673 research outputs found

    The Occurrence of Insects and Fungi, and Aflatoxin B Contamination of Stored Sorghum in Demak and Wonogiri Regencies, Central Java

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    The objectives of this study were to collect informations on the method of postharvesthandling of sorghum and to investigate the moisture contents, insects infestation, fungalinfection, and aflatoxin B contents of stored sorghum grains collected from various stagesof the delivery chain in Demak and Wonogiri regencies, Central Java. In Demak regencysorghum cultivation was monoculture, variety cultivated was UPC-S1. In Wonogiri regencysorghum cultivation was intercropping with secondary crop and cassava. Sorghum varietiescultivated were Kawali, Numbu, ZH30, Mandau and Hibrida hybrids. There was a differencebetween the method of postharvest handling of sorghum at farmer and collector levels inDemak andWonogiri regencies. In general the method of postharvest handling of sorghum inDemak regency was more appropriate and more advance compared to that in Wonogiriregency. The moisture contents of sorghum at farmer as well as at collector level in Demakregency (13.0%) and Wonogiri regency (12.9%) were still lower that that of normal (safe)moisture content of sorghum. The number of insect species associated with sorghum invarious distribution level in Demak andWonogiri regencies was 10 and 17 species, respectively.The dominant insects species were and . The number offungal species found in sorghum at various distribution level in Demak andWonogiri regencieswas 23 species, respectively. In general, the dominant fungal species were ,and . In Demak regency aflatoxin B contents of sorghum atfarmer and collector levels were 22.50 and 15.45 ppb, respectively, while in Wonogiri regency2.27 and 10.28 ppb, respectively.insects, fungi, aflatoxin B , stored sorghum, Demak and Wonogiri regencies,Central Jav

    Dietary Exposure Assessment for Aflatoxin B From Processed Peanut Products in Municipality of Bogor 1

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    A research on dietary exposure assessment for aflatoxin B (AFB1) fromprocessed peanutproducts in Municipality of Bogor was carried out. The objectives of this study were todetermine the contents of AFB1 in processed peanut products at retail levels, and to obtaininformation whether there is a risk to public health caused by the consumption of processedpeanut products contaminated by AFB1. Survey of processed peanut product consumptionwas carried out by interviewing each respondent using a questionnaire of weekly processedpeanut product consumption. Sampling of processed peanut products was conducted at thelocations where the respondents obtained processed peanut products. The number of roastedpeanuts with skin pods, flour-coated peanuts and or sauces samples was 33,respectively, while the number of and sauces samples was 18 and 12, respectively.The total number of processed peanut product sampleswas 129.AFB1contentwas determinedusingThin LayerChromatographymethod.Estimation of the dietary exposure assessmentwasdetermined using the actual survey data consisting of AFB1 content, consumption data andbody weight. The highest contaminated sample percentage and mean of AFB1 content wasfound in roasted peanuts with skin pods i.e. 42% of 33 samples and 43.2 μg/kg, respectively,followed by flour-coated peanuts (30% of 33 samples and 34.3 μg/kg), and or(21%of 33 samples and 17.1 μg/kg).Mean of estimated dietary exposure for AFB1 found inchildren was 15.2 ng kg bw day and 95 percentile exposure was 38.9 ng kg bw day , while inadults 9.0 ng kg bw day and 95 percentile exposure was 27.0 ng kg bw day . The excesscancer risk of AFB1 exposure in Bogor fromthis study on children and adults was calculated as193 and 115 cancers/year, respectively-1 -1 th -1 -1-1 -1 th -1 -1pecel gado-gadosiomay sataipecel gado-gado1

    The Occurrence of Insects, Fungi and Organoleptic Characteristics in Stored Coffee Beans in Lampung

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    A survey on postharvest handling and technology processing of coffee beans at farmer, trader and exporter levels was conducted in West Lampung and Tanggamus regencies of Lampung province during harvest time (July 1998). Interviews and sampling of coffee beans were carried out during the survey. The number of respondents at farmer, trader and exporter levels was 22, 20 and 4, respectively, while the number of samples collected from each level was 20. All samples were analyzed for moisture content, physical quality, insect and fungal infestation, reducing sugar content, and coffee cupping. The results of the interviews indicated that postharvest handling and technology processing became better from farmers to exporters. Moisture contents of coffee beans collected from farmers and traders were higher than the tolerable limit recommended by SNI (13%). Physical quality of coffee beans collected from exporters was higher than that collected from farmers and traders. Insects were found on coffee beans collected from farmers, traders and exporters, but the number of species and the percentage of samples infested by insects from each level were relatively low. The predominant species was Liposcelis entomophila. The number of fungal species on coffee beans collected from farmers was higher than that collected from traders and exporters. The predominant species at the three levels was Aspergillus Niger, but the lowest percentage of beans infected by this fungus was found on coffee beans collected from exporters. The lowest percentage of samples infected by all fungi was also found on coffee beans collected from exporters. Reducing sugar content of coffee beans collected from exporters was lower than that from farmers and traders. Aroma and flavor values tended to increase from farmers through traders to exporters, while the body decreased. Some off-flavors (i.e. earthy, mouldy, fermented and woody) were encountered in a few coffee samples from farmers as well as from traders. There was no off-flavor encountered in the coffee samples from exporters

    Aspergillus Flavus Population and Aflatoxin B1 Content of Processed Peanut Products in Municipality of Bogor, West Java, Indonesia

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    The objectives of this study were to get informations on the population of A. flavus and aflatoxin B1 content of five processed peanut products collected from retailers in Kecamatan Bogor Tengah (Subdistrict of Central Bogor), Municipality of Bogor. A total of 129 samples of processed peanut products was collected. They consisted of roasted peanuts with skin pods (33 samples), flour-coated peanuts (33), siomay sauce (18), pecel/gado-gado sauce (33) and satai sauce (12). A sample each of 2 000 g roasted peanuts with skin pods as well as flour-coated peanuts, and a sample each of 1 500 g siomay sauce, pecel/gado-gado sauce as well as satai sauce was mixed homogenously. It was then divided two times manually to obtain working samples to determine A. flavus population, AFB1 content and a reserve sample. Peanut kernels of roasted peanuts with skin pods and flour-coated peanuts were obtained by peeling their skin pods and the batter coat of tapioca flour manually, respectively. Aspergillus flavus in peanut processed products was isolated using a serial dilution method, followed by pour plate method on Aspergillus Flavus and Parasiticus Agar (AFPA). AFB1 content was determined using Thin Layer Chromatography method. Two replicates were used for each sample. The results showed that the population of A. flavus in roasted peanuts with skin pods, flour-coated peanuts, siomay sauce, pecel/gado-gado sauce and satai sauce were 0.3, 0.1, 0.3, 13.2 and 0.4 cfu/g (wet basis), respectively. The highest AFB1 content of processed peanut products (43.2 ppb) was found in roasted peanuts with skin pods, followed by flour-coated peanuts (34.3 ppb), satai sauce (23.2 ppb), pecel/gado-gado sauce (17.1 ppb) and siomay sauce (4.4 ppb)

    Fungal Infection in Stored Arabica Coffee (Coffea Arabica) Beans at Various Stages of the Delivery Chain in South Sulawesi Province

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    Indonesia has retained its status as the world\u27s fourth largest coffee producer after Brazil, Vietnam and Columbia, in which one of its well-known coffee is originated from Toraja region, South Sulawesi. Because of this, Indonesia has to compete with these countries in producing good quality coffee beans. The objectives of this research were (a) to obtain information on the postharvest handling methods of Arabica coffee (C. arabica) beans in Tana Toraja and North Toraja Regencies, and Makassar Municipality, and (b) to investigate the occurrence of fungi (including ochratoxin A producing fungi) in stored Arabica coffee beans collected from various stages of the delivery chain. Methods used in this study included surveys, interviews and sample collections in each level of delivery chain, which were conducted in May and July 2016. The moisture content and physical quality of the beans were also measured to determine the quality of the beans. The total number of coffee bean samples was 64, consisting of 27 samples from farmers, 15 samples from collectors, 13 samples from traders, and 9 samples from exporters. The results showed that the moisture content of coffee beans collected from farmers and collectors was higher than the maximum tolerable limit determined by SNI (13%), while the moisture content of beans collected from traders and exporters were lower. Based on the total defective value, coffee beans collected from farmers had more diverse grades than those at other levels. Penicillium citrinum was the dominat fungus found in coffee beans collected from farmers, collectors and traders, while Aspergillus Niger was the dominant fungus found in coffee beans collected from exporters. At trader level, 46% of the samples was infected by Aspergillus ochraceus and A. Niger, which are known as OTA-producing fungi. At exporter level, 44% of the samples was infected by A. ochraceus, while 78% of the samples was infected by A. Niger. The postharvest handling methods of Arabica coffee beans conducted especially by farmers and collectors should be improved to minimize moisture content and to increase quality grade of coffee beans

    Keanekaragaman Serangga Hama Pala (Myristica Fragrans) dan Tingkat Kerusakannya di Penyimpanan

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    Pest attack in nutmeg is a cause of major damage both in the field and in storage. Information on the diversity of pest insects in storage, harvesting methods, and good drying needs to be known to reduce the level of damage to nutmeg. This study aims to determine the diversity of insect pests and the percentage of nutmeg damage due to various postharvest treatments. Nutmeg was packed in jute bag and stored for four months under warehouse conditions. Each jute bag containing nutmeg is treated based on the origin of nutmeg (picked from a tree or picked up on the ground), drying method (sunshine or fogging), and shell or without shells with each treatment replicated three times. Sampling of numtag was conducted after four month to calculate the number of each insect species found, determine the insect population, and determine the percentage of damaged seeds. Four insect species were found in nutmeg kernels in almost various treatments. They were Araecerus fasciculatus ((Degeer) (Coleoptera: Anthribidae), Carpophilus dimidiatus (Fabricius) (Coleoptera: Nitidulidae), Oryzaephilus Surinamensis (Linnaeus) (Coleoptera: Silvanidae), and Tribolium castaneum (Herbst) (Coleoptera: Tenebrionidae). The dominant species was A. fasciculatus. The percentage of damaged kernels derived from nutmeg kernels fallen on the ground, dried either using sun-drying or smoke-drying, either in-shell or without shell, were higher than the kernels derived from ripe fruitswith various treatments. The recommendation of this research result is good postharvest handling of nutmeg to prevent insect infestation should be conducted by collecting nutmeg derived from ripe fruits picked from the trees, nutmeg in-shell either sun-dried or smoke-dried, and storing nutmeg in-shell

    The effect of heat stress on the oxidative status of red hybrid tilapia (Oreochromis sp.) infected with Streptococcus Agalactiae

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    A commercial red hybrid tilapia was experimented with S. agalactiae infection under influences of heat stress which indicated by plasma malondialdehyde (MDA) and erythrocyte superoxide dismutase (SOD) as biomarkers of stress. To achieve these objectives, 110 red hybrid tilapia in good health were divided into five groups of 22 fish each. Group A was challenged with 2.3 109 CFU of S. agalactiae and exposed to heat stress at 33 ± 0.5C on day 1. Group B was challenged on day 1 as in Group A but heat stress was introduced on day 7 post challenge (pc). Group C was exposed to heat stress on day 1 and challenged on day 7 pc while groups D and E served as a positive and negative controls respectively. Blood samples were collected at days 0, 3, 7, 10 and 14 for MDA and SOD analysis. Groups A and B recorded high mortality following exposure to heat stress and bacteria inoculation, with group A reaching 100% mortality at day 7 post inoculation. Overall, Groups A, B, C and Group D showed pattern of increase in MDA level as early as day 3 and decrease pattern for SOD activity. Group E did not show any significant difference in MDA level throughout the study period. Clinical signs such as erratic swimming, exopthalmia, skin haemorrhage and cloudy eye were predominantly observed in group A 24 h post inoculation. Based on the findings of this study, it was concluded that heat stress plays crucial role in the pathogenesis of S. agalactiae, via alteration of the oxidant defence system
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