Some biological and chemical characteristics of damaged corn

The predominant fungi isolated from damaged kernels of corn (maize) plated on agar media were species of Aspergillus (mainly A. glaucus) and Penicillium. Masses of spores and mycelium of Aspergillus, Penicillium, Cladosporium and Fusarium were present in the cavities of the embryo of many kernels from which no fungi grew. Some samples had a high percentage of blue-eye kernels, evidently caused mainly by A. restrictus and A. glaucus. The embryos of all damaged kernels were decayed to some extent by fungi. Weight averaged 51 · 7 lb/bu, not much below that of sound corn. Fat acidity values ranged from 90–324. No aflatoxin was found in any of the 24 samples tested.     

Factors associated with fumonisin contamination of maize in Uganda

BACKGROUND: During production and handling, maize is attacked by many Fusarium species, some of which are prolific producers of fumonisins. Contamination of maize with fumonisins is influenced by climate, agronomic and postharvest practices. This study investigated the factors associated with the occurrence of fumonisins in maize produced in three agroecological zones of Uganda. RESULTS: All the maize samples were positive for fumonisins with levels ranging from 0.27 to 10 mg kg^?1. A positive and significant correlation (P < 0.01) was observed between fumonisin levels and agroecological zone. Maize from high altitude zone had significantly higher (P < 0.05) mean total fumonisin content (4.93 mg kg^?1) than maize from the mid altitude‐moist (4.53 mg kg^?1) and mid altitude‐dry (4.50 mg kg^?1) zones. Five farmer practices, namely intercropping, crop rotation, delayed harvesting, drying maize on bare ground and planting treated seeds were significantly associated with fumonisin production in maize. Intercropping, delayed harvesting and drying maize on bare ground increased fumonisin contamination whereas crop rotation and planting treated seeds reduced the contamination. CONCLUSION: All maize samples obtained from the three agroecological zones were contaminated with fumonisins. The study showed that some of the farmers' practices predispose maize to fumonisin contamination. The findings are important for future studies aimed at designing strategies to control and prevent contamination of maize with fumonisins. Copyright © 2009 Society of Chemical Industry     

Spectral analyses of fluorescences in dent maize infected with Aspergillus flavus and Aspergillus parasiticus

Bright greenish yellow (BGYF) and blue white (BWF) fluorescences were associated with Aspergillus flavus and A. parasiticus infected maize. The fluorescences were studied spectrofluorometrically, the BGYF exhibiting a peak wave length between 480–485 nm and the BWF between 440–445 nm. Neither fluorescence varied in maize stored under different moistures and temperatures.

BWF was similar spectrally to the fluorescence of the endosperm of sound kernels but × 5 20 more intense. The spectrum of BWF was similar to Aflatoxin G₁ or a mixture of aflatoxin B₁, B₂, G₁ and G₂ when they were spotted on endosperm tissue. A color reference for BGYF was similar in peak wave length to BGYF. Amsoy soybeans without the seed coat fluoresced with a peak 470–475 nm and the intensity was low compared to BGYF in maize. A fluorescence of maize kernels visually similar to BGYF but not associated with Aspergillus infection or aflatoxin contamination was also investigated. This “false BGY” fluorescence was spectrally similar to the BGYF in infected kernels.     

Insect pests, Aspergillus flavus and aflatoxin contamination in stored wheat: A survey at North Bihar (India)

Fifty stored wheat samples (25 each of insect pest free and infested) were collected from North Bihar (India). Of the four major pests recorded, Sitophilus oryzae was the dominant insect, followed by Tribolium castaneum, Rhizopertha dominica and Trogoderma granarium. Aspergillus flavus was recorded in all samples: infection in insect-damaged samples was 87% and in insect-free samples 25%. Aflatoxin contamination was found in 19 and 2 of the insect-damaged and insect-free lots respectively. The role of insect pests in making wheat grains vulnerable to A. flavus infection and subsequent aflatoxin production is discussed.     

Aspergillus flavus infection and aflatoxin production in mixtures of high-moisture and dry maize

High-moisture (26·6–27·9% m.c.) and dry (9·8% m.c.) fractions of white and yellow maize were examined for fungal development and aflatoxin production during an 8-week incubation at 25°C. Treatment procedures included blending of either high-moisture white with dry yellow or high-moisture yellow with dry white maize fractions (average moisture in blend, 14%) and inoculation of some test maizes with A. flavus spores. At sampling time white and yellow components of maize blends were manually separated and all of the maize samples were analyzed for levels of moisture, fungal infection and aflatoxin. Moisture levels in maize blends equilibrated rapidly during the initial 2–4 days of incubation; neither dry yellow nor dry white exceeded 13% moisture during the trial period. Only a limited incidence of A. flavus was observed on uninoculated maize. but in samples treated with A. flavus spores a high infection rate developed; from 58 to 98% of the kernels in dry fractions of inoculated blends were infected with A. flavus during the trial. Aflatoxin was detected in high-moisture maize and in both high-moisture and dry fractions of inoculated maize blends. Up to 500 μg aflatoxin B₁/kg of corn was found after the 8-week incubation in a dry fraction of inoculated maize blends.     

Aspergillus flavus and aflatoxin production in acid-treated maize

Isobutyric acid (IBA) and propionic-acetic acid (PA) were applied to comparable 52.8 m³ lots of freshly harvested yellow dent maize containing 27% moisture. After 6 months storage, 30% Aspergillus flavus infection and low levels of aflatoxin were detected in adjacent bins of IBA-treated and PA-treated maize. Extensive samples were taken after 7 months from moldy spots in each bin and evaluated for aflatoxin, zearalenone, ochratoxin and microorganisms. Aspergillus flavus (10⁶ propagules/g) was detected in 40% of the PA samples, but no aflatoxin was found. Also, counts of Aspergillus fumigatus, Absidia and Penicillia were high. In addition to the molds found on PA maize, Aspergillus niger was identified on IBA-treated maize. Aspergillus flavus (10⁴–10⁷ propagules/g) was present in 79% of the IBA samples; aflatoxin (from 2 to 857 ng/g) was detected in 57%. Aflatoxin contamination varied between locations within a moldy area. Among 20 individual kernels picked at random from each location, aflatoxin contamination ranged from 150 to 21.800 ng/g in positive kernels. Evidently, bulk quantities of maize must be appraised on the basis of individual kernels because toxin-free kernels often are adjacent to highly contaminated kernels.     

Survey of mycoflora counts, aflatoxin production and induced biochemical changes in walnut kernels

Fungal infection and mycotoxin contamination in fresh and stored kernels of walnut (Juglans regia) collected from different localities of Uttaranchal (India) were investigated. Fresh samples carry a combination of field as well as storage fungi. Species of Alternaria, Aspergillus and Penicillium were predominant. Thirty-nine percent of Aspergillus flavus isolates were toxigenic and produced up to 2170 μg/l of aflatoxin B₁ in the liquid media. Aflatoxin B₁ was the most common mycotoxin encountered as a natural contaminant in the stored samples. Twenty-one percent of fresh samples contained aflatoxin B₁ in low concentrations. The concentration of aflatoxin B₁ in fresh as well as stored samples was in the range of 140–1220 μg/kg. Characteristic rotting was observed in fresh as well as stored samples. The walnut kernels exhibited significant reductions in the levels of oil, starch and protein content during fungal infection.     

The influence of storage practices on aflatoxin contamination in maize in four agroecological zones of Benin, west Africa

Aflatoxin level in 300 farmers’ stores in four agro-ecological zones in Benin, a west African coastal country, were determined over a period of 2 years. At sampling a questionnaire was used to evaluate maize storage practices. Farmers were asked what storage structure they used, their storage form, storage period, pest problems in storage and what was done against them. Beninese farmers often changed their storage structures during the storage period, transfering the maize from a drying or temporary store to a more durable one. Most of the farmers complained about insects damaging stored maize. Often, storage or cotton insecticides were utilized against these pests. Regression analysis identified those factors that were associated with increased or reduced aflatoxin.

Maize samples in the southern Guinea and Sudan savannas were associated with higher aflatoxin levels and the forest/savanna mosaic was related to lower toxin levels. Factors associated with higher aflatoxin were: storage for 3–5 months, insect damage and use of Khaya senegalensis-bark or other local plants as storage protectants. Depending on the agroecological zone, storage structures that had a higher risk of aflatoxin development were the “Ago”, the “Secco”, the “Zingo” or storing under or on top of the roof of the house. Lower aflatoxin levels were related to the use of storage or cotton insecticides, mechanical means or smoke to protect against pests or cleaning of stores before loading them with the new harvest. Fewer aflatoxins were found when maize was stored in the “Ago” made from bamboo or when bags were used as secondary storage containers.     

Fungal contamination and aflatoxin content of maize,moringa and peanut foods from rural subsistence farms in South Haiti

Mycotoxins are toxic, low molecular weight compounds produced by fungi. Among them, aflatoxins are the most carcinogenic and they mainly impact on rural communities of developing countries. The present study supplies data on mycobiota and aflatoxin contamination in the most common food products consumed in Haiti. The study concerns analyses performed on 49 samples of meals and seeds collected in South Haiti and tested for fungal occurrence and aflatoxin content by HPLC-DAD technique. The results revealed that three main fungal genera affected Haitian food products: Aspergillus spp. (Section Flavi and Nigri), followed by Penicillium spp. and Fusarium spp. Aflatoxin was present in more than half of the samples of maize (Zea mays L.) kernels (55%), maize meal (57%) and moringa (Moringa oleifera Lam.) seeds (64%), and in 25% of peanut (Arachis hypogaea L.) samples. The tested food products were mostly contaminated by aflatoxin B₁ (AFB₁) followed by aflatoxin B₂ (AFB₂), while no aflatoxins type G were detected. The total concentration of aflatoxins in the positive samples was 228 μg/kg on average, i.e., fifty-seven and eleven times higher than the maximum levels allowed in Europe and USA, respectively. Both the presence of aflatoxigenic fungi and aflatoxin contamination in maize kernels seemed to be related to agricultural practices, such as weed control, irrigation and growing cycle length. These findings suggest that the Haitian population is strongly exposed to aflatoxin risk. This risk could be reduced by exploiting simple and accessible farming strategies for minimizing mycotoxin contamination, at least for maize.     

Aflatoxin formation and gene expression in response to carbon source media shift in Aspergillus parasiticus

Aflatoxins are toxic and carcinogenic polyketide metabolites produced by fungal species, including Aspergillus flavus and A. parasiticus. The biosynthesis of aflatoxins is modulated by many environmental factors, including the availability of a carbon source. The gene expression profile of A. parasiticus was evaluated during a shift from a medium with low concentration of simple sugars, yeast extract (YE), to a similar medium with sucrose, yeast extract sucrose (YES). Gene expression and aflatoxins (B₁, B₂, G₁, and G₂) were quantified from fungal mycelia harvested pre- and post-shifting. When compared with YE media, YES caused temporary reduction of the aflatoxin levels detected at 3-h post-shifting and they remained low well past 12 h post-shift. Aflatoxin levels did not exceed the levels in YE until 24 h post-shift, at which time point a tenfold increase was observed over YE. Microarray analysis comparing the RNA samples from the 48-h YE culture to the YES samples identified a total of 2120 genes that were expressed across all experiments, including most of the aflatoxin biosynthesis genes. One-way analysis of variance (ANOVA) identified 56 genes that were expressed with significant variation across all time points. Three genes responsible for converting norsolorinic acid to averantin were identified among these significantly expressed genes. The potential involvement of these genes in the regulation of aflatoxin biosynthesis is discussed.     

Population ecology of Aspergillus flavus associated with Mississippi Delta soils

Understanding the source of Aspergillus flavus is required to manage aflatoxin contamination of maize (Zea mays L.). Studies assessed A. flavus propagules, Fusarium spp., and total fungi associated with Mississippi Delta soils. Soils from 12 and 15 sites were collected in 2000 and 2001, respectively. The propagule density of A. flavus ranged from log(10) 2.0 to 4.3 colony-forming units (cfu) g^-1 soil, while total fusaria ranged from log(10) 3.0 to 5.4 cfu g^-1 soil. The highest populations of A. flavus were associated with soils containing higher organic matter, especially in sites under a no-tillage management. The frequency of aflatoxin production in isolates ranged from 13 to 81% depending on soil. In 2001, there was a highly significant correlation between A. flavus and the history of maize cultivation. Soil fertility factors such as organic matter content, nitrate and extractable phosphorus correlated with the density of Aspergillus, Fusarium spp., and total fungi. The relationship between soil parameters and Aspergillus populations may be useful in predicting the contribution of soil microflora to aflatoxin contamination.     

Preliminary studies of the effects of heat and gamma irradiation on the production of aflatoxin B1 in static liquid culture,by Aspergillus flavus link NRRL 5906

Aflatoxin B₁ production by a strain of Aspergillus flavus NRRL 5906 was examined in static liquid culture in maize meal broth (MMB) and maize meal broth supplemented with 2% glucose and 2% peptone (AMMB). Erlenmeyer flasks were inoculated with 1.0 ml aliquots of fungal spores which had been heat-treated (60°C for 30 min) under low humidity (< 45% R.H. dry heat) or high humidity conditions (>85% R.H., moist heat) followed by gamma irradiation with either 0.0, 3.5 or 4.0 kGy. AMMB supported 6–17 times more vegetative growth (depending on the heat and dose combination) than spores incubated in MMB alone. High inoculum size of control unheated spores (log CFU/g, 6.9) yielded the least aflatoxin B₁ in flasks containing AMMB (8.2–19.3 μg/ml). A dose of 3.5 kGy reduced by 3.2–3.8 log cycles the viable inoculum of control unheated spores, resulting in 2–5 fold increase in aflatoxin B₁ formed in flasks containing AMMB. Increasing the applied load to 4.0 kGy, however, reduced aflatoxin B₁ levels formed in AMMB to similar or lower levels than found in flasks inoculated with control unirradiated spores. Combination treatment of A. flavus with dry heat and 3.5 kGy reduced the spore inoculum size by about 4 log cycles and yielded the highest amount (41.1 μg/ml) of aflatoxin B₁ in AMMB. However, moist heat treatment of spores receiving the same dose (3.5 kGy) reduced toxin level formed by 25%. Aflatoxin B₁ formation by A. flavus spores incubated in AMMB was completely prevented by a combination treatment of moist heat and 4.0 kGy of gamma irradiation. This same treatment attenuated aflatoxins B₂, G₁ and G₂ production which are formed with B₁ by A. flavus NRRL 5906. Spores raised in all flasks containing MMB did not form aflatoxin except when the medium MMB was autoclaved twice at 121°C for 15 min.     

Detecting Aspergillus parasiticus in cereals by an enzyme-linked immunosorbent assay

An enzyme-linked immunosorbent assay (ELISA) was used for the specific detection of Aspergillus parasiticus molds in artificially contaminated corn, rice, wheat and peanut, and also to detect naturally occurring aflatoxigenic molds in the same form cereals. After inoculation of Aspergillus parasiticus in the cereals, the growth of A. parasiticus was monitored by both plate count and ELISA, and the aflatoxin content was measured. Water activity (a_w) affected the fungal growth, aflatoxin production and degradation. The higher a_w level (a_w=0.98 vs. a_w=0.92) resulted in higher fungal growth rates and fungal masses in corn, rice and wheat, and the plate count and ELISA measurements were better correlated, with correlation coefficients of 0.94, 0.93, 0.96 and 0.86, respectively for corn, rice, wheat, and peanuts. Aflatoxin was also both produced sooner and degraded more rapidly at a_w=0.98. Although standard plate counting techniques detected A. parasiticus/A. flavus in 5 out of the 40 cereal samples bought from retail stores, ELISA did not give a positive result in any of them. After moisturization and incubation of these commercial samples at 28°C for 29 days, the incident rates of aflatoxigenic molds increased to 65% and 52% by plate count and ELISA, respectively.     

Mycotoxin occurrence and Aspergillus flavus soil propagules in a corn and cotton glyphosate-resistant cropping systems

The effects of cotton-corn rotation and glyphosate use on levels of soil-borne Aspergillus flavus, aflatoxin and fumonisin contamination in corn and cotton seed were determined during 2002-2005 in Stoneville, Mississippi (USA). There were four rotation systems (continuous cotton, continuous corn, cotton-corn and corn-cotton) for both glyphosate-resistant (GR) and non-GR cultivars-herbicide system arranged in a randomized complete block design with four replications. Aspergillus flavus populations in surface (5-cm depth) soil, sampled before planting (March/April), mid-season (June) and after harvest (September), ranged from 1.47 to 2.99 log (10) cfu g^-1 soil in the four rotation systems. Propagules of A. flavus were higher in the continuous corn system compared to the continuous cotton system on three sample dates, and cotton rotated with corn decreased A. flavus propagules in three of nine sample dates. Propagules of A. flavus were significantly greater in plots with GR cultivars compared to non-GR cultivars in three samples. In cotton seed, aflatoxin and fumonisin levels were similar (≤4 µg kg^-1 and non-detectable, respectively) regardless of rotation and glyphosate. In corn grain, aflatoxin was above the regulatory level (≥20 µg kg^-1) only in GR cultivar in 2004 and 2005. Fumonisin was higher in non-GR cultivar (4 mg kg^-1) regardless of rotation in 2004; however, in 2002, 2003 and 2005, aflatoxin and fumonisin levels were similar regardless of rotation and glyphosate. These results indicate the potential for increased aflatoxin and fumonisin levels (1 of 4 years) in corn; however, climatic conditions encountered during this study did not allow for mycotoxin production. In laboratory incubation studies, fairly high concentrations of glyphosate were required to inhibit A. flavus growth; however no short-term effect of soil treatment with glyphosate on A. flavus populations were observed. These data suggest that altered populations of A. flavus or higher aflatoxin concentrations in corn grain were due to indirect effects of the GR cropping system.     

Distribution and toxigenicity of Aspergillus species isolated from maize kernels from three agro-ecological zones in Nigeria

Maize samples were collected during a survey in three agro-ecological zones in Nigeria to determine the distribution and aflatoxin-producing potential of members of Aspergillus section Flavi. The three agro-ecological zones were, Derived Savannah (DS) and Southern Guinea Savannah (SGS) in the humid south and North Guinea Savannah (NGS) in the drier north. Across agro-ecological zones, Aspergillus was the most predominant fungal genera identified followed by Fusarium with mean incidences of 70 and 24%, respectively. Among Aspergillus, A. flavus was the most predominant and L-strains constituted >90% of the species identified, while the frequency of the unnamed taxon S(BG) was <3%. The incidence of atoxigenic strains of A. flavus was higher in all the districts surveyed except in the Ogbomosho and Mokwa districts in DS and SGS zones, respectively, where frequency of toxigenic strains were significantly (P<0.05) higher than that of atoxigenic strains. The highest and lowest incidence of aflatoxin positive samples was recorded in the SGS (72%) and NGS (20%), respectively. Aflatoxin contamination in grain also followed a similar trend and the highest mean levels of B-aflatoxins were detected in maize samples obtained from Bida (612 ng g(-1)) and Mokwa (169 ng g(-1)) districts, respectively, in the SGS. Similarly, the highest concentrations of G-aflatoxins were detected in samples from Akwanga district in the SGS with a mean of 193 and 60 ng g(-1), respectively. When agro-ecological zones were compared, B-aflatoxins were significantly (P<0.05) higher in SGS than in NGS, and intermediate in maize samples from the DS agro-ecological zone.     

Impact of habitats on toxigenic potential of Aspergillus flavus

Toxigenic potentials of Aspergillus flavus strains isolated from different organic substrates, air and soils were evaluated. The frequency of occurrence of A. flavus ranged from 76% in maize to 87% (coconut and groundnut) and 92% in makhana (Euryale ferox indica.) Incidence was lowest in green gram (42%). Analysis of variance showed that the percentage incidence of A. flavus in the aerosphere of maize fields was significantly affected by season × location. In soil samples the frequency of occurrence of A. flavus was high during the monsoons (76% in non-diara land soils, 69% in diara land soil). Among 1706 isolates of A. flavus obtained from different sources, 826 (48.4%) were found to be toxigenic. The frequency of non-toxigenic strains of A. flavus was comparatively higher (ratio = 1.07:1) than the toxigenic strains. Percentage incidence of the toxigenic strains of A. flavus was the highest (73.3%; ratio = 0.36:1) in the soil samples. No attempt was made to differentiate A. flavus and A. parasiticus and therefore all references to A. flavus include A. parasiticus.     

Fungal colonists of maize grain conditioned at constant temperatures and humidities

Fungal colonization of shelled maize (Pioneer 3320) harvested from a field near Furman, South Carolina, in 1992 was determined after 348 and 751 days of continuous storage at each of seven temperatures (10, 15, 20, 25, 30, 35, or 40°C) and four constant relative humidities, giving equilibrium grain moisture contents ranging from 9.4% to 17.5% m.c. in 28 grain conditioning environments. Twenty fungal species infected surface sterilized seeds and were recorded from these conditioned grain treatments, including species commonly found in preharvest maize [e.g. Acremonium zeae, Aspergillus flavus, Fusarium moniliforme (syn. F. verticillioides), Penicillium pinophilum (syn. P. funiculosum), etc.]. Eupenicillium cinnamopurpureum and Monascus ruber were recorded only from conditioned grain treatments. Eurotium chevalieri colonized 50–96% of the kernels from grain conditioning treatments with the highest moisture content for each incubation temperature. Grain samples with>33% E. chevalieri infection had a decreased occurrence of F. moniliforme and A. zeae, and no kernels from these samples germinated. No fungi colonized more than 50% of the kernels conditioned at 30–40°C and 9.4–14.2% m.c. The results of this study indicate that individual patterns of fungal colonization during grain conditioning were a function of the survival rates for preharvest fungal colonists and their potential replacement by E. chevalieri.     

INFLUENCE OF OTHER FUNGI ON AFLATOXIN PRODUCTION BY ASPERGILLUS FLAVUS IN MAIZE KERNELS

Experiments were designed to determine whether certain nontoxigenic fungi commonly isolated from maize kernels can affect aflatoxin B₁ development when inoculated with A. flavus onto individual unsterilized, and autoclaved maize kernels . Trichoderma viride and Aspergillus niger were found to be strongly antagonist inhibiting the growth of A. flavus by 87 and 66% respectively, whereas Aspergillus versicolor, Fusarium moniliforme, Paecilomyces variotii and Emericella quadrillineata inhibited the growth of A. flavus by less than 51%. Less aflatoxin B₁ was detected when A. flavus was paired with A. niger or T. viride than with the other test fungi. When A. niger or T. viride was introduced onto the kernels 72 h before inoculation with A. flavus, no aflatoxin B₁ was detected in unsterilized kernels and the levels of aflatoxin B₁ were greatly reduced from 700 ppb to 160 and 140 ppb in autoclaved kernels, respectively. When inoculation of A. flavus followed 72 h of incubation of either A. niger and T. viride, no aflatoxin B₁ was detected. However, when both A. niger and T. viride were introduced 72 h after inoculation with A. flavus, the levels of aflatoxin B₁ were reduced to 385 and 560 ppb, respectively in unsterilized and autoclaved maize kernels . Trichoderma viride and Aspergillus niger may be useful in biological control of aflatoxin contamination of maize kernels .; Accepted for Publication June 11, 1997     

Factors influencing fungal and aflatoxin levels in Turkish hazelnuts (Corylus avellana L.) during growth, harvest, drying and storage: A 3-year study

The levels aflatoxins in Turkish hazelnuts have been monitored over a 3-years period (2002-2004). Periodical sampling was made in 72 different orchards at different locations representative of the hazelnut-growing areas and post-harvest applications. Various parameters (aflatoxins, water activity, moulds) were analysed and environmental conditions (temperature and relative humidity) recorded during growing and at different stages of harvest and post-harvest processing, involving three different harvesting methods (collection in nets, from the ground, etc.) and four drying techniques (traditional sun-drying, mechanical drying, etc.). Fungal and aflatoxin analyses (HPLC) showed no significant difference except between samples which had been in contact with the ground and those which had not (at 95% confidence level). Aflatoxins levels from the orchard recorded a maximum of 0.77 ± 0.08 ng g^-1 from a total of 1624 samples. Regarding harvesting and post-harvest processes, the only application where aflatoxins were detected was in samples which had been in direct contact with the ground (max. 3.18 ± 0.03 ng g^-1). Aflatoxin formation was low during storage (max. 0.34 ± 0.003 ng g^-1). As a result of mycological studies, a total of 5546 Aspergillus flavus (89%) and A. parasiticus (11%) species were isolated and identified from samples. The results indicated that harvesting hazelnuts into a canvas by shaking the trees, manual harvesting of mature hazelnuts where possible, use of jute instead of nylon sacks and mechanical drying technique would minimize aflatoxin levels in hazelnuts. These recommendations have been implemented and about 4000 people in the hazelnut industry have been trained in these practices.     

Aflatoxin levels in raw and processed hazelnuts in Turkey

Aflatoxin levels in hazelnut samples obtained from exporter companies were monitored over a 3-year period. A total of 3188 samples of raw and processed hazelnuts were analysed using an HPLC method. The total aflatoxin content of the contaminated samples was in the range of 0.02–78.98?µg?kg^?1 for hazelnut kernels, 0.07–43.59?µg?kg^?1 for roasted hazelnut kernels, 0.02–39.17?µg?kg^?1 for roasted sliced hazelnut kernels, and 0.02–11.20?µg?kg^?1 for hazelnut purees, respectively, showing that the variations of aflatoxin contamination were very high. The results of aflatoxin analysis revealed that the aflatoxin contamination in the hazelnut samples was at a tolerable level. A total of 3147 samples were contaminated with aflatoxins, although below the legal limits. However, the aflatoxin contents of 41 samples exceeded the legal limits. Therefore, aflatoxin contents of hazelnuts should be monitored regularly to minimise the risk of aflatoxin hazard, and pre- and post-harvest strategies should be developed to prevent aflatoxin formation.