OK so I nearly kill my plants and these were stunted and bonsai like.. Only got 30grams dry weight but were not all cbd and definitely contained thc.. Not so good for what the intended use.. But it's like opium...

I love this strain to pieces man! Another high quality genetic by original sensible seeds, very very hard dense nuggets like rocks, sticky, stinky as hell, high quality, as always by original sensible seeds. 100% organic grown

Yooooo what is up guys! Welcome back - in to week ten and the zkittlez has been harvested. Cloudy trichs all over and about 10/15% amber so went with a chop today. Wet weight of 628g for the plant roughly. Including a bit of stalk weight, which I’m chuffed with. 🙌🏼 She’s on to dry now, so stay posted for post dry weights. I’ve taken off the majority of fan leaves but left all the sugar leaves for a dry trim and to help slow the drying process. The Runtz still has a few days or weeks left in her. Just waiting for those pistils to stop sprouting and some further clouding up of the trichs and then chop chopppp! Thanks for stopping by 🤟🏻

Cut down at day 80. I cut the first plant at day 56 and washed a lot of it into FF live rosin. First time doing that’d got lower yields than I wanted but think I know how to bump them up on the next wash! The 56 tasted good but trichomes weren’t as mature as I wished they would be. I’m thinking the 80 day will be not enjoyable. This 80 day plant will be mostly for smoke.

was busy setting up new tent and light and fixing old one. plants are now in a more controlled environment. new setup has plants feeling better. higher temps and better humidity. probably going to top 2 out of 4 plants. they appear to be coming out of the stress from transplanting and moving and too cold environment. hoping to switch to flower in 2 weeks. big pots are 5 gal and others like 2.5

. The end of a nice run😊 The three big sisters dried for 8 days as colas and then 2 days as buds on a drying net. They ended up at 139g, 127g and 145g dry respectively; added to the 83g and 64g from the little sisters, that makes a total harvest of 558g. My best one so far! Adding the lights was clearly the decisive factor. I'm finally satisfied with my setup. Aside from the small ball of finger hash, I put the trim in the freezer; as soon as my Banana finishes its run, I’ll mix it with the WW for a nice bubble hash. EDIT : I took 85 g from my White Widow and 25 g from my Banana Purple Punch, frozen along with about fifty grams of leaves. The result for this third bubble hash run: 12.85 g, i.e. 8% of the material used. The first time I reached 3.0%, the second time 7.1% ; with this 8.0% I’m making progress, but I haven’t reached the 10% goal yet... I’ll keep working on it 😉 Thanks to all of you for following this diary ! 👋

Big Beautiful Budz 8th W/Flower: 8th Feed of #HumboldtCountysOwn Packed, Stacked Up and Lights Upgrading under way! Cloned with my Steady's Saliva!!! 8th w/ Flower: Budz getting Outstandingly Huge, Plump, Dense, Juicy and Everything is Supreme, Savory, Stinky, Sweet, Swelling Out, Skunky and Gasy at thier 8th week of Flower! 8th Week of Flower: 8th Flower Feed of #HumboldtCountysOwn and the Ladies Love the Bloom portion of Nutrients! They're Stacking Up Great and Filling Out thier Mighty Branches with Giant Gorgeous Budz! 5 Confirmed Females!!! It's been a few days since I gave the Ladies thier 8th Feed of #HumboldtCountysOwn Nutrients and they look Fantastically Divine!!! We'll definitely Grow back to everything here soon! 11th w/ Veg and Flowers Update #Pre-Sexed🚺 #SuperCropped #Defoliated #Lollipoped Good Day and Happy Growing Everyone! These Ladies were Growing into thier 11th Week of Veg and Looking Totally Tight and Phenomenally *Femed* from the Right! #Pre-Sexed 4/9/21 #Opium/#PabloEscobar *Fems* breed by Team #DivineSeeds #DivineSeedsSquad #DivineSeedsBreedingCompany and #SuperCropping continued! I'm Very Excited and Extremely Gracious!!! Heck Yeah Growmies and Growmets!!! Check Out these Confirmed Females with thier Wild Pistol Hairs popping and I'm still Training and Widening them Out with #SuperCropping Everything looks Expanded and Growing Great! After #SuperCropping the plant will Grow Bushier, Produce More Buds, and possibly even Produce More THC! This is how the plant naturally responses to danger and protects itself! Growers take advantage of this technique to get Bigger Yields and More Potent Buds than would be produced otherwise! Getting Trained out into thier 11th Week of Veg and Looking Mighty Fine!!! Thier getting Humongous and Hearty in thier 10 gallon Grow Bag from Broski #www.as420.ca These Cannabis plants are Camping out in the Closet for a week or so! Lol This is my 2nd run using the Osree.Light QB1000w and Everything is Mesmerizing!!! My #Opium and #PabloEscobar *Fems* from #DivineSeeds Regs: SalamiLegF3's×2 and FireAlienRomulan look$ Outstandingly Awesome and Growing Up Phenomenally Fine into thier 11th week of Veg in our 2- 10 gallon The Grow Bags from Broski #www.as420.ca and also 2- 5 gallons as Well! Our others are Super and Breed by #thehumancannabiniod #AlienBloodGenetix #TNBNaturals #Foop Yo!!! Thanks Again for All the Love and Support my fellow Growmies and Growmets!!! These Magnificent and Magical Ladies were Growing in our 48×24×60 ViparSpectra Official Club 🌿 ®️ Grow Tent and under our #Osree QB1000w and #GrowStarStore Kokokala QB1000w and our Purple Rose Cutting×2, Aloe Vera Cutting, Maters×3, Morel Mushroom, Lavender×3, Sunflowers×5 and The 5 Brand New and Fresh Starts are Wonderful with a Huge Hint of Fantastical Fire is my #SalamiLegF3×2 by Broski #thehumancannabiniod #DankFlowGenetics #EastCoastSeedBank #FireAlienRomulan by Broski #AlienBloodGenetix my #PabloEscobar and #Opium by Team #DivineSeeds #DivineSeedsBreedingCompany We Grow with #Growatt 600w with #FoopOrangicBioSciences and #TNBNaturals The Enhancer Co2 Despersal canister and ph'd them w/ Declorinated watering w/ TNB ph Up and Down! Totally Top Quality Topz all Around! Thanks Again #GallowGlas420 #HarleyGrower #thehumancannabiniod #AlienBloodGenetix #TNBNATURALS #FoopOrangicBioSciences #www.as420.ca #divineseeds #divineseedssquad #divineseedsbreedingcompany #BioFlux Family's and Teams!!! Your Genetics are Merry Magnificent, Mega Marvelous and Mighty Medical! Love um!!! I really Can't stress enough how Thankful and Grateful I am of All of you and what you've Shared with Us! Means the World!!! It's definitely a Pleasure being able to Grow with these Phenomenal Grow Lights! Please Enjoy! BudBrothers4-Life! Cheers Famz!!! Much Props and Much Topz!💯🔥 #Osree #GrowStarStore #Growatt #TNBNaturals #TNBTeam #FoopOrangics #GrowYourOwn #Bliss HumboldtCounty'sOwn: Email: [email protected] Phone: (707) 725-4119 Toll free: (866) 872-9434 Humboldt Bottling Po Box 429 · Fortuna, CA 95540 HumboldtCounty'sOwn Website Link: https://humboldtcountysown.com/ HumboldtCounty'sOwn Instagram Link: https://instagram.com/humboldtcountysown?igshid=1qj809qkkwych https://instagram.com/osree.light?igshid=1vrsbdyhzg2h8 https://instagram.com/growstarstore?igshid=2yjn0r00r6ru https://instagram.com/divine.seeds?igshid=1r90iwe9xiwz8 https://instagram.com/thehumancannabinoid?igshid=17k159pumklkq https://www.instagram.com/alienblood_genetix_official/ https://instagram.com/as420.ca?igshid=1f116alw054wp The Grow Bags: https://www.as420

Raised lights a bits. 2 seeds one 2 gal pot in a 2 gal bucket. Same structure 2 very different smells one turns color. It's tricks for your fucking mind! Left one is very sweet smell. Right one that is turning darker is very rotten skunky. Gavem a prune job cause the lower buds all bleached lookin and need a tan.

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.

Generative steering Day 30 sprayed with Jas Day 31 noticed spider mites

8/20 Looking real good did a small bit of defoliation but this thing real leafy and frosty at the same time

Holy god ... brothers .... I was growing of the magnificent raw diamonds of Sierra Leone and I didn't realize it !!!! Magnificent look gems covered with a huge frosted layer of resin so pearlescent to make them look from white appearance. Of course it was not at all easy to grow them given their multiple ramifications and not having a containment network installed. In a short time they filled all the cultivation sweats, even the little ones and this to ensure that the lower gems did not have the same compactness as the upper ones, but they still came very resinous! My advice and to contain this very powerful plant and try to concentrate all its exposure with a scrog technique and remove all the lower bulbs

16 Diciembre: El runoff ha alcanzado los 10EC, las plantas siguen creando puntos de floración con espacio internodal corto, gracias al stress generativo, están de 80~85cm de alto aprox. Hay una sola planta que tiene más de 90cm. En unos 2 días más se alcanzarán los 21 días de floración, ese día se hará una defoliacion grande y Lollipop, después de esa defoliacion se volverá a riego vegetativo para estimular el engorde de los cogollos. 18 Diciembre: hoy la EC del runoff alcanzó los 12EC, mañana se harán más disparos de riego para bajar la EC del sustrato. Hoy también se realizó una defoliacion agresiva + Lollipop, para que haya mejor penetración de luz en el Canopy y mejor flujo de aire. Queda solo una semana de riego Generativo, después de eso se vuelve al riego vegetativo para engordar los cogollos.

👍 10/15/2020 It's been 3 weeks since last update so 33 weeks got 2 weeks I think ? Feed some 4-9-3 happy frog 3 tbls and 3 tbls of (DE). 3 weeks left at most. 10/16/2020 There is some nasty weather on the way so I am going to bring her in for the finish going to get out a scope tonight and have a good look at her. But I think two weeks left, also will be under a 11-14 cycle till done. Her mother plant thrived under this light and microclimate. Ps. She's expected to be (FLOWERING!) 10-12 week strain So calyx swelling soon🙏 I almost forgot, she smells like Juicy Fruit gum. Smoked something similar in the 1980's and been searching ever since! Hope she tastes as good as she smells 10/26/2020 Its been 9 weeks and 4 days since start of flower buds are getting harder everyday maybe a week to go. 10/29/2020 10 weeks on the nose. Just water,water and water this week took some branches 2 weeks ago very good for no cure just dried, but With a good trim, and cure should improve over the next couple weeks. Harvest may come this week but we will see🙏

Day 48 of flower just cruising along.

Resin is increasing and looks like bud sites are ready to start putting on some bulk. Issue with low ph drift reaching 5.2 so I decreased 50ppm with distilled water without calmag to soften the water and counter the drift. After decreasing ppm, ph drift continues, so I flushed for 2 days with distilled water and added back nutrients at half strength to increase to 800 ppm over time.