Direct-use value of smallholder crop production in a semi-arid rural South African village
- Authors: Dovie, Delali B K , Witkowski, Ed T F , Shackleton, Charlie M
- Date: 2003
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/181595 , vital:43750 , xlink:href="https://doi.org/10.1016/S0308-521X(02)00124-5"
- Description: The monetary value of natural resources used by rural communities for subsistence is important when addressing issues affecting the livelihoods of impoverished rural households. There is therefore the need to attribute monetary values to non-marketed products from smallholder production systems in order to reliably account for resource availability and usage to further sound policy decisions. The objective of this paper is to present an empirical analysis of the direct-use and traded values of crop production by households, and to discuss the implications for policy development. The study was undertaken in combination with an evaluation of other livelihood sectors in Thorndale, a semi-arid rural village in the Limpopo province of South Africa. The net direct-use value of crops was estimated at $443.4 per household per annum across the village. Maize (Zea mays), watermelon (Citrullus, vulgaris), peanuts (Arachis hypogaea) and common beans (Phaseolus vulgaris) contributed over 90% to the total direct-use value of crops. Maize alone contributed 40% of this value per household at an estimated $652/ha. Marketing of resources was not a common practice, limited to only maize and peanuts. Farming was basically a rain-fed–mixed cropping system with low production inputs. Farmer support services, human capital development and tenure security were major areas identified for policy development.
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- Date Issued: 2003
Electrochemical behavior and detection of dopamine and ascorbic acid at an iron (II) tetrasulfophthalocyanine modified carbon paste microelectrode
- 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.
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- Date Issued: 2003
Electrochemical behaviour of thiol-derivatised zinc (II) phthalocyanine complexes and their self-immobilised films at gold electrodes
- Authors: Ozoemena, Kenneth I , Nyokong, Tebello
- Date: 2003
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/290295 , vital:56737 , xlink:href="https://doi.org/10.1016/j.microc.2003.08.002"
- Description: Electrochemical properties of novel, peripherally substituted zinc phthalocyanine complex, octa(4-methylphenylthio-) phthalocyaninatozinc(II) [ZnPc(SC6H4CH3)8] (1a) in DMF solution are presented. This complex showed five quasi-reversible/reversible, diffusion-controlled redox couples. Solution voltammetry of 1a showed little contrast with that of its alkythiol-derivative, octabutylthiophthalocyaninatozinc(II) [ZnPc(SC4H9)8] (1b) in that both thiol-substituents tend to show electron-withdrawing influence on the phthalocyanine ligands; complex 1a showing easier reduction and more difficult to oxidation when compared to 1b and other alkyl derivatives. The voltammetric features of the solid ultrathin films of 1a and 1b, immobilized on gold electrodes via the self-assembling technique, are also presented. Interestingly, the self-assembled films are stable and reproducible and provide good suppression to the following Faradaic processes; gold surface oxidation, solution ion species and underpotential deposition (UPD) of copper.
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- Date Issued: 2003
Phthalocyanines and related complexes as electrocatalysts for the detection of nitric oxide
- Authors: Nyokong, Tebello , Vilakazi, Sibulelo
- Date: 2003
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/290346 , vital:56741 , xlink:href="https://doi.org/10.1016/S0039-9140(03)00356-4"
- Description: Metallophthalocyanine (MPc) and metalloporphyrin complexes as well as some metalloproteins including myoglobin, hemoglobin, cyanocobalamin and cytochrome c catalyse the detection of nitric oxide (NO). The catalytic process often involve changes in the oxidation state of the catalyst. These complexes catalyse both the reduction and oxidation of NO. MPc complexes containing electroactive central metals such as CoPc and FePc generally show better catalytic activity towards the detection of NO than complexes containing electroinacive central metals. However, the involvement of ring based redox processes was confirmed for the homogenous NO catalysis using CoPc.
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- Date Issued: 2003
Synthesis, spectroscopy and photochemistry of octasubstituted thiol-derivatized phthalocyaninatozinc (II) complexes
- Authors: Ozoemena, Kenneth I , Nyokong, Tebello
- Date: 2003
- Subjects: To be catalogued
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/290401 , vital:56746 , xlink:href="https://doi.org/10.1016/S1387-7003(03)00218-1"
- Description: Synthesis, spectroscopic and photochemical characterization of phenylthiol-derivatized zinc phthalocyanine complex: 2,3,9,10,16,17,23,24-octa(4-methylphenylthio-)phthalocyaninatozinc(II) [ZnPc(SC6H4CH3)8] (3a) and its alkanethiol derivative, 2,3,9,10,16,17,23,24-octabutylthiophthalocyaninatozinc(II) [ZnPc(SC4H9)8] (3b) are described. Spectroscopic analyses show that 3a has a higher aggregation tendency than 3b in organic solvents. Photochemical studies indicate that 3b is more photostable and more efficient at singlet oxygen generation than 3a.
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- Date Issued: 2003