After 7-8 weeks of flower she is ready to harvest. I give an update when she is dry and trimmt. I hope you enjoyed my little grow report. stay healthy

Esta semana estamos empezando a ver los primeros pelos de los cogollos ! Muy contentos con las semillas que pev seeds nos ha mandado !

Week 7 of Flower- We have stopped feeding these plants nutrients and began the flushing process. April 4th we will give them 2 days of darkness and then April 6th we will start the drying process.

* ***************** Week 3 of Growth From Seed, April 25 to May 1, 2020 - Days 15 to 21 from germination ********************** * Started the head scratching more this week and wondering what is going on with the slower growth she has experienced the last 4 days or so. She is looking good and not dark....environment is good.....what the heck is the pH so high when been given feed well inline and below 6.0......why runoff numbers in low 7's so early in the run?? A number of heavy feedings this week so that I can read the runoff numbers for her. Going to keep staying the course with feeding but lower the pH because she is still progressing and its still pretty early in the run........not much veg time for an auto though so I need to get this figured out pretty soon. Gave her some Epsom salts this week as well as I have been battling Magnesium deficiency the last run or two. Always just used CalMag but I don't think the girls always want as much Calcium as they are given this way though. Fed at a rate of 1tsp/gal in a two litre feed early on in the week. Little more Detail........... Apr 25/20, Day 15 - 500ml feed - VitaThrive and Dual Fuel @ 1.5ml - 700ppm and 6.0pH - small feed of base nute to try and perk her up. - noticed the lower leaves are droopy while the upper leaves are perky still. - Still working on dialing the light for these girls as they are happier at 30" away from canopy. Apr 26/20 - Day 16 - 500ml feed - AN Sensi Cal @ 1.5ml, Sensyzime @ 2ml, Epsom Salt @ 1tsp/gal - 700ppm and 6.0pH - The Epsom Salt alone shot the ppm to 500 - Only have the veg switch on for the UnitFarm light. - feeling some of the other girls are showing some magnesium deficiency with the yellowing perimeter of the leaves. Apr 27/20 - Day 17 - dry out day - Cut slits in the bottom of the bag today to let more water out, more quickly when feeding. - Wondering if the root zone is staying too wet and therefore causing some stunted growth. - She has been falling a sleep too early in the day so either too much light or getting root bound? Apr 28/20 - Day 18 - needing some runoff numbers to see what the hell is going on - fed 3L - Piranha @ 1ml, VooDoo @ 2ml, Dual Fuel @ 1ml - going in was 575ppm and 5.3pH - runoff numbers were 1450ppm and 6.9pH - WTF......bring it down......next feed at only 500ppm and 5.0pH to lower her?? - leaf colour is perfect. Stems are a little immature yet, but side branching is coming out stronger. Apr 29/20 - Day 19 - 8L feed - Dual Fuel @ 1.5ml = 325ppm and 5.0pH - runoff after the watering was 500ppm and 7.0pH - WTF.....expected it to be more in the 6.5pH range and not that high still? - KK looked worse off, still droopy, after this than the other girls did. Lack of oxygen in root zone with so much water? Its coco though shouldn't be for too long. Apr 30/20 - Day 20 - dry out day - KK likes it a little dryer in her medium.....she perked up more today and looking a lot better. - She has had more vertical growth the last day and she is spacing out some of her nodes. - Her stem is thicker and she is getting stronger. - Still a week behind though in my opinion and they should have been this size a week ago. Apr 31/20 - Day 21 - dry out day - she has done very well the last two days and going to keep riding that wave, didn't water today. - She has certainly gotten taller and wider.......getting her back on track? That will wrap up this puzzling week........pH is not staying low after being brought down......shoots back up over 7 in only 24 hours idea. Working on it Growmies. Have a great week and thanks for checking out the girls🙏👌

The ladies have loved the fish sh!t so far, I am currently feeding about every 48-72 hours and they seem to be doing great They are getting thick but I really hope to get some FAT colas at the end of harvest, damn they are starting to smell so good!

420Fastbuds-Greenhouse Grow 2025 The feminized strains RainbowMelon, GorillaMelon, LemonPaya, PapayaSherbet, LemonMandarin, the FastFlowering GG4/Sherbet from Fastbuds are doing amazing for there first full week in the greenhouse. The heat in SoCal is warming up with temps in the low 90's in the daytime and 60's for nighttime. Over all they're starting to reach for the stars after being topped. Besides a couple of yellow leafs I snipped at the soil level, I'm seeing growth almost daily. I'll start feeding this week Grow A & B as well as Calmag from AthenaBlendedLine. Since being transplanted into the 5gal fabric pots they've only got well water. Happy Growing.

These were just used for dry sift, together with the poor Iced Outs and the small Sugar Cane. Don't grow this freebie if your space/time is limited.

Bruce Banner #3 fast is growing great under the Hortibloom Solux 350. Everything is looking really good. She is starting to bulk, and get a nice resin layer going. Not much else to report at the moment. Thank you Hortibloom, and Tge Orginal Sensibile Seeds Company. 🤜🏻🤛🏻🌱🌱🌱 Thank you grow diaries community for the 👇likes👇, follows, comments, and subscriptions on my YouTube channel👇. ❄️🌱🍻 Happy Growing 🌱🌱🌱 https://youtube.com/channel/UCAhN7yRzWLpcaRHhMIQ7X4g

Due to construction and revamping of our space, we had to leave all seedlings in their germination dome for approximately a month before getting them into veg. In order to not run into any space issues within the small dome, these young plants were kept under a low-wattage fluorescent tube to avoid any growth which may have been "too vigorous." VEG WEEK 1: 03/09/2021: (Image 1) Each plant was potted into, and fed with the following nutrients during transplant: 1. 5l FF F1 medium 2. GHF: Biogrow - 15g worked into medium 3. Wormcastings (workd into medium and astop dress) 4. Organics Matter Mycoroot Supreme -placed at the bottom of the planting hole. 5. Watered each plant with a Silicon Plus feed solution . 07/09/2021: (Image 2) - All plants are now in 5l pos with Freedom Farms F1 medium, and are in their new veg home under a 3500K 320W Quantum Board. - The 3 weakest seedlings of the total 19 seeds (1x Crit and 2x PC) were placed on the left side of the tent, and in different pots, as they are obviously struggling and may not even make it into our final flower room.

D61 (21/01/2021): First day for week 5 of flowering. It's incredible how the buds are forming and getting bigger. It easily doubled (if not more) in size in the last 7 days. Since beginning of bloom, I normally gave water every other days. I make sure the soil is dry and the pots feel light when I lift them before giving any water. But it's not ideal cause it means that the plant drank all the water at his disposal and maybe it missed some. I will try a different watering schedule by giving water every 36 hours instead of every 48 hours. I will still make sure the soil his not wet and the pot not heavy (soil full of water) when I will give water. At this stage, they need a lot of nutrients to produce big buds. I will give nutrients every other feeding and only Max Minerals the others. Today I gave 1/2 of the recommended dose of Max Minerals. - temp: 24-26C light ON ; 21-22C light OFF - water: PH6.3 , 329PPM , less then a gallon each - run off: PH6.9 and 1090PPM for Glue Gelato ; PH6.9 and 940PPM for Banana Kush - RH: 50% light ON ; 48-49% light OFF D62 (22/01/2021): Nothing special for today. The lamps are now at 12 inches from higher colas. - temp: 24-25C light ON ; 20-21C light OFF - no water - RH: 50-52% light ON ; 48-52% light OFF D63 (23/01/2021): I gave full dose of Max Minerals and Max Bud and 1/2 of Max Grow. All base on mid late flower recommended dose. Relative humidity % was difficult to maintain low last night. It is normal since I give water more often. I removed leaves to help reduce humidity. Both look and smell sooooo good! 😋 - temp: 24-26C light ON ; 21-22C light OFF - water: PH6 , 940PPM , less then a gallon each - run off: PH6.7 and 1270PPM for Glue Gelato ; PH6.7 and 1100PPM for Banana Kush - RH: 50% light ON ; 55% light OFF D64 (24/01/2021): I gave half dose of Max Minerals. - temp: 24-26C light ON ; 21-22C light OFF - water: PH6.4 , 360PPM , less then a gallon each - run off: PH6.9 and 950PPM for Glue Gelato ; PH6.9 and 1030PPM for Banana Kush - RH: 50% light ON ; 45-47% light OFF D65 (25/01/2021): I'm at day 65 and base on the website I bough the seeds, they are close to harvest. They say 65-75 day from seed. My girls are not ready. I guess maybe 2 more weeks. The trichomes are all cloudy for Glue Gelato and 90% cloudy 10% clear for Banana Kush. I think it is time to start flushing. I will only give tap water at proper PH for the next 10-14 days and keep looking at trichomes. I consider also reducing air temperature and humidity for the rest of the grow. We are getting close! 😍😎 - temp: 24-26C light ON ; 20-22C light OFF - no water - RH: 49% light ON ; 49-50% light OFF D66 (26/01/2021): I decided not flushing today. I gave only full dose of Max Bud. Glue Gelato is getting very frosty! She has approximately 50% white pistils and 50% brown pistils but she keep growing new pistils. Banana Kush is less frosty but thicker and look a bit behind in maturity compared with Glue Gelato. - temp: 24-25C light ON ; 21-22C light OFF - water: PH6 , 440PPM , less then a gallon each - run off: PH6.8 and 930PPM for Glue Gelato ; PH6.8 and 1220PPM for Banana Kush - RH: 48% light ON ; 47-50% light OFF D67 (27/01/2021): The electric breaker where all the equipment of my tent is plug tripped. It took me around 20 min to notice it. During that time the relative humidity % went up around 75%. I don't think it will cause anything bad but I wanted to document it. I started the flush today by giving tap water at proper PH. The tap water of my city is around 130-140 PPM. I always let it sit in a bucket for 24h. - temp: 24-25C light ON ; 20-21C light OFF - water: PH6, 135PPM, less then a gallon each - run off: PH6.9 and 625PPM for Glue Gelato ; PH6.9 and 725PPM for Banana Kush - RH: 48% light ON ; 52-55% light OFF

Lots of foliage growth over the last week. Not much height growth though. Little sister is now nearly twice the height of her but with much less foliage. Not sure if the height thing is something i should be worried about. Ive only got a 60cm x 60cm x 140cm grow space for 2 plants so short plants would be great, so long as they still produce a decent crop.

This plant has CRAZY stacking on it. It hasn't grown up as much as it has branched out. This is a strain I'm growing to treat symptoms of MS, so with the stacking it may turn into a mom plant for cloning, but we'll see. It's received some feedings of liquid seaweed, black strap molasses, and URB in R/O water.

Week 10 (3/21/22 - 3/27/22)

8th days/Flowering /little change 10TH DAYS OF FLOWERING DUE TO RAIN HAD TO TRIM BOTTOM -LITTLE EARLY MY HUM WAS HEATING 70 TO 76 BLOWING FANS.... AND CHECKING FOR SEX POP 9 SEEDS 100% SUCESS AND ALL FEMALE THANKS TO COPY CAT GENTICS. 11TH DAYS -FLOWERING RAINING SEASON HAD TO TRIM BOTTOM FOR AIR VENTILATION MY HUM HITTING 72%.......T T DUE TO RAIN RUNNING EXTRA FAN FOR AIR VENTILATION. EVERYDAY PLANTS GROWING ABOUT 2 TO 3 INCHES LET'S GO GOOMIES

Flowering process going very well, buds smelling very well and growing. She is in very good health. Hope buds start turning purple soon, still, they are filling with trichomes. Mollases: 5 mL/L

31/10 Voilà, voilà ! Alors, il ne faut pas se moquer de sa petite taille 😂 Elle a eu des ennuis à la naissance. 😂👍 Divine Seeds : https://divineseeds.net/ _ils ont des petites plantes bien sympathiques.

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.

È stato un piacere coltivare questa genetica fantastica peccato per aver perso strain 2 causa ermafroditismo!! Molto profumata e resinosa asciutta 12g ma in un vaso da 6,5l penso sia un ottimo risultato anche perchè i fiori sono compatti!! Grazie @Barneys per la collaborazione e grazie a tutti voi per il supporto! Ne vedremo delle belle!! ❤️🔥🌲

Things are abit hectic at the moment in the garden as all my tents are currently occupied so these guys have to share for the next few days.... More information on the video I have uploaded.... Sorry I couldn't give you guys a better update

Two of the smallest trees I have grown..but these where some light brown seeds and they did well....part 2 on the way .....#happy growing