The ladies are looking good 3 had a rough start but it was either ph or nitro deficiency somehow...im using nftg#4 for base soil and building a living soil...I topdressed 1/4 cup craft blend and 2 tbls Bokashi...

Vegetacion (Tiempo estimado 28 dias) Segunda Semana de Vegetacion 14/12/2023 - 5:00hrs y 22hrs: Se Hace cambio de solucion nutritiva y se limpia el recipiente, se verifican parametros basicos del agua, mantener cuidados especificos, el Ec y PPm Varean por los aditivos. Agua de osmosis: Ph 6.0, PPm 650-800, Ec 1.3-1.6, Temperatura 22°C - 26°C, Humedad 65% Ambiente: Temperatura 22 °C, Humedad 65%, Ventilacion 15%, 18 hrs de luz , 6 hrs de obscuridad. 15/12/2023 - 5:00hrs y 22hrs: Se verifican parametros basicos del agua, mantener cuidados especificos. Agua de osmosis: Ph 6.0, PPm 650-800, Ec 1.3-1.6, Temperatura 22°C - 26°C, Humedad 65% Ambiente: Temperatura 22 °C, Humedad 65%, Ventilacion 15%, 18 hrs de luz , 6 hrs de obscuridad. 16/12/2023 - 5:00hrs y 22hrs: Se verifican parametros basicos del agua, mantener cuidados especificos. Agua de osmosis: Ph 6.0, PPm 650-800, Ec 1.3-1.6, Temperatura 22°C - 26°C, Humedad 65% Ambiente: Temperatura 22 °C, Humedad 65%, Ventilacion 15%, 18 hrs de luz , 6 hrs de obscuridad. 17/12/2023 - 5:00hrs y 22hrs: Se verifican parametros basicos del agua, mantener cuidados especificos. Agua de osmosis: Ph 6.0, PPm 650-800, Ec 1.3-1.6, Temperatura 22°C - 26°C, Humedad 65% Ambiente: Temperatura 22 °C, Humedad 65%, Ventilacion 15%, 18 hrs de luz , 6 hrs de obscuridad. 18/12/2023 - 5:00hrs y 22hrs: Se verifican parametros basicos del agua, mantener cuidados especificos. Agua de osmosis: Ph 6.0, PPm 650-800, Ec 1.3-1.6, Temperatura 22°C - 26°C, Humedad 65% Ambiente: Temperatura 22 °C, Humedad 65%, Ventilacion 15%, 18 hrs de luz , 6 hrs de obscuridad. 19/12/2023 - 5:00hrs y 22hrs: Se verifican parametros basicos del agua, mantener cuidados especificos. Agua de osmosis: Ph 6.0, PPm 650-800, Ec 1.3-1.6, Temperatura 22°C - 26°C, Humedad 65% Ambiente: Temperatura 22 °C, Humedad 65%, Ventilacion 15%, 18 hrs de luz , 6 hrs de obscuridad. 20/12/2023 - 5:00hrs y 22hrs: Se verifican parametros basicos del agua, mantener cuidados especificos. Agua de osmosis: Ph 6.0, PPm 650-800, Ec 1.3-1.6, Temperatura 22°C - 26°C, Humedad 65% Ambiente: Temperatura 22 °C, Humedad 65%, Ventilacion 15%, 18 hrs de luz , 6 hrs de obscuridad.

This was a effortless week 🐱👌 all plants (except 1runt) were topped and given their first feeding..new growth has already developed on most.. A few plants are distinct from all the others, there's only 2 different strains but it looks like way more at the moment. We're expecting a bunch of vegetative growth this week, will update..thank for dropping by growmies and happy harvests ❤️

la resa è ottima, la resistenza di questa genetica altrettanto. Ho avuto problemi con le mosche bianche e nonostante ciò non hanno accusato molto lo stress.

Started flowering on 7/9/2021

2 weeks left according to breeder info. I'm getting excited @female_seeds . ..

Halfway through week 7. Couple pictures from Tuesday. Gonna upload more when I get back home to her. Can’t raise the lights anymore. Hoping she is done stretching. She takes up every bit of that 4x5 box. Couldn’t be happier with this grow so far. I think next time I’ll go down to 5 gal smart pots this way I can pump out two of them. Still in disbelief she has grown this fast and started budding that fast as well!! I’m feeding her 2 gallons every 2 or so days. She is a very thirsty girl and let’s me know when she is hungry too (leaves curl down). I’ve been slowly defoliating the bottom of her. I cut a couple under grown budds from underneath as well. Not sure how she’d respond if I went scissor happy. I also can’t say enough about Advanced Nutrients. Since I made the switch I can tell her leaves are always praying up and overall health seems through the roof! She really is a monster. 31 inches wide by 36 inches tall. She is stacking nicely. Did my best with pictures. Can’t tell if the flash on the phone helps or hurts the pictures. End of the week- She is doing awesome. Blowing up pretty fast and there is a serious citrus pine smell coming off her when you bump into a budd or it wipes on your finger. For the most part it seems as if she is loving life!!

Det går fint det kommer nok lige lidt an på hvordan man ser på det;) jeg prøver dobbelt topping og pt går det virkelig godt og jeg kan også se på bladenes stilke de er helt RØD/LILLA 👌💚😘🤗🙏🏼💚glæder mig til at se 👀 hvordan den kommer til at se ud u fuld blomst og med buds

hello to all I share with pleasure this fantastic variety, excellent structure, grows very vigorous. as regards lengthening in the first weeks not more than 50% of its size. this week I will make the last thinning. thanks to all the friends who follow me. make it grow

Photoperiod buds 🤩 The smell is absolutely divine very fruity,sweet & tropical🍋🍊🍉🍌 Solid like a diamond 💎 Bay harbor butcher’s trim to show the density

Aún las tenía metidas en casa por la noche, por qué las plante en pretemporada y no quería que se congelarán.

📅 D85- 26/01 📜 Only fresh water from now on. She's not yet ready - 3-4 days more I think. ✍️ 0.1 EC ♒ 6 pH 🌊 10 L 📏 95 cm 📅 D90- 29/01 📜 Not yet Ready ✍️ 0.1 EC ♒ 6 pH 🌊 10 L 📏 95 cm

With no doubt these plants have not produced much more quantity and density of buds due to the 2 serious mistakes I've made (those who have read the weeks will know what I mean). However, I can say that I am happy with the production obtained given the mistakes made. Between the 2 plants, the one that has produced more and generated the most dense buds has been the Gorilla with the Man-lining technique applied, it has also loosed a bit less weight drying than the non man-lining one. In comparison with the Money Makers with which they have grown the result is the same. Both Gorillas have each produced more than any of the Moneys comparing them 1 to 1. Also buds are a bit dense than the moneys, but none of them is really desde at all. *****ESPAÑOL***** Sin duda estas plantas no han producido mucha mas cantidad y densidad de cogollos debido a los 2 graves errores que he cometido (quien se haya leído las semanas sabrá a que me refiero). No obstante, puedo decir que estoy contento con la producción obtenida dados los errores cometidos. Entre las 2 plantas, la que más a producido y ha generado cogollos más densos ha sido la Gorilla con la técnica de Man-lining aplicada, y también ha perdido un poquito menos de peso en el secado que la otra. En comparación con las Money Maker junto a las que han crecido el resultado es el mismo. Las Gorillas han producido cada una más que cualquiera de las Moneys comparándolas 1 a 1. Así mismo, los cogollos de las Gorillas presentan un pelín más densidad que el de las Moneys, aunque realmente ninguna de las 4 plantas ha generado cogollos densos del todo.

Day 14, some supercropping Day 15 .. it’s under control 😂🤣 Day 19 lights almost maxed to tent height unless I zip tie led to the top ceiling frame, last bit of monster cropping. Lost 2 top nugs to physical led burn but it’s ok. Everything is fine. Still going very hard on soluble N, and Pk along with b+, fishsh!t, microbial mass, humic acid. Carbs every day with organic booster

💩Holy Crap💩 That was so much fun , it's full on winter where I am and it kept me busy , and come on there's nothing like growing your own stuff. I had a blast as it's been at least over 10 years since my last indoor grow , and it was fun , I had used all of my old techniques and equipment and it worked out just fine , so I was glad I had a ruff idea of what to expect...... Final thoughts Gonna be honest about that grow , it should me just how far Genetics have come, 10 plus years ago before I stopped growing indoors , all we had was like lowrider auto and greenomatic auto and maybe few others but they were horrible...... but this auto produced quite well as expected it should with the size of my medium and my soil base and very little nutrients, which is what I had hoped for from the start , cause I didn't really know where to start in terms of Genetics as I have been out the game for awhile but I'm super glad with the results and some gratitude needs to be sent to CanukSeeds , they came through as it always starts and ends with elite Genetics👌 ........... I can't wait to start my next grow diary, so keep an eye out , there's gonna be more to come , I'm going to try some really interesting cultivars........ PS. Can anyone tell me this , back in the day like 2003-4-5-6 wasn't growdiaries.com just a private forum cause if memory serves me , I was among those lucky enough to find a community that did complete grow logs, fourm style, which is where I found my growmie and Mentor Franco Loga from Greenhouse seeds , RIP BUDDY 😃 CANT WAIT TO START MY NEXT GROW 👉I HAVE CREATED A PLACE FOR GROWMIES TO VISIT , SHOW OFF THERE GROWS , AND JUST HANG OUT .....👈 👉ALL YOU NEED IS TO JOIN THE GROWDIARIES DISCORD SERVER !!!!!!!!!!!👈 LINK IS 👉 https://discord.gg/zQmTHkbejs

Managed to break a main stem, tried my best to get her back on in rapid fashion, but it was a 95% clean break, so I can't expect 🙃 much. Oh well, that's what I get for cracking bad jokes. Genetics is the study of heredity, the passing of traits from parents to offspring, while photomorphogenesis is the developmental process in plants where light influences growth and development. Genetics focuses on the fundamental principles of heredity and gene expression, while photomorphogenesis specifically investigates how light signals affect plant morphology, including growth, elongation, and overall development. Photomorphogenesis, the light-mediated developmental process in plants, involves complex gene expression regulation. This regulation occurs at multiple levels, from the initial perception of light signals by photoreceptors to the activation of specific gene networks and post-transcriptional modifications. https://onlinelibrary.wiley.com/doi/full/10.1111/pce.12934 Photomorphogenic responses to ultraviolet-B light Gareth I. Jenkins First published: 09 February 2017 https://doi.org/10.1111/pce.12934 Citations: 173 A further response involving UVR8 and auxin signaling is leaf epinasty, which is the downward curling of leaf edges away from incident light. A recurrent theme in recent research is that UVR8 often functions through interaction with other signaling pathways. In particular, several studies highlight an interaction between UVR8 and the hormonal pathways that regulate extension growth. One example is the role of UVR8 in suppressing the shade avoidance response. Many plant species respond to the presence of neighbouring vegetation by stimulating extension growth as a result of increased auxin biosynthesis. Leaves absorb red light but reflect far-red light, and therefore shading by vegetation leads to a relative decrease in the ratio of ambient red:far-red light, which is detected by phytochrome, causing a decrease in Pfr relative to Pr (Casal 2013; Fraser et al. 2016). In turn, the decrease in Pfr/Pr leads to an increase in stability and activity of several PHYTOCHROME INTERACTING FACTOR (PIF) transcription factors, notably PIFs 4, 5 and 7, which stimulate expression of auxin biosynthesis genes, leading to extension growth (Hornitschek et al. 2012; Li et al. 2012). Hayes et al. (2014) showed that UV-B antagonizes shade avoidance responses in Arabidopsis elicited by low red:far-red light, and the UV-B effect was strongly impaired in uvr8 mutant plants. UV-B, detected by UVR8, inhibited the increase in expression of auxin biosynthesis and signaling genes promoted by reduced red:far-red light. Furthermore, UVR8 signaling stimulated GA2OXIDASE1 expression, which causes reduced levels of gibberellic acid and consequent stabilization of DELLA proteins, which antagonize PIF activity (De Lucas et al. 2008; Feng et al. 2008). Whereas the effect of UV-B on GA2OXIDASE1 expression required HY5/HYH, that on the auxin related genes did not. The experiments further showed that UV-B elicited destruction of PIFs 4 and 5 and the stabilization of DELLA proteins, although it remains to be established directly whether the effects on these proteins are mediated by UVR8. Thus, UV-B, detected by UVR8, signals to plants that they are in sunlight and negates shade-induced extension growth by antagonizing PIF action and auxin biosynthesis. UV-B also inhibits the morphogenic responses caused by exposure to elevated temperature, which include hypocotyl extension in seedlings and petiole extension and leaf elevation in mature plants; again, the effect of UV-B is substantially mediated by UVR8 (Hayes et al. 2016). However, in contrast to the action of UV-B in suppressing shade avoidance, UV-B inhibition of thermomorphogenesis does not involve either PIF destruction or an effect on DELLA proteins. PIF4 is a key regulator of thermomorphogenesis, promoting expression of genes concerned with auxin biosynthesis and signaling. UV-B inhibits PIF4 transcript accumulation, consequently preventing an increase in PIF4 protein, and also stabilizes the LONG HYPOCOTYL IN FAR-RED 1 transcription factor, which binds to PIF4, impairing its ability to bind to DNA. Together, these mechanisms block the accumulation and activity of PIF4 at elevated temperature (Hayes et al. 2016). The inhibition of thermomorphogenesis by UV-B is likely to be advantageous for plants, as it will prevent detrimental extension growth under natural conditions where elevated temperature is often accompanied by exposure to relatively high levels of UV-B. Another auxin-regulated growth response is phototropism. It is well established that phototropism in response to unilateral UV-A/blue light is mediated by phototropins, which direct accumulation of auxin on the non-illuminated side of the stem, causing localized extension and hence bending towards the light source (Christie & Murphy 2013). Vandenbussche et al. (2014) reported that UV-B can also induce phototropic bending and that the UV-B response in phot1phot2 mutant plants requires UVR8. However, UV-B-induced bending is slower in phot1phot2 than in wild type, indicating that phototropin action is involved in the wild-type UV-B response, and that the phototropin-mediated response is faster than that mediated by UVR8 (Vandenbussche & Van Der Straeten 2014; Vandenbussche et al. 2014). Moreover, the response mediated by phototropin is initiated at lower fluence rates than that mediated by UVR8 (Vanhaelewyn et al. 2016b). The UV-B-induced phototropic response involves the establishment of an auxin gradient across the hypocotyl, as in the UV-A/blue light response, but formation of the gradient in UV-B does not require phototropins and involves some different auxin signaling components to phototropism mediated by UV-A/blue light (Vandenbussche et al. 2014). UVR8 mediates repression of genes involved in auxin biosynthesis and signaling, which likely contributes to the generation of the auxin gradient across the hypocotyl. Vandenbussche & Van Der Straeten (2014) showed that the accumulation of HY5 on the UV-B exposed side of the hypocotyl (demonstrated using a HY5-YFP fusion) correlated with UVR8 response kinetics and is likely to mediate the repression of auxin biosynthesis genes on the illuminated side. A further response involving UVR8 and auxin signaling is leaf epinasty, which is the downward curling of leaf edges away from incident light. Epinasty is stimulated by UV-B exposure (Wilson & Greenberg 1993; Jansen 2002) and also by the action of phyB, whereas phototropins promote leaf flattening (Kozuka et al. 2013). Fierro et al. (2015) showed that the epinastic response to UV-B in Arabidopsis is mediated by UVR8, most likely through the regulation of auxin transport. Moreover, they found considerable overlap in the sets of genes regulated by UVR8 and phyB, notably in the repression of genes involved in auxin action. The phyB action in epinasty involves the regulation of specific PIFs (Johansson & Hughes 2014), and there is evidence that PIFs are required for the UV-B-induced response (Fierro et al. 2015). A possible scenario is that UV-B de-stabilizes PIFs, as in the inhibition of shade avoidance, causing the repression of auxin response genes and consequently initiating the changes in auxin transport associated with the epinastic response. Fasano et al. (2014) highlighted the potential interactions between UVR8 and abiotic stress signaling pathways and proposed that the cross-talk may involve auxin signaling. They reported that high salt and osmotic stress stimulate UVR8 expression and that a uvr8 mutant has increased salt tolerance under UV-B conditions. In addition, the reduced extension growth of plants over-expressing UVR8, previously observed by Favory et al. (2009), was enhanced under osmotic stress. Fasano et al. (2014) found that the UVR8 over-expression phenotype is due to reduced cell expansion and suggested that the phenotype could be explained by altered auxin signaling. Abiotic stresses such as drought, salinity and high temperature will often be accompanied by relatively high fluence rates of UV-B in nature, and the interplay between UVR8 signaling and auxin signaling could be modulated under such conditions to regulate growth and promote survival. The stimulation of stomatal closure by UV-B involves interaction of UVR8 with different signaling pathways to those that regulate growth responses. In species such as Vicia faba (Jansen & Noort 2000) and Arabidopsis (Eisinger et al. 2003; He et al. 2013; Tossi et al. 2014), low fluence rates of UV-B stimulate stomatal opening whereas higher fluence rates promote closure. He et al. (2013) showed that the closure response in Arabidopsis is mediated by an increase in H2O2, generated through NADPH oxidase activity. UV-B-induced cytosolic alkalinization is involved in mediating the increase in H2O2 production (Zhu et al. 2014). In turn H2O2 stimulates NO production (He et al. 2013). Inhibition of endogenous NO accumulation prevents closure even under conditions where H2O2 remains high (Tossi et al. 2014). Tossi et al. (2014) found that UV-B-induced stomatal closure is impaired in uvr8, with a concomitant reduction in H2O2 and NO accumulation in the guard cells. Nevertheless, the mutant stomata were viable, and they closed when either a NO donor or abscisic acid was added. It is likely that UVR8 acts to promote H2O2 and hence NO accumulation, but it is not clear how it does so. The UVR8 action likely involves gene expression, because a mutant lacking the HY5/HYH transcription factors is impaired in the closure response (Tossi et al. 2014), but the relevant target genes are not known. The ability of UVR8 to influence auxin and gibberellic acid signaling, as well as redox signaling, is likely to affect a larger number of physiological processes than reported to date. Furthermore, it is likely that interactions between UVR8 and additional signaling pathways will be discovered. UVR8 photoreception leads to sequestration of COP1 and stimulation of HY5 accumulation, and both these proteins participate in a range of cellular processes (Lau & Deng 2012; Huang et al. 2014a; Gangappa & Botto 2016). For instance, COP1 is involved in controlling abundance of the flowering time regulator CONSTANS (Jang et al. 2008; Liu et al. 2008; Sarid-Krebs et al. 2015), and hence UVR8 activation might influence flowering time, as suggested in some studies (Morales et al. 2013; Fasano et al. 2014). HY5 binds to over 9000 genomic loci in Arabidopsis (Zhang et al. 2011) and regulates genes in numerous processes (Gangappa & Botto 2016). Thus, regulation of HY5 provides a potential mechanism for UVR8 to influence several aspects of plant physiology. Figure 3 illustrates some of the known and potential interactions involving UVR8.

That was the first and definite not last grow of Greenhouse Seeds Lemon Orange. She has grown very wide with strong and heavy branches, buds also really crazy exploded. The taste should satisfy every fruity lover out there , the high is uplifting , not too much body, for me a pretty nice allday smoke. I also find a medical aspect in it , i suffer under depression and it gave me nice moments. Update: After a time with it , i'm even more convinced, it also give me energy to get started / going. I thank Arjan and all Greenhouse employees, especially Georgia from CS , for this wonderful plant.