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Robimy nasiona feminizowane - FOTORELACJA

cannabis sativa

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jakie dać steżenie ga3 i ile razy powtarzac aplikacje. Chce połaczyć to z sts przepisem forumowym gdzie jest 3.5g/l albo stosowac na przemian w celu wydłuzenia kwiatostanow
 

sub23

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jakie dać steżenie ga3 i ile razy powtarzac aplikacje. Chce połaczyć to z sts przepisem forumowym gdzie jest 3.5g/l albo stosowac na przemian w celu wydłuzenia kwiatostanow​

1 oprysk w fazie gdy zaczynają się pokazywać męskie 50 mg/l bardzo delikatny powinien ładnie już rozbić.
Jak dasz dwa na etapach pośrednich trochę możesz zmienić str. wygląd kwiatów męskich które się pojawią : ogonki _ bardziej przypominają prawdziwe męskie, ale po samym Ga3 są mniejsze niż normalne. Ga3 samo z siebie jest niepewne i daje karkołomne efekty uboczne w większych dawkach. Gdzieś na początku watka masz stare foty Grzecha z łączenia z agno3 ale bez podania pełnej procedury: porównaj wygląd żeńskiej i męskiej po : hermieniu taka mieszanka. Imo. 2 opryski niezbyt stężonymi r. 1 po dwu tygodniach od aplikacji srebra + drugi przy pierwszych objawach hermienia to max. Mały wydatek cieczy i nie wysokie stężenie _ granica podane up. są imo. nie warte przekraczania. W zależności od tego jak dużo pryśniesz wyniki zmienne nawet przy tak samo st. roztworach.

Opryskiwacz po próbniku perfum taki 2 ml jest wyst tutaj moim zdaniem : delikatnie i ostrożnie z tym : Może także opóźniać kwitnienie : redukować ilość "palcy" w liściach _ powodować wyrastanie łodyg do absurdalnych długości + kasować ząbkowanie z liści. Jak by dobrać dobrze dawki i terminy zapewne łączeniem STS czy azotanu z Ga3 dało by się zrobić fenkopie wypisz wymaluj prawdziwa męska wiecha. Ale dokładnych danych ile nie mam ;]. Dawno temu i nieprawda.

Ga3. jest wredne _ silne efekty _ przy opryskach łatwo podać 2 czy 3x więcej niż się zakładało. Ze zwilżaczem się lepiej wchłania + odmiana niekoniecznie tak samo reaguje jak druga. Lepiej dać za mało niż przeginać zaraz foty z tego tematu. Nie pamiętam dawek zbyt dokładnie. To powoduje nawet wtórny przyrost łodyżek w dojrzewających już szczytach.

temat jest długi gdzie to cholera było : grzecha na początku... Zdjęcia Kota z mieszaniem : zaginęły : tam dawka podziałała mniej więcej zgodnie z założeniami : nieco rozciągnęło jedynie. Podawane miejscowo.

jest fota Grzecha: Raczej wczesny oprysk po całości : i ga3 spowodowało przyrost up jak diabli ale w momencie gdy powstawały męskie kwiaty już przestało zapewne działać. Tego można się spodziewać przy podawaniu razem : w większej dawce nie miejscowo

grzech_srebro-i-ga3.jpg


Kocich fot jak wspomniano nie ma z miejscowego.
Foty z testów innych także gdzies znikły zara sie poszuka.
łatwo znalexc te od mohana ;)

Nomercy : dawka około 600 mg/l _ prawdopodobnie kawałek "waty" nasączonej roztworem lub podobnie w bardzo później fazie kwitnienia.
Kot miał także mniej więcej miejscowe działanie przy podaniu mieszanki na sam szczyt pędu. [ połowa kwitnienia mniej więcej ??]

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Efekty podania Ga3 jako stymulatora wzrostu : dawka zbyt duza do tego : i za mała dla tej odmiany aby wywołac hermienie [ mniej skuteczne od srebra ] widac efekt o którym była mowa : liście zredukowane do 1 bez ząbkowania. Rozumiem, że tu zależy na wywołaniu nieco podobnego efektu. [ zdjęcie ma z 20 lat ]

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Tu połączeniu agno3 z ga3 uzyskano właśnie coś podobnego ale bez aż takiego wpływu na liście. Dawka zagineła w pamięci : nie było podawane razem Ga3 później. Mix out. e/lr1 F1

ga3_agno3.jpg


Było tego kapkę więcej. Może w wiki sie zachowały sekundę.

Wiki : jeszcze jedna z nomercy : bardziej efektywne hermienie _ procedura mniej wiecej jest w wiki :

Ga3_cannabis.jpg


Oraz efekt oprysku Ga3 : rozbicie str. szczytów : Bez hermienia. Dawka pewnie ze 100 mg/l ale ilość cieczy przy oprysku nieokreślona _ można pewnie odnaleźć źródło jak się bardzo postarać.

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Nigdy nie było procedury ze stężeniami opracowanymi tak aby : można było pryskać roślinę do całkowitego zamoczenia i spłynięcia roztworu z : Bez tego trudno o jakakolwiek powtarzalność bo przy podobnie st . roztworach można podać zdecydowanie odmienne dawki. Ja bym raczej unikał oprysku łodyg i starał się bardziej miejscowo. Strzelając w procedurę podana na początku.
Jeśli ma wpłynąć także na budowę męskich kwiatów silniej. Pierwsza dawka zanim zaczną się formować. łączenie dwu środków do zmiany płci może działać nieco synergiczne dodatkowo większy stopień zmiany : a jak tu sie w wątku przewijało odporność na opryski w zależności od odmiany czy nawet sztuki bywała nieco inna. Nawet czasem mocno.

Foty z ekstremalnie wydłużonym dziwnym szczytem po Ga3 i bardzo małymi nie do końca rozwiniętymi męskimi nie mogę w tym śmietniku namierzyć. Duże z tego co była zaginała i są puste kwadraciki zamiast dokumentacji ;(. Może i ta fota także ?? chgw.​
 
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sub23

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Dawno dawno temu : problemy z płodnością : =>
Podejrzewano o to zbyt wysokie dawki srebra : lub czynniki genetyczne : próbowano obchodzić przy pomocy suplementu Ga3 dodanego do STS : Identyczna obserwacja : teraz w erze gdy na rynku są praktycznie wyłącznie nasiona femi zapewne rzadziej problem występuje : potomstwo roślin które wytworzyły płodny pyłek na tyle aby otrzymać nasiona. [ takie uzupełnienie po dziesięcioleciu mniej więcej od startu tematu popularyzacyjnego ]


na link natrafiono przypadkiem na forum IC mag :

w początku watka :


Gdzie Ktoś w zasadzie powtarza doświadczenia które tu zostały wykonane.​

Pollen Appearance and In Vitro Germination Varies for Five Strains of Female Hemp Masculinized Using Silver Thiosulfate

in HortScience
Online Publication Date: 06 Mar 2020

Abstract
Genetically female seed is sought for cannabidiol (CBD) hemp production because CBD is extracted from the flowers of female hemp plants. The production of all female seed requires masculinization of female plants to produce genetically female pollen that reliably generates female seed. Of the five female hemp genotypes that we masculinized using foliar sprays of silver thiosulfate (Abacus, Cherry Wine, Mountain Mango, Youngsim10, Wife), all genotypes produced fewer large and more irregular or misshapen pollen grains than genetically male plants. The masculinized female genotypes Wife and Cherry Wine produced pollen with germination rates similar to those of the male genotype Kentucky Sunshine. Female hemp genotypes vary in their ability to produce usable pollen that disperses well, is easily collected, and germinates as well as pollen from genetically male hemp plants.

Keywords: Cannabis sativa; feminized seed; foliar sprays
Hemp is an annual dioecious species with separate male (XY) and female (XX) plants (Moliterni et al., 2004). Dioecious hemp seed will generate ≈50% male and 50% female plants (Schaffner, 1921). Female plants are preferred over males for CBD hemp production because female inflorescences accumulate significantly greater cannabinoid content than male inflorescences (Small, 2015). Monoecious plants, which have both male and female flowers, occur occasionally in hemp, and cultivars have been selected for use in the production of industrial hemp fiber and grain. Male and monoecious plants are problematic for CBD production because of their pollen, which is produced in copious quantities because hemp is a wind-pollinated species (Small and Naraine, 2016). A single male hemp flower can produce hundreds of thousands of pollen grains (Faegri et al., 1989), and hemp pollen can travel long distances by wind (Clarke, 1977).

Although female plants produce greater CBD content than male plants, pollination and subsequent fertilization of female plants lead to seed development, which significantly reduces the CBD content and, thus, the CBD yield, of female plants (Meier and Mediavilla, 1998). Therefore, CBD hemp growers must be vigilant when scouting for and removing male or monoecious plants from production fields before the plants release pollen (DeDecker, 2019). Scouting and removing males are highly labor-intensive for growers and result in the loss of ≈50% of harvestable land area per production cycle.

In an effort to eliminate male plants in production, growers can use feminized hemp seed, which contains only female embryos (Soler et al., 2017). However, feminized hemp seed is currently difficult to source and prohibitively expensive for many growers (Lee, 2019). Feminized seed is more labor-intensive to produce than nonfeminized seed because it requires the masculinization (induction of male flowers) of female plants. Male flowers induced on genetically female plants will produce pollen grains that contain only X gametes that, when crossed with eggs from female plants, result in all-female seed (Mohan Ram and Sett, 1982). Female plants can be masculinized by treatment with silver nitrate or silver thiosulfate (STS). Lubell and Brand (2018) demonstrated that foliar sprays of STS at 0.3 to 3 mm concentrations are effective for inducing male flowers on female plants. They noted that pollen output for masculinized female plants may be reduced compared with pollen output from genetically male plants. We have observed that some female hemp strains make better pollen parents than others following masculinization with STS. The objective of this study was to evaluate differences in germination of pollen from five masculinized female hemp genotypes.

Materials and Methods

In vitro pollen germination was evaluated for five masculinized female hemp genotypes, Abacus, Cherry Wine, Mountain Mango, Wife, and Youngsim10, and two male hemp genotypes, Kentucky Sunshine and Youngsim10. Plants were grown in a greenhouse with set points of 21 °C/17 °C day/night. They were well-established in 3-gallon containers and between 1 and 1.5 m tall, depending on the strain when the flowering stage was initiated. Plants were potted in a peatmoss-based grower mix (ProMix BX; Premier Tech Horticulture, Quakertown, PA) and top-dressed with controlled-release fertilizer (Osmocote Plus 15N–3.9P–10K 5- to 6-month formulation; Everris NA, Dublin, OH) at 64 g/container. During the vegetative stage, plants received a soluble fertilizer (Peters 20N–8.7P–16.6K; Scotts, Marysville, OH) providing 100 ppm nitrogen at every irrigation as needed. Beginning on 26 Sept. 2019, plants were provided short-day conditions of 12 h using a blackout curtain to initiate the flowering stage. Silver thiosulfate solution at a concentration of 3 mm was prepared according to Lubell and Brand (2018). Female plants were sprayed to runoff (≈400 mL/plant) on three occasions, 7 d apart, on 26 Sept., 3 Oct., and 10 Oct. 2019. During the flowering stage, plants received a soluble fertilizer (Peters 15N–12.9P–12.5K; Scotts) providing 100 ppm nitrogen at every irrigation (8 L/day).
Pollen grains were collected in 2-mL centrifuge tubes from male plants on 14 Oct. 2019 and from masculinized female plants on 21 Oct. 2019, except for Abacus, which was collected on 28 Oct. 2019. Immediately after collection, pollen was spread on petri dishes containing a gelled medium using a soft bristled brush. The germination medium, described by Zottini et al. (1997), was composed of 17% sucrose, 30 mg·L−1 Ca(NO3)2, 100 mg·L−1 H3BO3, and 0.7% agar, with pH adjusted to 6.4. Three petri dishes were prepared per genotype. Petri dishes with pollen were maintained for 18 h at 24 °C in a growth chamber with a 16-h photoperiod (25 umol·m−2·s−1). Pollen grains were visualized using a compound microscope (Microphot-FXA; Nikon Instruments, Melville, NY) and microscopy camera (Infinity3; Teledyne Lumenera, Ottawa, ON). For each petri dish, up to 200 pollen grains for male plants and 200 to 700 pollen grains for masculinized female plants were scored for germination. Pollen grains were counted as germinated if any organized tip was observed emerging from the pollen wall. Nongerminated spherical pollen grains were counted as large if their diameter was larger than 35 μ and small if their diameter was smaller than 34 μ. The pollen grain diameter was measured for the longest axis using ImageJ (National Institutes of Health, Bethesda, MD). Nonspherical irregular pollen grains were also counted. Data were subjected to an analysis of variance (PROC ANOVA) and mean separation using Fisher’s least significant difference test (P ≤ 0.05) using SAS software (version 9.2; SAS Institute, Cary, NC).

Results

All five female genotypes produced male flower buds following treatment with STS. Figure 1 shows terminal inflorescences with male flowers for the five masculinized female genotypes. Flowers on male genotypes began opening and releasing pollen 18 d after short-day conditions were initiated. Male flowers on all masculinized female genotypes, except Abacus, required 25 d of short-day conditions before opening. Nearly all flowers on male genotypes opened and released pollen; however, many flowers on masculinized female genotypes did not open, and few flowers opened on Abacus.

full-547fig1.jpg


Fig. 1.
Terminal inflorescences consisting of male flowers for masculinized female genotypes (A) Abacus, (B) Cherry Wine, (C) Mountain Mango, (D) Wife, and (E) Youngsim10.
Citation: HortScience horts 55, 4; 10.21273/HORTSCI14842-20
Of the five masculinized female genotypes, Wife produced the most visible pollen, which was similar in consistency to pollen from male genotypes. Mountain Mango and Youngsim10 also produced visible pollen. Cherry Wine flowers did not produce visible pollen as consistently as the other masculinized genotypes, and Abacus did not produce visible pollen. Wife, Mountain Mango, and Youngsim10 pollen was easy to collect in centrifuge tubes for storage or use in hand pollinations.

Masculinized genotypes Wife and Cherry Wine had pollen germination rates similar to those of genetically male Kentucky Sunshine (Table 1). Wife had the greatest pollen germination percent compared with the other four masculinized female genotypes. Plants produced large-diameter (average 40 μ) and small-diameter [average 26 μ; P = 0.0001 (n = 30)] pollen grains (Fig. 2). Male genotypes produced significantly more large pollen grains than did masculinized female genotypes (Table 1). All masculinized female genotypes produced a significant number of irregular or misshapen pollen grains (Fig. 2; Table 1), whereas male strains produced none. Abacus produced the greatest percent of irregular pollen grains at 83% (Table 1). No pollen germination was observed for Abacus.

Table 1.
Percent of pollen grains germinated, of large and small diameter, and of irregular shape for five masculinized female strains and two male strains of hemp.
tabelka.png
full-547fig2.jpg


Fig. 2.
Freshly collected pollen of masculinized female Wife (A) and 18-hr germinated pollen of masculinized female Wife (B), Cherry Wine (C), Mountain Mango (D), Youngsim10 (E), and Abacus (F), and male Wife (G) and Kentucky sunshine (H). SM = small pollen grain; LG = large pollen grain; IR = irregular pollen grain; GE = germinated pollen grain.
Citation: HortScience horts 55, 4; 10.21273/HORTSCI14842-20

Discussion

We observed two different pollen grain sizes, large and small. The difference in pollen grain size could indicate that large grains had undergone microspore mitosis I, which can result in increased grain diameter, and that small grains did not (McCormick, 1993). Irregular or misshapen pollen grains were commonly observed for masculinized female genotypes. Irregular pollen grains could be the result of many things, including abnormal meiosis, improper exine formation, and problems with the tapetal cells (Baghali et al., 2011; Small, 1972). The pollen germination rates we observed were less than those reported for hemp by Zottini et al. (1997) using the same germination media. This contrast may be attributable to differences in genotype and growing conditions. Zottini et al. (1997) evaluated pollen germination for the fiber variety Carmagnola, which was grown outdoors in the field. Our pollen germination rates for CBD hemp are similar to those reported for five cultivars of tea hybrid rose (Voyiatzi, 1995).
Overall, those interested in masculinizing female plants to produce all female pollen should generally expect to see lower production of usable pollen than is found with genetically male plants. Pollen output from masculinized females can range from complete failure of some genotypes to other genotypes that yield usable pollen, which is comparable to that from a genetic male. For example, female Abacus did not produce obvious viable pollen, but Wife produced pollen that was essentially equivalent to male pollen because it could be collected and had similar germination percentage. Production of viable pollen from female Cherry Wine, Mountain Mango, and Youngsim10 plants was intermediate. Masculinized female plants can be expected to produce fewer large pollen grains and more misshapen pollen grains than male plants. Pollen from masculinized plants will not disperse as well, will be more challenging to collect in bulk, and may not germinate as well as pollen from genetically male plants.

Literature Cited

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