Present International Status of Microwave Power Standards

Agrawal, Govind P.; Kothari,; Chandra,

doi:10.1109/cpem.1988.671246

Cited by 1 publication

(2 citation statements)

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“…The genus Capsicum is a member of the Solanaceae family that includes tomato, potato, tobacco, and petunia. So far, there exist approximately 22 wild species and five domesticated species of chilli: C. annuum L., C. baccatum L., C. chinense Jacq., C. frutescens L., and C. pubescens R. & P. [1,2]. The one attribute most typical of chillies is pungency and must be considered one of its most important traits.…”

Section: Introductionmentioning

confidence: 99%

“…This highly supports the fact that its extinguishing germplasm should be conserved urgently Commensurate with this, intervention of biotechnology or to be more precise, plant tissue culture for accelerating clonal multiplication of desired clones and strains of medicinal plants through micropropagation and their conservation through establishing Tissue Banks or Gene Banks are warranted in the right earnest. Even though there are several reports of In vitro regeneration on different domesticated species of Capsicum [1][2][3][4][5][6][7][8][9][10][11][12][13][14][15], there is no such report on indirect organogenesis of C. chinense cv. Lota Bhot however.…”

Section: Introductionmentioning

confidence: 99%

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MICROPROPAGATION OF Capsicum chinense Jacq. cv. LOTA BHOT VIA INDIRECT ORGANOGENESIS

Bora¹,

HK²,

PJ³

2014

Int J of Agri Scie

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Capsicum chinense Jacq. is well known for its pungency factor, "capsaicin". An attempt has been made to maintain the desired pungency of Capsicum chinense Jacq. cv. Lota Bhot through in vitro propagation via callusogenesis from leaf explants under the influence of different plant growth hormones and an additional component, Silver nitrate (AgNO3). The combination of Kinetin (45µML -1 ) along with 2,4-Dichlorophenoxy Acetic Acid (2,4-D) and AgNO3 at 3.5µML -1 and 35µML -1 respectively was found optimum for callus induction as well as multiple shoot induction whereas maximum shoot length was recorded at Kin (40µML -1 ), 2,4-D (3.0 µML -1 ) and AgNO3 (30µML -1 ). In vitro flower induction and fruit development was most observed under the influence of Gibberellic Acid (GA3) at 30µML -1 . Murashige and Skoog (MS) medium fortified with Benzyl Amino Purine (BAP) 1 and 2,4-D at 4.0µML -1 and 5.5 µML -1 correspondingly was standardized for maximum induction of roots in vitro. Healthy in vitro regenerated plantlets were acclimatized in the potting substrate containing half strength MS medium enriched with soil, sand, vermicompost and vermiculite in all equal proportion and 78.56% of total acclimatized plants were successfully transferred to the main field.

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Section: Introductionmentioning

confidence: 99%