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Propagating some commonly-used South African medicinal plants with compost and vermiteaFaulconbridge, Steven Craig January 2013 (has links)
The use of many of South Africa’s medicinal plants has shown marked increase with over 27 million users in South Africa alone. Most plants are still being unsustainably wild-harvested, a major concern for biodiversity conservation. Commercial interest in certain more commonly-used species has increased, with potential to cultivate medicinal plants on a more sustainable basis. Focus has shifted from conventional use of synthetic fertilisers, pesticides and fungicides to more organic methods of plant propagation. Aqueous extract derived from earthworm composted food waste (vermitea) was used to study the germination and rooting success of selected species. Also survival and growth performance of selected plants grown in a medium amended with commercial NPK fertiliser was compared to those grown in the same medium amended with compost and to those grown in the same medium amended with compost with weekly applications of vermitea. No change in germination success was noted. Vermitea showed promising results on the rooting of cuttings. The application of NPK improved growth performance (biomass) significantly for all species tested. However, they had lower root:shoot ratios as well as lower survival rates compared to plants under the compost and compost/vermitea treatments. The improved survival of these plants highlights the potential of these organic treatments on the propagation of selected medicinal plants.
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Medicinal properties and micropropagation of Cussonia species.Tetyana, Pokazi. 18 December 2013 (has links)
Cussonia species (commonly known as Cabbage trees) are indigenous to
South Africa and are used in traditional medicine to treat an assortment of
diseases. Due to their attractive growth form, they are assets in gardens.
However, there are no developed methods for propagating these species. The use of three selected species, Cussonia paniculata (Eckl. & Zeyh.), C. spicata (Thunb.) and Schefflera umbellifera (Sond.) Baill, = C. umbellifera), in
traditional medicine was validated. Rapid propagation protocols for C.
paniculata and C. spicata were investigated and ultimately developed for the former species. Cussonia paniculata, C. spicata and C. umbellifera were screened for their medicinal properties, mainly focussing on anti-bacterial, anti-inflammatory and anti-malarial activities. In the anti-bacterial screening, C. spicata bark and root extracts showed activity against selected Gram-positive and Gram-negative bacterial strains at a concentration of 50 mg ml ¯¹ . The highest inhibition was observed with ethanol and ethyl acetate root extracts against Staphylococcus aureus. The other two species did not show anti-bacterial activity. Ethanol and
ethyl acetate extracts of all species showed anti-inflammatory activity in the
cyclooxygenase assay (COX-1) at a concentration of 8 μg ml ¯¹, These active extracts showed an inhibition percentage that was greater than 50 % against cyclooxygenase. In the anti-malarial screening , bark extracts were screened. C. umbellifera bark extracts exhibited the best inhibition against P. falciparum, a malaria-causing agent in humans. The percentage inhibition of these extracts was up to 100% at a concentration of 200 μg ml ¯¹ . While C. spicata is known to be used to treat malaria, the screening results showed much less activity (less than or equal to 35 %) as compared to C. umbellifera, which is preferably used to treat malaria. The results obtained from screening these three species validated their use in traditional medicine. This means that the people or traditional healers use these species for different treatments by possibly relying on past knowledge about the effects after administering the medicine.
Fingerprinting using Thin Layer Chromatography (TLC) was used in an attempt to determine whether there are any chemical differences or similarities between the three species. There were similarities between the plant parts across the species as well as some differences. However, this method cannot be used as an unequivocal test to deduce that compounds that are present in a certain species and not in others are the ones responsible for bringing about a certain biological activity. That can only be achieved by a bioassay-guided isolation of possible compounds. A tissue culture protocol was developed to produce a large -number of plants
of C. paniculata. Explants were derived from nodal explants of in vitro
germinated seeds and cultured on Murashige and Skoog (MS) (1962) medium supplemented with 3% sucrose, 2.5 mg l ¯¹ BA and solidified with 3 g l ¯¹ Gelrite. These explants produced multiple shoots. The average number of shoots per explant ranged between 1 to 3.5. Multishoots were subcultured on to rooting media and roots were produced on MS with 0.75 mg l ¯¹ IBA and 1 mg l ¯¹ NAA. Callus from zygotic embryos also produced plantlets on MS supplemented with 1.5 mg l ¯¹ 2,4-D and 0.5 mg l ¯¹ BA. Hyperhydricity was encountered in this study. This problem was reversed successfully by transferring the shoots from medium solidified with 3 g l ¯¹ Gelrite to medium solidified with 8 g l ¯¹ agar. Plantlets were successfully acclimatized for planting ex vitro. The percentage
of healthy plants after a 35-day acclimatization period was 63 %.
C. spicata was not successfully micropropagated from shoot-tip explants.
However, a protocol was developed for decontaminating shoot-tips from the mother plants. The plant material was successfully decontaminated with 0.01% HgCl₂ for 15 min. The decontamination percentage was up to 80 %. Browning of the explants was observed and it was successfully treated with soaking the explants in a 15 mg l ¯¹ ascorbic acid solution for 15 min. A high percentage of shoot-tip regeneration (80 %) was observed when they were cultured on MS medium supplemented with 2 mg l ¯¹ BA, 1 mg l ¯¹ IAA and 1 mg l ¯¹ GA₃. However, multishoots were not observed as in C. panicualata. Shoot elongation in vitro was similar to shoot elongation as it occurs in nature. The shoots elongated and a flush of palmitately arranged leaves were produced. Further research is required to investigate a commercially viable protocol for rapid propagation and conservation of the germplasm of Cussonia species. / Thesis (M.Sc.)-University of Natal, Pietermaritzburg, 2000.
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Rooting of buchu cuttings (Genus : Agathosma)Karsen, P. A. 12 1900 (has links)
Copies no. 3007841664 and 3007841665 are photocopies of the original. / Thesis (MScAgric)-- University of Stellenbosch, 2003. / ENGLISH ABSTRACT: Buchu (Agathosma betulina and A. crenulata) are grown commercially as an aromatic
crop and are endemic to the Western Cape of South Africa. Poor rooting of cuttings have
limited the development of superior clones. Under standard mist bed conditions terminal,
sub-terminal or basal stem cuttings were taken from March to August. When not treated with
an auxin, rooting percentages of between 20 and 25 were obtained. Rooting percentages
increased to between 40 and 45 after treatment with 500-1000 ppm indolebutyric acid (lBA).
Substituting lBA with naphthaleneacetic acid (NAA) did not improve rooting. There was a
tendency for cuttings with fewer than four leaf pairs to give lower rooting percentages.
Plants of Agathosma betulina x A. crenulata, grown in Paarl, and A. betulina, grown in
Piketberg, were used as source plants for making cuttings. Paarl plants were shaded with 80
percent shade and Piketberg plants with 60 or 80 percent shade respectively from February to
October 2002. Plants in full sun served as a control. Plants were pruned back initially in
February and then two months before samples were taken in March, June, August and
October at both locations. New shoots were used as cuttings. Terminal cuttings for rooting
and for carbohydrate analyses were collected on four different dates (March, June, August
and October). Cuttings were treated with 500 ppm indolebuteric acid (lBA) and placed in
misting beds with bottom heating (18-25°C) for a period of three months.
Shading reduced rooting of cuttings from the Paarl plants. However, it did not
significantly increase rooting of cuttings taken from Piketberg plants. Rooting percentage
was the highest in August (43%) for cuttings from sun grown plants in Paarl. No consistent
relationship between, respectively, dry mass or carbohydrate content of cuttings and rooting
could be established.
Terminal current years' growth, taken from Agathosma crenulata x A. betulina (hybrid)
softwood cuttings, collected in January 2002, were extracted with methanol and fractioned by
thin layer chromatography (Silica gel) in isopropanol: acetic acid: water (4: 1:1 v/v). The
chromatographs were divided in ten fractions and were bio-assayed for a rooting co-factor with the mung bean rooting test. Extracts from buchu cuttings showed significant activity at
the Rf values of co-factor 3. Co-factors 1,2 and 4 do not seem to be present in significant
quantities. However, co-factors with Rf values different from previous reported values were
present in significant quantities. No inhibition was found in buchu. In fact, all Rf values
stimulated rooting. / AFRIKAANSE OPSOMMING: Boegoe (Agathosma betulina x A. crenulata) word kommersieël verbon as 'n
aromatiese gewas en is endemies tot die Wes-Kaap. Die ontwikelling van superieure klonale
materiaal word beperk deur swakbeworteling. Terminale, sub-terminale en basale steggies is
gesnyonder standaard misbed toestande van Maart tot Augustus. Beworteling was tussen 20
en 25 persent as geen ouksien gebruik word nie. As indolebottersuur (IBS) gebruik word
tussen 500-1000 dpm, verhoog die bewortelingspersentasie tot tussen 40 en 45 persent. Die
gebruik van naftaleen asynsuur (NAS) in plaas van IBS het nie beworteling verbeter nie.
Daar was a tendens dat steggies wat minder as vier blaarpare gehad het 'n verlaging in
bewortelingspersentasies gehad het.
Plante van Paarl, A. betulina x A. crenulata, en Piketberg, A. betulina, is gebruik as
plantmateriaal vir steggies. Plante in die Paarl was onder 80 persent skadu geplaas en plante
in Piketberg onder 60 en 80 persent skadu van Februarie tot Oktober 2002. Plante in vol son
was as 'n kontrole gebruik. Plante was eers in Februarie teruggesny en dan weer twee mande
voor monsters geneem is. Die monsters is in Maart, Junie, Augustus en Oktober geneem in
beide liggings. Terminale steggies is vier keer ingesamel (Maart, Junie, Augustus en
Oktober) vir beworteling en koolhidraat analises. Die steggies is met 500 dpm IBS behandel.
Daarna is die steggies vir drie maande in die misbed geplaas met bodem-verhitting (18-
25°C).
Dit is gevind dat die gebruik van skadu die beworteling in Paarl verminder het
alhoewel die beworteling in Piketberg nie beduidend beinvloed is nie. Die hoogste
bewortelingspresentasies is waargeneem in Augustus (43%) in Paarl van plante wat in vol
son was. Geen verband tussen onderskeidelik die droe massa of koolhidraat inhoud en
beworteling kon gevind word nie.
Terminale steggies van dieselfte jaar se groei van Agathosma betulina x A. crenulata
(hibried) is in Januarie 2002 ingesamel. Die materiaal is geëkstraheer en gefraksioneer deur
dunlaag kromatografie in isopropanol: asynsuur: water (4: 1:1 v/v). Die kromograaf is in 10 fraksies verdeel. Die fraksies was bioassaieer VIr beworteling ko-faktore met die
mungboontjie bewortelingstoets. Die ekstrakte van boegoe het beduidende aktiwiteit by die
Rf waardes van ko-faktor 3 getoon. Ko-faktore 1, 2 en 4 is nie in groot genoeg hoeveelhede
waargeneem nie. Ko-faktore, wat nie voorheen gevind is nie, is waargeneem in beduidende
hoeveelhede. Geen inhibitors is in boegoe gevind nie en al die getoetste ko-faktore het
beworteling gestimuleer.
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