Comparison of plant diversity in protected and communal lands in the Bushbuckridge lowveld savanna, South Africa
- Authors: Shackleton, Charlie M
- Date: 2000
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/181885 , vital:43777 , xlink:href="https://doi.org/10.1016/S0006-3207(00)00001-X"
- Description: Patterns of higher plant species richness and beta diversity were assessed using standard Modified-Whittaker plots in relation to land use, slope position and mean annual rainfall across a rainfall gradient in the savanna areas of the Bushbuckridge lowveld, South Africa. In particular, comparison of communal areas with adjacent protected areas was important in showing the impacts of potential changes in land use within an overarching catchment management plan. Although most of the protected areas considered preservation of biodiversity as their primary goal, they were characterised by significantly fewer plant species than the adjacent, highly utilised, communal lands, at both the plot and point scale. Slope position also had a significant effect on plant species richness, with eutrophic bottomlands having c. 30% more species than the dystrophic toplands. This adds weight to the need for greater public awareness for the judicious use and management of the sensitive bottomlands, which fringe the primary drainage lines that are vital for sustained supplies of good quality surface water in this semi-arid environment. The total number of species increased with increasing mean annual rainfall across the rainfall gradient. This suggests that, if the catchment management plan aims to identify additional areas for conservation, the higher rainfall areas should be the first to be assessed. Species turnover was greater along the rainfall gradient than the catenal gradient between toplands and bottomlands.
- Full Text:
- Date Issued: 2000
- Authors: Shackleton, Charlie M
- Date: 2000
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/181885 , vital:43777 , xlink:href="https://doi.org/10.1016/S0006-3207(00)00001-X"
- Description: Patterns of higher plant species richness and beta diversity were assessed using standard Modified-Whittaker plots in relation to land use, slope position and mean annual rainfall across a rainfall gradient in the savanna areas of the Bushbuckridge lowveld, South Africa. In particular, comparison of communal areas with adjacent protected areas was important in showing the impacts of potential changes in land use within an overarching catchment management plan. Although most of the protected areas considered preservation of biodiversity as their primary goal, they were characterised by significantly fewer plant species than the adjacent, highly utilised, communal lands, at both the plot and point scale. Slope position also had a significant effect on plant species richness, with eutrophic bottomlands having c. 30% more species than the dystrophic toplands. This adds weight to the need for greater public awareness for the judicious use and management of the sensitive bottomlands, which fringe the primary drainage lines that are vital for sustained supplies of good quality surface water in this semi-arid environment. The total number of species increased with increasing mean annual rainfall across the rainfall gradient. This suggests that, if the catchment management plan aims to identify additional areas for conservation, the higher rainfall areas should be the first to be assessed. Species turnover was greater along the rainfall gradient than the catenal gradient between toplands and bottomlands.
- Full Text:
- Date Issued: 2000
Electrocatalytic behavior of substituted cobalt phthalocyanines towards the oxidation of cysteine
- Maree, Suzanne, Nyokong, Tebello
- Authors: Maree, Suzanne , Nyokong, Tebello
- Date: 2000
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/293268 , vital:57070 , xlink:href="https://doi.org/10.1016/S0022-0728(00)00281-3"
- Description: Ring substituted cobalt phthalocyanine complexes of the form CoPc(X)4, (where X=NH2, NO2, C(CH3)3, SO3H and COOH) are compared for their catalytic activities towards the oxidation of cysteine. The potential for the electrocatalytic oxidation of cysteine is closely related to the CoIII/CoII couple of the CoPc(X)4 complexes in acidic media and to the CoII/CoI couple in basic media. The catalytic currents and the oxidation potential for cysteine are dependent on the pH of the solution, the potential becoming less positive as the pH increases and the catalytic currents decreasing with increase in pH, for the same concentration of cysteine. The magnitudes of the catalytic currents (after ten scans) for cysteine oxidation at pH 8.3 and on electrodes modified with the CoPc(X)4 complexes increased with the nature of the ring substituent as follows: NO2 less than NH2 less than SO3H less than C(CH3)3 less than COOH.
- Full Text:
- Date Issued: 2000
- Authors: Maree, Suzanne , Nyokong, Tebello
- Date: 2000
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/293268 , vital:57070 , xlink:href="https://doi.org/10.1016/S0022-0728(00)00281-3"
- Description: Ring substituted cobalt phthalocyanine complexes of the form CoPc(X)4, (where X=NH2, NO2, C(CH3)3, SO3H and COOH) are compared for their catalytic activities towards the oxidation of cysteine. The potential for the electrocatalytic oxidation of cysteine is closely related to the CoIII/CoII couple of the CoPc(X)4 complexes in acidic media and to the CoII/CoI couple in basic media. The catalytic currents and the oxidation potential for cysteine are dependent on the pH of the solution, the potential becoming less positive as the pH increases and the catalytic currents decreasing with increase in pH, for the same concentration of cysteine. The magnitudes of the catalytic currents (after ten scans) for cysteine oxidation at pH 8.3 and on electrodes modified with the CoPc(X)4 complexes increased with the nature of the ring substituent as follows: NO2 less than NH2 less than SO3H less than C(CH3)3 less than COOH.
- Full Text:
- Date Issued: 2000
Electrocatalytic behavior of substituted cobalt phthalocyanines towards the oxidation of cysteine
- Maree, Suzanne, Nyokong, Tebello
- Authors: Maree, Suzanne , Nyokong, Tebello
- Date: 2000
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/293185 , vital:57063 , xlink:href="https://doi.org/10.1016/S0022-0728(00)00281-3"
- Description: Ring substituted cobalt phthalocyanine complexes of the form CoPc(X)4, (where X=NH2, NO2, C(CH3)3, SO3H and COOH) are compared for their catalytic activities towards the oxidation of cysteine. The potential for the electrocatalytic oxidation of cysteine is closely related to the CoIII/CoII couple of the CoPc(X)4 complexes in acidic media and to the CoII/CoI couple in basic media. The catalytic currents and the oxidation potential for cysteine are dependent on the pH of the solution, the potential becoming less positive as the pH increases and the catalytic currents decreasing with increase in pH, for the same concentration of cysteine. The magnitudes of the catalytic currents (after ten scans) for cysteine oxidation at pH 8.3 and on electrodes modified with the CoPc(X)4 complexes increased with the nature of the ring substituent as follows: NO2 less than NH2 less than SO3H less than C(CH3)3 less than COOH.
- Full Text:
- Date Issued: 2000
- Authors: Maree, Suzanne , Nyokong, Tebello
- Date: 2000
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/293185 , vital:57063 , xlink:href="https://doi.org/10.1016/S0022-0728(00)00281-3"
- Description: Ring substituted cobalt phthalocyanine complexes of the form CoPc(X)4, (where X=NH2, NO2, C(CH3)3, SO3H and COOH) are compared for their catalytic activities towards the oxidation of cysteine. The potential for the electrocatalytic oxidation of cysteine is closely related to the CoIII/CoII couple of the CoPc(X)4 complexes in acidic media and to the CoII/CoI couple in basic media. The catalytic currents and the oxidation potential for cysteine are dependent on the pH of the solution, the potential becoming less positive as the pH increases and the catalytic currents decreasing with increase in pH, for the same concentration of cysteine. The magnitudes of the catalytic currents (after ten scans) for cysteine oxidation at pH 8.3 and on electrodes modified with the CoPc(X)4 complexes increased with the nature of the ring substituent as follows: NO2 less than NH2 less than SO3H less than C(CH3)3 less than COOH.
- Full Text:
- Date Issued: 2000
Electrocatalytic properties of vitamin B12 towards oxidation and reduction of nitric oxide
- Vilakazi, Sibulelo Lea, Nyokong, Tebello
- Authors: Vilakazi, Sibulelo Lea , Nyokong, Tebello
- Date: 2000
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/293196 , vital:57064 , xlink:href="https://doi.org/10.1016/S0013-4686(00)00628-9"
- Description: This paper reports on the catalytic behaviour of cyanocobalamin (VB12) towards the reduction and oxidation of nitric oxide. When VB12 is adsorbed on glassy carbon electrodes, it catalyses the reduction of nitric oxide (NO) in pH 4 and 9 buffers. In the absence of NO, cyclic voltammetry shows that VB12 is reduced by a one-step two-electron reduction from CoIII to the CoI species. Addition of NO at pH 9 to solutions of VB12 resulted in the splitting of the cyclic voltammetry peaks as a result of a consecutive one-electron reduction of the central CoIII metal in VB12 to CoII and finally to CoI. The catalytic peak for oxidation of NO on a glassy carbon electrode modified with VB12 was observed at 1.21 V versus Ag∣AgCl, at pH 9. The products of the catalytic reduction of nitric oxide include ammonia and hydroxylamine.
- Full Text:
- Date Issued: 2000
- Authors: Vilakazi, Sibulelo Lea , Nyokong, Tebello
- Date: 2000
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/293196 , vital:57064 , xlink:href="https://doi.org/10.1016/S0013-4686(00)00628-9"
- Description: This paper reports on the catalytic behaviour of cyanocobalamin (VB12) towards the reduction and oxidation of nitric oxide. When VB12 is adsorbed on glassy carbon electrodes, it catalyses the reduction of nitric oxide (NO) in pH 4 and 9 buffers. In the absence of NO, cyclic voltammetry shows that VB12 is reduced by a one-step two-electron reduction from CoIII to the CoI species. Addition of NO at pH 9 to solutions of VB12 resulted in the splitting of the cyclic voltammetry peaks as a result of a consecutive one-electron reduction of the central CoIII metal in VB12 to CoII and finally to CoI. The catalytic peak for oxidation of NO on a glassy carbon electrode modified with VB12 was observed at 1.21 V versus Ag∣AgCl, at pH 9. The products of the catalytic reduction of nitric oxide include ammonia and hydroxylamine.
- Full Text:
- Date Issued: 2000
Interaction between iron (II) tetrasulfophthalocyanine and the neurotransmitters, serotonin and dopamine
- Oni, Joshua, Nyokong, Tebello
- Authors: Oni, Joshua , Nyokong, Tebello
- Date: 2000
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/293223 , vital:57066 , xlink:href="https://doi.org/10.1016/S0277-5387(00)00421-6"
- Description: This work reports on the kinetics of interaction of iron(II) tetrasulfophthalocyanine, [FeTSPc]4−, with dopamine (DA) and serotonin (5-HT). The interaction results in the coordination of dopamine and serotonin to [FeTSPc]4−, followed by internal electron transfer and the formation of [(DA+)FeITSPc]4− and [(5-HT+) FeITSPc]4− complexes, respectively. The rate constants for the coordination of dopamine or serotonin to [FeTSPc]4− and the formation of the FeITSPc species were found to be kf=6.8 and 9.3 dm3 mol−1 s−1, respectively. The equilibrium constants were 2.2×103 and 1.5×103 dm3 mol−1, respectively, for the interaction of dopamine or serotonin to [FeTSPc]4−.
- Full Text:
- Date Issued: 2000
- Authors: Oni, Joshua , Nyokong, Tebello
- Date: 2000
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/293223 , vital:57066 , xlink:href="https://doi.org/10.1016/S0277-5387(00)00421-6"
- Description: This work reports on the kinetics of interaction of iron(II) tetrasulfophthalocyanine, [FeTSPc]4−, with dopamine (DA) and serotonin (5-HT). The interaction results in the coordination of dopamine and serotonin to [FeTSPc]4−, followed by internal electron transfer and the formation of [(DA+)FeITSPc]4− and [(5-HT+) FeITSPc]4− complexes, respectively. The rate constants for the coordination of dopamine or serotonin to [FeTSPc]4− and the formation of the FeITSPc species were found to be kf=6.8 and 9.3 dm3 mol−1 s−1, respectively. The equilibrium constants were 2.2×103 and 1.5×103 dm3 mol−1, respectively, for the interaction of dopamine or serotonin to [FeTSPc]4−.
- Full Text:
- Date Issued: 2000
Interaction of nitric oxide with cobalt (II) tetrasulfophthalocyanine
- Vilakazi, Sibulelo, Nyokong, Tebello
- Authors: Vilakazi, Sibulelo , Nyokong, Tebello
- Date: 2000
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/293235 , vital:57067 , xlink:href="https://doi.org/10.1016/S0277-5387(99)00373-3"
- Description: The interaction of nitric oxide (NO) with cobalt(II) tetrasulfophthalocyanine [Co(II)TSPc]4−) has been studied. Coordination of NO is accompanied by electron transfer from the central metal in [Co(II)TSPc]4−, the resulting complex being represented as [(NO−)Co(III)TSPc]4−. The rate constant for the formation of this species is kf=142±7 dm3 mol−1 s−1 and an equilibrium constant of 3.0±0.5×105 dm3 mol−1 was obtained. When adsorbed to a glassy carbon electrode, [Co(II)TSPc]4− catalyses the oxidation and reduction of NO, with a detection limit of the order of 10−9 mol dm−3. Ammonia and hydroxylamine are some of the reduction products obtained for the reduction of NO on [Co(II)TSPc]4−-modified glassy carbon electrodes.
- Full Text:
- Date Issued: 2000
- Authors: Vilakazi, Sibulelo , Nyokong, Tebello
- Date: 2000
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/293235 , vital:57067 , xlink:href="https://doi.org/10.1016/S0277-5387(99)00373-3"
- Description: The interaction of nitric oxide (NO) with cobalt(II) tetrasulfophthalocyanine [Co(II)TSPc]4−) has been studied. Coordination of NO is accompanied by electron transfer from the central metal in [Co(II)TSPc]4−, the resulting complex being represented as [(NO−)Co(III)TSPc]4−. The rate constant for the formation of this species is kf=142±7 dm3 mol−1 s−1 and an equilibrium constant of 3.0±0.5×105 dm3 mol−1 was obtained. When adsorbed to a glassy carbon electrode, [Co(II)TSPc]4− catalyses the oxidation and reduction of NO, with a detection limit of the order of 10−9 mol dm−3. Ammonia and hydroxylamine are some of the reduction products obtained for the reduction of NO on [Co(II)TSPc]4−-modified glassy carbon electrodes.
- Full Text:
- Date Issued: 2000
Photocatalytic properties of neodymium diphthalocyanine towards the transformation of 4-chlorophenol
- Nensala, Ngudiankama, Nyokong, Tebello
- Authors: Nensala, Ngudiankama , Nyokong, Tebello
- Date: 2000
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/${Handle} , vital:58491 , xlink:href="https://doi.org/10.1016/S1381-1169(00)00283-1"
- Description: Photolysis of aqueous solutions of 4-chlorophenol (4-Cp) in the presence of solid neodymium diphthalocyanine ([Pc(−2)NdPc(−2)]−) and oxygen using visible and ultraviolet (UV) radiation resulted in the formation of a number of products. For photolysis in the visible region, phenol, benzoquinone, hydroquinone were observed as intermediates and 4-chlorocatechol (4-CC) as the main product; intermediates similar to those observed for visible photolysis were obtained. Langmuir–Hinshelwood kinetic model was used for treatment of photochemical data.
- Full Text:
- Date Issued: 2000
Photocatalytic properties of neodymium diphthalocyanine towards the transformation of 4-chlorophenol
- Authors: Nensala, Ngudiankama , Nyokong, Tebello
- Date: 2000
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/${Handle} , vital:58491 , xlink:href="https://doi.org/10.1016/S1381-1169(00)00283-1"
- Description: Photolysis of aqueous solutions of 4-chlorophenol (4-Cp) in the presence of solid neodymium diphthalocyanine ([Pc(−2)NdPc(−2)]−) and oxygen using visible and ultraviolet (UV) radiation resulted in the formation of a number of products. For photolysis in the visible region, phenol, benzoquinone, hydroquinone were observed as intermediates and 4-chlorocatechol (4-CC) as the main product; intermediates similar to those observed for visible photolysis were obtained. Langmuir–Hinshelwood kinetic model was used for treatment of photochemical data.
- Full Text:
- Date Issued: 2000
Stump size and the number of coppice shoots for selected savanna tree species
- Authors: Shackleton, Charlie M
- Date: 2000
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/181896 , vital:43778 , xlink:href="https://doi.org/10.1016/S0254-6299(15)31074-7"
- Description: Management of coppice dynamics of indigenous savanna trees could assist in increasing the regrowth rates or number of coppice shoots produced. This would be useful in natural resource management programmes to promote sustainable resource management. This study examined the influence of cutting height, stem size and surface area on the number of coppice shoots produced for twelve savanna species from a communal land in the Bushbuckndge lowveld. All species exhibited a strong coppicing ability following cutting. The number of shoots per stump was most frequently related to cutting height, although this was not always the most significant predictor. There were clear differences between species with respect to the number of shoots per unit surface area, the highest being for Albizia harveyii and the least Piliostlgma thonningii. The taller the potential height of a species, the fewer were the coppice shoots per stump surface area.
- Full Text:
- Date Issued: 2000
- Authors: Shackleton, Charlie M
- Date: 2000
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/181896 , vital:43778 , xlink:href="https://doi.org/10.1016/S0254-6299(15)31074-7"
- Description: Management of coppice dynamics of indigenous savanna trees could assist in increasing the regrowth rates or number of coppice shoots produced. This would be useful in natural resource management programmes to promote sustainable resource management. This study examined the influence of cutting height, stem size and surface area on the number of coppice shoots produced for twelve savanna species from a communal land in the Bushbuckndge lowveld. All species exhibited a strong coppicing ability following cutting. The number of shoots per stump was most frequently related to cutting height, although this was not always the most significant predictor. There were clear differences between species with respect to the number of shoots per unit surface area, the highest being for Albizia harveyii and the least Piliostlgma thonningii. The taller the potential height of a species, the fewer were the coppice shoots per stump surface area.
- Full Text:
- Date Issued: 2000
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