D92/F48 - 01/07/23 - 👉👉👉 First Havest, I cutted the main buds and left the others for one more week. Now I'm going to put only the timelapse video and then all details in the next week D93/F49 - 02/07/23 - Secondary grow with flushing D94/F50 - 03/07/23 - Secondary grow with flushing D95/F51 - 04/07/23 - Secondary grow with flushing D96/F52 - 05/07/23 - Secondary grow with flushing D97/F53 - 06/07/23 - Secondary grow with flushing D98/F54 - 07/07/23 - Secondary grow with flushing

Hello. This is the last week for these plants. I don't know if I'll start harvest in the first 2 tents or in here first. Flip a coin I guess.... Turned down the lights to 60% yesterday. Getting ready for harvest the plants are getting a break from the intense lights. The plants are looking a bit more yellow as they pull what they need from the fanleaves as they mature before harvest. I'll show pre harvest pics next week. OK. Be Great... Chuck.

Week 8 and she’s looking super amazing with her low structure 👨‍🌾🏻 Buds are fatten up really fast right now and she is literally full of trichomes ❄️ The smell is amazing

💩Alrighty Then Growmies We Are Back At it 💩 Well folks we just finished up the last run and so we are back to do it all over again 😁 So what do you say we have some fun 👈 We got some Gorilla Punch 👊 👊 👊 DAY 7 👉 Its been a really good week , ive had to boil water the last week as its been so dry , and even with my Humidifier its been tuff 👌 Never the less we are moving along and so far so good folks👌 FC4800 from MarsHydro Lights being readjusted and chart updated .........👍👉Added an RU45 too the mix 👍 www.marshydro.ca 👉I used NutriNPK for nutrients for my grows and welcome anyone to give them a try .👈 👉 www.nutrinpk.com 👈 NutriNPK Cal MAG 14-0-14 NutriNPK Grow 28-14-14 NutriNPK Bloom 8-20-30 NutriNPK Bloom Booster 0-52-34 I GOT MULTIPLE DIARIES ON THE GO 😱 please check them out 😎 👉THANKS FOR TAKING THE TIME TO GO OVER MY DIARIES 👈

This is the fresh frozen wash from two of the four apricot autos grown, It’s smelling and tasting beautiful, with sharp lime/lemon notes mixed with a tropical pineapple and guava mixed drink, So far test pressed 5g of the 159u-73u live heads and it’s return around 71% with a 3.56g give back, For anyone who cares about whole plant fresh frozen yields, I washed 800g and gained 12/13g of 159u-73u heads

Day 9 I had no choice but to defoliate, the canopy was getting way to dense and humidity was hard to control even with my 30 pin dehumidifier. Hopefully will not affect to much. Probably I will do another defoliation on day 21. TDS stays at 550PPM this week and CO2 at 1200PPM.

X

Smooth sailing, watered once every three days

FLOWERING WEEK 1 - 4TH DAY FLOWERING/WORM TEA

In dieser Woche wurde die Düngemenge Hesi Coco auf 4ml/l erhöht. Der EC Wert steht somit auf 1.0 Ich habe die Ladies in dieser Woche 1 mal austrocknen lassen und dann mit der erhöhten Menge Dünger stark gegossen (aber nicht geflusht). Das Wachstum hält sich in Grenzen.... ca. 1,5 cm pro Tag, das ist nicht sehr viel aber ok wenn Sie jetzt hoffentlich noch 1 Woche etwas weiter wächst. Da es draußen immer noch scheisse kalt ist, keine aktive Zuluft sondern nur aktive Abluft nach draußen. Temperatur zwischen 18-24 Grad. Luftfeuchtigkeit könnte ein bisschen besser sein... ich werde aber noch nicht nervös. RLF zwischen 38und 45 %. Die ersten Blüten treiben aus und ich werde bald noch ein bisschen mehr füttern. Blätter sehen gesund aus, keine Mangelerscheinungen. Die Lichtmenge der HID Lampe wurde von 500 Watt auf 530 Watt erhöht.

Hey everyone :-) This week it smells more and more sweet and fruity in the whole room 😍. There is actually not much to report, everyone is now under 12/12 :-). This is the last grow that comes in the entire diary. From now on, each plant will be added to the diary 👍. I wish you all a lot of fun watching, stay healthy 🙏🏻 and let it grow 😎👌

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.

Non metterò la germinazione me la sono scordata e non metterò nemmeno tante foto,a fine ciclo vi dimostrerò come far uscire 6 autofiorenti da almeno 200g l'una Ho 2 hps da 600w e 6 vasi/buste da 40 litri 20/4 di luce più luce naturale che entra dalla finestra,la terra é stata fatta da me perche mi ero rotto il cazzo di quella con i moscerini 30% terriccio/ 30% fibra di cocco/ 20% lapillo vulcanico/ 10% humus di lombrico/ 10% perlite e torba bionda

May 3- I picked up my clones for this season today. Plants appear very healthy and are currently under two 150 Watt HPS until these plants can survive the cold Maine temps which won't be for a few weeks. From here the will go in fabric pots ranging from 30 to 50 gallons and trellised. The soil mixture that I use is 1/3 happy frog 1/3 FFOF and 1/3 roots organic. When I get good weather I need to clean up last year's mess and wash my bags. I couldn't take pictures due to low memory but I will. I'm going to start hardening the plants off a few hours each day. 5/9 Watered everything and started LSTing but I need more room. Weather is going to be great so I think I'll hold off on training others. I pinched a few and I'm going to try to get the plants out side some so they can harden off. Planning on dumping soil and washing bags today. I got most of the cleaning done. Bags are dumped and soaking. Soil needs have been established and I'm planning on either ordering from Amazon or picking up in person the next couple days. Plants never made it outside today as it was rather windy.

It's growing...

Everything seems to be doing well, they are all sticky and stinky!

12/20 - 12/26: Busy week...Merry Christmas! I'll add more detail later- Last fed on 12/26..started Beastie Bloomz

Even in the version worked with main lining and sent into flowering a little later, Zamnesia's Tangerine Dream remains one of the fastest plants to flower and is surprising because it is the most solid flower of all, it is a boulder, stone, pure marble. ** We remind all users that we grow two plants per variety, one worked with techniques and the other left to grow freely and beautifully to preserve its speed and the classic Christmas tree shape in height. Below in this diary we have the Main lining plant. Description // This plant had a fast flowering like its sister left to go without techniques. The phenotype is practically identical, solid flower, excellent resin production even in the great heat, structure of the super thick ones that drive me crazy. The smell is always that of mandarin while it is peeled perfectly in line with that declared I imagine the magnificent taste. Why? I tasted the hash that remained on my gloves and I was going crazy. For citrus lovers who are a bit tired of the forced lemon scent. Trichomes and maturation // We looked carefully under the 10x microscope (and 10x x 1.6) and noticed a good percentage of milky/clumpy trichomes, still many transparent but also many golden amber. It is mainly sativa, but only 60/40, so guys, if we want to maintain a more sativa effect, we need to harvest with a majority of cloudy/milky trichomes if we want a more indica effect, remembering that THC oxidizes too much, amber is the right color. I use it during the day and therefore I look for a more sativa effect when the plant is sativa. Fertilizers and soil // We used the Plagron range of organic nutrients the whole time, all the recommended additives and the Pro Mix soil, unfertilized and organic. Calculate the dosage that best suits your needs on the website ------ https://plagron.com/ Nutrients are available in convenient packs on the Zamnesia website --------- https://www.zamnesia.io/en/11457-plagron-easy-pack-natural.html I love this strain, I love its mandarin scent and its hard, potent flowers ---- https://www.zamnesia.io/en/10966-zamnesia-seeds-tangerine-dream.html Zamnesia Short Description // Whether you're new to the fascinating world of cannabis cultivation or an expert, Tangerine Dream by Zamnesia Seeds will give you great satisfaction both in growing and smoking. Carefully selected from G13, Afghan and Neville's A5 Haze clones, this strain boasts a slight sativa dominance of 60% and offers a relaxing yet uplifting effect. She’s also easy to grow and is suitable for both indoor and outdoor growers. As we’ve just seen, Tangerine Dream is a pleasure to grow, but she’s even more enjoyable to smoke. With 25% THC and a pungent blend of exotic terpenes, Tangerine Dream smells incredible, tastes delicious, and delivers a balanced, long-lasting effect. When you open a jar full of these dense, resinous buds, you’ll be hit with a delicious citrus aroma reminiscent of freshly peeled mandarins and grapefruits. With hints of citrus, spice, and incense, each hit is a sensory delight reminiscent of sipping a refreshing juice on a sunny porch. Finally, as the effects kick in, you’ll be treated to a long-lasting, balanced, positive cerebral buzz, followed by a gentle physical relaxation. Perfect for weekends away or social gatherings. Order your Tangerine Dream seeds today and grow this invigorating hybrid. The whole world of growing and much more is on Zamnesia: take a look at the site and you will find "the best that nature has to offer" in various shapes and colors. --------------- www.zamnesia.com

(11/11-11/17) ***All feeds with nutes use either a whole ratio or combination of "Veg Mix" and "Bloom Mix"concentrates DILUTED in water until a total ppm of add-in is reached using a (Total Dissolved Solids) TDS Meter measured in PPM (parts per million). The "Veg Mix" concentrate will eventually be added in smaller ratios and "Bloom Mix" concentrate will eventually replace the "Veg Mix" concentrate entirely. The ppm and ratios of each feed will be listed when I feed. Veg mix recipe is on week 2. Bloom Mix recipe will be noted in this top message of the week that I make it.*** Week 1 Notes & Observations: Both plants are coming along pretty good. No concerns rolling into week 2, I will be starting nute supplements in the diet this week but plan to add them slowly to the regular routine. Day 18, WOW what a difference the feed made with Plant 1!? She was a good inch behind plant 2 at the start of the week and today she 'looked' bigger, so I measured, 2 days after the deep nute feed, and now she's an inch taller than plant 2.😮 VPD this week will reduce the humidity in the tent to about 70-75% and temps will be monitored for 75- 78F daytime and 68-70F overnight. Lights should adjusted to provide 300 max, but will try to hold the 280 setting as long as I can this week. Meaning no increase over last week other than growth. Feed & Monitor: Day 16 (last feed was day 11) Tested and Calibrated my ph pens. Starting weight from each pot was 18 lbs and 8 oz, P1 weighed 15lbs 9oz and P2 was 15lbs 15oz before feed. Each plant got 1 gallon of purified water with 75ppm Veg Mix (recipe above and makes 1 gallon at about 3600 to 4000ppm concentrate to dilute each feed, i.e. I only fed 75ppm above the purified water ppm this feed) The ph on this feed was balanced to 5.75ph to combat the higher runoff ph from the last feed. P1 weighed 21lbs even and P2 weighed 21lbs 5oz after feed. I got about 5 cups of runoff on P1 and 6 cups on P2. Top soil tested at: P1 (6.37, 6.37, 6.37, 6.32) avg 6.357 and P2 (6.55, 6.61, 6.52, 6.42) avg 6.525 - Runoff for P1 ph was 6.29 with 1530ppm and P2 was 6.29 with 1580ppm. Hope everyone enjoys the daily progressions of overhead and side profile (Organized Chaos). I will try to add a video and black back or cover pics by end of week every week.