 weeks flowering cycle. This terpene powerhouse produces loads and loads of mouth-watering vanilla-creamy-cookie-scented terps with hints of citrus and cinnamon. In addition to its delicious aromas, this variety grows very well in both indoor and outdoor setups, yielding up to 650 g/m2 without extra maintenance, making it the ideal strain for beginners as it allows you to maximize yields while minimizing work. This super-fast feminized photoperiod version offers upbeat and energetic yet deeply relaxing effects that are perfect for consumers looking for a heavily focused, motivating, and creative high. It’s the ideal strain for those needing that extra energy boost to start a busy day on the right foot. Wedding Cheesecake FF boasts chunky, large-sized buds with a thick layer of silvery-white resin and bright orange hairs scattered all over: that just screams ‘quality’. The lime-green flowers sparkle with an array of hues ranging from dark to light green, to magenta and purple, and reek of a delicious aroma that’ll remind you of fresh store-bought cheesecake. This is an XXL hybrid that grows extremely tall in height, reaching up to 3m with one huge main cola and multiple long side branches that can withstand enormous yields of up to 650 g/m2 with ease. Wedding Cheesecake FF is extremely resilient to the elements and can be grown in almost every climate as long as you’ve got the space and basics covered, making her an excellent choice for those looking for large-scale harvests with a quick turnaround time without much effort." ________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________ The Setup: This is going to be an outdoor grow, but I have started the Wedding Cheesecake FF indoors as our weather is still too cold to put her outside (nighttime temp's dipping regularly into the 30's℉). The plan is simple... let her grow inside under a 19/5 light schedule until the nighttime temperatures stay above the mid 40's℉, at which point she'll be moved outside and transplanted into the soil which I have already setup and inoculated with beneficial microbes, and then let the fun begin!🤪💚 ________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________ Weekly Updates: 9/6- Well, Week Five of flower is here and the Wedding Cheesecake FF by FastBuds is rockin-n-rollin! Well fam, the 'Beast From The East' is going strong, and so far has not encountered any issues with any bud rot but is showing signs of the beginnings of Septoria. Luckily, this far into flower it shouldn't be too much of a concern at this point. This late in our growing season I always worry about Boytris, especially with cultivars that have really dense and tightly grouped flowers as our weather is now turning cooler and wetter. 9/8- I'm continuing to water the Wedding Cheesecake FF in the mornings on days that we do not get any substantial rain with well water via the garden hose. Today I went through the plant and removed a bunch of old dead leaves, along with any shade leaves that were totally yellow. I did not water today as we had a good amount of rain yesterday and the soil is still really moist. 9/10- My daily routine of watering, removing dead foliage and checking over the flowers continues. The aroma coming off of the Wedding Cheesecake FF is really loud now and you can definitely pick up some subtle hints of her Cheese lineage in it! 9/12- With Five weeks of flowers now behind her, the FastBuds Wedding Cheesecake Fast Flower only has 2-3 more weeks to go (weather permitting) and she's on track to be an enormous yielding plant! I can't wait!!! Thank you for checking out my diary, your positive comments and support make it all worthwhile! 💚Growers Love!💚😎🙏

Smell is amazing even though yield is low. I blame the super hot 90+ degree days. Then we had lots of rain to flush out all the nutes in the pot- so Mother Nature is really trying to help here Regardless- I’ll get 4 good nugs and they smell amazing

Couldn’t manage the stretching anymore ... heartbreaking but this is the end for this G14.

Semana 2 Flora: Liguei o segundo painel, uma Quantum Board Lmb 301 da Samsumg - 120W / 3000K. Continuo alimentando a planta apenas com água e fertilizantes orgânicos. O desenvolvimento da planta foi enorme nessa primeira semana de flora, ja comecei a fazer umas desfoliações. Translate by Google Week 2 Flowering Stage: I connected the second light, a Samsumg Quantum Board Lmb 301 - 120W / 3000K. I continue to feed the plant only with water and organic fertilizers. The development of the plant was huge in that first week of flora, I started to do some defoliation. Hugs from Brazil

Flower is upon us and now the journal is caught up. I will be giving weekly updates at this point as they happen, playing catch-up is over but I did want to get my journey started on this site. Still a relatively new grower and I have plenty to learn.

Another week has flown by! The girls are doing great, cruise control this week as I have just been monitoring RH and temps. Trying to keep them as low as possible, I’ve been getting as low as 74 during the day and 68 at night. I finally took a look a look at the trichomes with my jewellers loop, lots of cloudy, and a few amber around the leaves and top colas, but still lot’s of clear trichomes. I’ve ordered myself a wireless/usb digital microscope to assist with the process, and looks like it will be here just in time to determine harvest day. 😎🎄 I started by eliminating the nutrients at the beginning of the week. I typically allow for 3-4 pure water feeds before I harvest, and at the rate they have been drinking, this should be enough to get through the 7-12 days they have before harvest. I don’t flush, but rather “rinse” with normal water amounts, allowing the plant to use up the remaining nutrients in the soil. This also allows me to recover most of the soil from my grows and reuse ♻️ with other soil mix. There has been great debate and a great deal of bro science out there for many years, but the recent studies suggest there is no difference in end result when it comes to flushing or using nutrients right until the end, if a proper dry and cure is performed. What do you think? What do you prefer to do? Thanks for reading this far, leave me a comment with your preferred method 👊🇨🇦❤️

I do not know how it happened but it did… She has decided she want to reveg herself. I hope you can see what I mean, if you compare week 18 and this 23rd week. She’s now bush and showing off her new growth, I am caught between defoliation or letting her grow wild and uninterrupted, the problem lies with blocking other new growth from getting enough sunlight, I remember change her position to try get both sides growing at an equal rate but all I did is made the one lacking to be the one leading in growth. Loving her scent, fruity sweet, though has a slight hint of diesel.

7/19: Started new nutrients today. Filled gallon jug with new nutes. Poured half of new nute mix in half gallon jug. Poured the entire half gallon jug into reservoir. 7/20: Bumped light intensity to 50% 7/21: Filled reservoir to the 2nd line today. Added a total of 1 gallon to res to get it to that line. Poured the rest of the mixed nutes for this week (half gallon) and then another half gallon of just plain water. 7/24: Bumped light intensity to 55% 7/25: Sadness today 😞.. While in the process of doing more LST today I accidentally snapped the main stem. I Panicked! Moved plant back in opposite direction to counteract the split. Will be monitoring very closely! 🙏🏾 ***** For this Grow****** “Day Air Temperature” will be the max temp of tent for the week. “Substrate Temperature” will be the average temp of tent for the week. “Night Air Temperature” will be the lowest temp of the tent for the week.

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.

64.nap Valami nagy robbanás volt az ak47 lányokon.. Nagyon meleg van és szeretik 4 naponta itatomm őket Ma nagyon meleg volt 34fok a fólia sátorban gondolom több

Hallo liebe Gartenfreunde 🙂 Es geht in die letzte Runde. Wie im letzten Update schon mal angesprochen, mussten wir von einer Seite des Haupttriebes was weg nehmen da es eher abgreift ist. Der Trieb wurde durchgehend nicht so gut versorgt wie der Rest der Pflanze. Dennoch, dafür dass sie sehr viel sich selbst überlassen war, ist es soweit ok. Wir hoffen sehr, dass sie nicht alt zu sehr vermännlicht. Ab und zu sieht man mal ein Vermehrungssamen. Olle Zicke sie 🤭 Im ganzen trotzdem ein tolles Experiment(9 Monate), tolle Erfahrungen, was zum Beispiel das Thema Erbgut angeht und insgesamt hätte es viel schlechter für solch ein Vorhaben über 2 Generationen und 2 mal kurzer Blüte registration laufen können. Die Reife der Trichome bei dem schon abgenommen sind Milchig und 10 Prozent ca. dunkle bzw. Lilafarbende Drüsenköpfe. Passt soweit, aber man kann schon mit bloßem Auge sehen, dass sie kaum Blüten Volumen aufgebaut haben. Aber es ist halt so 😇 Wir werden ab jetzt ins Spülen über gehen und zum Wochenende wahrscheinlich komplett Ernten. Alle zwei Tage wird Sie Wasser mit CalMag bekommen ca. 0.6 l und ab Freitag wahrscheinlich für 48 Stunden trocken und dunkel stehen. In diesem Sinne wünschen wir allen eine angenehme neue Woche und viel Erfolg bei euren Vorhaben! 🙌 Falls, vielen Dank für das vorbeischauen 😉 Viele Grüße an alle Gartenfreunde 😎✌️

Things are really starting to smell strong and getting fun. Seeing some frosty Trichomes. Excited!

Hello Growmies, Our week 13 marks the harvest of the Watermelon Candy strain, a reflective moment that encapsulates our journey. With a wet harvest tallying at 419 grams from three plants, it's evident that the repotting process played a pivotal role in our yield outcome. Despite this, the harvest, although modest, is a testament to our plant's resilience. Throughout this grow, our meticulous environment control, courtesy of the Mars Hydro setup and TrolMaster's precision, ensured our plants thrived in stability. This experience has highlighted the delicate balance of growth, particularly how repotting can significantly impact our plants' performance, with only one plant weathering the change successfully. This cycle's standout plant serves as a beacon for what could be achieved. It exemplifies the sheer potential of a well-timed and well-executed grow strategy, paving the way for future harvests that align with our high standards. A heartfelt shoutout to Patricia from the Zamnesia Family is in order. Her consistent support has been instrumental throughout our growing endeavors, enabling us to share our story with a wider community. Let’s also appreciate the stellar TrolMaster team—Sascha, Ying, and Caren—for their expertise and guidance, which has been integral in refining our grow environment. As we bid farewell to this cycle, we carry with us the valuable lessons learned and an eagerness to apply them moving forward. We embrace the quality of our Watermelon Candy harvest as a clear indicator of our dedication. Looking ahead, we anticipate future grows with optimism, ready to optimize and advance our methods for even greater success. Stay lifted, stay curious, Salokin P.S. Reflecting on this harvest's scale, we're inspired to strive for excellence, fueled by the guidance and support of remarkable individuals like Patricia and the TrolMaster team. Here's to the promising yields ahead that they'll help foster.

Week 9...coming down the home stretch. The buds keep adding more frost by the day. My dehumidifier stopped working in the middle of the night yesterday, I didn't catch it until evening. I hope it didnt start mold growth. The tent was 80% humidity for about 8 hours! The smell in the air is starting to become very dank like a very fruity diesel.

Monday Gave her some enzyme, I think it's supposed to help the plant break down nutrients so we'll see. I'm exactly 70 days from seed, 63 days since I transplant it to the 10 gallon pot, it should be a 10 week auto flower so I'm hoping I'm close to harvest. The flowers are really starting to turn purple now, I suspect its a sign that it's finishing, looks really cool close up! Tuesday No work done today, dry day. I think the buds are ripening, that purple is really starting to come out right across the canopy, can wait to see what it's like right before cutting 😀 Wednesday Gave her 5l of water with 5ml of plagron pure enzyme, I'm checking the trichromes under a glass every day now to try catch the right time to harvest, the buds are so frosty, still clear trics I thunk. Thursday Dry day today, its very nearly finished, trics are stating to turn Amber, I reckon I will give it a week more, maybe less and then I'm cutting! Friday Just clean water today, nearly at the point of cutting! Saturday No work done today, tomorrow is the last watering, its going into 2 days of darkness and then I'm cutting, so much work now so close! Sunday OK, so I think I've given it the last watering, I've just turned off the light and I'm going to leave it in complete darkness for 48hrs, then it's cutting time! 😀 I'm going to hang the plant whole, I'm only going remove some of the bigger fan leaves then dry trim, I've read that it's better that way, we'll see

The looks on this one are sexy! It also burns even. Effects wise, first 15 mins you perceive a high cerebral rush that peaks at 30 mins. Makes you feel creative and with energy. Later on, the cerebral effect dissipates and leaves you feeling all giggly and relaxed in da body. The smell is all about sweetness and gas with a funky grapey smell hugging and keeping those close. Colors didn't showed much cause of the 24/0 light cycle but it ended up showing some purple hues during late bloom. Overall this girl was so fn grateful with the treatment she received.

9 out of 10 seeds germinated 4 x WW and 5 CSC. Germinated in paper towel then moved to easy plug sowing kit then to small pots coco coir 30/70 ph water only. Bit of stretch as under a low powered led that was set too high. Now under Spider Farmer 300 watt led set at 25% at 12 inches. Best of the bunch will go to Autopots x 6 running GT nutrients veg 2 part and Great White Premium Mycorrhizae. Under Mars FCE 8000 and CO2 system with inkbird icc-500t controller. Controller is a nightmare to program with the poor manual. Hoping to set at 800 ppm for veg stage.