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Medicinal plants have bioactive compounds which are used for curing of various human diseases and also play an important role in healing. Phytochemicals have two categories i.e., primary and secondary constituents. Primary constituents have chlorophyll, proteins sugar and amino acids. Secondary constituents contain terpenoids and alkaloids. Medicinal plants have antifungal, antibacterial and anti-inflammation activities. The present study involves medicinal plant Meconopsis aculeta which is locally available in Kashmir Himalaya. The aerial and rhizome parts of the selected medicinal plant were washed, air dried and then powdered for qualitative and quantitative analysis. Different extracts of aerial and rhizome parts were used to find out the phytochemical constituents in the Meconopsis aculeta. The main objective of the research work was to check the presence or absence of the phytochemical constituents and quantitative analysis in different extracts of Meconopsis aculeta. The results of the phytochemical analysis of Meconopsis aculeta showed that the terpenoids, phlobatannins, flavonoids and alkaloids were present. The phytochemical analysis of medicinal plants is very important commercially and has great interest in pharmaceutical companies for the production of the new drugs for curing of various diseases. It is expected that the important phytochemical constituent recognized in Meconopsis aculeta found in Kashmir Himalaya will be very useful in the curing of various diseases of this region.

Categorization of species under different threat classes is a pre-requisite for planning, management and monitoring of any species conservation programme. However, data availability, particularly at the population level, has been a major bottleneck in the correct categorization of threatened species. Till date, threat assessments have been mostly based on expert opinion and/or herbarium records. The availability of primary data on distribution of species and their population attributes is limited in India because of inadequate field survey, which has been ascribed to resource constraints and inaccessibility. In this study, we demonstrate that ecological niche modelling (ENM) can be an economical and effective tool to guide surveys overcoming the above two constraints leading to the discovery of new populations of threatened species. Such data lead to improved threat assessment and more accurate categorization. We selected 14 threatened plants comprising 5 trees (Acer hookeri Miq., Bhesa robusta (Roxb.) Ding Hou, Gynocardia odorata Roxb., Ilex venulosa Hook. f. and Lagerstroemia minu-

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Aconitum chasmanthum Stapf ex Holmes, a highly valued medicinal plant, is a critically endangered plant species with restricted global distribution. Because there is no published report on the in vitro micropropagation of A. chasmanthum, the present study was undertaken to contribute to the development of an efficient micropropagation protocol for its conservation. Seeds collected from the wild showed enhanced germination after being given a chilling treatment (−4 °C and −20 °C) for different durations (10, 20, 30 and 40 days). Seeds given a chilling treatment of −4 °C for 10 days showed enhanced germination rates of 47.59 ± 0.53% with a mean germination time of 10.78 ± 0.21 days compared to seeds kept at room temperature when grown in an MS basal medium. Nodes, leaves and stems, taken from 20–40-day-old seedlings, were used as an explant for micropropagation. An MS medium supplemented with different concentrations of cytokinins (BAP, Kn), auxins (2,4-D, NAA), and an additive adenine sulphate were tested for callusing, direct shoot regeneration and rooting. Only nodal explants responded and showed direct multiple shoot regeneration with 7 ± 0.36 shoots with an elongation of 5.51 ± 0.26 cm in the MS medium supplemented with BAP 0.5 mg/L, and with a response time (RT) of 10.41 ± 0.51 days and a percentage culture response of 77.77 ± 2.77%. Rhizome formation was observed after 8 weeks, with the highest culture response of 36.66 ± 3.33% in the MS basal media with an RT of 43.75 ± 0.50 days. These rhizomes showed a 60% germination rate within 2 weeks and developed into plantlets. The present in vitro regeneration protocol could be used for the large-scale propagation and conservation of A. chasmanthum.

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