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.

Only just cut them down so will update on taste and effects in a couple of weeks 💚 So the sherbs are dried enough to jar still stinking of sweet candy and she is still very sticky 😁👌💚 got 28.4 grams from this grow as a beginner I'm very proud thankyou for following and supporting me throughout growmies 🙏😁💚

Overall, I am really impressed with the quality of this grow. Impressed by Barney Farms and the quality of this seed! Overall it was pretty easy to grow, with great yield, and great tasting buds!

🌿 **Moby Dick Auto Grow Week 9 Update: Harvest Time Approaches!** 🌱 Greetings, fellow growers! It's time for an exhilarating update on the progress of our Moby Dick Auto adventure as we hit Week 9 of the grow cycle. With excitement mounting and buds maturing, let's delve into the latest developments: 🌟 **Abundant Bud Growth**: At Week 9, our Moby Dick Auto marvels are truly showcasing their potential, with buds swelling and resin production reaching its peak. The once-tiny flowers have evolved into dense, resinous clusters, promising a generous harvest in the near future. Trichomes are abundant, signaling optimal cannabinoid potency and aromatic richness. 📏 **Final Phase of Flowering**: As we enter the final phase of the flowering period, our focus is on maximizing bud development while ensuring ideal ripening conditions. By meticulously managing environmental variables such as temperature, humidity, and airflow, we're creating the perfect environment for our plants to flourish and achieve their utmost potential. 🍃 **Leaf Aging and Nutrient Management**: As anticipated in the late flowering stage, some leaves may exhibit signs of aging as the plant redirects its energy towards bud formation. This natural progression indicates that the plant is nearing maturity. Meanwhile, our nutrient regimen remains carefully calibrated, providing essential elements to support vigorous flowering without risking imbalances or deficiencies. 🔍 **Monitoring Trichome Ripeness**: With harvest drawing near, we're closely monitoring trichome development to determine the optimal time for harvest. Using magnification tools like jeweler's loupes or digital microscopes, we're scrutinizing trichomes for signs of ripeness, aiming for a blend of cloudy and amber trichomes to achieve the desired balance of cannabinoids, as well as flavor and aroma complexity. 🌞 **Preparation for Harvest**: As we gear up for harvest day, our checklist includes gathering essential tools such as trimming shears, drying racks, and storage containers, as well as ensuring a hygienic and organized workspace to preserve the integrity of our precious buds. We'll employ proper post-harvest techniques and curing methods to safeguard terpene profiles and enhance overall quality. In summary, Week 9 signifies a pivotal juncture in our Moby Dick Auto grow expedition, where patience and precision converge in anticipation of the impending harvest of our prized buds. Stay tuned for the forthcoming update as we rejoice in the culmination of months of dedicated cultivation, yielding a bounty of premium-grade cannabis ready for enjoyment and sharing. Happy growing! 🌿✨

10th week of flowering: week from 23/10 to 29/10 This is the last week of flowering for this strain. Unfortunately here in north eastern Italy the outdoor climate isn’t so kind in this period. So even If I wanted to let them mature a bit more, the temperature at night goes to 10°C. It hasn’t perfectly matured, but that’s what I have. I noticed some trichomes have lost the head or sphere at the top. I read that’s due to low temperature, so I see myself forced to harvest it now. Also it’s better to get them out the rain since bud rot and mold are still spreading in some branches.

settimana soddisfacente ad inizio settimana ho travasato la pianta,nel travaso ho trovato una parte delle radici un po' piu scura del normale,come avevo scritto ho usato del coco vecchio e in quella parte rimaneva piu umido e compatto..naturlmente ho aggiunto coco nuovo quindi ho aggiuto micorizze sulle radici prima di reinvasare ho aspettato un giorno che il cocco si asciugasse un po' di piu e h bagnato con il doppio dell'acido umico che metto normalmente LST continua con piccoli aggiustamenti e una defogliazione limitata a qualche foglia ,al buio,ogni tanto le dimensioni iniziano ad aumentare

Hey Growers, End of week 3 from seed :) - From the start of the grow Ive been experiencing small issues with plant #2 but everyday I learn new things and try to figure out what she wants and try to adapt to it. looks like its working slowly. 1st time of transplanting, it was a success. 1st week of nutrients, I will feed 1/3 to start

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. Flowering day 21 since the time change to 12/12 h. Hi everyone :-) . She has developed really well this week. it grows super in height 😀. I am very curious how it will develop. It was poured twice with 1.2 l per watering. Otherwise the tent was cleaned as usual and everything checked. Stay healthy 🙏🏻 You can buy this Strain at https://www.amsterdamgenetics.com/product/super-silver-haze/ Type: Super Silver Haze ☝️🏼 Genetics: Haze x Skunk #1 x Northern Lights Type: 70% Sativa – 30% 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 .

Dwc was flushed for 4 days, coco mix was flushed for a week. Dry was too fast (under a week) learned a lot can't wait to apply it

Weekly update for these girls. They got a defoliated and lollipopped this week. Also went full on into preflower showing pistols and flower sites everywhere. Over all they're growing like champs. Happy Growing.

I cannot believe how bushy she is! Very very short internode length. I'm wondering if I have an indica dominant plant? 😭 But anyway, she is doing her thing this week. She only grew 9cm this week. Nutrients this time are 20-20-20 NPK powdered fertiliser I'm trying this time around. About 1.2 grams mixed with 10L of water makes ~1000ppm. My clean water alone is ~350ppm of that. I do have a CO2 bag generator thing... It's not doing a lot though. My CO2 meter reads barely over 400ppm.........

Wow what a week. We are at 48” as of day 20 on the Enemy of The State plants (both are the same height now). The two White Criticals were 36 and 38 inches from the top of the tanks and the taller tops on Purple Purple are about 34”. Wedding cake is about 30” now. All my plants seem to love the 5.2 pH. Enemy of the state are on a lighter feed of about 950ppm and wedding cake is still eating from a vegetive reservoir at 1125ppm. Thanks for looking!

Las plantas siguen creciendo y formando flores. A la mitad les e aplicado una defoliacion selectiva de hojas primarias para abrir paso a las ramas bajas y agrupar la planta de esta forma consigues plantas mas compactas al no tener que alejarse tanto las ramas del tallo para recibir luz. La otra mitad no lo a necesitado al ser un fenotipo mas xativo y corto. El aporte de co2 las hace trabajar bastante y aguantar la dosis de nutrientes diaria. Solo se riega una vez a la semana con sensizym. La distancia internodal de algunas plantas es espectacularmente corta. Llos cogollos ya estan unidos y apenas han comenzado a salir. Muy ansioso por ver como continua esta variedad de barneys farm. En el ultimo video podeis ver el plano general y la diferencia que hay entre el fenotipo mas xativo y el fenotipo indico a pesar de ser todas dos si dos 33 y estar bajo las mismas condiciones.

For LIQUIDS & NUTES ******GREEN BUZZ NUTRIENTS***** organic. Also i’m using their LIVING SOIL CULTURE in powder form! MARSHYDRO ⛺️ has large openings on the sides which is useful for mid section groom room work. 🤩 ☀️ MARSHYDRO FC 3000 LED 300W 💨MARSHYDRO 6” in-line EXTRACTOR with speed-variation knob, comes complete with ducting and carbon filter.

Going great trying to train to best suit my grow tent. There will be 3 other strains so I need to make sure they all get enough light. The water volume in the plants is less then what I have in the conditions. More like 2L every two days

The first day of the sixth week flowering🤗

hace tiempo tenia ganas de cultivar esta cepa, de buen crecimiento y aroma dulce. muy buena produccion de cogollos y resina, resistio muy bien algunos problemas al inicio del cultivo en la poda apical y posterior LST, buena cepa para LST muy frondosa

Day 57 Update: Plants got water yesterday with tiger bloom. First few orange pistils noticed last night, not very many yet. Yellowing is predominately in the fan leaves so maybe that is normal? Things are about to get crowded in the tent as the other three plants are starting to get big. Day 58 Update: I read up on cal-mag deficiencies. As it's my first grow, I can't know for sure how heavy/light-handed I've been with nutrients, but it feels like I've erred on the side of less is more. The "bar graph" thing is not accurate for what I've done feeding-wise. Either way, I can't image there's any actual deficiency but more likely a pH issue causing problems with magnesium uptake. I'm not too sure how accurate the 3-in-1 pH/Light/Moisture meter is, but the pH reads close to 8 in every insertion location. I'm going to order pH down, but was reading about lemon juice as a SHORT TERM fix to lower pH. Two significant issues were inevitable with this grow: 1) traveling and leaving it unattended for a week & 2) using soil that other plants were grown in. Knowing how much these two issues caused me, my future grows will honestly be way better for it. Notably how to handle extended time away as well as consistently testing pH/soil. Depending on how serious I get with this, I'd invest in more precise measurement tools, but not yet. Obviously I want big yields, but I wasn't expecting to get pounds, so I'm okay with learning how issues affect yield. My other grow is actually a really interesting study in how different stresses affect plants, but I digress. Point is, I know there are problems, I'm trying to learn to fix them, but if things go totally pear shaped, I'm not going to be too disappointed. Day 59 Update: Working on lowering the pH that feels more like the cause of deficiencies than underfeeding. In another diary I read, the grower used lemon juice in dechlorinated tap consistently in each feeding without nutrients to control pH. That's my plan until Monday when the GH ph Up/Down will be delivered. One of my plants in my other grow has pretty obvious signs of necrosis on some leaves, but it doesn't seem to be spreading. I'm pretty sure I've had wonky pH levels since I went out of town and I never got those fixed so now I'm dealing with it. Having never grown any cannabis before, but also expecting some purple in the plant, the purple/reddish hues some of the leaves initially developed seemed more normal than I should have realized. Trial by fire!! Day 60 Update: So, thinking it was a pH issue causing uptake irregularities. Many of the yellow/reddish leaves have the FEEL of a healthier leaf even if they’re still discolored. Many fan leaves fell off with minor contact/pulling. I used lemon juice last night to flush with water in the 6.0 pH range and health may be returning. I’m not going to say it’s fixed, but the damage is hopefully contained for the time being. Pics and video show damages pretty well. Knowing it may creep back up, I'll keep feeding with closer to 6.0 pH water until pH Up/Down arrives and I can re-flush for the last week or two. Day 61 Update: Nothing new to report. Feels healthier than a few days ago still, but the countermeasures deployed seem to be holding for now. Buds seem to be filling out, I’m content for the night. Day 62 Update: Water and nutrients, maybe for the last time, tonight. New soil pH meter from Home Depot is hopefully more accurate. All water was pH'd to around 6 as the soil meter showed slightly alkaline still. I'm doing the best I can to keep this under control for another week, two at the most. I also got some soil acidifier amendments for the other plants because the readings were slightly alkaline for those pots. Day 63 Update: Got a set of mobile camera lenses to take macro photos of the trichomes. Its a work in progress. Otherwise, things seem okay today. Gonna press on keeping an eye on pH, but whatever shall be, shall be.