Info: Unfortunately, I had to find out that my account is used for fake pages in social media. I am only active here on growdiaries. I am not on facebook instagram twitter etc All accounts except this one are fake. Have fun with the update. Hey everyone 😃. Another week of beautiful growth goes by 😀. She continues to develop very well and beautifully. All shoots were topped up again. I think I'll go back a few more times do topping before it goes into bloom :-). The tent was cleaned and the humidifier refilled 👍. Otherwise nothing exciting happened this week. I wish you all the best and have fun with the update 👍. Stay healthy 🙏🏻 You can buy this Strain at : https://www.zamnesia.com/de/4532-zamnesia-seeds-gorilla-glue-feminisiert.html Type: Gorilla Glue ☝️🏼 Genetics: Chem's Sister x Chocolate Diesel 50% Sativa/50% Indica 👍 Vega lamp: 2 x Todogrow Led Quantum Board 100 W 💡 Bloom Lamp : 2 x Todogrow Led Cxb 3590 COB 3500 K 205W 💡💡☝️🏼 Soil : Canna Coco Professional + ☝️🏼 Fertilizer: Green House Powder Feeding ☝️🏼🌱 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 5.5 - 5.8 .

26.1.25: I have had a mistake 😕 i spilt some Fish Mix as I was experimenting with a syphon from some aquarium tubing I have. Unfortunately, I forgot to take the syphon out! Ugh 😣 However, it is fish emulsion and very thick consistency. Therefore, I was able to scrape it up with 2 of my business cards up off the counter. So added this extra into the next 2 ltr solution I mixed. All plants were watered with at least 1ltr of dechlorinated water PH'd to 6.3. Containing the following nutrients;- ♡ 3ml Seachem Seaweed ♡ 4ml Biobizz Fish Mix ♡ 4ml Biobizz Bio-Grow ♡ 3ml Biobizz Bloom ♡ 2ml Xpert Nutrients Bloom Booster ♡ 2ml Xpert Nutrients Cal-Mag ♡ .25g Ecothrive Biosys. ♡ 2.5g of Bicarbonate of Soda as PH UP. Unfortunately I have broken my PH pen too. Accidentally submerged it under water, then the readings went crazy. I'm leaving it to dry by standing it up but I'm most likely going to need a new one, which is extremely annoying 😑 I'm going start implementing the Scrog net probably some point next week if I let the plants that are in flower to just grow up now, as I do believe that I stunted Watermelon 🍉 by using too strenuous LST. Hopefully the plants still are able to grow upwards at this stage during flower for all the Purple Punch P1, P2 and P3. We will soon see! 28.1.25: My PH pen has packed up 😣 I've got to wait to get another. It's super annoying 😑 so I'm just judging by memory how to regulate it. Unfortunately, that's my only choice! I'm also out of the dechlorinator 😕 things are not going very well this week so far 😅 I guess we will have to make do, until I can get replenished. 29.1.25: I removed all the plants, hoovered, and disinfected the tent. There were several accidents when watering, causing some debris and splashes. I decided to just go ahead and get a few other things done. It's crazy how quickly things can become neglected! 😣 So I defoliated moderately on all plants except Gorilla Cookies seedling. I have absolutely dropped the ball on my lighting situation! My light was much further away than I thought! I turned it up to 100% and dropped it down to just under 2 feet away. After I reset the tent, I set up my scrog net. I removed 80% of all LST pegs. I am planning on letting the scrog net take over the training from here. I really want to minimise the risk of mould, so I decided to start using my dehumidifier. It has raised up to 73% RH this week, so it's necessary. Hopefully, I will be able to get my dechlorinator and PH pen soon! That's kind of essential to me. It's been a little bit of a stressful day in the garden, to be honest 😅 30.1.25: So I am expecting the arrival of my new PH pen today, as well as my new bottle of Ecothrive neutralise. It is supposed to measure the TDS and EC in addition to the standard TEMP and PH, which I had previously. Obviously, time will tell if it's any good or not. I realise, much too late now, that my lighting is very insufficient for this many plants. I need double the watts at least, and coverage is very poor. I remembered I had an old LED floor lamp, which was in a corner being unused. I decided to take the stand off, and Zip tied the pole onto the tent pole at the back left corner. I have no idea what the wattage is, and it's quite pathetic 😅 but I mean, I might as well use it, being as I definitely cannot afford more lights! 😣 Next grow, I will probably only grow 2 plants, max 4, and just use larger 7-10 Gallon pots. Being as I ran out of dechlorinator, I only watered some plants properly because I only had enough to make 6 litres. When my pen arrives, I will get everything properly watered. 31.1.25: The leaves of several plants are showing signs of iron deficiency. This is likely due to my PH pen packing up earlier. I now have a new pen. Due to this, I decided to use my Seachem Prime, which I use for my aquariums. As I wanted to get them watered properly, and my Ecothrive Neutralise hasn't arrived yet. I watered each plant with 1ltr of dechlorinated water PH'd to 6.0. I added .25g Ecothrive Biosys to the water. May give them a breather on the nutes and just use the Cal-Mag and Biosys. Being as I've just topped dressed with rich fertilisers, I'm sure that will be OK for the next several waterings. Bubble Kush

Week 10 Day 1 11/25/2023 Walked in the door, dropped everything and rushed in to check on the ladies, it was past lights out so I couldn't check on the plants but checked on the pH. The PH was down to 5.19... noooooo..I adjusted it to 6.0 and crossed my fingers the plants looked good, will check on them in the morning. Week 10 Day 2 11/26/2023 Well She looked great and I think she is ready for Chop, Chop, so debating the 48 hours of darkness, or chopping today.. so going to get some breakfast and give it a think. Afternoon update: So I gave it a think and I decided to do a split harvest this run. I took the top half and left the bottom half to mature for another week. I did run out of hooks so I was forced to freeze dry some and will have that to try in 48 hours. The problem is that I will have to remember the weights that I get when I get the final harvest and all the numbers but since I am doing a split harvest anyways it will be three sets of numbers to track over the next few weeks. Week 10 Day 3 11/27/2023 Got my first little bit out of the freeze dryer and trimmed up: I got 48 grams of bud and 7.4grams of shake. Smoke is smooth will see what kind of high comes with it.. Week 10 Day 4 11/28/2023 I let them bottom half recover and get another week under their belt to color and get some trichomes on them. I will be cutting 12/2/2023 Week 10 Day 5 11/29/2023 Ground Hogs day.. Recovery/ Trichome build of lower buds. Week 10 Day 6 11/30/2023 Ground Hogs day.. Recovery/ Trichome build of lower buds. Week 10 Day 7 12/01/2023 Ground Hogs day.. Recovery/ Trichome build of lower buds.

Had very good growth this week in height and pistils. Roots are also doing well with more growth and nice color so I will keep my fingers crossed that they continue to do well. The MP3 player was not working again. I used a MicroSD card and put a Velvet Underground Album on it and stuck that into the newest speaker. This one is the smallest and easiet yet plus it has continuous play so the album plays all the time without stopping like the MP3 player did. Am getting a bigger SD card to put more Velvet Underground on. I also defoliated a small amount and don't expect to cut anymore. The Grow Chamber continues to perform nicely and I hope to start building the first real Model Type soon. I also had to make a new top drip system because the older one was not dripping water. I am also CO2 enriching the Chamber for a couple of hours every two days. Looking to see more pistil growth this week. I've also added my data charts for January. Everything was in range and moving forward.

This was their last week! They had 4 full water feeds till runoff, and the trichomes we’re looking just right by Thursday (day 67). Throughout the week I had been increasing the light intensity and ended up running at 95% of what the SF4000 can do. I have stopped doing the 48 hours of darkness awhile back, so Harvest to come! Happy Gardening 🇨🇦❤️😎

The buds are starting to form. The smell is strong when I open the cabinet, but with the filter, it doesn't smell. I corrected the deficiencies I had correctly. I defoliated a bit to allow good light penetration. I'll let you judge how they look now. I did a week of stretching, lowering the light by 1 hour each day.

Today is day 57 for these Wedding Cheesecakes and they are looking great ! 2 of them decided to stretch out on me so had to tie one of them down even more an looks like she might be a little stressed out from it or might lacking something I’m not too sure if anybody can tell please let me know if anything I would really appreciate it ! Other then that we are going into week 8 and these ladies are putting off some delicious smells can’t wait to see what they do this week! Hope you all enjoy ! Keep them eyes peeled for next week!! ✌️Cheers

Another week of decent growth 🌱 All three plants seem to be healthy and are growing quite a lot each day. Having to adjust the light on a daily basis to avoid too much light exposure. Some little deficiencies showing here and there but for the most part they are looking good. 🤞🏻👨‍🌾🏻🤞🏻 ✌️

Finally I meet you… she’s flowering and guess what I’ve done, due to an foreseen circumstance, going to be away for a month, and all I know is my babies will get water and rain if it does rain, Sad days ahead, however at least the are sheltered from the rising temperatures. As good as it is, guess what this genius does… you guessed it, i defoliated my babies. I hope my decision rewards me, I will surely find out when I return in September, I thought of getting my assistant to send me pictures so I can keep posting, however I think it’s best I stay completely away from posting. This will truly test my growing skill, not forgetting my building skill when it comes to the greenhouse, with temperatures rising I will finally see if this self ventilate design will keep humidity at a desirable level to promote adequate growth, I have not encountered any fungal or pest isssues, but usually problems arise during the hot seasons.

These coming along excellent started some lst this week and there looking healthy :-) good feeling about these can’t wait to see how they turn out

Update to fo

🌱 Week 3 – Gorilla Cookies Auto Pheno Hunt Another week down and the differences between the phenos are becoming more obvious every day 👀🔥 The environment stayed very stable this week with temperatures, humidity, and VPD remaining consistent. Because all plants are growing under the exact same conditions, it’s really interesting to see how differently each phenotype develops genetically. 📈 Current observations: Several phenos are already reaching close to 30 cm in height Meanwhile, some smaller phenos — especially Pheno #6 — are still around 13 cm Leaf structure and overall plant shape continue to vary a lot between phenos Growth vigor is clearly different from plant to plant now 💧 Feeding & maintenance: This week the plants received their first proper feeding with around 4 liters of nutrient water. Some phenos seem to react more sensitively to the nutrients, as a few plants are starting to show slight brown leaf tips, so I’ll keep a close eye on them over the next days 👀 I also removed more large fan leaves to improve light penetration and allow the lower branches to develop more evenly. 📊 Current environment: Temperature stable around 26°C Humidity staying between 63–65% VPD maintained around 1.3 kPa Light intensity remaining at 35% Now I’m really curious to see when the first flowering signs will appear 🌸🔥 💬 Which pheno would you pick so far?

Eccoci qui... Siamo quasi alla fine del cultivo, odore, resina e colore ci sono. Attendiamo solo la maturazione delle cime che richiederà 1/2 settimane.... NON VEDO L'ORAAAA... Seguiranno aggiornamenti, grazie a tutti per il supporto🔥🌲❤️

A lot of stretching happened the first week. Week 2 so far so good. I will lollipop at the end of week 2. Thanks for watching.

Girls will get a feed of 400 ppm 0.8 ec of Massive Bloom Formulation, 600 ppm 1.2 ec of Flora Nova Bloom, and 200 ppm 0.4 ec of Floranova grow for a grand total of 1200 ppm 2.4 ec. Girls are stacking, node spacing is close. Smell is amazing and she is a very healthy big bush.😍

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.

She's doing OK, certainly not jumping up in height though.

Day 60 Notes Today I water with 2lt tap water with Bio Bizz Calmag 1ml per 2lt Bio grow 3.5ml per 2lt Bio bloom 2.5ml per 2lt Bio heaven 2.5ml per 2lt Monkey Nutrients Root shoot 5 drops per 2 Lt I firstly bottom fed around 300-400ml The pour the rest on the top.. Seeing some lovely growth Day 61 Notes really seeing them bud sites form now Even seeing alot of trics