The plant started drinking a lot of water, but the flowering is going well. 🌸

Hello! Thank you again for stopping in! Last week was a great and exciting week. I learned a lot to say the least. Biggest lesson LESS WATER!! Haha the plants seem to be growing slower than I expected, but that could just be me rushing things along. 😅 I also added a metal grid to half of the ceiling of tent this week. The panels were only $6 each at Menards and makes hanging and organizing all the needed equipment much easier and not to mention it brings a cleanliness to the work/grow area. I highly suggest them. Day 1 Feb 1st- no water Day 2 Feb 2nd- Watered as needed. Approximately 15ML/plant distilled water. Day 3 Feb 3rd- Watered each plant with 15ml Coconut water mixed at 50ml/gallon. 1 Tahoe OG is growing nicely while other one continues to yellow. Im lost for what to do to correct issue as both are in same environment? Day 4 Feb 4th- watered 20 ml per plant. Moved two more super skunk seedlings to tent. Ordered a humidity controller so I can keep a more consistent humidity. Day 5 Feb 5th- watered all plants with distilled water at a PH of 6.3. Flushed Tahoe OG #2... notnsure why it was yellowing when all other conditions are.same.and Tahoe OG #1 is flourishing.  Tahoe #1 60 ml Tahoe #2 flushed 150 ml SS #1  75 ml SS #2 60 ml SS #3 90 ml SS #4 75 ml SS #5 75 ml SS #6 50 ml SS #7 50 ml SS #8 20 ml Day 6 Feb 6th- no water today. SS #8 died. It honestly never really lived. It sprouted but no leaves ever opened. Added metal grating and humidity controller. The humidity controller is amazing.. well worth the $. It keeps my tent between 67-73 relative humidity. Will be able to dehumidify when the time comes as well. I like a clean tent as well as save. All electrical cords minus 1 are at the top of tent and the 1 is well above the water line. I know this isn't a huge deal as I self water, but better safe than sorry. Day 7 Feb 7th- all plants got 30 ml of coconut water and a healthy foliar spray of distilled water. I've seen some good growth this week and hope to see it continue through next week. I did have one SS seedling not make it this week and one Tahoe OG hasn't shown any growth and is completely yellow/golden brown. I still have it going but not sure what to do or if there is any hope. As always thank you for stopping in. Please like and comment so I know whose following along so I csn reciprocate the kindness. Keep growing!

Que pasa familia, actualizamos la semana de la farm cheese, la trasplantamos a su maceta definitiva, utilizamos sustrato Plagron. Ph controlado en 6,5 humedad algo baja pero pronto pasaremos a floración, temperatura ideal, el led hace si función y aparte no da calor. Los nutrientes los seguimos echando en dosis muy bajas para que no sobre fertilize. Hasta la semana que viene fumetillas.

Put on alot of size, I think they are coming to the end of the stretch now, loads and loads of bud sites and both look so healthy, roll on next 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.

Hey Grow Diaries fam, Welcome back to another update on our PCR adventure! We're at Week 9, which marks Week 4 of the flowering stage, and things are getting exciting! Overview The PCRs are flourishing, and the transformation is nothing short of spectacular. The tent is buzzing with energy, and every day brings new developments. The buds are swelling beautifully, and the trichome production is off the charts. This week has been all about maintaining optimal conditions and ensuring our ladies get everything they need to reach their full potential. Environment and Conditions Tent: 3x3, cleaned and prepped from top to bottom to ensure a pristine environment. Lighting: ViparSpectra P2000, delivering a perfect spectrum for this stage of growth. The balanced PAR output and efficient energy use keep our girls happy and thriving. Watering: TDS at 410, pH 5.8, and water temperature at 21°C. This ensures the nutrients are perfectly balanced and readily available. Nutrient Regimen We’ve kept up with our Aptus Holland feeding schedule, and it's paying off big time. Here's the current mix: Nutritional Spray: Aptus Holland NutriSpray to keep those leaves lush and healthy. TopBooster: Replaced StartBooster with TopBooster to promote flower development. P-Boost: Added to the mix for that extra phosphorus kick, crucial for blooming. K-Boost: a must for them to go fat as we like. The results speak for themselves – lush green foliage and robust bud formation. Defoliation At the end of this week, we performed a mass defoliation. It's always a bit nerve-wracking, but the results are worth it. Removing excess leaves ensures better light penetration and airflow, reducing the risk of mold and pests. Plus, it allows the plant to focus its energy on bud production. And let me tell you, after the defoliation, the PCRs look sexy as ever with their long legs and sculpted structure! Clones Update Our clones are thriving, showing the longest and whitest roots I've ever seen. We treated them with a water mix that included K-Boost and Mycor Mix at 1 gram per liter. This combination has worked wonders, promoting vigorous root development and overall plant health. Reflections This week has been a testament to the importance of a clean environment and precise nutrient management. The PCRs are responding exceptionally well, and I couldn’t be more thrilled with their progress. We're well on our way to an incredible harvest, and I can't wait to see these beauties in full bloom. A huge shout out to: Aptus Holland: For the top-notch nutrients and constant support. You guys rock! Art Genetix: For creating such an incredible strain. The PCRs are truly something special. Grow Diaries Community: Your support and feedback are invaluable. Keep the positive vibes coming! Here’s to another fantastic week of growing! Stay positive, keep pushing forward, and enjoy every moment of this beautiful journey. Genetics - P.C.R. @Art_Genetix_Team https://artgenetix.world/ Nutricion @aptusholland https://aptus-holland.com/ LED Power @Lumatek and @viparspectra As always thank you all for stopping by , for the love and for it all, i fell blessed to have you all with me for one more love journey Thank you Thank you Thank you , you guys are great and have been amazing , thank you for everything ! #aptus #aptusplanttech #aptusgang #aptusfamily #aptustrueplantscience #inbalancewithnature #trueplantscience #dogdoctorofficial #growerslove
 With true love comes happiness , Always believe in your self and always do things expecting nothing and with an open heart , be a giver and the universe will give back to you in ways you could not even imagine so ! Growers love to you all

Soaked seeds all in peroxide solution for effortless germination 48 hours or until root pops out 1mm, than I paper towel them for 2 days for tap roots before planting in the medium. Note: Smile now Cry Laterz and FX3 were started one week later. Not pictured in this post. The first 6 popped were lemon cherry pop, which are from S1 seeds I made from 2 females using the stress method. I just raised my flowering temps for one day at 92 degrees during week 4 flowering to make them herm as an experiment and it worked😅! This was during a hot summer and I just shut off the a/c for a day in the room which I usually keep at 77-82 degrees! So I basically tricked them!

1 woche noch ca. +/- 3-4 tage je nachdem wie es ausschaut.... bin mega gespannt... habe vor 2 tagen schon ein kleinen trieb abgeschnitten um es vorab testen zu können und die sieht schon mega aus 😋😋😋👌😉

I like colorful plants very much, let's see what they look like

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After 20 days in seedling stage. I stopped watering. Planted into bigger pots using new organic soil.

Hi fellow growers, another week and a half has passed so this diary update is a bit over due. As i said in my last update that i was growing on 24 hours of light and thinking about switching them to 18-6, right after writing last weeks diary i made the switch to 18-6 and left it for the past week and a half and that made a huge difference in growth the plants where nice and bushy from the 24 hours of light and they are now stretching towards the light just like we want to see yesterday i made the switch to 12-12 so the next update will be in flowering fase. The day before i made the switch to 18-6 we topped the plants and did a little defoliation but that is hardley noticable in the pictures i added because the new fan leaves developed quick and now they are nice and bushy again, enough leaf surface to take in a lot of light. I think i will be taking out my scrog net somewhere in the next week or so to train them a little but no full on scrog. lighting is now on full power 330 watts full spectrum but is still hanging on 50 cm above the canopy. I give them a little more water every day they get half a liter with hy-pro nutes and rootbastic (the amount added is in the nutes section above) That is all for now. Cheers, Nibameca

------GENERAL COMMENT------ This week was very flat and steady, girls are growing very well and leafs got sharper. They have got a new defoliation session, and a bit of supper cropping to make steams stronger. Nothing fancy, just training to an even or more even canopy. ------GG.AK47 COMMENT------ Girl is growing with intensity, shooting various bud spots, i'm having a very good feeling about the outcome from her! Tips are a bit lighter, nothing to get overwhelm.

Какое же красивое растение!!! Аромат яблока 🍏 и сладостей, есть нотки дизеля.

******************************************** Week 11 mid flower (flower week 5) ******************************************** Light cycle=12/12 Light Power=150w 63% Extractor controller settings High temp= Day 26c, Night 20c Low temp= c Temp step=0c High Rh= Day 50%, Night 55% Low Rh= % Rh step=0% Speed max=10 Speed min=2 Smart controller settings (during lights on). Lights on=9.00am Top fan on=+22.5c Top fan off=-22.0c Dehumidifier on=+50% and -26c Dehumidifier off=-50% or +26c Smart controller settings (during lights off). Lights off=9.00pm Dehumidifier on=+55% and -20c Dehumidifier off=-55% or +20c VPD aim=0.6-1.6 DLI aim=30-45 EC aim=0.2-2.0 PH aim=6.0-6.5 NPK(10.45/9.9/28) 💧💧💧💧💧💧💧💧💧💧💧💧💧💧💧💧 Method= Autofeed 6 drippers. Feed=Flower Nutes. Neutralise=0.1ml/L Bloom=3.0ml/L Silicon=1.0ml/L Calmag=0.25ml/L Pk=0.5ml/L Boost=2.0ml/L Volume=12L Easy Ph down= 0.166ml/L Ec=1.6 PH=6.4/6.5 Runs=14 Run times=5min (275ml each) Gap times=15min Total runtime=70mins (3.85L each) Total flowrate= 110ml/min (55ml/min each) Auto start time=10.00am Auto stop time=2.25pm 💧💧💧💧💧💧💧💧💧💧💧💧💧💧💧💧 ******************************************** ******************************************** 📅28/7/24 Sunday (day 71, day 29 flower) 📋 Hot day. 💧 Method= automatic Feed=Nutes flower Volume=12L Ec=1.6 PH=6.4/6.5 Volume left=L Volume used=L (125ml/min) Volume each=L (62.5ml/min) Runoff. Total runoff=0L Ec= PH=/ Feed=manually @2.55pm 5 mins Feed=manually @3.50pm 5 mins Volume left=2.5L Volume used=9.5L (125ml/min) Volume each=4.75L (62.5ml/min) Runoff. Extra runoff=0.3L Ec=3.2 PH=/6.4 💧 📅29/7/24 Monday (day 72, day 30 flower) 📋 Hot day. Defoliation 📅30/7/24 Tuesday (day 73, day 31 flower) 📋 Hottest day of the year again 📅31/7/24 Wednesday (day 74, day 32 flower) 📋 Hottest day of the year again She's got a bit to much nitrogen in her. 💧 Method= automatic Feed=water Volume=13L Ec=0.2 PH=6.3/6.3 (PH D=0.02ml/L) 7d Volume left=L Volume used=L (105ml/min) Volume each=L (52.5ml/min) Runoff. Total runoff=0L Ec=PH=/ Water=manually @3.55pm 5 mins Water=manually @5.00pm 5 mins Water=manually @5.30pm 5 mins Water=manually @6.35pm 5 mins Water=manually @7.20pm 5 mins Volume left=2.5L Volume used=10.5L (105ml/min) Volume each=5.25L (52.5ml/min) Runoff. Extra runoff=0.5L Ec=3.2 PH=/6.4 💧 📅1/8/24 Thursday (day 75, day 33 flower) 📋 mega hot again. 📅2/8/24 Friday (day 76, day 34 flower) 📋 Hot day 📅3/8/24 Saturday (day 77, day 35 flower) 📋 H=99cm D=16cm Dli=64.9 Ppfd=1489 Slight defoliation. 💧 Method= automatic Feed=water Volume=13L Ec=0.2 PH=6.2/6.3 (PH D=0.025ml/L) 8d Volume left=5L Volume used=8L (110ml/min) Volume each=4L (55.ml/min) Runoff. Total runoff=0L Ec=PH=/ Water=manually @4.10pm 5 mins Water=manually @4.40pm 5 mins Water=manually @6.15pm 5 mins Water=manually @6.35pm 5 mins Water=manually @7.05pm 5 mins Volume left=2.5L Volume used=10.5L (110ml/min) Volume each=5.25L (55ml/min) Runoff. Extra runoff=0.7L Ec=4.1 PH=/6.2 💧 ******************************************** Weekly roundup. 📋 Been a tough week conditions wise. Had consecutive hottest days of the year, so I had a battle keeping temps below 30c in the lung room. She's looking good but a bit over fed on nitrogen, I still have faith this one is going to produce a decent amount of solid nugs. Take it easy. Back soon. ********************************************

This is my largest indoor plant I've ever had! I'm super happy. I have a lot to do with trimming now. Thanks to canna the whole growing process was quite easy!! It took her three weeks longer than the breeder stated but that's okay considering the low night temperatures and the fact that she only got 12H light.

So far everything is going great. I water every 4 days and trying to use as little nutrients as possible as these plants don't like nutrients that much. I haven't faced major problems yet. They getting bigger and bigger each week..

Super frosty looks good

Hey guys :-) She is growing great and will be ready for the flowering tent in the coming days :-) A few cuttings are taken beforehand. Was poured 2 times with 1 .2 l each. have fun and stay healthy 🙏🏻 👇🏼👇🏼👇🏼👇🏼👇🏼👇🏼👇🏼👇🏼👇🏼👇🏼👇🏼👇🏼 You can buy this Nutrients at : https://greenbuzzliquids.com/en/shop/ With the discount code: Made_in_Germany you get a discount of 15% on all products from an order value of 100 euros. 👇🏼👇🏼👇🏼👇🏼👇🏼👇🏼👇🏼👇🏼👇🏼👇🏼👇🏼👇🏼 You can buy this strain at : https://www.ripperseeds.com/en/feminized/kmintz-feminized-cannabis-seeds Water 💧 💧💧 Osmosis water mixed with normal water (24 hours stale that the chlorine evaporates) to 0.2 EC. Add Cal / Mag to 0.4 Ec Ph with Organic Ph - to 5.8 - 6.5 MadeInGermany