We start week 3 of bloom!! Goofiez 2 amor compound genetics it’s the champions!!

Mucha humedad vía foliar primer riego con fertilizante día 8 dosificación muy leve 👍🏻

Day 39 of flower. Noticing more bulk daily. Smells like sugary jelly donuts/bakery.

Looks a litle purple 💜

This week went by well, I will start checking the trichomes on the Runtz at the end of this week. It should be ready for harvest in the next 2 to 3 weeks The G13 is still smelling like magic, looking majestic. The GDP buds are starting to put on weight

Everything has gone really well up till now , She is start too show the beginning of pre flower , I wasn't expecting that for a couple of weeks so not sure if this is normal ? But she is growing fast and strong , I picked of a few select large leaves that where coving the side branches , but very minimal , mabey one or two leaves of each plant , and also pulled down the branches too help with light getting down into the center of the girl ,

Starting to really fill out smell is 6/10 so far very sweet some pine as well

At the start of week 9 The end of the feeding schedule for two out of the three ladies for "Cath" & "Lorna" 5 litres of dechlorinated tap water only, for the remaining amount of time ripening up. "Anna-Marie" is still on the normal feeding schedule as she's several weeks behind the other two so fed her 13mls of Bio Flores and 20 mls of Bio Boost diluted in 5 litres of dechlorinated tap water. Chopped off a couple of LARFY branches to sample. I then gave them a quick couple of days speed dry in front of the fire 🔥 😅 Yes I know they need to cure but temptation be dammed, needs must lol 😆

9/24 Busy as fuck and personal emergencies always hit during harvest season. I took a few tops from my favorite gmo just so I have some if the weather fucks me. I'll take more today probably. WATERED YESTERDAY. I'll post pictures of dry flowers and do the reports. Three are still standing. That huge gmo is going to extracts though. 9/25 9/26 We are getting a week of rain. After looking at my trichs I decided to pull the GMO's I had left. I was sick of cutting branches due to grey mold and I was starting to lose buds to botrytis. Trichs got to about 10% amber on most. Maybe more. I worked like a mule. I was going to leave my favorite gmo and the sherb pie. However, my wife had multiple medical emergencies that required hospitalization. I couldn't risk letting my girls turn to mush if she had to stay. I'm glad with my decision. Everyone now I see is asking about bud rot and pm cures. This happened at the same time last year. She was hospitalized during late late flower. I couldn't keep this updated and I took the plants ad quickly as I could and rough wet trimmed some of them. Some plants got hung whole. I have been in trim jail. I have finished two plants and that is working my balls off. The one in the fifty and the event horizon. I'll do the harvest reports and add pictures but with my wife how she is and the work load I'm going to have to wait. I also left buds to ripen right before the rain and got lots of nice amber flowers that I froze to make a temple ball. I have lots of content. I just need time and a place to do it. I have one lone survivor. The seedling in the ten that seems to be a sativa hybrid. She's a beast and I think can handle the rain due to the fluffy buds. If I see problems I could easily carry it inside. I'll be back with some pics and videos but for now breaks. 9/28 Busy as FUCK. SICK. Been in and out of the hospital with the wife. Looking back on diaries she's in the hospital when I'm harvesting the past few years. I got two strains curing right now. I got a shit ton drying and I'm in trim jail. I haven't taken picturesor been on here but ill be more active i just havent hadcthe time. I'll wait until shits dry and I can do my harvest reports. I'll look to see if I have any pictures I can upload My sativa hybrid survived the rain. All this rain has made its leaves turn yellow and start to drop. It needs food I think. I'll check the trichs but I know it's not ready. The buds are like soda bottles but they are loose. Like a string of calyxes. I don't flgrow sativas so I'll have to ask for some help. I'm trying to decide if I should feed it. It looks hungry. I'm going to have to scope it and then I'll feed if necessary. I'll take pictures and a video when I have the chance. 9/29 Rain stopped and the sun came out. I need to take some pictures and put them up here and do a harvest report. My little BIG Sativa hybrid in the ten got scoped today. It's weird it's starting to foxtail some. . I've had tons of emergencies but I've bern kicking asses and taking names. I've got one GMO (one pheno was much faster flowering than the others), one event horizon and the sherb pie all curing. I'm just waiting on the others to dry. I've got a couple gmos that are just going to extract. One is really nice though and I'm keeping it for smoke. That's trimmed too. I have been working on the other event horizon which will be done today because it's time for it to be cured. I am sick and sore as fuck but I know how important this is and it's mine and my wife's medicine for the year. Sherb pie was a let down quantity wise but I let it get eaten by ear wigs for too long. I've got to get back to it but when I get it done I'll take the pictures and do the reports reports but this breaks over. I've got a BUNCH of fresh frozen too that I'm planning on running bubble hash with and aging a temple ball.

At day 10 today 9/19 so fucking excited they are really started to take off now just fed again with some sweet candy added this time fucking love greenleaf nutrients so easy to manage. The price on this stuff is fucking dirt cheap and the results show !!! C4 first time growing second week looking good healthy green no issues at all. Almost at the end of the week.and I got my little trooper with me. I love when my cat always taking a look into the garden with me. She always been apart of weed since day 1 her birthday is even on 420 :)!

Balanced compare tea given this week, but nothing else amendment wise and no other watering needed still. Nice stretch gone on in the first week of flowering, plant still looking nice and healthy, will see how things are looking for a defol on day 14 or so.

Flo 22: Arrosage engrais complets Flo 26: Arrosage engrais complets

Hi all the happy people here in GrowDiaries. This is my second cultivation ever and it will be fun to try a bigger space than my closet grows First, I'm just going to say I'm done with the construction of my new growroom. I put some pictures on the construction here in week one. The room is 2.14 meters by 1.7 meters and has a ceiling height of 2 meters. It provides a floor area of ​​3.6 square meters. I use a 54 Watt Lightwawe T5 for germination and 2 Pcs 400 Watt HPS lamps. I have a channel fan that replaces the room air about 40 times an hour to get a comfortable theme in the room, the air enters a fresh air intake from the outside. The air is purified through a carbon filter to then leave the room to the rest of the basement. Then I use that heat to heat the rest of the basement. I will use 8 pcs 15 liter Autopots to grow with and a 100 liter water tank that supplies the pots of water and nutrition. I will grow completely organically in soil and will watercure my buds to get the best possible medicine for me. But there are no cultivation rooms to be displayed here, so I continue with what is most important. Today I have put my seeds in my moisture dome and hope the seeds have germinated within a few days. I am very excited to see how the new growroom will work and how this CBD Fast Eddy plant from Royal queen seeds will turn out. CBD Fast Eddy Automatic is combining Cheese x Juanita la Lagrimosa x Ruderalis, Fast Eddy is a rapid growing, flavourful, and CBD-rich auto strain that goes from seed to harvest in 8-9 weeks, produce generous yields, and induce a clear, mellow, and most importantly, functional high. THC: 9% CBD: High Yield Indoor : 400 - 450 gr/m2 Yield Outdoor: 80 - 130 gr/plant Height Indoor: 60 - 100 cm Height Outdoor: 80 - 120 cm Flowering: 6 - 7 weeks Harvest month: 8-9 weeks after sprouting Genetic Background: Cheese x Juanita la Lagrimosa x Ruderalis Type: Sa 50% In 40% Ru 10% Effect: Clear, Painrelief Climate: Mild .............................................................................................................................................................................................................................................................................................................................................. Update 2017-08-15. Both seeds have germinated and planted in small pots inside the humidity dome. I'm so glad it worked so well and now it's just hoping they'll start growing and become 2 big healthy girls :) ............................................................................................................................................................................................................................................................................................................................................... Update 2017-08-16. I have mixed my own soil today. Its 40% sieved peat harrow H2-H4 0-30 mm, 45% sieved peat harrow H4-H6 0-30 mm. 5% sand and 10% of compost soil. And i use 15% of perlite and mix it all together. ............................................................................................................................................................................................................................................................................................................................................... Update 2017-08-20. These girls are much slower to germinate and to start growing than the other 6 girls I started at the same time. One of the germinated seeds split in half, so I had to take a new seed and germinate it. It took 2 days. It was just a smal taproots after germination with this strain as opposed to my Fastbuds cbd. But I hope everything goes well from now and that they live up to their name, Fast Eddy. ................................................................................................................................................................................................................................................................................................................................................ Update 2017-08-21. New pics. ................................................................................................................................................................................................................................................................................................................................................ 2017-08-22. Nr1 dident make it and died. Started germinate a new seed to get another Nr1. .............................................................................................................................................................................................................................................................................................. 2017-08-27. Nr 1 is in a small pot in humidity dome and i hope shes going to break the surface soon. Nr 2 is slow but doing fine. --------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------- 2017-08-28. Nr2 is transplanted in 15 liter autopot. --------------------------------------------------------------------------------------------------------------------------------------------------------------------- 2017-08-29. New movie of the girls Nr2. Its no water for 3 days now so the roots develop more and match the plant above the soil. The temp controlled fan is awesome, its easy to set what temp you like to have in the room. Right now its 28 celcius. And humidity is 56%. ----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------- 2017-08-29. Hello to you who read my diary, I just want to say that I am pleased that you have chosen to check in with me and in my diary. I just want to say that I do this for myself and for a steady flow of my medicine. Everything you read and see in my diary is 100% honest and I will never distort or beautify anything here. I document my crops so that I can learn from my mistakes and also to look back at those different crops. I try to update with pictures every day and with text if something special has happened in the garden. This is my strainhunt for the best medicine and the beginning of my journey with cannabis and the cultivation of it. ----------------------------------------------------------------------------------------------------------------------------------------------------------------------- 2017-08-30. Cleaned the room this morning, just vacuuming and cleaning with chlorine solution. Im testing the fan to control temp and humidity, it works great. Added a movie. Everything is looking great right now. ------------------------------------------------------------------------------------------------------------------------------------------------------------------------ 2017-08-31. 3 New pics. ------------------------------------------------------------------------------------------------------------------------ 2017-09-01. New pics and a video of the grow room from today.

11.10.2022 130 giorni dalla germinazione al raccolto 70 giorni fioritura in totale Pianta molto bella, sexy, 2 semi su 2 germinati con successo. di due piante, ho avuto 2 fenotipi leggermente diversi, entrambe le piante mostrano una struttura ibrida tendenzialmente sativa, con rami lunghi e boccioli densi e duri, ricoperti da tricomi. Ho laciato le piante crescere con un Lst applicato un po in ritardo, ma entrambe le piante hanno reagito benissimo e formato delle belle chiome a cespuglio. Profumo tendente al dolce, note di lavanda ed erbe aromatiche, una delle 2 in fase avanzata di fioritura profumava di ananas maturo, semplicemente uno spettacolo! La resa sembra buona, le cime sono di ottima qualita, aggiornerò con peso tra poche settimane!

Week 9 for Kalini Asia by Zamnesia seeds, She really bounced back from her last topping to 16 tops. now just keeping her levelled in height. Because of the messed up light schedule + massive shifts of temps from 28+ to 6... outside the tent so really for 7 hours their growth is completely stunted, but I'm making due with what I have 😂

Here we are :) the are finished

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.

Last lap ! This is the biggest plant a grew, def

Well My friends gave me a bigger tent so I got a little more time to let them develop! I'm very ready to take them down just waiting a bit longer for a few more amber trichomes. I'm still feeding them ripen but i wish last week i'd given them a feed in addition too. They look nice in the new tent, there is loads more room, and while the lighting didn't go up as much as I'd like, They have a nice big fan oscillating on them now and room to stretch. ________________________________________________________________ I suppose I'm glad I waited. I wanted to take a few more pics and get one last video in! I'm def seeing a bit more amber in the trics and i think it will make em a bit better for these 2 extra waterings! Probably gonna chop them soon!!!!