This week I decided to change MH 250w to HPS 250w, at same time I changed light schedule to 12/12. So I have 250w HPS plus 120w 2 cree cobs 3500k now. It's first time I use this light setup. Last times I used MH 250w and HPS 400w without the LEDs. I also removed some of popcorn buds. Maybe I'll remove more next week and also I'll remove some leaves in the future. I watering every 2nd/3nd day, every 2nd time with nutrients. I give about 3 liters for Lemon and about 2 liters for Diesel. Lemon shining silver haze is huge in my opinion. I pretty sure if I didn't top it and didn't train it now it should be somewhere between 1-1,2 meters or maybe even more! 😮Looking very strong and healthy. Very good genetic. The seed was the smallest I ever saw, about 2mm and so much power in this little baby 😀 I can't say same about Diesel. It's like 2-3 times more compact than Lemon. I think it's not genetics that course growth like this. I have a theory. I think I didn't put (sit) the plant in the soil mix well enough when I had transplanted it or maybe I damaged the root. Because the main stem was very loose in the base. BTW Diesel looking healthy now.

hello, quick update.. I got another fan which is amazing.. čubičky (my plants) looks healthy and that's most important.. <3

Starting off week 7. Gotta love the holidays! Good to catch up with family, but sucks when you can't get time to water. Water deprived 2 more times this week. Also had several bleached buds on various plants and my favorite light was now done with the other tent, so swapped it over now. led. Spaectra has much better even par distribution than my king leds. Got about a month or so to go. Still not bad given the neglect and over use of light they've recieved over last couple weeks. Hoping to get everything dialed back in for the remaining month.

New week! Tips and help from last week, I had around 1500 ppm and I did flush my roots in water and change everything. Now is around 1000 ppm and dropping 150 ppm a day. Did read about water level in DWC and how to increase the grow with water. I had the water almost up to the root or the level of there the basket is. Now I have 1-2 inch (2-5 cm) below where the roots come out. This create air roots. I'm not sure if it's the air roots or the ppm but my flower is boosting. Can se buds grow!! Trimming so I can keep the same hight. Have any tips or rekomandation? Only have one question for next week and this is: it's looking a bit thigth between the buds and all of the leaf is cristal on it. Should I cut some more leaf? And what leaf should I trim? Is so thigth in there. Or will it grow fine?

The plant on the right got chopped down the hairs were 90% dark brown while left was fully white last week when it got taken down it had only one day flush. This plant I will flush for a week and see which is better. It has decent size buds all the way to the bottom but this one growing still doesn't have as many crystals as the harvested plant which was definitely cut down way to early 😕 shame it must have forced to finish early from shock when I snapped a main branch clean off. This plant I will flush with plain filtered water for 7 days and even if it doesn't have as much crystals as the other plant, the bud size is 2x-3x the size of the plant that was cut down last week so I hope they will look a lot better size wise after they shrink when they are cut down and dried. I have also noticed some medium sized fan leads turning from green into a beautiful dark purple colour over the last 2-3 days slowly and it's spreading to other leaves the buds on this plant are also purple bits it's hard to see on here but looking sweet so far I have uploaded pic of the frost one which has been drying for a week now

LJ 2Q24 Flower Week 6 Start of Week: - [Sun Aug 4, 2024, LJ 2Q24 36:F:6:1] - Plant Heights: [ 25, in] End of Week: - [Sat Aug 10, 2024 LJ 2Q24 42:F:6:7] - Plant Heights: [ 26, in] EC: 2.4. # Until Week 10 __ Sun Aug 4, 2024 LJ 2Q24 36:F:6:1 Add 7.5 ml of Dr. Zymes to 1 PT of Last Two Plants Feed (Ran out last night) THIS CHART FOR WEEKS 7 - DEHU Water, Reducing Lush Green (N), Eliminating Root Anchor + PSP, 1 Drop Beauvaria Bassiana Soluble __ Mon Aug 5, 2024 LJ 2Q24 37:F:6:2 RLA Week 6 +BioAg TM-7 Nik wonders if it might actually be a molybdenum deficiency w/ Lemon Jeffery. __ Tue Aug 6, 2024 LJ 2Q24 38:F:6:3    Environmental: - LightIntensityAvg: [ 836, µMol/m2/s] - TempAvg: [ 78.4, °F] - RHAvg: [ 65.7 , %] - VPDAvg: [ 0.90 , kPa] - EC: [ 2.4, mS] Note: - Nik @TheRootedLeaf mentioned Molybendum as an ESSENTIAL µNutrient participating in Nitrogen Reduction. - The BioAg TM-7 contains Mb, Apply @ 1 tsp/gal  __ Wed Aug 7, 2024 LJ 2Q24 39:F:6:4 __ Thu Aug 8, 2024 LJ 2Q24 40:F:6:5 Note: - We really need at least 2 Fertigations/day, @2000 & @0130 - We’ll water to saturation each event (10% Pot Volume, 440 ml/plant/event) - We need 440 * 2 * 7: 6.16 Liters,Need 1.62 Liters, Will mix 1.75 - Need to increase daily total from 1.5 to 2 Gallons - 1.1 L/Plant/Day - 440 ml/plant/event * 2 Per Event - Estimate Minimal Runoff - Pot Size 4.4 Liters - Saturation: 440 ml - 0% Runoff 1.75 Gal, 5700 ml, 814 ml - [x] Light Defoliation (as needed/lowers) Feed Chart for 1.75 Gallons Apply 440 ml/plant @ 2000 & @ 0130 - [x] Mixed! 2024-08-08T16:03:01-0500   __ Fri Aug 9, 2024 LJ 2Q24 41:F:6:6 - [ ] Collect Dehu Water - [ ] Water 440/plant @ 2000 - [ ] Water 440/plant @ 0130 880 ml/plant/day * 7 : 6160 ml, 1.62 Gal __ Sat Aug 10, 2024 LJ 2Q24 42:F:6:7

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.

Hallo zusammen 🤙. Sie wächst sehr schön und macht keine Probleme

Wir starten in die BW 5 Pflanzen sehen sehr gesund aus. LST ein wenig nachjustiert. Richtiger gesamt Bericht Ende der Woche

Welcome to Bud Boutique Grow Diary - really appreciate all your love and support :) Dont forget to check out my other current grows! 🗓️ This Week: - Day 52: the end is near - Day 53: Trichomes check from #1 and #2 - looking super good almost all cloudy, a few amber and clear. perfect point to chop - Day 54: this one is finished, let's chop them both #1 & #2 !! ✂️✂️✂️ - both phenos got still super purple beautiful leaves - now its time to dry inside the tent at about 60%rh and less than 20°C/68°F trying to get it even lower for the next 10-14 days ___________________________________________ --- 🌱 Strain (Sponsor) --- 🏷️ P.C.R. by Art Genetix https://www.artgenetix.world/product-page/p-c-r --- 🥗 Nutrients and Feeding (sponsored by APTUS: APTUS Ambassador) --- 🍸 APTUS: full nutrient schedule extreme -- Regulator, N-Boost, P-Boost, CaMg-Boost, K-Boost, Allin1 Liquid, Startbooster, Topbooster, Enzym+ every feeding -- Fulvic-Blast, NutriSpray as Foliar each once a week 🔗 https://aptus-holland.com/ --- ♻️ Grow Control (Sponsor) --- TROLMASTER: TENT-X + LM14 Light Adapter to dim/sunrise/sunset lights + Temp & rH Sensor all remote on App 🔗 https://www.trolmaster.eu/ --- 🚿 PetraGrow (Sponsor) --- CannaFogger Foliar Spray 🔗 https://www.petratools.com/product/petragrow-cannafogger-atomizer-new-mini-fogger --- 🏭 Grow Setup --- 💡LUMATEK Zeus Pro 600 * 🏠🌿 Indoor: Homebox 120x120x200cm (4x4) * 📐🌀 PrimaKlima exhausting Fan 1180m3/h (running on 60-80%) * 🌀 Can Light Filter 800m3/h & 1x Fanbox 1x Dyson fan for Air circulation 🔗 https://lumatek-lighting.com/zeus-600w-pro-29/ 🔗 https://primaklima.com/de/shop/ventilatoren-de/ec-ventilatoren/pk160ec-tc/ 🔗 https://canfilters.com/products/filters/ All Likes and comments are highly appreciated!!! 👨‍🌾 don't forget to check out my Instagram for daily educational content: budboutiquee - Bud Boutique

These ladies are getting humongous, honestly scared to see how big they get in flower since the still have roughly a month before I will have room in the tent!😅😅

3 ml npk in 2 l water And given half of it! Plant seems to like it And pruning worked wonder! Leaves are healthy and getting much bigger in size! 15 cms+ excited!!

34g und 32g

Week 1 flowering is just over for our melonade Runtz from Dutch Passion The stretching is amazing, they really doubled the size or even tripled the size. We are adding some bloom nutrients now and lets see the buds starting to appear the next weeks.

this week I was a lil happy because I pollinate my C4matic with a Male pink kush the feminizing spray tiresias mist didn't work the way I thought it would. thank God I had a Male coming up in my outdoor garden...I can already see seeds a little more than I expected, for some reason I only wanted to pollinate 1 bud but got seeds on the main and a few lower buds still happy for that will update images .

Another easy week for the Runtz ladies ❤️ I’ve been watching closely and counting down, they are getting so close but could still go a little further without getting too much amber. I’m trying to time the harvest to go along with my other strain I have going as I have no other space available 🙈 I switched to straight PH water the end of last week, and they have gotten three feeds with runoff since, there will probably be 2 more. They are taking less water now, or rather, it’s lasting longer now. RH was dropped to between 48-50 % and temps have been between 76-79 degrees, and about 69 degeees at night. Thanks for checking the grow out, Happy Gardening 🇨🇦👊❤️🌱

Hey guys! Thanks for stopping in to check out my babies! This is week 2 of flower (days 8-14). This week things really seemed to take off! 🔥 Plants were happy all week long and seemed to grow almost an 1” per day if not more. Buds are developing nicely, no smell yet but nice to see them stackin’. I cut out anything under the trellis that would end up being popcorn buds so the plants could focus on the main colas. Hoping I’ll just have to pull a few leaves here and there from now on. The New Floraflex drip system has been nice! 💯 It has made watering easier and more automated. Water distribution isn’t perfect but I’m sure they aren’t 100% level either. Plants should stop stretching after this next week and should start putting on some size! Stoked to see what these girls can do in week 3! Day by day break down: Day 8 Cut out some lower growth/ leaves blocking bud sites Day 9 Fed all 6 plants. PH: 6.11, PPM: 1136 Day 10 Plants look great. Let them do their thing. Day 12 Fed al 6 plants. PH: 6.05, PPM: 1264 Day 14 sitting at 29” tall right now. Not so stressed on height being be issue. Thinking they might be around 35-40” tall at the max. Stay tuned for next weeks post to see how much these ladies have thickened up!