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1

Amano, Junji, Sachiko Kuwayama, Yoko Mizuta, Masaru Nakano, Toshinari Godo, and Hajime Okuno. "Morphological Characterization of Three Intergeneric Hybrids Among Gloriosa superba ‘Lutea’, Littonia modesta, and Sandersonia aurantiaca (Colchicaceae)." HortScience 43, no. 1 (2008): 115–18. http://dx.doi.org/10.21273/hortsci.43.1.115.

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Three intergeneric hybrids among colchicaceous ornamentals, Gloriosa superba ‘Lutea’ (2n = 2x = 22), Littonia modesta (2n = 2x = 22), and Sandersonia aurantiaca (2n = 2x = 24), were subjected to morphological characterization and chromosome observation. Hybrid plants produced flowers 2 to 3 years after transplantation of ovule culture-derived plantlets to the greenhouse. All the hybrid plants, L. modesta × S. aurantiaca, L. modesta × G. superba ‘Lutea’, and S. aurantiaca × G. superba ‘Lutea’, showed a climbing habit like those of L. modesta and G. superba ‘Lutea’. Plants of L. modesta × S. aur
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2

ADE, RAVINDRA. "Current Advances in Gloriosa superba L." Biodiversitas, Journal of Biological Diversity 10, no. 4 (2009): 210–14. http://dx.doi.org/10.13057/biodiv/d100409.

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3

R, Sri Indah, Ari Susilowati, Yuli Widyastuti, and Ahmad Yunus. "ARTEMISININ CONTENT ON ARTEMISIA ANNUA L. TREATED BY GLORIOSA SUPERBA SEEDS’ WATER EXTRACT." Asian Journal of Pharmaceutical and Clinical Research 11, no. 8 (2018): 147. http://dx.doi.org/10.22159/ajpcr.2018.v11i8.25738.

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Objective: The aim of this study was to determine the artemisinin content on Artemisia annua L. treated by water extract of Gloriosa superba seeds.Methods: G. superba seeds obtained naturally on Krakal Beach, Gunung Kidul, and extraction used a maceration method by water solvent (1:1). A. annua L. sprouts were obtained from B2P2TOOT Tawangmangu. Treatment variables done on sprouts using various water extract concentration of G. superba seeds and soaking time on A. annua L. sprouts. Determination of artemisinin content in leaf extract of A. annua L. was done using KLT-densitometric method with
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4

Ghosh, Seemanti, Biswajit Ghosh, and Sumita Jha. "Polymorphism in Gloriosa superba." Plant Genetic Resources 7, no. 1 (2009): 9–15. http://dx.doi.org/10.1017/s1479262108995125.

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Gloriosa superba L. is a highly valued indigenous medicinal plant. It is available throughout India with noticeable variations in morphology and colchicine content. In the present study, morphological, phytochemical, cytological and molecular data are employed to screen the polymorphism, if present, in five different populations of G. superba L. Based on gross morphological traits, the plants can be grouped into two clusters: Amtala (AM) and Baruipur (BR) plants belonging to one cluster, and Siliguri (SG), Darjeeling (DJ) and Sikkim (SK) plants belonging to the other. Colchicine content of the
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5

Shobha, M., K. K. Sampath Kumara, and H. S. Prakash. "Fungal Endophytes Associated with Gloriosa superba (L.)." Proceedings of the National Academy of Sciences, India Section B: Biological Sciences 89, no. 4 (2018): 1335–42. http://dx.doi.org/10.1007/s40011-018-1053-2.

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6

S, Padmapriya, Rajamani K, and A. Sathiyamurthy V. "Glory Lily (Gloriosa superba L.) - A Review." International Journal of Current Pharmaceutical Review and Research 07, no. 01 (2015): 43–49. https://doi.org/10.5281/zenodo.12739621.

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ABSTRACT Gloriosa superba is an herbaceous or semi-woody climber with v- shaped tubers. The plant is highly valued for its medicinal properties, more importantly for the treatment of cancer related diseases, arthritis, gout, rheumatism and impotency, containing the alkaloids, colchicines and colchicosides.  Colchicine also acts as an anti-mitotic agent by inhibiting mitotic cell division. Thiocolchicoside (TCC), is a semi-synthetic derivative of naturally occurring colchicoside with anti-inflammatory and analgesic effects. The fascinating bright coloured flowers and hercogamous nature fav
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7

Maroyi, Alfred, Den Berg Ronald Van, and Der Maesen Jos Van. "Systematic studies in the Gloriosa superba complex (Colchicaceae): a re-assessment of species boundaries." Plant Ecology and Evolution 146, no. (2) (2013): 212–18. https://doi.org/10.5091/plecevo.2013.694.

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<b>Background and aims</b> – <i>Gloriosa superba</i> L. is a highly variable species occurring in a wide range of ecological habitats in South Africa, tropical Africa and Asia. The morphological variation in <i>G. superba</i> was found to be complicated and therefore numerical methods were used to re-evaluate morphological variation and species delimitation in the <i>G. superba</i> complex. <b>Methods</b> – This study was based on 79 herbarium specimens from B, BM, BR, C, COI, F, K, L, SRGH, U, UPS and WAG (abbreviations follow Holmgren et al. 1990). Cluster and ordination analyses were used t
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8

Le Roux, L. G., and P. J. Robbertse. "Aspects relating to seed production in Gloriosa superba L." South African Journal of Botany 63, no. 4 (1997): 191–97. http://dx.doi.org/10.1016/s0254-6299(15)30743-2.

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9

Geetha., K. "TLC AND GC-MS ANALYSIS OF GLORIOSA SUPERBA L." International Journal of Advanced Research 7, no. 7 (2019): 703–8. http://dx.doi.org/10.21474/ijar01/9414.

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10

Lipipun, Vimolmas, Wanchai De-Eknamkul та Malai Luempol. "Determination of Colchicine in Gloriosa superba L. by Enzyme-Linked Immunosorbent Assay(การวิเคราะห์หาปริมาณ, Colchicine ในดองดึง(Gloriosa superba L.) โดยวิธี Enzyme - Linked Immunosor..." Thai Journal of Pharmaceutical Sciences 20, № 2 (1996): 119–26. http://dx.doi.org/10.56808/3027-7922.1195.

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11

Ariyomo, T. O., B. B. Isaiah, B. P. Omobepade, and A. A. Fabusoro. "Toxicity of crude extract of <i>Terminalia superba</i> sawdust to <i>Clarias gariepinus<i/> (Burchell 1822)." Biological and Environmental Sciences Journal for the Tropics 20, no. 2 (2023): 25–33. http://dx.doi.org/10.4314/bestj.v20i2.4.

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The study examined the toxicity of Afara tree (Terminalia superba) sawdust extract to African catfish, Clarias gariepinus. The fish were exposed to four concentrations 55 ml/L, 60 ml/L, 65 ml/L, 70 ml/L and the control for 96 hours. C. gariepinus juveniles exposed to sublethal concentrations of T. superba extract were examined in a static bioassay with reference to behavioural, haematological and histopathological changes. Early observations of fish exposed to T. superba extract showed erratic swimming, loss of equilibrium and respiratory distress. The behavioural response was dose-dependent a
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12

Chitra, R., K. Rajamani, and M. Jawaharlal. "Variability for Qualitative and Quantitative Traits in Glory Lily (Gloriosa superba L.)." Journal of Horticultural Sciences 5, no. 1 (2010): 38–41. http://dx.doi.org/10.24154/jhs.v5i1.493.

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Glory lily (Gloriosa superba L.) is one of the major medicinal plants of India cultivated for its seeds which are exported to developed countries for pharmaceutical use. Identifying germplasm is an important component for efficient and effective management of plant genetic resources. Variability for qualitative and quantitative traits was investigated in 18 genotypes of G. superba collected from different regions of Tamil Nadu and Andhra Pradesh. For qualitative traits, these genotypes were subjected to diversity analysis based on NBPGR descriptors. Fourteen qualitative and twenty quantitative
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13

Hastami, Eria Rosanti Nugrahening, and Purnomo Purnomo. "Variasi dan Analisis Fenetik Aksesi Kembang Sungsang (Gloriosa superba L.) di Daerah Istimewa Yogyakarta Berdasarkan Karakter Morfologi dan Anatomi." Jurnal Biologi Indonesia 19, no. 2 (2023): 99–110. http://dx.doi.org/10.47349/jbi/19022023/99.

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Kembang sungsang (Gloriosa superba L.) is a member of Colchicaceae family and distributed in tropical areas such as India, Malaysia, and Indonesia. G. superba has a high colchicine content, so it is widely used as a traditional medicine and biomutagen. The diverse habitats of G. superba have potential to create variations. The aims of this study were to determine the morphological, anatomical variations, and phenetic relationship of G. superba in Yogyakarta. A sample of 12 accessions was taken from 4 regencies in Yogyakarta: Bantul, Sleman, Kulon Progo, and Gunungkidul. Morphological character
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14

Vaikos, N. P., and R. M. Pai. "The floral anatomy ofGloriosa superba L. andTricyrtis pilosa Wall. (Liliaceae)." Proceedings / Indian Academy of Sciences 96, no. 3 (1986): 233–39. http://dx.doi.org/10.1007/bf03053307.

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15

Patel, AI, BS Desai, BN Chaudhari, and JM Vashi. "Genetic improvement in glory lily (Gloriosa superba L.): A review." International Journal of Chemical Studies 8, no. 4 (2020): 255–60. http://dx.doi.org/10.22271/chemi.2020.v8.i4d.9701.

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16

le Roux, L. G., and P. J. Robbertse. "Tuber ontogeny, morphology and vegetative reproduction of Gloriosa superba L." South African Journal of Botany 60, no. 6 (1994): 321–24. http://dx.doi.org/10.1016/s0254-6299(16)30586-5.

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17

Ghosh, Seemanti, Biswajit Ghosh, and Sumita Jha. "In vitro tuberisation of Gloriosa superba L. on basal medium." Scientia Horticulturae 114, no. 3 (2007): 220–23. http://dx.doi.org/10.1016/j.scienta.2007.06.008.

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18

Ninomiya, C., T. Nishiuchi, M. Hiraishi, and S. Fukai. "GA3 FOLIAGE SPRAYING ENHANCES TUBER DORMANCY IN GLORIOSA SUPERBA L." Acta Horticulturae, no. 886 (January 2011): 193–96. http://dx.doi.org/10.17660/actahortic.2011.886.26.

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19

Eti Ernawiati, Rochmah Agustrina, and Mohammad Kanedi. "Kembang sungsang (Gloriosa superba L.): A potential plant as a source of biomutagens." Magna Scientia Advanced Biology and Pharmacy 7, no. 1 (2022): 036–43. http://dx.doi.org/10.30574/msabp.2022.7.1.0088.

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Gloriosa superba (Kembang Sungsang, local name) belongs to the monocotyledoneae class and the Liliaceae family. This plant is known as a medicinal plant and its pharmacological effects have been developed both traditional and modern. All parts of the Gloriosa superba, especially the tubers and seeds, contain alkaloids namely colchicine and gloriosine. The content of colchicine and colchicides in tubers and other parts of plants is about 0.1 - 0.9% and 0.8% respectively. Colchicine has a strong affinity for tubulin so it is often used in biological studies and plant breeding to induce mutations
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20

Madhavan, Manju, and Joy P. Joseph. "Histological Marker to Differentiate Organogenic Calli from Non Organogenic Calli of Gloriosa superba L." Plant Tissue Culture and Biotechnology 20, no. 1 (2010): 1–5. http://dx.doi.org/10.3329/ptcb.v20i1.5957.

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A histological study of the indirect organogenesis from internodal cultures of Gloriosa superba L. showed that the callus initiated from the subepidermal cells. The organogenic and non organogenic callii are the result of hormonal variation in the medium. In non organogenic callus cells redifferentiated into xylem elements forming clusters of nest like structures. In organogenic callus, cells redifferen-tiated into nodules of meristemoids which further differentiated into shoot apical meristem. Keywords: Histological marker, Gloriosa superba, Organogenic calli D.O.I. 10.3329/ptcb.v20i1.5957 Pl
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21

Efenberger-Szmechtyk, Magdalena, Agnieszka Nowak, Agata Czyżowska, Alicja Z. Kucharska, and Izabela Fecka. "Composition and Antibacterial Activity of Aronia melanocarpa (Michx.) Elliot, Cornus mas L. and Chaenomeles superba Lindl. Leaf Extracts." Molecules 25, no. 9 (2020): 2011. http://dx.doi.org/10.3390/molecules25092011.

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The purpose of this study was to investigate the composition of leaf extracts from Aronia melanocarpa, Chaenomeles superba, and Cornus mas, and their antimicrobial activity against typical spoilage-causing and pathogenic bacteria found in meat and meat products. The highest total phenolic content (TPC) was detected in C. superba extract, followed by C. mas and A. melanocarpa extracts. The antioxidant capacity of the extracts was measured by DPPH and ABTS assays. The lowest IC50 values were found for C. superba extract, followed by C. mas and A. melanocarpa extracts. LC-MS and HPLC analysis rev
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22

Soltani, G. A., and V. I. Malyarovskaya. "Bioresource potential of chaenomeles (Chaenomeles L.) in the humid subtropics of Russia." Bulletin of the State Nikitsky Botanical Gardens, no. 136 (January 8, 2021): 67–77. http://dx.doi.org/10.36305/0513-1634-2020-136-67-77.

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The taxonomic composition of the genus Chaenomeles L. was determined in the conditions of the Sochi Black sea region. Morphological and biological description was made and fruiting was evaluated for 19 taxa. Decorative cultivars Ch. japonica, Ch. speciosa, Ch. × superba, Ch. × vilmoriniana are of interest for cultivation in the humid subtropical zone of Russia. Fruit cultivars are not represented. Ch. sinensis is recommended as a fruit crop of Chaenomeles and a promising form of Ch. × superba has been identified. The cultivar Ch. speciosa ‘ Kermesina ' is universal and recommended for use in b
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23

Soltani, G. A., and V. I. Malyarovskaya. "Bioresource potential of chaenomeles (Chaenomeles L.) in the humid subtropics of Russia." Bulletin of the State Nikitsky Botanical Gardens, no. 136 (January 8, 2021): 67–77. http://dx.doi.org/10.36305/0513-1634-2020-136-67-77.

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The taxonomic composition of the genus Chaenomeles L. was determined in the conditions of the Sochi Black sea region. Morphological and biological description was made and fruiting was evaluated for 19 taxa. Decorative cultivars Ch. japonica, Ch. speciosa, Ch. × superba, Ch. × vilmoriniana are of interest for cultivation in the humid subtropical zone of Russia. Fruit cultivars are not represented. Ch. sinensis is recommended as a fruit crop of Chaenomeles and a promising form of Ch. × superba has been identified. The cultivar Ch. speciosa ‘ Kermesina ' is universal and recommended for use in b
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24

Yang, S. X., H. Deng, and M. S. Li. "Manganese uptake and accumulation in a woody hyperaccumulator, Schima superba." Plant, Soil and Environment 54, No. 10 (2008): 441–46. http://dx.doi.org/10.17221/401-pse.

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A wide-spread subtropical tree species, &lt;I&gt;Schima superba (Theaceae)&lt;/I&gt;, occurring in a Mn mine wasteland, was found to contain unusually high Mn content in the leaf tissues. A pot growth experiment with different Mn treatments was conducted to further illustrate its Mn tolerance, accumulation and relocation capacity. &lt;I&gt;Schima&lt;/I&gt; saplings grew well and showed no symptoms of Mn toxicity with Mn supply below 60 mmol/l. Total plant biomass decreased with the increase of Mn supply, but Mn contents in tissues increased significantly, and peaked (62 412.3 mg/kg) in stem at
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Ninomiya, Chitoshi, Seiichi Fukai, Takashi Nishiuchi, Maki Hiraishi, Keiko Takano, and Nobuhito Sasaoka. "Genotypic Differences in Floral Initiation and Development of Gloriosa superba L." Horticultural Research (Japan) 7, no. 2 (2008): 227–33. http://dx.doi.org/10.2503/hrj.7.227.

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26

Vijayavalli, B., and P. M. Mathew. "Karyomorphology of four morphotypes of Gloriosa superba L. from South India." CYTOLOGIA 55, no. 4 (1990): 531–33. http://dx.doi.org/10.1508/cytologia.55.531.

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27

Nagendra K, Chandrawanshi, S. K. Jadhav, K. L. Tiwari, and Quraishi Afaque. "In vitro Tuberization and Colchicine Content Analysis of Gloriosa superba L." Biotechnology(Faisalabad) 14, no. 3 (2015): 142–47. http://dx.doi.org/10.3923/biotech.2015.142.147.

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28

Padmapriya, S., and K. Rajamani. "Induced mutagenesis in glory lily (Gloriosa superba L.) for economic variability." Medicinal Plants - International Journal of Phytomedicines and Related Industries 9, no. 4 (2017): 231. http://dx.doi.org/10.5958/0975-6892.2017.00037.5.

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29

Putalun, Waraporn, та Boonyean Kitvijarn. "Production of colchicine from root cultures of Gloriosa superba L.(สารโคลชิซีนจากรากเพาะเลี้ยงดองดึง)". Thai Journal of Pharmaceutical Sciences 25, № 1 (2001): 75–80. http://dx.doi.org/10.56808/3027-7922.2306.

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30

Kitcharoen, Nudchanart, and Wanchai De-Eknamkul. "Distribution of Colchicine in Various Plant Parts of Gloriosa superba L." Thai Journal of Pharmaceutical Sciences 17, no. 3 (1993): 141–47. http://dx.doi.org/10.56808/3027-7922.1247.

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31

Désiré, Dzeufiet Djomeni Paul, Tadondjou Tchingo Cyrille D’Alex, Bilanda Danielle Claude, Aboubakar Oumarou BibiFarouck, Kamtchouing Pierre, and Dimo Théophile. "Endothelium-dependent and independent vasorelaxant effect of Terminalia superba (Combretaceae) on rat aorta." Journal of Phytopharmacology 2, no. 5 (2013): 21–27. http://dx.doi.org/10.31254/phyto.2013.2504.

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Terminalia superba (Combretaceae) is a plant which is used in Cameroon for the treatment of many diseases including arterial hypertension. The vasorelaxant effect of the aqueous stem bark extract of T. superba was evaluated on the isolated aorta rings of the rat constricted with KCl (60 mM) or norepinephrine (10-5 M). Cumulative concentrations (20-100 µg/mL) of T. superba provoked a dose-dependent relaxation of the thoracic aorta precontracted by norepinephrine or KCl. The maximum vasorelaxant activity of T. superba was 107.24 ± 7.01% on the intact aorta and 102.48 ± 19.09% on the denuded aort
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Schodde, R., L. Christidis, H. Batalha-Filho, P.G.P. Ericson, and M. Irestedt. "Why neotypification of Lophorina superba (Pennant, 1781) (Aves: Paradisaeidae) is justified-and necessary." Zootaxa 4951, no. 2 (2021): 304–20. https://doi.org/10.11646/zootaxa.4951.2.5.

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Schodde, R., Christidis, L., Batalha-Filho, H., Ericson, P.G.P., Irestedt, M. (2021): Why neotypification of Lophorina superba (Pennant, 1781) (Aves: Paradisaeidae) is justified-and necessary. Zootaxa 4951 (2): 304-320, DOI: 10.11646/zootaxa.4951.2.5
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Efenberger-Szmechtyk, Magdalena, Ilona Gałązka-Czarnecka, Anna Otlewska, Agata Czyżowska, and Agnieszka Nowak. "Aronia melanocarpa (Michx.) Elliot, Chaenomeles superba Lindl. and Cornus mas L. Leaf Extracts as Natural Preservatives for Pork Meat Products." Molecules 26, no. 10 (2021): 3009. http://dx.doi.org/10.3390/molecules26103009.

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The aim of this study was to investigate the possibility of using Aronia melanocarpa, Chaenomeles superba, and Cornus mas leaf extracts as natural preservatives for pork meat products. Pork sausages were stored in modified atmosphere packaging (MAP) (80% N2 and 20% CO2) at 4 °C for 29 days. The total psychrotrophic counts (TPC) were determined during the storage period, along with the numbers of Enterobacteriaceae and lactic acid bacteria (LAB). The extracts improved the microbial quality of the meat products but to a lesser extent than sodium nitrate (III). They reduced the amounts of Enterob
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Mahajan*, Ritu, Nisha Kapoor, and Pallavi Billowria. "Callus proliferation and in vitro organogenesis of Gloriosa superba : An endangered medicinal plant." Annals of Plant Sciences 5, no. 12 (2016): 1466. http://dx.doi.org/10.21746/aps.2016.12.003.

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Gloriosa superba L. an important medicinal plant has become endangered due to over exploitation, as the tubers are rich source of an alkaloid, colchicine. Poor seed germination and tuber dormancy restricts it multiplication and thus the germplasm available is very less. So, there is urgent need to develop a protocol for its conservation and commercial propagation. Only 10-15% of seeds germinated after three weeks following cold treatment. Best shoot multiplication in sprouted tubers (88.67%) was observed in MS supplemented with 2.0 mg/l BAP, 0.5mg/l Kn and 1.0 mg/l GA3 with 8.7±0.18 average nu
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S. Undal, Vinod. "Phyto Constituents and Pharmacology of Gloriosa superba L.: A Medicinally Potent Plant Species." International Journal of Science and Research (IJSR) 12, no. 10 (2023): 1150–55. http://dx.doi.org/10.21275/sr231012105054.

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Muthulakshmi, P., K. Rajamani, and K. Prabakar. "Bacillus spp. mediated management of soil borne diseases in Gloriosa superba L." Medicinal Plants - International Journal of Phytomedicines and Related Industries 13, no. 1 (2021): 137–44. http://dx.doi.org/10.5958/0975-6892.2021.00015.0.

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Chitra, R., and K. Rajamani. "Assessment of Different Glory Lily (Gloriosa superba L.) Accessions for Biochemical Traits." Research Journal of Medicinal Plant 4, no. 1 (2010): 21–25. http://dx.doi.org/10.3923/rjmp.2010.21.25.

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Zhang, Yiru, Haikui Li, Xiaohong Zhang, Yuancai Lei, Jinjin Huang, and Xiaotong Liu. "An Approach to Estimate Individual Tree Ages Based on Time Series Diameter Data—A Test Case for Three Subtropical Tree Species in China." Forests 13, no. 4 (2022): 614. http://dx.doi.org/10.3390/f13040614.

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Accurate knowledge of individual tree ages is critical for forestry and ecological research. However, previous methods suffer from flaws such as tree damage, low efficiency, or ignoring autocorrelation among residuals. In this paper, an approach for estimating the ages of individual trees is proposed based on the diameter series of Cinnamomum camphora (Cinnamomum camphora (L.) Presl), Schima superba (Schima superba Gardn. et Champ.), and Liquidambar formosana (Liquidambar formosana Hance). Diameter series were obtained by stem analysis. Panel data contains more information, more variability, a
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39

Singh, Satnam, Amandeep Saini, and R. G. Saini. "Antitumor and cytotoxic potential of various extracts of Gloriosa superba L. Centaurea behen L., Elaeocarpus ganitrus Roxb and Ficus religiosa L. against human breast cancer (MDA-MB 231) cell lines." International Journal of Research in Medical Sciences 12, no. 1 (2023): 103–9. http://dx.doi.org/10.18203/2320-6012.ijrms20233982.

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Background: Medicinal plants are rich in a wide variety of secondary metabolites such as tannins, alkaloids, phenolic compounds, flavonoids etc. which have the capability to inhibit many pathways that lead to cancer. The present study was conducted with the objectives to screen the extracts of dried roots Gloriosa superba L., dried roots of Centaurea behen L. dried fruits/beads of Elaeocarpus ganitrus Roxb., dried leaves of Ficus religiosa L. and investigate their antitumor activity on human breast cancer cell lines (MDA-MB 231). Methods: Cytotoxic activity was evaluated against non-cancerous
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40

Rajeswari, P., P. Samuel, D. N. P. Sudarmani, K. Amirtharaj, and R. Deenathayalan. "GLORIOSA SUPERBA L. – AN ENDANGERED PLANT OF TAMILNADU, YET TO BE EXPLORED AND NEED TO BE CONSERVED." INDIAN DRUGS 54, no. 07 (2017): 60–62. http://dx.doi.org/10.53879/id.54.07.10830.

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Gloriosa superba L. is commonly being called as glory lily. This perennial climber is designated as the State flower of Tamilnadu. It is extensively cultivated for colcichine, an alkaloid obtained from the seed being exploited for its medicinal properties. The present investigation on this climber was started with an intention to bring out the biomedical potentials with special reference to its anticancer properties. The plant was extracted with methanol and ethyl acetate using Soxhlet extraction unit and the extract was concentrated using vacuum rotavapor. The presence of 15 different compoun
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Mahajan, Yogesh Ashok, Balkrishna Ankush Shinde, Arun Torris, et al. "Pre-Sowing Treatments, Seed Components and Water Imbibition Aids Seed Germination of Gloriosa superba." Seeds 2, no. 1 (2023): 15–29. http://dx.doi.org/10.3390/seeds2010002.

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Gloriosa superba L. is a horticulturally and medicinally important plant. Its seeds have poor, erratic, and deferred germination. The detailed seed structure components and water imbibition mechanism facilitating the process of seed germination in G. superba remain unexplored. Therefore, it is essential to develop methods to ensure consistent and enhanced seed germination in G. superba. Various pre-sowing treatments along with the Brunauer‒Emmett‒Teller (BET) surface area analysis and 3D X-ray micro-tomography (micro-T) were employed to elucidate seed structure components, porosity network, an
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42

ELLIOTT, ANDY, NIGEL J. COLLAR, MURRAY D. BRUCE, and GUY M. KIRWAN. "The nomenclature of Lophorina (Aves: Paradisaeidae), with remarks on the type and type locality of L. superba." Zootaxa 4732, no. 1 (2020): 57–78. http://dx.doi.org/10.11646/zootaxa.4732.1.2.

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Based on molecular and morphological analyses, Irestedt et al. (2017) propose various taxonomic revisions for the genera Lophorina and Ptiloris (Paradisaeidae). Concerning Lophorina, which they recommend treating as three species rather than one, they hypothesize that the no longer extant type specimen of L. superba, heretofore believed to come from the Vogelkop in westernmost mainland New Guinea, in fact pertained to a different population (and different species, under their revised taxonomy), and they attempt to consolidate the nomenclatural repercussions of this by proposing a neotype for t
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Ninomiya, Chitoshi, Keiko Takano, and Nobuhito Sasaoka. "Development and Dormancy of Tuber of Gloriosa superba L. Grown in Different Season." Horticultural Research (Japan) 6, no. 3 (2007): 417–23. http://dx.doi.org/10.2503/hrj.6.417.

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Jothi, U., J. Angelin Jebamalar, and T. Sivakumar. "Study on Estimation and Antioxidant activity of Gloriosa superba L. Whole Plant Extract." International Journal of Scientific Research in Biological Sciences 6, no. 3 (2019): 50–55. http://dx.doi.org/10.26438/ijsrbs/v6i3.5055.

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Mary, A. Anitha Divya, S. Padmapriya, and K. Rajamani. "Anatomical and biochemical studies on tuber growth and development in Gloriosa superba L." Medicinal Plants - International Journal of Phytomedicines and Related Industries 12, no. 3 (2020): 422. http://dx.doi.org/10.5958/0975-6892.2020.00053.2.

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Cyriak, AMANI Yves Frédéric, M’BO Kacou Antoine Alban, CHÉRIF Mamadou, KONE Daouda, and KOUAME Christophe. "Mycorrhizal Interaction between Companion Trees and Cocoa Trees (Theobroma cacao L.) in Traditional Agroforestry Systems in Côte d’Ivoire." Microbiology Research Journal International 35, no. 3 (2025): 25–44. https://doi.org/10.9734/mrji/2025/v35i31548.

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Aims: The effective use of companion trees in agroforestry systems could improve the health and productivity of cocoa trees by understanding the interactions they promote. This study aims to decipher the characteristics of arbuscular mycorrhizal communities in the roots and soil of cocoa trees and their companion trees to understand the interaction between these two types of trees. Methodology: Five mycorrhization parameters measured in cocoa trees and nearby companion trees were compared. These were, shared species diversity, number of spores, mycorrhization frequency, mycorrhization intensit
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Majumdar, Moumita, Rakesh Arya, Soumya Prakash Sahu, Archana Tiwari, and Jong-Joo Kim. "Assessment of Genetic Diversity by Morphological, Biochemical, and Molecular Markers in Gloriosa superba Ecotypes Collected from Different Agro-Climatic Zones in India." Horticulturae 11, no. 7 (2025): 723. https://doi.org/10.3390/horticulturae11070723.

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Background: Gloriosa superba L., commonly known as Glory Lily, is a medicinally valuable perennial climber native to tropical and subtropical regions of India. It is known for its rich alkaloid content, including colchicine and colchicoside, which contribute to its therapeutic potential in treating various ailments. Despite its pharmacological significance, genomic research on G. superba remains limited due to the lack of genetic markers, hindering molecular studies and breeding advancements. Methods: This study utilized a previously reported de novo transcriptome assembly of G. superba, ident
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S. Megala, S. Megala, and R. Elango R. Elango. "Antifungal Activity of Tubers And Seeds Extracts of Gloriosa Superba L. Against in Human Pathogens." International Journal of Scientific Research 2, no. 5 (2012): 3–5. http://dx.doi.org/10.15373/22778179/may2013/2.

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Coulibaly, Kiyinlma, Sibirina Soro, Keassemon Herve Cedessia Kone, and Guede Noel Zirihi. "Antifungal effect of Ethanol Extracts 70% of Terminalia ivorensis and Terminalia superba on two phytopathogenic fungi." INTERNATIONAL JOURNAL OF AGRICULTURE AND BIOLOGICAL SCIENCES 4, Sep & Oct 2020 (2020): 91–98. https://doi.org/10.5281/zenodo.4286932.

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<em>Lumber is the raw material for the wood industry. Much of the bark from these logs is either buried or incinerated without any form of recovery. This study was carried out to verify the antifungal power of the trunk barks of two forest species: Terminalia ivorensis and Terminalia superba, on two fungal parasites, Fusarium oxysporum lycopersici and Sclerotium rolfsii of the tomato. They were tested in vitro using the double dilution method. Ethanol extracts from both species significantly inhibited the radial growth of both mycopathogens (100 &plusmn; 00 and 68.46 &plusmn; 5.35). T. superba
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TALUKDAR, JAYASHREE, and MANOJ BARTHAKUR AND NIJARA GOSWAMI. "Antifungal Activity of Pyocyanin like Compound of Pseudomonas aeruginosa JT25 Isolated from Gloriosa superba L." BIOPESTICIDES INTERNATIONAL 19, no. 02 (2023): 165. http://dx.doi.org/10.59467/bi.2023.19.165.

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Isolation of rhizobacteria from the rhizosphere of medicinal plants for screening antimicrobial compounds has paved an alternate way for a sustainable approach to agriculture. In our investigation, 109 isolates were obtained from the rhizosphere of Gloriosa superba L., commonly known as glory lily and screened for their antagonism against 6 test fungal pathogens. Three isolates showed promising antibiosis and were further screened for bioactive metabolite production. The present study was limited to the evaluation of antimicrobial properties of one of the isolates Pseudomonas aeruginosa JT25 a
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