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Cannabis Seed Storage

acespicoli

Well-known member

Product Description​

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Durable Insulin Fridge Holder​

Our 15-Slot Insulin Storage Case for Refrigerator fits Standard 10ml Vials. The 15 pre-cut holes in high density foam hold your vials snug, safe and secure from accidental drops from over 20+ft.

Multi-function Insulin Holder Storage Case​

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Qualified Material For Safety​

Insulin vial holder storage case made of high quality Oxford cloth, it is equipped with Pearl cotton cushion and EVA cushion. Protect your vials with double protections. Insulin vial cooler travel case is ideal and perfect for diabetes and professional.

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Product details​

  • Product Dimensions ‏ : ‎ 6.1 x 4.33 x 3.15 inches; 5.29 ounces
 

acespicoli

Well-known member
In earlier research, induction of hermaphroditism in marijuana plants was achieved experimentally by applications of gibberellic acid (Heslop-Harrison, 1956, 1957; Ram and Jaiswal, 1970, 1972, 1974; Galoch, 1978; Rosenthal, 1991; United Nations Office on Drugs and Crime [UNOCD], 2009). Other studies showed that male and female flower ratios in marijuana plants could be altered by applications of chemicals such as 2-chloroethanephosphonic acid, aminoethoxyvinylglycine, silver nitrate, silver thiosulfate, or cobalt chloride (Ram and Jaiswal, 1970, 1972; Ram and Sett, 1981). Silver nitrate inhibits ethylene action in plants (Kumar et al., 2009) and was reported to increase male sex expression in marijuana, cucumber and gourd plants (Atsmon and Tabbak, 1979; Ram and Sett, 1982; Stankovic and Prodanovic, 2002). In a recent study, applications of silver thiosulfate induced male flower formation on genetically female hemp plants (Lubell and Brand, 2018). These findings demonstrate that changes in growth regulator levels in treated plants can impact hermaphroditic flower formation.

Physical or chemical stresses can also have a role in inducing staminate flower development on female plants of marijuana. For example, external environmental stresses, e.g., low photoperiods and reduced temperatures in outdoor production, were reported to increase staminate flower formation (Kaushal, 2012). Some plants formed hermaphroditic flowers when female plants were exposed to extended periods of darkness early during growth or during altered photoperiods during the flowering stage, although the exact conditions were not described (Rosenthal, 1991, 2000). Such stress factors could affect internal phytohormone levels, such as auxin:gibberellin ratios (Tanimoto, 2005), which could in turn trigger hermaphroditic flower formation in marijuana plants. In Arabidopsis plants, auxin, gibberellin and ethylene interact with jasmonic acid (JA) to alter stamen production (Song et al., 2013, 2014). Consequently, jasmonic-acid deficient mutant Arabidopsis plants exhibited male sterility, with arrested stamen development and non-viable pollen (Jewell and Browse, 2016) while JA treatment restored stamen development in these mutants. In marijuana plants, environmental stress factors which enhance JA production could potentially promote hermaphroditic flower formation but this requires further study. Lability of sex expression may offer advantages in promoting seed formation in hermaphroditic plants subject to environmentally stressful conditions (Ainsworth, 2000).

In the present study, pollen germination and germ tube growth were observed in samples of hermaphrodite flowers and pollen transfer from male flowers to stigmas of female flowers showed germination in situ followed by germ tube growth and penetration of the stigmatic papilla. Small and Naraine (2015) and Small (2017) showed pollen grains attached to stigmatic papillae but the germination and penetration process was not described. We observed a row of bulbous trichomes forming along the stomium on the anthers in staminate flowers and in hermaphroditic flowers, confirming earlier descriptions by Potter (2009) and Small (2017) for staminate flowers. The function of these trichomes is unknown. The findings described here are the first to demonstrate viable pollen production and anther morphology in hermaphroditic flowers in marijuana.
 

acespicoli

Well-known member

Discussion​

Overall, STS at 3 mm was the most effective treatment for producing the greatest number of male flowers on female hemp plants. Green (2015) suggested that female hemp plants can be masculinized using a single foliar spray of 0.3 mm STS, but did not provide any information about the percent conversion to male flowers. We did not find three foliar sprays of 0.3 mm STS to be as effective for producing male flower formation as three foliar sprays of 3 mm STS. However, there may be specific strains, such as CBD hemp A, which produce primarily male flowers with STS concentrations less than 3mm.

Silver thiosulfate has been used to extend the vase life of cut flowers by blocking the effect of ethylene (Farnham et al., 1981; Veen and van de Geijn, 1978). A similar action of ethylene blocking by STS is likely responsible for the production of male flowers on female hemp plants in our study. It is generally believed that ethylene blocking is extended when a series of sprays of STS is used compared with a single spray of STS (Reid et al., 1980). It may be possible to induce male flowers on genetically female hemp using other ethylene perception inhibiting chemicals such as 1-methylcyclopropene.

Mohan Ram and Sett (1982), using 25 to 100 µg STS applied directly to the growing shoot tip of female hemp plants, were able to produce male flowers. However, they also noted severe necrosis on young leaves covering shoot tips and suspended apical growth for 20 to 25 d before lateral budbreak and subsequent flower formation. In comparison, we did not observe any plant phytotoxicity or delay in flower development. Furthermore, we were able to achieve 95% to 100% conversion to male flowers for all hemp strains, whereas Mohan Ram and Sett (1982) reported ≈60% to 80% conversion.

Producers and breeders should be able to masculinize female hemp plants routinely by using short-day conditions of ≈8 h and three foliar sprays of 3 mm STS at weekly intervals. We suspect that this method will be applicable for a broad range of genetically diverse hemp genotypes. Pollen produced by male flowers on genetically female plants can be used to produce all-female seed, but growers and breeders should be aware that pollen output may be reduced compared with pollen output from genetically male plants.

Foliar Sprays of Silver Thiosulfate Produce Male Flowers on Female Hemp Plants​


Article Category: Research ArticleOnline Publication Date: Dec 2018
Page(s): 743–747Volume/Issue: Volume 28: Issue 6
DOI: https://doi.org/10.21273/HORTTECH04188-18
 

acespicoli

Well-known member
RAM, HY. "Mohan; SETT, R. Induction of fertile male flowers in genetically female Cannabis sativa plants by silver nitrate and silver thiosulphate anionic complex."
Theoretical and Applied Genetics 62.4 (1982): 369-375.



Summary​

Apical application of silver nitrate (AgNO3; 50 and 100 μg per plant) and silver thiosulphate anionic complex (Ag(S2O3)3−2; STS; 25, 50 and 100 μg per plant) to female plants of Cannabis sativa induced the formation of reduced male, intersexual and fully altered male flowers on the newly formed primary lateral branches (PLBs); 10 μg per plant of AgNO3 was ineffective and 150 μg treatment proved inhibitory. A maximum number of fully altered male flowers were formed in response to 100 μg STS. The induced male flowers produced pollen grains that germinated on stigmas and effected seed set. Silver ion applied as STS was more effective than AgNO3 in inducing flowers of altered sex. The induction of male flowers on female plants demonstrated in this work is useful for producing seeds that give rise to only female plants.
 

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