Gotowe bibliografie tematyczne / Aristolochia cathcartii

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  1. Artykuły w czasopismach

Gotowa bibliografia na temat „Aristolochia cathcartii”

Autor: Grafiati
Data publikacji: 3 czerwca 2025
Data aktualizacji: 19 lipca 2025

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Artykuły w czasopismach na temat "Aristolochia cathcartii"

1

Upson, Tim, and Robert Brett. "554. Aristolochia Cathcartii. Aristolochiaceae." Curtis's Botanical Magazine 23, no. 1 (2006): 84–90. http://dx.doi.org/10.1111/j.1355-4905.2006.00518.x.

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2

Zhang, Hong-Chi, Rui Liu, Zhi-peng An, Hui Li, Rui Zhang, and Feng Zhou. "Aristolactam-type alkaloids and aristolochic acids from Aristolochia moupinensis and Aristolochia cathcartii." Biochemical Systematics and Ecology 65 (April 2016): 198–201. http://dx.doi.org/10.1016/j.bse.2016.02.028.

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3

Sarma, Bhaskar, and Bhaben Tanti. "Analysis of genetic diversity of certain species of Aristolochia using ISSR-based molecular markers." Current Life Sciences 3, no. 4 (2017): 47–53. https://doi.org/10.5281/zenodo.883637.

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Inter Simple Sequence Repeat (ISSR) polymor-phism was used to determine genetic diversity and phylogenetic relationship in 4 species of <em>Aristolochia </em>viz <em>A. indica </em>Linn.<em>, A. saccata </em>Wall.<em>, A. tagala </em>Cham. and <em>A. cathcartii </em>Hook.f &amp; T. A panel of 8 ISSR primers was screened representing di-nucleotide repeats, of which 57 polymorphic and informative patterns were selected to determine the genetic diversity. The consensus tree constructed using binary data from banding patterns generated by ISSR-PCR depicting that <em>A. indica </em>and <em>A. cathc
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4

Sarma, Bhaskar, and Bhaben Tanti. "In vitro regeneration of plantlets from nodal explants of Aristolochia saccata and Aristolochia cathcartii." European Journal of Biological Research 7, no. 3 (2017): 191–201. https://doi.org/10.5281/zenodo.825746.

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<em>In vitro</em> propagation of <em>Aristolochia saccata</em> and <em>A. cathcartii</em> were carried out using nodal explant. In both the plants, nodal explants showed direct somatic embryogenesis when cultured on MS medium using various concentrations of BAP (1.0-4.0) and 2iP (1.0-4.0) separately or in combination with low concentration (0.5 and 1.0 mg l<sup>-1</sup>) of auxin (NAA). It was observed that BAP in combination with NAA was more effective for shoot induction than the hormones used separately. Among different combinations of NAA and BAP, 3.0 mg/l BAP + 1.0 mg/l NAA showed better
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5

Sarma, Bhaskar, and Bhaben Tanti. "Ecological niche modeling for reintroduction and conservation of Aristolochia cathcartii Hook.f. & Thomson (Aristolochiaceae), a threatened endemic plant in Assam, India." Journal of Threatened Taxa 14, no. 2 (2022): 20597–605. http://dx.doi.org/10.11609/jott.6999.14.2.20597-20605.

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Aristolochia cathcartii Hook.f. &amp; Thomson is a medicinal plant species native to Assam (India). Karbi people have traditionally used the plant to treat a variety of ailments. The population stock of this species has been rapidly depleting in its natural habitats due to over-utilization, habitat fragmentation, and other anthropogenic activities. Extensive field surveys were carried out to investigate the population status of A. cathcartii in various forest areas of Assam’s Karbi Anglong district. In 20 km of transects, a total of 36 quadrats were observed. A. cathcartii density, frequency o
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6

Borah, Punam Jyoti, and Ruma Sarma. "Phytoconstituents of Aristolochia cathcartii Hook.f. Leaf Extract; an Analysis through FTIR and GC-MS." Biomedical and Pharmacology Journal 18, no. 2 (2025): 1457–62. https://doi.org/10.13005/bpj/3183.

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FTIR and GC-MS were carried out to reveal the phytocompounds and their functional groups present in the methanolic leaf extracts of A. cathcartii. FTIR analysis resulted a total of five peaks indicated the presence of alcohol, amines, amino acids, alkynes, aldehyde, aliphatic groups, aromatics, unsaturated heterocycles, amides, nitro compound, alkanes, alkenes, phosphorous, and organosilicon compounds. GC-MS analysis resulted a total of 70 peaks consisting different compounds with different retention time, area percentage where 2,6,10,14-Hexadecatetraen-1-ol, 3,7,11,15-tetramethyl-, acetate, (
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