Ok Growers! Check it out. Week one, you can tell it's a slow start due to the light that I have. Not much to say about this week, DONT WATER! unless you plant it's definitely asking for it.. try not to over water the firsts weeks. Again, they might be some Spanish in the videos 😅 let me know if something like this but in English would be good around here.

Day 36, 25th of October 2021: Hi there and welcome to the first lovely day of the 6th week that is i beleive the last week of their vegetative stage because I am planning to switch the lamp to 12/12 from next week :) This week is not about LST anymore it is FIMing week that means all of them have FIMmed on all of their "heads" so like each plant approx 6-8 times.... Together, they have strong smell even without flowering lol 😆 Well, CBD Medi Kush is my favourite lady from here she will be another strong and big plant I think. Very cool I like this one even the smell already amazing! Afghani Gold typical bushy midget Indica with fan big leafs 🍃 nice creation she will be nice as well, I don't reckon with big strech :) Spliffs Strawberry 🍓 the typical Sativa with that saw leaves well, here I am afraid a bit of streching as she just FIMmed and Sativa however, I beleive she will be cool with that :) She looks pretty a bit lighter in colour. Blue Berry she is the hybrid lady and still looks a bit pale for me obviously she has got some deficiency but she will make it let's see what comes when she turns to flower.... I am excited 😁 I wanna give them several days before the darkness period which is 3 days and the from next week switching to 12/12. They are FIMmed only so it doesn't really stress them to give them much extra time to recover before flowering. I think it will be the right time to switch on the next week because I can see they really want to flower 🌼 ☺️ 😅 But for now lamp is still 18 hours on, set to be on 150W (approx 60% of the max) ventilation is on for 10 minutes in every 2 hours but the extraction fan is 18 hours on with the lamp... Humidity approximately is the same 50% and the temperature as well +/- 1-2 Celsius. Water intake increased approx 0.12-0.15L per day per plant. Fertilization is the same Epsom salt once a week, and then 2x a week Biobizz Family included BioGrow, BioBloom, TopMax and of course - Vitalink bat gunao also. Ratio is above. Happy Growing 👀

Day 23 of flowering. They are still suffering from trips attack. Did a last EM5 foliar spray today. They receive almost every day 1ml/l from Flowermind, 2 time a week 5ml/l from a banana fermented fertilizer, and 1 time a week 10% of the dosage of a flowering mineral fertilizer.

Note: Moisture and Temp readings are done in the mornings. Lights are on an 18/6 schedule on most days. Unless stated otherwise. 📏: AK1: 22 in (55.88 cm), AK2: 26 in (66.04 cm), North: 17 in (43.18 cm) Quick Notes: At the beginning of the week I was tending to the AKs deficiencies, all plants received a lot of extra nutrients this week. I think it was related to being underfed or underwater. Midway through the week, they started to recover and grow taller. North is on the verge of flowering. I also lollipopped all plants to try and clear the lower region so it's easy to water and so the plants can focus growth on the important parts. Overall the AKs have been drinking up a storm (watering almost every day at this point), I'm trying to keep an eye out for overfeeding. I'm feeding every watering for now until I see issues pop up, then I'll slow down. Next week may be the week I start flower (guessing since these are autos). Day 42 (Jul 8) - Plants look the same as yesterday pretty much, AK1 & AK2 are doing less of the 'preparation droop'. The major yellow leaves are starting to crust off and it seems like the mid/upper leaves are not getting paler / translucent. Watering with a lot of Nutrients this morning. 💧: Tap: x pH (Forgot to measure tap) Adjusted with Concentrated Lemon Juice AK1: 1 liter (5.7 pH, 2.5 ml FloraMicro, 2 ml FloraGro, 1ml FloraBloom, 1.5 ml CalMag) AK2: 1 liter (6.1 pH, 2.5 ml FloraMicro, 2 ml FloraGro, 1ml FloraBloom, 1.5 ml CalMag) North: 1 liter (5.6 pH, 2 ml FloraMicro, 2 ml FloraGro, 1 ml FloraBloom, 1.5 ml CalMag) 💦: 41% (36-58) - 🌡️: 28C (25-34) Day 43 - Lights out overnight, starting 7 hrs from 130am. Lights on, AL1 & AK2 perky, surprised AK2 is perky. The yellowing seems to have slowed on both plants. AK2 developed salty spots on random leaves. *AK2 grew 4 inches in 2 days. 💦: 52% (36-65) - 🌡️: 28C (23-31) Day 44 - Lights 24 hours. Watering in the morning, pots are light and the soil is pretty dry. Giving a little less Nitrogen / Micro and more Bloom to North since she's clearly showing some white pistols (and it doesn't seem to be suffering from the same things as the AK's). 💧: Tap: 8.15 pH Adjusted with pH Down AK1: 1.5 liter (6.1 pH, 2.5 ml FloraMicro, 2 ml FloraGro, 1.5 ml FloraBloom, 1.5 ml CalMag, 1.5 ml Voodoo Juice) AK2: 1.5 liter (5.8 pH, 2 ml FloraMicro, 2 ml FloraGro, 1.5 ml FloraBloom, 1.5 ml CalMag, 1.5 ml Voodoo Juice) North: 1.5 liter (6 pH, 1.5 ml FloraMicro, 2 ml FloraGro, 2 ml FloraBloom, 1.5 ml CalMag, 1.5 ml Voodoo Juice) 💦: 41% (35-65) - 🌡️: 31C (23-31) Day 45 - Soil pretty dry, a little damp ¾ inch below surface. Got 3-in-1 pH / Light / Moisture reader in mail, pH is reading pretty alkaline soil (need to investigate, not sure if accurate). 💧: Tap: 7.10 pH Adjusted with pH Down AK1: 1.5 liter (7? pH [forgot to record the exact amount], 2 ml FloraMicro, 2 ml FloraGro, 1.5 ml FloraBloom, 1.5 ml CalMag) AK2: 1.5 liter (6.15 pH, 2 ml FloraMicro, 2 ml FloraGro, 1.5 ml FloraBloom, 1.5 ml CalMag) North: 1.5 liter (6.15 pH, 1.5 ml FloraMicro, 2 ml FloraGro, 2 ml FloraBloom, 2 ml CalMag) 💦: x% (34-37) - 🌡️: xC (28-30) Day 46 - Lights off overnight (9 hrs), with exhaust fan on so watered pots don't humidity tent. Plants look relatively fine, North's bud sites are developing (think I see 2 new sites). Placed Oscillating fan in tent for more circulation, average temps decreased overall. 💦: 62% (34-34) - 🌡️: 24C (23-31) Day 47 - Lights off overnight (~9 hrs). Spent some time Lolipopping the plants, then watered. *North soil wasn't completely dry yet. 💧: Tap: 7.30 pH Adjusted with pH Down AK1: 1.5 liter (5.9 pH, 2 ml FloraMicro, 2 ml FloraGro, 1.5 ml FloraBloom, 2 ml CalMag, 1.5 ml Voodoo Juice) 875 PPM AK2: 1.5 liter (5.75 pH, 2 ml FloraMicro, 2 ml FloraGro, 1.5 ml FloraBloom, 2 ml CalMag, 1.5 ml Voodoo Juice) 1050 PPM North: 1.5 liter (6? pH, 1 ml FloraMicro, 2 ml FloraGro, 2 ml FloraBloom, 2 ml CalMag, 2 ml Voodoo Juice) 💦: 54% (40-64) - 🌡️: 27C (23-29) Day 48 (Jul 14) - Lights dimmed overnight. Not watering North since the soil is still moister than the AKs. AK soils are not completely dry. All plants are beginning to flower, especially North so I'm lowering FloraMicro for now to see the response and upping FloraBloom. 💧: Tap: 7.60 pH Not adjusted AK1: 1 liter (6.2 pH, 1.5 ml FloraMicro, 2 ml FloraGro, 2 ml FloraBloom, 2 ml CalMag, 1.5 ml Voodoo Juice) ~1200 PPM AK2: 1 liter (6.2 pH, 1.5 ml FloraMicro, 2 ml FloraGro, 2 ml FloraBloom, 2 ml CalMag, 1.5 ml Voodoo Juice) 💦: 72% (41-74) - 🌡️: 25C (24-30)

Last week I confused Blue Mystic #1 and #2, and reported #2 data instead of #1 one. No problem, I’ll be updating with these values from today (just to know, Blue Mystic #1 is 68cm and it’s 57cm far away from the lamp). By the way, #2 is higher and bigger. The same happened with my Dance World #2. Blue Mystic is a beautiful strain. If I touch sugar leaves, I can smell a powerful grape and in general very fruity aroma. Of course it smells like weed, but a sweet fruity weed. It’s really nice. Can’t wait to smoke her flowers!

So I'm doing a little experiment with the clones: took the 2 lowest viable branch pairs and put 1 of each pair into a Jiffy pellet and a rockwool cube. All preloaded with Roots Excelurator and SuperVit at 5.5pH and added some mycorrhizae to boot. Only had 2 days to prespray the branches with Clonex Mist and have been spraying the clones every other day with it. It's been a week with no roots showing yet but the clones have looked healthy throughout and never showed signs of wilting (which I remember happening for a short period the last time I cloned). I expect roots to show in the next day or 2 but who knows. And now for our main story: LSSH1 is showing white bud tips! This is most likely due to the ridiculously close proximity to the light. Not sure what to make of it yet but I guess we'll see if it has any effect on quality 😏 The buds have expanded a very tiny amount and I expect much more this coming week but from my understanding this strain does not produce really dense nugs to begin with. From the results so far I would say the plants have liked the switch to Canna nutes although I would recommend going with the light feeding schedule at least to start with. PK1 still with very tiny buds but it's getting more light now. PK2 seems to be growing faster now on Canna nutes. BTW: on the rare occasion I get my hands on some trichs, my fingers have an unmistakable lemon candy smell 😍

This didn’t save Monday. Thurs: refill Earthbox 2.5 gallons. I put a 2nd trellis net up. - set VPD 1.1 Fri: finished pollen collection for NL #1. Repotted clones 2 of 6 had roots out side of Root Riot. Had more success with a glass of on window ledge. Earthbox BB #2&3: defoliated, tucked trellis. Seeing nice frost.

Smelling lovely These ladies are looking fantastic

yield over 800gs dry . germany grown

I will be careful every time I encounter an insect problem and use an insecticide, I will eventually get rid of it with a water care method

Top-dressed the pots today and watered in the amendments so they can start breaking down and feeding. Took off a few leaves to open airflow and ease the humidity. The fresh intake is bringing in some muggy air, so conditions are still on the damp side—might be time to pick up a dehumidifier to keep things steady. I’m no expert, but the color looks good so far. Just trying to stay on top of things and give the nutrients time to kick in. Tent is starting to smell a bit dank.

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.

26.12.2021 Everything is fine. Finally i have my lamps so now we waiting. The plants feel good. I make a lot of humidity. Happy growing guys

In middle of ripening faze,Girls getting huge and drinks about 2,5 L of water per day nice and sweet smel coming from tent just about 4 am when I waking up 😄 even these are all autos I got them nearly 3 months running and see it on another month or so also still no sings for any colours yet got 2 purple strains in lol next week 3 of them start flush week

Really just a video from this week but I think I was a week or 2 behind anyways lol just so y’all can see some real color of my girls. Still haven’t named em but I’ll be doing that in the next week I’m switching em to 12 gradually within the next week to experiment with some stretching during the transition compared to a straight 12 switch

Phénotype hermaphrodite je viens de trouver une 1ere fleur mal JeCroise les doigtsPour qUe J'en ai peu Phénotype coloré cool j'ai hâte de voir l'évolution !!!!!! merci a tous ceux qui sont passés !!! 👍 Watermelon Automatic: Meet the Offspring of Tropicanna Cookies and Lemon OG Our talented breeders wanted to create a strain that tickled the taste buds to the highest point. To achieve such a terpene profile, they selected two incredibly tasty parent varieties: Tropicanna Cookies and Lemon OG. These two varieties are full of limonene, myrcene and other fruity and earthy molecules. After back-cross and stabilization of these varieties over several generations, Watermelon Automatic appeared with a genetic composition of 75% indica, 20% sativa and 5% ruderalis. This fast autoflowering strain has managed to inherit the delicious terpenes of its ancestors. Growing Watermelon Automatic: A Real Delight On All Plans Watermelon Automatic has a fast life cycle that will deliver some rewarding yields. In addition, its compact and discreet nature allows growers to grow it in places with limited space or environments hidden outside. Indoor plants reach heights of 70—110 cm and if left to their own devices, they will form a broad central branch of heads. If subjected to low-stress trellising techniques, this variety will grow closer to the ground and form a more uniform and productive canopy. Expect a satisfactory harvest of 500 g/m² in just 8-9 weeks post-germination. Plants grown outdoors reach slightly higher heights of 90—120 cm and produce a respectable yield of 100 g/plant. They thrive well in containers, raised beds or directly in the ground. Watermelon Automatic's Aromas, Flavors and Effects: A Triple Threat on All Fronts Although compact and cute, its resinous buds have a heavy striking force. A 20% THC level will smash the body with a superb comforting indica effect that will soothe body, mind and soul. Average levels of CBD come into synergy with the psychotropic cannabinoid to balance the slightest shattering ounce. Take advantage of this strain in the evening to fully enjoy its enjoyable euphoria. By doing this, you will encounter a real armada of divine flavors and aromas from its superb terpene profile. Typical scents of watermelons come to mix with other tropical fruits and earthy notes sublimate an undeniably refreshing smoke. Watermelon Automatic data sheet Variety type: Auto flowering THC: 20 CBD: Medium Indoor Yield: 450 - 500 gr/m2 Outdoor Yield: 50 - 90 gr Indoor Height: 80 - 110 cm Outdoor Height: 100 - 120 cm Flowering Time: 6 - 7 Weeks Harvest Month: 8-9 Weeks after germination Origin & Breeding History: Tropicanna Cookies x Lemon OG Type: 20% Sativa, 75% Indica, 5% Ruderalis Effect: Calming Climate: Summer Long Taste: Fruity, Watermelon https://marshydro.eu/products/100x100x180cm-grow-tent/ https://marshydro.eu/collections/ts-series/products/ts-1000/

Día 88 y penúltimo antes del corte. Ya se aplicó Flawless Finish para un acabado impecable como su nombre lo indica. Siempre prefiero hacer el lavado de raiz solo aplicando agua en las últimas 2 semanas, pero esta vez lo hice aplicando el finalizador y luego los últimos riegos con agua purificada. La verdad es que estoy contento con los resultados de esta nena, que es hermosa por cierto, desprende olores ácidos, cítricos, dulces. Los colores son hermosos y las flores están rebosantes de tricomas, lo que la vuelve muy vistosa. Es todo por ahora, estaré manteniendoles informados en estos últimos días. Buenos humos! 👽

Its amazing how tall these plants are getting, the topped one is just as tall as the non-topped. Flipped these to 12/12 last weekend, no sign of flower yet, added some p/k to the last watering. Slight burning on top leaf tips which I'm guessing is because of it growing closer to the light, I'll have to work out a way to shorten the light hangers.