68 research outputs found
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Digitally: Piloting offline payments for phones
Mobile payments support a range of services in many less developed countries including everyday payments, migrant remittances, credit, tax collection, and welfare benefits. These services depend entirely on the mobile phone network as their carrier, so they stop where the network does. This leaves millions of the very poorest people stranded - people living in remote areas where there is little to no network service. It also leaves urban users at the mercy of network congestion. We developed a prototype system, DigiTally, which lets users make offline payments by copying short strings of digits from one mobile handset to another. Offline payments are already used for electricity (both in prepayment meters and pay-as-you-go solar); can we extend them into a general-purpose payment system, to increase service resilience in the face of network congestion or outage, and provide service to currently excluded areas? We report the results of a preliminary study with an early prototype of DigiTally, tested on participants from a university in Nairobi (Kenya). The code-sharing process presented a possible usability challenge. To explore this and other aspects of an early prototype, DigiTally was introduced to Kenyan participants in order to resolve any major issues before a later field trial. We discuss the lessons learned from our field visits and initial evaluation; we hope that this contribution is helpful for researchers and policy makers interested in mobile payments and financial inclusion. We also present our findings and observations. We found that, although offline payments involve copying codes in both directions between the payer's phone and the payee's, the extra workload was acceptable to most users.This work was supported by a grant from the Bill & Melinda Gates Foundatio
Changes in fungal population and aflatoxin levels and assessment of major aflatoxin types in stored peanuts (Arachis hypogaea Linnaeus)
Peanut kernels of Homabay Local, Valencia Red, ICGV-SM 12991 and ICGV-SM 99568 cultivars were storedfor six months in jute, polypropylene and polyethylene bags to assess the effect of storage bags, temperature andR.H. on fungal population and aflatoxin contamination. Moisture content (M.C.), fungal population and aflatoxinlevels were determined before storage and after every 30 days during storage. Isolates of Aspergillus flavus andA. parasiticus were assayed for production of aflatoxin B1, B2, G1 and G2. The correlation between MC,population of A. flavus and A. parasiticus and aflatoxin levels in peanuts was also determined. Six fungalpathogens were commonly isolated from the peanut samples and occurred as follows in decreasing order:Penicillium spp. (106.6 CFU/g), A. flavus L-strain (4.8 CFU/g), A. flavus S-strain (2.9 CFU/g), A. niger (2.6CFU/g), A. parasiticus (1.7 CFU/g) and A. tamarii (0.2 CFU/g). The overall population of A. flavus L-strain was66% higher than that of A. flavus S-strain. Ninety one percent of A. flavus and A. parasiticus isolates produced atleast one of the four aflatoxin types assayed, with 36% producing aflatoxin B1. Total aflatoxin levels rangedfrom 0 - 47.8 μg/kg with samples stored in polyethylene and jute bags being the most and least contaminated,respectively. Eighty nine percent and 97% of the peanut samples met the EU (≤ 4 μg/kg) and Kenyan (≤ 10μg/kg) regulatory standards for total aflatoxin, respectively. Peanuts should be adequately dried to safe moisturelevel and immediately packaged in a container - preferably jute bags - which will not promote critical increasesin fungal population and aflatoxin contamination
Occurrence of Aspergillus species and aflatoxin contamination in raw and roasted peanuts from formal and informal markets in Eldoret and Kericho towns, Kenya
Published Online: August 2013.The population and diversity of fungal species and levels of aflatoxin contamination were investigated in 228 marketed peanut samples; 140 from formal and 88 from informal markets, in Kericho and Eldoret towns of Kenya. Ground pea- nut samples were cultured on Modified Dichloran Rose Bengal (MDRB) agar while aflatoxin level was quantified based on indirect competitive ELISA. Correlation between the incidence of major aflatoxin-producing fungal species and aflatoxin levels was also established. Fungal species commonly isolated from the peanut samples included Asper-gillus flavus L strain, A. flavus S strain, A. parasiticus, A. tamarii, A. caelatus, A. alliaceus (all of Aspergillus section Flavi) and A. niger. Fungi isolated in low frequency included Fusarium spp., Penicillium spp., Mucor spp. and Rhi- zopus spp. Aflatoxin levels in peanut products ranged from 0 to 2345 μg/kg in raw peanuts, 0 to 382 μg/kg in roasted coated peanuts, and 0 to 201 μg/kg in roasted de-coated peanuts. Overall, levels of total aflatoxin were higher in sam- ples from informal (mean = 97.1 μg/kg) than formal (mean = 55.5 μg/kg) market outlets. There was a positive and sig- nificant correlation (R2 = 0.63; p ≤ 0.05) between aflatoxin levels and the major aflatoxin producing fungi in raw pea- nuts from formal markets in Eldoret town. Additionally, total aflatoxin in raw peanut samples from informal markets in Kericho was positively and significantly correlated (R2 = 0.81; p ≤ 0.05) to the population of A. flavus (L and S strains). In roasted coated peanuts sampled from formal market outlets in Eldoret, aflatoxin levels correlated positively and sig- nificantly (R2 = 0.37; p ≤ 0.05) with A. flavus S strain. There is need to create awareness among peanut traders and con- sumers on proper handling of peanuts and health risks associated with consumption of unsafe peanut products
Science-based decision support for formulating crop fertilizer recommendations in sub-Saharan Africa
Open Access Article; Published online: 31 Jan 2020In sub-Saharan Africa, there is considerable spatial and temporal variability in relations between nutrient application and crop yield, due to varying inherent soil nutrients supply, soil moisture, crop management and germplasm. This variability affects fertilizer use efficiency and crop productivity. Therefore, development of decision systems that support formulation and delivery of site-specific fertilizer recommendations is important for increased crop yield and environmental protection. Nutrient Expert (NE) is a computer-based decision support system, which enables extension advisers to generate field- or area-specific fertilizer recommendations based on yield response to fertilizer and nutrient use efficiency. We calibrated NE for major maize agroecological zones in Nigeria, Ethiopia and Tanzania, with data generated from 735 on-farm nutrient omission trials conducted between 2015 and 2017. Between 2016 and 2018, 368 NE performance trials were conducted across the three countries in which recommendations generated with NE were evaluated relative to soil-test based recommendations, the current blanket fertilizer recommendations and a control with no fertilizer applied. Although maize yield response to fertilizer differed with geographic location; on average, maize yield response to nitrogen (N), phosphorus (P) and potassium (K) were respectively 2.4, 1.6 and 0.2 t ha−1 in Nigeria, 2.3, 0.9 and 0.2 t ha−1 in Ethiopia, and 1.5, 0.8 and 0.2 t ha−1 in Tanzania. Secondary and micronutrients increased maize yield only in specific areas in each country. Agronomic use efficiencies of N were 18, 22 and 13 kg grain kg−1 N, on average, in Nigeria, Ethiopia and Tanzania, respectively. In Nigeria, NE recommended lower amounts of P by 9 and 11 kg ha−1 and K by 24 and 38 kg ha−1 than soil-test based and regional fertilizer recommendations, respectively. Yet maize yield (4 t ha−1) was similar among the three methods. Agronomic use efficiencies of P and K (300 and 250 kg kg−1, respectively) were higher with NE than with the blanket recommendation (150 and 70 kg kg−1). In Ethiopia, NE and soil-test based respectively recommended lower amounts of P by 8 and 19 kg ha−1 than the blanket recommendations, but maize yield (6 t ha−1) was similar among the three methods. Overall, fertilizer recommendations generated with NE maintained high maize yield, but at a lower fertilizer input cost than conventional methods. NE was effective as a simple and cost-effective decision support tool for fine-tuning fertilizer recommendations to farm-specific conditions and offers an alternative to soil testing, which is hardly available to most smallholder farmers
Potential of Grain Legume Fallows to Address Food Insecurity and Boost Household Incomes in Western Kenya
A pigeonpea fallow-maize crop rotation trial was carried out over a period of 4 seasons in western
Kenya. The trial compared six high altitude long duration pigeonpea varieties i.e. ICEAP 00020,
ICEAP 00040, ICEAP 00048, ICEAP 00053, ICP 9145 and ICP 13076 and a medium duration
variety i.e. ICP 13211 for productivity, post fallow maize crop yield and financial returns
indicators. Long duration pigeonpea varieties take 140-180 days to mature while medium duration
varieties take >200 days to mature. Continuous maize cropping acted as a control. Depending on
the variety, pigeonpea grain yield ranged between 1.3 and 1.9 t ha-1. Post fallow maize grain yield
from each of pigeonpea variety plot was approximately 3 fold higher than yield from continuous
maize plots. The medium duration pigeonpea plots yielded significantly higher maize grain than
the long duration (ICEAP 00053, ICEAP 00040) pigeonpea variety plots. Relative to the control,
incremental returns to land were highest for medium duration pigeonpea fallow plots (619
USD ha-1) and lowest for ICEAP 00040 fallow plots (305 USD ha-1). We estimated that by
selecting an appropriate pigeonpea variety for a fallow-maize rotation system, a household could
produce sufficient food for consumption and remain with a surplus of approximately 2.8 tons for
sale. For widespread adoption of pigeonpea based technologies in western Kenya, there is a need
for policy improvement on issues related to improved seed production systems, cost of fertilizers,
extension services, and market for the end products
Biological control of aflatoxins in Africa: current status and potential challenges in the face of climate change
Article purchased; in PressAflatoxin contamination of crops is frequent in warm regions across the globe, including large areas in sub-Saharan Africa. Crop contamination with these dangerous toxins transcends health, food security, and trade sectors. It cuts across the value chain, affecting farmers, traders, markets, and finally consumers. Diverse fungi within Aspergillus section Flavi contaminate crops with aflatoxins. Within these Aspergillus communities, several genotypes are not capable of producing aflatoxins (atoxigenic). Carefully selected atoxigenic genotypes in biological control (biocontrol) formulations efficiently reduce aflatoxin contamination of crops when applied prior to flowering in the field. This safe and environmentally friendly, effective technology was pioneered in the US, where well over a million acres of susceptible crops are treated annually. The technology has been improved for use in sub-Saharan Africa, where efforts are under way to develop biocontrol products, under the trade name Aflasafe, for 11 African nations. The number of participating nations is expected to increase. In parallel, state of the art technology has been developed for large-scale inexpensive manufacture of Aflasafe products under the conditions present in many African nations. Results to date indicate that all Aflasafe products, registered and under experimental use, reduce aflatoxin concentrations in treated crops by >80% in comparison to untreated crops in both field and storage conditions.
Benefits of aflatoxin biocontrol technologies are discussed along with potential challenges, including climate change, likely to be faced during the scaling-up of Aflasafe products. Lastly, we respond to several apprehensions expressed in the literature about the use of atoxigenic genotypes in biocontrol formulations. These responses relate to the following apprehensions: sorghum as carrier, distribution costs, aflatoxin-conscious markets, efficacy during drought, post-harvest benefits, risk of allergies and/or aspergillosis, influence of Aflasafe on other mycotoxins and on soil microenvironment, dynamics of Aspergillus genotypes, and recombination between atoxigenic and toxigenic genotypes in natural conditions
Fungal species isolated from peanuts in major Kenyan markets: Emphasis on Aspergillus section Flavi
A survey was conducted in Nairobi, Nyanza and Western provinces in Kenya between March and July
2009 with 1263 peanut products sampled out of which 705 samples underwent microbial analysis. The
study aimed at determining the incidence of fungal species e emphasis on Aspergillus section Flavi e
associated with peanut products. A 0.5 kg representative sample was obtained from each surveyed
vendor and the colony forming units (CFU) of fungal species determined. The samples were also analyzed
for total aflatoxin level while isolates of Aspergillus flavus and Aspergillus parasiticus were screened for
production of aflatoxin B1, B2, G1 and G2. Eight fungal species were detected in the samples and were in
decreasing order of CFU/g of sample: A. flavus S-strain (467), A. flavus L-strain (341), Penicillium spp.
(326), Aspergillus niger (156), Aspergillus tamari (27), Aspergillus alliaceus (21), A. parasiticus (10), and
Aspergillus caelatus (5). The overall incidence of A. flavus S-strain in samples from Nairobi was 92 and
1425% higher than samples from Nyanza and Western regions, respectively. The combined incidence of
A. flavus and A. parasiticus was varied significantly (p ≤ 0.05) with peanut product: peanut flour (69%),
shelled raw peanuts (53%), spoilt peanuts (49%), boiled podded peanuts (45%), podded peanuts (39%),
peanut butter (31%), fried peanuts (22%) and roasted peanuts (20%). Seventy three percent of A. flavus
and A. parasiticus isolates produced at least one of the aflatoxin types, with 66% producing aflatoxin B1.
The total aflatoxin level among peanut products ranged from 0 to 1629 mg/g; and there was a positive
correlation (r ¼ 0.2711) between the incidence of A. flavus and A. parasiticus, and total aflatoxin level. The
high incidence of aflatoxin producing fungi in peanuts traded in Kenyan markets implies a risk of aflatoxin contamination, highlighting the need for stakeholders to promote sound practices at all stages of
the peanut value chain in order to minimize market access by non-complying products
Morphological Variation in the Wild-Weedy Complex of Sorghum Bicolour In Situ in Western Kenya: Preliminary Evidence of Crop-To-Wild Gene Flow ?
Crop wild relatives are important components of agroecosystems and have over the years been exploited in
breeding programs as sources of genes for novel traits. Information on the extent and patterns of variability is
important in formulating effective conservation and utilization strategies for existing crop wild relative
populations. We conducted surveys and collections of wild and weedy accessions of Sorghum bicolor
(L.) Moench in Lambwe Valley in western Kenya in order to investigate occurrence, distribution, and
morphological variability in the wild-weedy complex of S. bicolor under local agroecological conditions. We
also attempted to understand the role, if any, of crop-to-wild gene flow in structuring variability within and
among populations. The morphological data presented here showed wide variability within wild-weedy
sorghum populations with respect to habitats and morphotypes. True wild sorghum populations in national
parks and the sugarcane belt were clearly distinguishable from the putative hybrids or intermediate forms
found in sorghum fields, in sorghum field margins, and, to some extent, by the roadside near sorghum fields.
The existence of these intermediate forms is empirical evidence of introgression between cultivated sorghum
and its wild-weedy relatives. Extensive introgression, especially within in situ conservation areas and/or in
areas of high diversity, would lead to genetic erosion and possible depletion of these important wild sorghum
genetic resources
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