Cyclic voltammetry and spectroelectrochemistry of osmium phthalocyanines in aqueous and non-aqueous solvents
- Sekota, Mantoa, Nyokong, Tebello
- Authors: Sekota, Mantoa , Nyokong, Tebello
- Date: 1996
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/293358 , vital:57078 , xlink:href="https://doi.org/10.1016/0277-5387(95)00581-1"
- Description: Cyclic voltammetry of osmium phthalocyanine complexes, [(CN)2OsIIPc]2− and (py)2OSIIPc (PC = phthalocyanine dianion), show two oxidation couples and two reduction couples in acetonitrile and dimethy1formamide. Oxidation and reduction in these complexes occur at the ring to form cation and anion radical species, respectively. The [(CN)2OsIIPC]2− complexes show a remarkable ease of ring oxidation with oxidation potentials that are much lower than is typical for metallophthalocyanines. Half-wave potentials of 0.25 and 0.67 V (versus saturated calomel electrode, SCE) were obtained for the first and second ring oxidations, respectively. The [(CN)2OSIIPc]2− complex is soluble in water at pHs greater than 4. This complex shows one oxidation couple in pH 9 buffer at −0.11 V versus SCE.
- Full Text:
- Date Issued: 1996
- Authors: Sekota, Mantoa , Nyokong, Tebello
- Date: 1996
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/293358 , vital:57078 , xlink:href="https://doi.org/10.1016/0277-5387(95)00581-1"
- Description: Cyclic voltammetry of osmium phthalocyanine complexes, [(CN)2OsIIPc]2− and (py)2OSIIPc (PC = phthalocyanine dianion), show two oxidation couples and two reduction couples in acetonitrile and dimethy1formamide. Oxidation and reduction in these complexes occur at the ring to form cation and anion radical species, respectively. The [(CN)2OsIIPC]2− complexes show a remarkable ease of ring oxidation with oxidation potentials that are much lower than is typical for metallophthalocyanines. Half-wave potentials of 0.25 and 0.67 V (versus saturated calomel electrode, SCE) were obtained for the first and second ring oxidations, respectively. The [(CN)2OSIIPc]2− complex is soluble in water at pHs greater than 4. This complex shows one oxidation couple in pH 9 buffer at −0.11 V versus SCE.
- Full Text:
- Date Issued: 1996
Perceptions of affirmative action
- Scott, Judith, Amos, Trevor L, Richard Scott, W
- Authors: Scott, Judith , Amos, Trevor L , Richard Scott, W
- Date: 1996
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/270914 , vital:54491 , xlink:href="https://hdl.handle.net/10520/EJC-67e7bffd2"
- Description: Private and public South African employers have instituted affirmative action policies meant to provide employment opportunities to Black South Africans. A body of literature suggests that because of affirmative action policies Black hopes have been raised while Whites view such policies as having a negative impact on their opportunities. However, no extant literature details an empirical investigation of these suggestions. Therefore, this study focusses on the affirmative action perceptions held by 350 South African university commerce students.
- Full Text:
- Date Issued: 1996
- Authors: Scott, Judith , Amos, Trevor L , Richard Scott, W
- Date: 1996
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/270914 , vital:54491 , xlink:href="https://hdl.handle.net/10520/EJC-67e7bffd2"
- Description: Private and public South African employers have instituted affirmative action policies meant to provide employment opportunities to Black South Africans. A body of literature suggests that because of affirmative action policies Black hopes have been raised while Whites view such policies as having a negative impact on their opportunities. However, no extant literature details an empirical investigation of these suggestions. Therefore, this study focusses on the affirmative action perceptions held by 350 South African university commerce students.
- Full Text:
- Date Issued: 1996
Photosensitization reactions of neodymium, dysprosium and lutetium diphthalocyanine
- Nensala, Ngudiankama, Nyokong, Tebello
- Authors: Nensala, Ngudiankama , Nyokong, Tebello
- Date: 1997
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/${Handle} , vital:57084 , xlink:href="https://doi.org/10.1016/S0277-5387(97)00045-4"
- Description: Photolysis, using a visible radiation, of diphthalocyanine complexes of NdIII, DyIII and LuIII ([Pc(−2)NdIIIPc(−2)]−, [Pc(−2)DyIIIPc(−2)]− and [Pc(−2)LuIIIPc(−2)]−, respectively) in the presence of pentachlorophenol (PCP) or SO2 results in the one-electron oxidation of the diphthalocyanine species to Pc(−1)NdIIIPc(−2), Pc(−1)DyIIIPc(−2) and Pc(−2)LuIIIPc(−2), respectively. The PCP is reductively dechlorinated to tetra- and trichlorophenols. The quantum yields for the photosensitization reactions are of the order 10−4.
- Full Text:
- Date Issued: 1997
- Authors: Nensala, Ngudiankama , Nyokong, Tebello
- Date: 1997
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/${Handle} , vital:57084 , xlink:href="https://doi.org/10.1016/S0277-5387(97)00045-4"
- Description: Photolysis, using a visible radiation, of diphthalocyanine complexes of NdIII, DyIII and LuIII ([Pc(−2)NdIIIPc(−2)]−, [Pc(−2)DyIIIPc(−2)]− and [Pc(−2)LuIIIPc(−2)]−, respectively) in the presence of pentachlorophenol (PCP) or SO2 results in the one-electron oxidation of the diphthalocyanine species to Pc(−1)NdIIIPc(−2), Pc(−1)DyIIIPc(−2) and Pc(−2)LuIIIPc(−2), respectively. The PCP is reductively dechlorinated to tetra- and trichlorophenols. The quantum yields for the photosensitization reactions are of the order 10−4.
- Full Text:
- Date Issued: 1997
Use of cobalt (II) phthalocyanine to improve the sensitivity and stability of glassy carbon electrodes for the detection of cresols, chlorophenols and phenol
- Mafatle, Tsukutlane J, Nyokong, Tebello
- Authors: Mafatle, Tsukutlane J , Nyokong, Tebello
- Date: 1997
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/293335 , vital:57076 , xlink:href="https://doi.org/10.1016/S0003-2670(97)00464-9"
- Description: A cobalt(II) phthalocyanine-modified glassy carbon electrode (CoPc-GCE) was used for the detection of o-, m- and p-cresols, and of 2-chlorophenol, 4-chlorophenol and phenol. Modification of the glassy carbon electrode with CoPc increases the oxidation currents of these species and increases the stability of the electrode. CoPc-GCE showed less fouling by the oxidation products of these compounds than the unmodified GCE. Comparison of some first row transition metal phthalocyanines showed the following trend for the enhancement of the currents for the oxidation of cresols and phenols: Co(II)Pc > Mn(II)Pc > Fe(II)Pc > Ni(II)Pc > Cu(II)Pc > H2Pc > Zn(II)Pc > GCE. When [Co(II)TSPc]4− (TSPc=tetrasulfo Pc) was added to aqueous solutions containing the cresols and phenols, an enhancement of the oxidation currents was also observed.
- Full Text:
- Date Issued: 1997
- Authors: Mafatle, Tsukutlane J , Nyokong, Tebello
- Date: 1997
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/293335 , vital:57076 , xlink:href="https://doi.org/10.1016/S0003-2670(97)00464-9"
- Description: A cobalt(II) phthalocyanine-modified glassy carbon electrode (CoPc-GCE) was used for the detection of o-, m- and p-cresols, and of 2-chlorophenol, 4-chlorophenol and phenol. Modification of the glassy carbon electrode with CoPc increases the oxidation currents of these species and increases the stability of the electrode. CoPc-GCE showed less fouling by the oxidation products of these compounds than the unmodified GCE. Comparison of some first row transition metal phthalocyanines showed the following trend for the enhancement of the currents for the oxidation of cresols and phenols: Co(II)Pc > Mn(II)Pc > Fe(II)Pc > Ni(II)Pc > Cu(II)Pc > H2Pc > Zn(II)Pc > GCE. When [Co(II)TSPc]4− (TSPc=tetrasulfo Pc) was added to aqueous solutions containing the cresols and phenols, an enhancement of the oxidation currents was also observed.
- Full Text:
- Date Issued: 1997
The use of optimal foraging theory to assess the fishing strategies of Pacific Island artisanal fishers: A methodological review
- Authors: Shankar, Aswani
- Date: 1998
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/440038 , vital:73730
- Description: Artisanal fisheries play a major role in the social, cultural, and economic life of most Pacific Islanders, particularly in rural communities where people are highly dependent on marine resources for subsistence and commercial purposes. Yet, marine resources are being threatened by pressure from exploding human populations and the increasing commercialisation of the subsistence fishery—circumstances which are now forcing researchers to find novel ways to examine issues of coastal management and marine resource conservation. Among the most recent approaches to coastal management has been to study marine ecological processes in conjunction with those of the contiguous shoreline and upland habitats, or what has been termed Integrated Coastal Zone Management (ICZM). From the standpoint of maritime anthropology, any comprehensive study of the integration of marine and terrestrial biotic components requires the parallel consideration of human activities, including existing property regimes, resource access and distribution rules, and resource exploitation strategies. Although numerous studies have concentrated on the social aspects of Pacific Island artisanal fisheries (eg Johannes, 1981; Hviding, 1996; Lieber, 1994), few have dealt explicitly with the micro-ecology of daily humanmarine interactions (see Aswani, 1997; Bird and Bird, 1997). Such neglect has hampered attempts to fully integrate studies of environmental coastal processes with those of human activities. In this paper, I examine the utility of optimal foraging theory and its methodology, as applied to the study of Pacific Island artisanal fishers. The inclusion of foraging theory can contribute to building a clearer anthropological model to describe the relationship between human foraging and fishery management.
- Full Text:
- Date Issued: 1998
- Authors: Shankar, Aswani
- Date: 1998
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/440038 , vital:73730
- Description: Artisanal fisheries play a major role in the social, cultural, and economic life of most Pacific Islanders, particularly in rural communities where people are highly dependent on marine resources for subsistence and commercial purposes. Yet, marine resources are being threatened by pressure from exploding human populations and the increasing commercialisation of the subsistence fishery—circumstances which are now forcing researchers to find novel ways to examine issues of coastal management and marine resource conservation. Among the most recent approaches to coastal management has been to study marine ecological processes in conjunction with those of the contiguous shoreline and upland habitats, or what has been termed Integrated Coastal Zone Management (ICZM). From the standpoint of maritime anthropology, any comprehensive study of the integration of marine and terrestrial biotic components requires the parallel consideration of human activities, including existing property regimes, resource access and distribution rules, and resource exploitation strategies. Although numerous studies have concentrated on the social aspects of Pacific Island artisanal fisheries (eg Johannes, 1981; Hviding, 1996; Lieber, 1994), few have dealt explicitly with the micro-ecology of daily humanmarine interactions (see Aswani, 1997; Bird and Bird, 1997). Such neglect has hampered attempts to fully integrate studies of environmental coastal processes with those of human activities. In this paper, I examine the utility of optimal foraging theory and its methodology, as applied to the study of Pacific Island artisanal fishers. The inclusion of foraging theory can contribute to building a clearer anthropological model to describe the relationship between human foraging and fishery management.
- Full Text:
- Date Issued: 1998
An investigation into the neuroprotective properties of ibuprofen
- Lambat, Zaynab Y, Conrad, Natasha, Anoopkumar-Dukie, Shailendra, Walker, Roderick B, Daya, Santylal
- Authors: Lambat, Zaynab Y , Conrad, Natasha , Anoopkumar-Dukie, Shailendra , Walker, Roderick B , Daya, Santylal
- Date: 2000
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/184335 , vital:44209 , xlink:href="https://doi.org/10.1023/A:1011115006856"
- Description: There is increasing evidence suggesting a protective role for anti-inflammatory medications in neurological disorders such as Alzheimer's disease (AD). While there has not been any direct evidence for this, a number of clinical studies indicate that those patients who have had a history of nonsteroidal anti-inflammatory use, have a lower incidence of AD. Since there is currently no evidence on the mechanism by which these agents offer possible neuroprotection, we investigated the potential neuroprotective properties of the nonsteroidal anti-inflammatory drug, ibuprofen, by examining whether this agent could reduce lipid peroxidation and superoxide radical generation. Quinolinic acid and cyanide, known neurotoxins, were used to induce lipid peroxidation and superoxide anion formation respectively, in rat brain homogenate. The results show that ibuprofen significantly (p more than 0.05) reduced quinolinic acid-induced lipid peroxidation and cyanide-induced superoxide production. The results of the present report therefore suggest a possible mechanism for the neuroprotective effect of ibuprofen.
- Full Text: false
- Date Issued: 2000
- Authors: Lambat, Zaynab Y , Conrad, Natasha , Anoopkumar-Dukie, Shailendra , Walker, Roderick B , Daya, Santylal
- Date: 2000
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/184335 , vital:44209 , xlink:href="https://doi.org/10.1023/A:1011115006856"
- Description: There is increasing evidence suggesting a protective role for anti-inflammatory medications in neurological disorders such as Alzheimer's disease (AD). While there has not been any direct evidence for this, a number of clinical studies indicate that those patients who have had a history of nonsteroidal anti-inflammatory use, have a lower incidence of AD. Since there is currently no evidence on the mechanism by which these agents offer possible neuroprotection, we investigated the potential neuroprotective properties of the nonsteroidal anti-inflammatory drug, ibuprofen, by examining whether this agent could reduce lipid peroxidation and superoxide radical generation. Quinolinic acid and cyanide, known neurotoxins, were used to induce lipid peroxidation and superoxide anion formation respectively, in rat brain homogenate. The results show that ibuprofen significantly (p more than 0.05) reduced quinolinic acid-induced lipid peroxidation and cyanide-induced superoxide production. The results of the present report therefore suggest a possible mechanism for the neuroprotective effect of ibuprofen.
- Full Text: false
- Date Issued: 2000
Comparative Spectroscopic and Electrochemical Properties of Bis (octakis (dodecylthio) naphthalocyaninato) europium (III) and Bis (tetra-tert-butylnaphthalocyaninato) europium (III) Complexes
- Nyokong, Tebello, Furuya, Fumio, Kobayashi, Nagao, Du, Daming, Liu, Wei, Jiang, Jianzhuang
- Authors: Nyokong, Tebello , Furuya, Fumio , Kobayashi, Nagao , Du, Daming , Liu, Wei , Jiang, Jianzhuang
- Date: 2000
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/293174 , vital:57062 , xlink:href="https://doi.org/10.1021/ic990483b"
- Description: Bis(substituted-2,3-naphthalocyaninato)europium(III) complexes: bis(octakis(dodecylthio)-2,3-naphthalocyaninato)europium(III) {Eu[2,3-Nc(SC12H25)8]2, 1} and bis(tetra-tert-butyl-2,3-naphthalocyaninato)europium(III) {Eu[2,3-Nc(t-Bu)4]2, 2} have been synthesized by cyclic tetramerization of naphthalonitriles with Eu(acac)3·H2O in the presence of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) in refluxing n-octanol. These compounds were characterized by UV−visible, magnetic circular dichroism (MCD), near-IR, IR, EPR, and mass spectroscopies. The absorption and MCD spectra of 1 showed splitting of the Q band, with peaks at 700 and 784 nm, red shifted from the Q band of 2 at 763 nm. The absorption and MCD spectral band deconvolution calculations of complex 1 gave two A terms in the Q-band region. The A terms are assigned to 2A2 → 2E1 transitions. Cyclic voltammograms of 1 and 2 showed reversible oxidation couples at E1/2 = −0.28 V (for 2) and −0.25 V (for 1) vs ferrocenium/ferrocene (Fc+/Fc). The second oxidation exhibited a complicated behavior for both complexes. The reduction couples for 2 were observed at E1/2 = −0.61, −1.64, −1.97, and −2.42 V, and for 1 they were observed at E1/2 = −0.62, −1.60, −1.86, and −2.27 V vs Fc+/Fc. Spectral changes observed on chemical oxidation and reduction of the complexes are presented, and the behaviors of 1 and 2 are compared.
- Full Text:
- Date Issued: 2000
- Authors: Nyokong, Tebello , Furuya, Fumio , Kobayashi, Nagao , Du, Daming , Liu, Wei , Jiang, Jianzhuang
- Date: 2000
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/293174 , vital:57062 , xlink:href="https://doi.org/10.1021/ic990483b"
- Description: Bis(substituted-2,3-naphthalocyaninato)europium(III) complexes: bis(octakis(dodecylthio)-2,3-naphthalocyaninato)europium(III) {Eu[2,3-Nc(SC12H25)8]2, 1} and bis(tetra-tert-butyl-2,3-naphthalocyaninato)europium(III) {Eu[2,3-Nc(t-Bu)4]2, 2} have been synthesized by cyclic tetramerization of naphthalonitriles with Eu(acac)3·H2O in the presence of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) in refluxing n-octanol. These compounds were characterized by UV−visible, magnetic circular dichroism (MCD), near-IR, IR, EPR, and mass spectroscopies. The absorption and MCD spectra of 1 showed splitting of the Q band, with peaks at 700 and 784 nm, red shifted from the Q band of 2 at 763 nm. The absorption and MCD spectral band deconvolution calculations of complex 1 gave two A terms in the Q-band region. The A terms are assigned to 2A2 → 2E1 transitions. Cyclic voltammograms of 1 and 2 showed reversible oxidation couples at E1/2 = −0.28 V (for 2) and −0.25 V (for 1) vs ferrocenium/ferrocene (Fc+/Fc). The second oxidation exhibited a complicated behavior for both complexes. The reduction couples for 2 were observed at E1/2 = −0.61, −1.64, −1.97, and −2.42 V, and for 1 they were observed at E1/2 = −0.62, −1.60, −1.86, and −2.27 V vs Fc+/Fc. Spectral changes observed on chemical oxidation and reduction of the complexes are presented, and the behaviors of 1 and 2 are compared.
- Full Text:
- Date Issued: 2000
Cyanide-induced free radical production and lipid peroxidation in rat brain homogenate is reduced by aspirin
- Daya, Santylal, Walker, Roderick B, Anoopkumar-Dukie, Shailendra
- Authors: Daya, Santylal , Walker, Roderick B , Anoopkumar-Dukie, Shailendra
- Date: 2000
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/184346 , vital:44210 , xlink:href="https://doi.org/10.1007/BF02674529"
- Description: The neuroprotective properties of aspirin were investigated using cyanide-induced neurotoxicity as model. Cyanide, a known neurotoxic agent significantly increased lipid peroxidation and superoxide anion levels in rat brain homogenate in a concentration-dependent manner (0.25–1.0 mM). When homogenate, containing 1.0 mM KCN was cotreated with aspirin (1.0 mM) there was a significant decrease in lipid peroxidation. Aspirin (0.5 mM and 1.0 mM) also significantly reduced KCN-induced superoxide anion generation. The results of the present report therefore indicate a neuroprotective role for aspirin.
- Full Text:
- Date Issued: 2000
- Authors: Daya, Santylal , Walker, Roderick B , Anoopkumar-Dukie, Shailendra
- Date: 2000
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/184346 , vital:44210 , xlink:href="https://doi.org/10.1007/BF02674529"
- Description: The neuroprotective properties of aspirin were investigated using cyanide-induced neurotoxicity as model. Cyanide, a known neurotoxic agent significantly increased lipid peroxidation and superoxide anion levels in rat brain homogenate in a concentration-dependent manner (0.25–1.0 mM). When homogenate, containing 1.0 mM KCN was cotreated with aspirin (1.0 mM) there was a significant decrease in lipid peroxidation. Aspirin (0.5 mM and 1.0 mM) also significantly reduced KCN-induced superoxide anion generation. The results of the present report therefore indicate a neuroprotective role for aspirin.
- 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
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
Effect of oligomerization on the photochemical properties of silicon octaphenoxyphthalocyanine
- Maree, M David, Nyokong, Tebello
- Authors: Maree, M David , Nyokong, Tebello
- Date: 2001
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/291542 , vital:56885 , xlink:href="https://doi.org/10.1016/S1010-6030(01)00485-3"
- Description: The photochemical properties of silicon octaphenoxyphthalocyanines (SiOPPc) oligomerized were studied in dimethylsulfoxide (DMSO) solutions. Oligomers containing 2–5 and 9 SiOPPc rings linked with terephthalate linkages were synthesized. Singlet oxygen quantum yields were found to be in the range 0.11–0.34, and increased with the number of rings up to five rings, a decrease in the quantum yield was observed for nine rings. This is explained in terms of the high aggregation of the oligomer containing nine rings.
- Full Text:
- Date Issued: 2001
- Authors: Maree, M David , Nyokong, Tebello
- Date: 2001
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/291542 , vital:56885 , xlink:href="https://doi.org/10.1016/S1010-6030(01)00485-3"
- Description: The photochemical properties of silicon octaphenoxyphthalocyanines (SiOPPc) oligomerized were studied in dimethylsulfoxide (DMSO) solutions. Oligomers containing 2–5 and 9 SiOPPc rings linked with terephthalate linkages were synthesized. Singlet oxygen quantum yields were found to be in the range 0.11–0.34, and increased with the number of rings up to five rings, a decrease in the quantum yield was observed for nine rings. This is explained in terms of the high aggregation of the oligomer containing nine rings.
- Full Text:
- Date Issued: 2001
Photochemical studies of tetra-2, 3-pyridinoporphyrazines
- Seotsanyana-Mokhosi, Itumeleng, Kuznetsova, Nina, Nyokong, Tebello
- Authors: Seotsanyana-Mokhosi, Itumeleng , Kuznetsova, Nina , Nyokong, Tebello
- Date: 2001
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/291580 , vital:56889 , xlink:href="https://doi.org/10.1016/S1010-6030(01)00427-0"
- Description: Tetra-2,3-pyridinoporphyrazines and the corresponding water-soluble N,N′,N′′,N′′′-tetramethyl-tetra-2,3-pyridinoporphyrazine complexes, containing central metal atoms; M=Ge, Sn, Si and Zn, were synthesized and their photochemical properties were investigated. The reductive quenching of pyridinoporphyrazines excited states, enhanced relative to phthalocyanines, was considered as the first photochemical step of dyes phototransformation in dimethylformamide (DMF) and dimethylsulfoxide (DMSO) solutions under irradiation with visible light. Efficiency of singlet oxygen photosensitization decreases significantly in the row phthalocyanines, unquaternized, quaternized tetra-2,3-pyridinoporphyrazine metallocomplexes.
- Full Text:
- Date Issued: 2001
- Authors: Seotsanyana-Mokhosi, Itumeleng , Kuznetsova, Nina , Nyokong, Tebello
- Date: 2001
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/291580 , vital:56889 , xlink:href="https://doi.org/10.1016/S1010-6030(01)00427-0"
- Description: Tetra-2,3-pyridinoporphyrazines and the corresponding water-soluble N,N′,N′′,N′′′-tetramethyl-tetra-2,3-pyridinoporphyrazine complexes, containing central metal atoms; M=Ge, Sn, Si and Zn, were synthesized and their photochemical properties were investigated. The reductive quenching of pyridinoporphyrazines excited states, enhanced relative to phthalocyanines, was considered as the first photochemical step of dyes phototransformation in dimethylformamide (DMF) and dimethylsulfoxide (DMSO) solutions under irradiation with visible light. Efficiency of singlet oxygen photosensitization decreases significantly in the row phthalocyanines, unquaternized, quaternized tetra-2,3-pyridinoporphyrazine metallocomplexes.
- Full Text:
- Date Issued: 2001
Spectroscopic studies of the interaction of cobalt (II) N, N', N ″, N‴-tetramethyltetra-3, 4-pyridinoporphyrazine with amino acids and nitrogen oxides
- Thamae, Mamothibe A, Nyokong, Tebello
- Authors: Thamae, Mamothibe A , Nyokong, Tebello
- Date: 2001
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/291617 , vital:56892 , xlink:href="https://doi.org/10.1002/jpp.551"
- Description: The interaction of histidine, cysteine, NO and nitrite with cobalt(II) N,N',N″,N‴-tetramethyltetra-3,4-tetrapyridinoporphyrazine ([CoIItmtppa]4+) is reported. Metal-based autoreduction of [CoIItmtppa]4+ occurs with the formation of the [CoItmtppa(-2)]3+ species in the presence of histidine and cysteine. Kinetic data for the auto reduction of [CoIItmtppa]4+ in the presence of these amino acids gave the rate constants kf = 2.1 × 101 and 2.8 dm3 mol-1 s-1, for cysteine and histidine, respectively. One molecule of NO or nitrite was found to coordinate to the [CoIItmtppa]4+ species. The equilibrium and rate constants for the coordination of the nitric oxide were K = 2.3 × 104dm3mol-1 and kf = 7.5 dm3mol-1s-1, respectively. The coordination of nitrite to [CoIItmtppa]4+ occurred with an equilibrium constant of K = 2.0 × 102dm3mol-1 and a rate constant of kf = 4.0 × 10-3dm3mol-1s-1. There was no evidence for the coordination of two molecules of nitrite to the [CoIItmtppa]4+ species.
- Full Text:
- Date Issued: 2001
- Authors: Thamae, Mamothibe A , Nyokong, Tebello
- Date: 2001
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/291617 , vital:56892 , xlink:href="https://doi.org/10.1002/jpp.551"
- Description: The interaction of histidine, cysteine, NO and nitrite with cobalt(II) N,N',N″,N‴-tetramethyltetra-3,4-tetrapyridinoporphyrazine ([CoIItmtppa]4+) is reported. Metal-based autoreduction of [CoIItmtppa]4+ occurs with the formation of the [CoItmtppa(-2)]3+ species in the presence of histidine and cysteine. Kinetic data for the auto reduction of [CoIItmtppa]4+ in the presence of these amino acids gave the rate constants kf = 2.1 × 101 and 2.8 dm3 mol-1 s-1, for cysteine and histidine, respectively. One molecule of NO or nitrite was found to coordinate to the [CoIItmtppa]4+ species. The equilibrium and rate constants for the coordination of the nitric oxide were K = 2.3 × 104dm3mol-1 and kf = 7.5 dm3mol-1s-1, respectively. The coordination of nitrite to [CoIItmtppa]4+ occurred with an equilibrium constant of K = 2.0 × 102dm3mol-1 and a rate constant of kf = 4.0 × 10-3dm3mol-1s-1. There was no evidence for the coordination of two molecules of nitrite to the [CoIItmtppa]4+ species.
- Full Text:
- Date Issued: 2001
Voltammetric determination of nitric oxide on cobalt phthalocyanine modified microelectrodes
- Vilakazi, Sibulelo Lea, Nyokong, Tebello
- Authors: Vilakazi, Sibulelo Lea , Nyokong, Tebello
- Date: 2001
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/291629 , vital:56893 , xlink:href="https://doi.org/10.1016/S0022-0728(01)00583-6"
- Description: The catalytic activity of a carbon fiber microelectrode modified with cobalt phthalocyanine (CoPc-ME) for the detection of nitric oxide in the presence of possible interfering molecules (dopamine and serotonin) is examined. A linear plot is observed for the variation of the catalytic currents with NO concentration in the presence of excess dopamine and serotonin, showing that NO may be determined in the presence of these molecules. However, oxidation currents due to serotonin were found to decrease with increase in NO concentration. The CoPc-ME could also detect NO added to blood or its components, the oxidation currents for NO, however, decreased rapidly with time. The decrease in currents was slower in blood serum, followed by whole blood, with a faster decrease being observed in blood plasma.
- Full Text:
- Date Issued: 2001
- Authors: Vilakazi, Sibulelo Lea , Nyokong, Tebello
- Date: 2001
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/291629 , vital:56893 , xlink:href="https://doi.org/10.1016/S0022-0728(01)00583-6"
- Description: The catalytic activity of a carbon fiber microelectrode modified with cobalt phthalocyanine (CoPc-ME) for the detection of nitric oxide in the presence of possible interfering molecules (dopamine and serotonin) is examined. A linear plot is observed for the variation of the catalytic currents with NO concentration in the presence of excess dopamine and serotonin, showing that NO may be determined in the presence of these molecules. However, oxidation currents due to serotonin were found to decrease with increase in NO concentration. The CoPc-ME could also detect NO added to blood or its components, the oxidation currents for NO, however, decreased rapidly with time. The decrease in currents was slower in blood serum, followed by whole blood, with a faster decrease being observed in blood plasma.
- Full Text:
- Date Issued: 2001
Woodlands or wastelands: Examining the value of South Africa's woodlands paper
- Shackleton, Charlie M, Willis, C B, Scholes, Robert J
- Authors: Shackleton, Charlie M , Willis, C B , Scholes, Robert J
- Date: 2001
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/182158 , vital:43805 , xlink:href="https://hdl.handle.net/10520/EJC33869"
- Description: The savanna woodlands are the largest biome in the country, constituting one-third of South Africa. They are also home to one-quarter of the population, with 70 % of the former homelands being in the savanna biome. Consequently, they have the potential to make a marked contribution to the national economy, both in the formal and informal sector. They are also valuable on a national scale in terms of the ecosystem services they provide, such as carbon storage, biodiversity and water yield. Until recently the real and potential values attached to South Africa's savannas have not been recognised in policy fora and government institutions. Recent policy changes, especially the National Forestry Action Programme and the National Forest Act, have attempted to remedy this situation. These policies have not filtered down to land owners and managers, nor have they resulted in a redirection of government resources. Thus, large areas remain subject to unsustainable use. It is necessary that the true value of woodlands be determined and acknowledged as a stimulus to government agencies, the private sector and local users to use this valuable resource sustainably.
- Full Text:
- Date Issued: 2001
- Authors: Shackleton, Charlie M , Willis, C B , Scholes, Robert J
- Date: 2001
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/182158 , vital:43805 , xlink:href="https://hdl.handle.net/10520/EJC33869"
- Description: The savanna woodlands are the largest biome in the country, constituting one-third of South Africa. They are also home to one-quarter of the population, with 70 % of the former homelands being in the savanna biome. Consequently, they have the potential to make a marked contribution to the national economy, both in the formal and informal sector. They are also valuable on a national scale in terms of the ecosystem services they provide, such as carbon storage, biodiversity and water yield. Until recently the real and potential values attached to South Africa's savannas have not been recognised in policy fora and government institutions. Recent policy changes, especially the National Forestry Action Programme and the National Forest Act, have attempted to remedy this situation. These policies have not filtered down to land owners and managers, nor have they resulted in a redirection of government resources. Thus, large areas remain subject to unsustainable use. It is necessary that the true value of woodlands be determined and acknowledged as a stimulus to government agencies, the private sector and local users to use this valuable resource sustainably.
- Full Text:
- Date Issued: 2001
Fuel wood use in South Africa: Where to in the 21st Century?
- Williams, Anthony, Shackleton, Charlie M
- Authors: Williams, Anthony , Shackleton, Charlie M
- Date: 2002
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/183026 , vital:43905 , xlink:href="https://doi.org/10.1080/20702620.2002.10434611"
- Description: South Africa is well known for the dichotomous nature of its economy, with its juxtaposed first and third world characteristics, perhaps nowhere more starkly evident than in the energy sector. South Africa produces and consumes over 60% of the total electrical energy on the African continent, and is ranked twelfth in the world in terms of carbon emissions (EIA, 2002). Yet the majority of the South African population does not have access to electricity, and despite the enormous strides taken since 1994 to increase household access to electricity (NER, 2001), newly electrified households, more often than not, cannot afford the appliances nor the monthly costs required to significantly improve their quality of life (White et al., 1997). Thus, most rural and many peri-urban households continue to use fuelwood as their primary energy source (Griffin et al., 1992; Dyer, 1996; Kotze, 1996; Williams et al., 1996). Fuelwood use presents both opportunities and risks.
- Full Text:
- Date Issued: 2002
- Authors: Williams, Anthony , Shackleton, Charlie M
- Date: 2002
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/183026 , vital:43905 , xlink:href="https://doi.org/10.1080/20702620.2002.10434611"
- Description: South Africa is well known for the dichotomous nature of its economy, with its juxtaposed first and third world characteristics, perhaps nowhere more starkly evident than in the energy sector. South Africa produces and consumes over 60% of the total electrical energy on the African continent, and is ranked twelfth in the world in terms of carbon emissions (EIA, 2002). Yet the majority of the South African population does not have access to electricity, and despite the enormous strides taken since 1994 to increase household access to electricity (NER, 2001), newly electrified households, more often than not, cannot afford the appliances nor the monthly costs required to significantly improve their quality of life (White et al., 1997). Thus, most rural and many peri-urban households continue to use fuelwood as their primary energy source (Griffin et al., 1992; Dyer, 1996; Kotze, 1996; Williams et al., 1996). Fuelwood use presents both opportunities and risks.
- Full Text:
- Date Issued: 2002
Interaction of sulfur dioxide and cyanide with cobalt (II) tetrasulfophthalocyanine in aqueous media
- Thamae, Mamothibe, Nyokong, Tebello
- Authors: Thamae, Mamothibe , Nyokong, Tebello
- Date: 2002
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/289595 , vital:56652 , xlink:href="https://doi.org/10.1016/S0277-5387(01)00968-8"
- Description: Kinetic and equilibrium studies for the coordination of cyanide or sulfur dioxide to the cobalt(II) tetrasulfophthalocyanine ([CoTSPc]4−) complex are reported. The equilibrium constant for the coordination of the cyanide under pH 11 conditions and an oxygen atmosphere, and the formation of [(CN−)2Co(III)TSPc]5− species, was found to be 2.1×101 dm3 mol−1 and the rate constant, kf was found to be 7.4 dm3 mol−1 s−1. Similarly, the coordination of SO2 to [CoTSPc]4− occurred with an equilibrium constant of 8.7×101 dm3 mol−1 and a rate constant of 2.1×102 dm3 mol−1 s−1, at pH 11. These rate and equilibrium constants represent the coordination of the second cyanide or sulfur dioxide ligands to the [CoTSPc]4− species. Coordination of the first ligand occurred faster than that of the second ligand in both cases. The coordination is accompanied by the oxidation of the central Co(II) metal with the formation of a Co(III) tetrasulfophthalocyanine species.
- Full Text:
- Date Issued: 2002
Interaction of sulfur dioxide and cyanide with cobalt (II) tetrasulfophthalocyanine in aqueous media
- Authors: Thamae, Mamothibe , Nyokong, Tebello
- Date: 2002
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/289595 , vital:56652 , xlink:href="https://doi.org/10.1016/S0277-5387(01)00968-8"
- Description: Kinetic and equilibrium studies for the coordination of cyanide or sulfur dioxide to the cobalt(II) tetrasulfophthalocyanine ([CoTSPc]4−) complex are reported. The equilibrium constant for the coordination of the cyanide under pH 11 conditions and an oxygen atmosphere, and the formation of [(CN−)2Co(III)TSPc]5− species, was found to be 2.1×101 dm3 mol−1 and the rate constant, kf was found to be 7.4 dm3 mol−1 s−1. Similarly, the coordination of SO2 to [CoTSPc]4− occurred with an equilibrium constant of 8.7×101 dm3 mol−1 and a rate constant of 2.1×102 dm3 mol−1 s−1, at pH 11. These rate and equilibrium constants represent the coordination of the second cyanide or sulfur dioxide ligands to the [CoTSPc]4− species. Coordination of the first ligand occurred faster than that of the second ligand in both cases. The coordination is accompanied by the oxidation of the central Co(II) metal with the formation of a Co(III) tetrasulfophthalocyanine species.
- Full Text:
- Date Issued: 2002
Electrochemical behavior and detection of dopamine and ascorbic acid at an iron (II) tetrasulfophthalocyanine modified carbon paste microelectrode
- Oni, Joshua, Westbroek, Philippe, Nyokong, Tebello
- Authors: Oni, Joshua , Westbroek, Philippe , Nyokong, Tebello
- Date: 2003
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/290279 , vital:56735 , xlink:href="https://doi.org/10.1002/elan.200390104"
- Description: In this article the electrocatalytic behavior of an iron(II)tetrasulfophthalocyanine modified carbon paste microelectrode for the oxidation of dopamine (DA) and ascorbic acid (AA) is described. Although the oxidation potential of ascorbic acid is shifted by over 100 mV to more positive potentials, no peak separation could be obtained. This can be explained by the immediate homogeneous reduction of the oxidation product of dopamine by ascorbic acid in solution. However, this reaction induces a shift of the half-wave potential as a function of ratio of concentration of dopamine to ascorbic acid (cDA/cAA). Therefore it was possible to determine the cAA and cDA from this potential shift and the experimental peak current. Detection limits of 4.5±0.2×10−7 and 7.5±0.5×10−7 mol L−1 were obtained respectively for dopamine and ascorbic acid for cDA/cAA>0.01.
- Full Text:
- Date Issued: 2003
- Authors: Oni, Joshua , Westbroek, Philippe , Nyokong, Tebello
- Date: 2003
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/290279 , vital:56735 , xlink:href="https://doi.org/10.1002/elan.200390104"
- Description: In this article the electrocatalytic behavior of an iron(II)tetrasulfophthalocyanine modified carbon paste microelectrode for the oxidation of dopamine (DA) and ascorbic acid (AA) is described. Although the oxidation potential of ascorbic acid is shifted by over 100 mV to more positive potentials, no peak separation could be obtained. This can be explained by the immediate homogeneous reduction of the oxidation product of dopamine by ascorbic acid in solution. However, this reaction induces a shift of the half-wave potential as a function of ratio of concentration of dopamine to ascorbic acid (cDA/cAA). Therefore it was possible to determine the cAA and cDA from this potential shift and the experimental peak current. Detection limits of 4.5±0.2×10−7 and 7.5±0.5×10−7 mol L−1 were obtained respectively for dopamine and ascorbic acid for cDA/cAA>0.01.
- Full Text:
- Date Issued: 2003
Fuelwood availability and use in the Richtersveld National Park, South Africa
- Shackleton, Charlie M, Guthrie, G, Keirungi, J, Stewart, J
- Authors: Shackleton, Charlie M , Guthrie, G , Keirungi, J , Stewart, J
- Date: 2003
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/181461 , vital:43736 , xlink:href=" https://doi.org/10.4102/koedoe.v46i2.66"
- Description: Concern has been voiced about the possible over-use of fuelwood from the riparian fringe by pastoralist herders in the Richtersveld National Park (RNP). This coincided with the current examination and modelling of the supply and use of ecosystem goods and services in the Gariep Basin as part of the Southern African Millennium Assessment (SAfMA). This paper reports on a study to index the current availability of deadwood within the riparian zone of RNP, its relationship with proximity to human habitation, and species preferences of the local herders. Deadwood availability was assessed per woody species and on the ground in 12 transects within the riparian fringe. Herders were interviewed regarding their species preferences, and the composition of woodpiles was examined. There was no relationship between the percentage of attached deadwood on the tree, or the percentage deadwood ground cover, and the distance from herder stockposts. Euclea pseudobenus and Tamarix usneoides were the dominant species in the riparian fringe. There was strong selection for Ziziphus mucronata as a fuelwood species and only marginal or random selection for E. pseudobenus. Tamarix usneoides and Prosopis sp. were abundant in the riparian zone, but were not used for fuelwood. There was a significant difference between species with respect to the mean proportion of the stem that was dead, the highest being Z. mucronata (± 28 % deadwood), followed by T. usneoides (± 12 %). Most of the Prosopis trees had no deadwood. Across all species, the mean percentage dead per tree was approximately 15 %. Additionally, detached deadwood covered just less than 9 % of ground area, averaged across all plots and transects. All the variables measured indicated that there seems to be little need for concern over the current fuelwood extraction activities of pastoralists within the RNP. There was no clear evidence of cutting of branches or deadwood. The abundance of both attached and detached deadwood was not depleted close to human habitation. There was still abundant deadwood, even on preferred species. The most preferred species (Ziziphus mucronata) had the greatest mean proportion of deadwood. The herders stated that they only used deadwood, and that there was plenty. They rarely used driftwood washed down the river, although there was an abundance of it. Thus, overall, there was no sign of depletion of the deadwood resource, even on favoured species, or degradation of the productive capacity for deadwood.
- Full Text:
- Date Issued: 2003
- Authors: Shackleton, Charlie M , Guthrie, G , Keirungi, J , Stewart, J
- Date: 2003
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/181461 , vital:43736 , xlink:href=" https://doi.org/10.4102/koedoe.v46i2.66"
- Description: Concern has been voiced about the possible over-use of fuelwood from the riparian fringe by pastoralist herders in the Richtersveld National Park (RNP). This coincided with the current examination and modelling of the supply and use of ecosystem goods and services in the Gariep Basin as part of the Southern African Millennium Assessment (SAfMA). This paper reports on a study to index the current availability of deadwood within the riparian zone of RNP, its relationship with proximity to human habitation, and species preferences of the local herders. Deadwood availability was assessed per woody species and on the ground in 12 transects within the riparian fringe. Herders were interviewed regarding their species preferences, and the composition of woodpiles was examined. There was no relationship between the percentage of attached deadwood on the tree, or the percentage deadwood ground cover, and the distance from herder stockposts. Euclea pseudobenus and Tamarix usneoides were the dominant species in the riparian fringe. There was strong selection for Ziziphus mucronata as a fuelwood species and only marginal or random selection for E. pseudobenus. Tamarix usneoides and Prosopis sp. were abundant in the riparian zone, but were not used for fuelwood. There was a significant difference between species with respect to the mean proportion of the stem that was dead, the highest being Z. mucronata (± 28 % deadwood), followed by T. usneoides (± 12 %). Most of the Prosopis trees had no deadwood. Across all species, the mean percentage dead per tree was approximately 15 %. Additionally, detached deadwood covered just less than 9 % of ground area, averaged across all plots and transects. All the variables measured indicated that there seems to be little need for concern over the current fuelwood extraction activities of pastoralists within the RNP. There was no clear evidence of cutting of branches or deadwood. The abundance of both attached and detached deadwood was not depleted close to human habitation. There was still abundant deadwood, even on preferred species. The most preferred species (Ziziphus mucronata) had the greatest mean proportion of deadwood. The herders stated that they only used deadwood, and that there was plenty. They rarely used driftwood washed down the river, although there was an abundance of it. Thus, overall, there was no sign of depletion of the deadwood resource, even on favoured species, or degradation of the productive capacity for deadwood.
- Full Text:
- Date Issued: 2003