Smells crazy on this now! Just had 3 days of dark and a flush of flawless finish. Chopped and drying in tent this week Not took any thing off as i want it to be slow dry and try and keep some of that weight. Harvest very soon🔥🔥

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.

Plant A seems to be packing weight on now had to tie a few branches up, Plant B seems behind i think its because it just kept on stretching done abit more defoliation on it throughout this week, Plant C is A lot smaller than the other 2 and is looking a lot more closer to harvest its currently 5 days into a flush, the best pictures i could get of the trichomes i have added can anyone tell me what they think from my pics how much longer i think a few days but this is my first grow? Would appreciate anyone comments thanks

So far she is staying small as I wished. Will start raising nutes little by little this week as more leaves come. At the third set of descent true leaves formed I plan to move her to the flower tent at 12/12 with more red spectrum. Attempting a candelabra trained tiny grow with one top and two side trained colas. I have to say this is the first time I ever strived for small. Usually I am trying to fill the tent.

everything changed on week 4 grow tent and cob led came to show how a good light is important. from now til last 2 weeks, only indoor growing goodbye CFL's, you worked well. + LST and ferts (2ml + 0.25) Defoliation started Removed branches from 1st node

12/25/2023-Germination Day 1 Merry X-mas 2023 I decided to start a run of SolFIre Gardens Hoodz Candyz S1. I am going to do a cup filled with RO water a touch of Hydrogen peroxide and let it sit for 24-48 hours until I see tap root then I am going to put it into a rapid rooter.. Tap root Down and put it about 1/4 of the say down the Rapid rooter. I made some modifications to my basket on this run.. I have taken a few Pods that I use for my cloning machine and decided that I am going to try and use them as sure plants, so that I can take my water right up to the bottom of the basket this time and see if these can make my planting more consistent.   12/26/2023-Germination Day 2 Tap root achieved Planting Commencing 12/27/2023-Germination Day 3 Misted the dome lightly misted the rapid rooter and added a little water to the bottom of the pan to encourage root growth to the pan. 12/28/2023-Germination Day 4 Ground Hogs day 12/29/2023- Germination Day 5 She is up, she has broken surface, I misted the root riot, and around the bottom of the tray to try and entice root growth down rapidly. 12/31/2023- Germination Day 6 Ground Hogs Day 1/1/2024-Germination Day 7 HAPPY NEW YEARS!!.. I did it I planned it out so my planting day would fall on New Years and it worked.. Yay!!! 1/2/2024- Germination Day 8 Since the roots are not to the water yet, I am pouring one cup of water lightly on the hydroton around the lady to try and encourage root growth down to the water.. 1/3/2024- Germination Day 9 Ground Hogs day, will continue until roots hit the water. 1/4/2024- Germination Day 10 Ground Hogs day, will continue until roots hit the water. I will just continue to top feed until roots are in the water.. Shouldn't be more than a few more days. 1/5/2024- Germination Day 11 Ground Hogs day, will continue until roots hit the water. I am going to change the water Sunday and kick off Week 1, I will just continue to top feed until roots are in the water.. Shouldn't be more than a few more days. 1/6/2024- Germination Day 12 Ground Hogs day, will continue until roots hit the water. I will just continue to top feed until roots are in the water.. Shouldn't be more than a few more days. 1/6/2024- Germination Day 13 Ground Hogs day, will continue until roots hit the water. 1/7/2024- Germination Day 14 Ground Hogs day, will continue until roots hit the water.

There loving the 12/12 light cycle thays forsure!

Switched from 24/0 to 12/12 at the end of day 14, also switched the 730nm Led's on. Its been 7 days the plants have started growing a lot faster but there's still no pistils showing. I started feeding biobizz grow @ 2ml/l At the moment there getting watered every 3-4 days. The light is showing 25000lux on a lux meter app.

Week 2 began very routine so far I have only watered with pH adjusted water and no nutrients yet. But looking to do a 1/4 strength feeding the next time I water. 10/26/2018 - Catzilla damaged 3 plants!!! I left the tent open for 5mins to get some water and by the time I was back the damage had been done. I am hoping they will still pull through. Any suggestion on what I can do to help save them??? Ironically the culprit appears to be my cat called Poison.... 10/28/2018 - 1/4 Strength of Nutes 3gallons (11355ml) - 6ml Micro/12ml Bloom/3.75mlCaliMagic 10/30/2018 Two days into first feeding. Plants seem to be pulling through and look good "Disco" still has some discolouration in the leaves, still unsure what is causing it. 10/31/2018 - Final day of week 2 Lots of growth since giving them nutes. On to week 3!

2/1/2024- Pre-Germination Activities Day 1 I have 21 weeks until final photo is do.. I took 3 seeds out of cold storage and will let them get to room temp for the next 48 hours before I go with Glass of water for germination. I have 3 beans because I will start from the very beginning helping ensure I present the best Pheno. This is going to be a fun one.. I am a few days away from being able to clear my tent out for this run.. I have a breeding run in right now and the Seeds are a few days away from being mature enough for me to take down the girls. Once I get them down I will need to get my tent cleaned up and turned over right away. This is going to be close, I will have to time them to the water and into the tray at the right time.. because I will need to get lighting on them right away.. I have my 2X2 and my light ready incase I need to hold them in the cloning machine if the others are not done in the next few days.. Glad I have options that can stretch me out for a week or 2 to give me a little more time. 2/2/2024- Pre-Germination Activities Day 2 I checked on my breeding run to see how close the seeds are and if the tent is ready for me to clear and clean but alas I am still going to need a few days. I setup the emergency 2X2 and that should give me 2-3 weeks. The plan is to still wait one more day to allow the beans to warm up to room temp and then drop them in Water sometime tomorrow. Form my Emergency 2X2 I have the following: 4" inline fan and carbon filter Fan VS-2000 light 2/3/2024- Germination Activities Day 0 - Dropped the Beans in.. Today is 0 day.. Go.. Go .. Go.. 2/4/2024- Germination Activities Day 0-1 - Checked in on them this morning and no tap roots yet.. covered them back up and back in to the closet they went. I setup the Root Riots and the Seed tray for them. I Ensured my water that I was soaking the root riots in was PHed to 5.8 and I used RO water. Afternoon Update: Checked on my Breeders and they are done. I started to harvest them, I took down the one I had reversed with STS and I took down the Black African Magic- All but one bud, I wanted to get some pics of that one today. I was only able to get 2lbs into the Cannatrol because I had to be very careful to keep the bud from the plant that was treated with the STS separated from the other seeded bud that was pollenated from the plant I reversed. Cannatrol could have held an additional 2oz of wet but not today. Ideally I need 1 more Cannatrol so I can take an entire Tent, but will figure that out. I put an additional 1.5lbs into the freezer to wait it's turn into the Cannatrol, I would have left it on the plant and taken it in 4 days when the dry cycle gets done but wasn't sure how much 2.2 lbs was equivalent to chopped and wet trimmed. 2/5/2024- Germination Activities Day 0-2 - Checked in on them this morning and 2 of them have very small tap roots out.. one still doesn't going to give them some more time. I will check in on them this evening and see if they are more open if so I will transfer the ones that are ready to their medium and seed tray. 2/6/2024- Planting Day TRUE Germination Day 0- Checked in on them this morning and all 3 of them have tap roots out. I broke the bottom of the tap root for #1 which was the biggest.. pretty sad.. I hope she survives.. I tried to be careful it just snapped off when I was trying to get it in the root riot right. Other than that all three are now in their in-between home in the 2X2 while if finish clearing and cleaning out their forever homes. 2/7/2024- Germination Day 1- Checked in on them and no surprise no sprouts yet. Sprayed the dome to moist it and light spray to the tops of the Root Riots. 2/8/2024- Germination Day 2- #3 is popped and it looks like #2 will be popped by this evening.. I got my second Cannatrol today so now I can take down the rest of the tent and get it into the dry/cure. 2/9/2024- Germination Day 3- #2 is popped as well.. so I have #2 and #3 up and still waiting to see on #1 but that might be a loss since I accidently broke off some of the Tap root when transplanting. 2/10/2024- Germination Day 4- #1 has Popped... We have ignition on all 3.. YAY!! I finished clean up and install of RDWC system, this time was unique the back left buckets 3 inch pipe wasn't seated correctly so I had to clean up about 12 gallons of water all of the floor. I also had two leaks coming from one of the Waterfall return junctions, this is why I do a full pressure test before I put anything in. I will continue to monitor it through tomorrow to ensure that I am good to go and then I will finish setting up the baskets and prepping the water to be ready for the ladies planting day!!! 2/11/2024- Germination Day 5- #1 Of course is going to be my trouble plant.. No matter what If she lives through planting in the system and making it, I think I might not cull her at all regardless, she has been such a problem, makes me wonder if she will be super worth it towards the end.. We will see as we go through this grow, but #1 has a piece of the shell on the leaves, Other than that I set up a new thing I have been doing since last grow converting my Baskets into Sure plants so I can see exactly where the water is when I plant them and ensure I have the water up high enough that they are able to access it and grow but not too high were they are drowning. 2/12/2024- Germination Day 6- Everything seems to be going good.. will just keep them moist and let the roots grow for a few more days before I transplant to forever home. 2/13/2024 - Germination Day 7- Just keeping them Moist. 2/14/2024 - Germination Day 8 - Planting day.. they are now in the system.. :-)I had to fill the water to the bottom of the basket where I could see water on the bottom rocks and just coming up where I had created my whole/ sure plant. 2/15/2024 - Germination Day 9- Top fed just a little to keep them moist and encourage root growth towards the water. I ensured the PH is right at 5.98-6.02 range. 2/16/2024 - Germination Day 10- Top fed just a little to keep them moist and encourage root growth towards the water.

Week 6 Report: Big Cheese Auto Flourishes in Bloom! Greetings once more, fellow cultivators! Week 6 with our illustrious Big Cheese Auto is like watching a floral masterpiece unfold, and the thrill is escalating. Kudos to Seeds Mafia for these genetics that keep delivering wonders. Our green queen is dancing through her second week of flowering, and oh, the elegance! It's like a choreography that only Mother Nature could compose. The Autopot system is still the unsung hero, allowing our star to sip on her terms. It's like the perfect rhythm for a flawless dance. P-Boost and Topbooster, our dynamic duo, continue to work their magic. Picture it like a nutrient wizardry, with organic nitrogen, L-amino acids, and a bouquet of trace elements and natural stimulants enhancing the bloom. The anticipation for those luscious, aromatic buds is becoming palpable. Our TDS is maintaining a harmonious 390, and the pH, a symphony at 6.0. It's like hitting the sweet spot in a musical composition. The Autopot and the nutrients are working together in a synchronized dance for our Big Cheese Auto. The leaf-bending symphony continues, creating an even canopy that basks in the natural light. Defoliation is on the horizon, like a spring cleaning for our green sanctuary. Ensuring she receives ample light for those inner buds to flourish. oh she is by far the biggest gir in the room , check the raw video OMG what a beast <3 <3 <3 As always, a colossal thank you to Seeds Mafia, Aptus Holland, Grow Diaries. Your collective support is the force behind this flourishing green odyssey. As we step into the next week, the excitement is electric. Our Big Cheese Auto is not just growing; she's thriving. I'm eager to witness the bloom spectacle that awaits. Let's continue to cultivate greatness together! Genetics -Seeds Mafia Big Cheese Automatic Light - LUMATEK ZEUS 465 COMPACT PRO 
Food - APTUS HOLLAND 
 
All info and full product details can be find in can find @ https://seedsmafia.com 

https://aptus-holland.com/
 

https://lumatek-lighting.com/ As always, thank you all for joining me on this journey, for your love, and for it all. My horticultural odyssey would never be the same without you. Your love and support are cherished, and I feel both honored and blessed to have you in my life <3 <3 <3 With true love comes happiness. Always believe in yourself and always do things expecting nothing in return, with an open heart. Be a giver, and the universe will respond in ways you can't even dream off. Friendly reminder: all you see here is pure research and for educational purposes only <3 <3 <3 Growers love to you all <3 <3 <3 P.S- I must extend my sincerest apologies for the missing video reports. Regrettably, Grow Diaries is still facing some technical issues that are preventing me from uploading them. Rest assured, as soon as the situation is resolved, I'll share those videos to give you an even closer look at this fascinating journey.( i can only upload 100 Mb files with is not enough for the most type of videos i do, and even the photos is hard sometimes )

Already set to 12/12 photoperiod; I have watered several times, aerating the water beforehand, and will continue like this until flowering begins. I also performed FIM pruning.👍

The buds on this plant seem very nice and tight, a nice purplish bud colour started to develop during the 48 hours producing some very pleasant looking buds.

~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_ 08/07/21: 😸Week 4!! (a day early, Sunday plans etc..).. We've been feeding lightly with every watering (we're in promix) but we may throw some EWC in their pots..the mainlined plant is sporting new growth and building symmetrically, she had almost no recovery downtime to speak of, i couldn't be happier 😻..the low stressed plants are starting to fill out, we've been doing a lot of leaf tucking with those 2. thanks for reading if you made it this far lol, we'll update midweek..happy growing folks! 😽💡🌱❤️ ~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_ 8/10/21: 🐱 The new growth seems to be coming light colored, they're definitely getting enough to eat for their size..idk..ill just keep doing the same routine and make changes if/when it gets worse..ty for stopping by ❤️💡🌱 ~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_~_

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Esta semana a estado marcada por un excelente desarrollo, ya esta culminando el desarrollo de los capullos para dar inicio al proceso de engorde de las flores.

Critical Cure is still happy and putting out good growth. Fertilized with a ring of the Coast of Maine around the base and watered it in with a little lime water. Bugs are getting hungry so the plants got some neem oil spray. Heat wave going through right now. Please forgive my slurring in the video, it's been a long week and my brain is addled😜