Next Article in Journal
Use of Insulated Covers over Product Crates to Reduce Losses in Amaranth during Shipping Delays
Next Article in Special Issue
Grain Sorghum: A Conundrum for Chicken-Meat Production
Previous Article in Journal / Special Issue
The Effect of Supplementing Air-Dried Moringa stenopetala Leaf to Natural Grass Hay on Feed Intake and Growth Performances of Arsi-Bale Goats
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Aflatoxins, Fumonisins and Zearalenone Contamination of Maize in the Southeastern and Central Highlands Provinces of Vietnam

1
Faculty of Animal Science and Veterinary Medicine, Nong Lam University, Linh Trung Ward, Thu Duc District, Ho Chi Minh City, Vietnam
2
Department of Animal Nutrition and Management, Swedish University of Agricultural Sciences, P.O. Box 7024, SE-750-07 Uppsala, Sweden
*
Author to whom correspondence should be addressed.
Submission received: 30 August 2015 / Revised: 20 November 2015 / Accepted: 26 November 2015 / Published: 4 December 2015
(This article belongs to the Special Issue Nutritional Toxicology and Animal Nutrition)

Abstract

:
A survey of the contamination of maize with aflatoxins, fumonisins and zearalenone was carried out in the Southeastern and Central Highland provinces in Vietnam. Four provinces were chosen for sampling maize: Dong Nai (22), Binh Phuoc (25), Dak Lak (30) and Dak Nong (20). Aflatoxin B1 (AFB1), B2 (AFB2), G1 (AFG1), G2 (AFG2), fumonisin B1 (FB1), fumonisin B2 (FB2) and zearalenone (ZEA) were analysed by HPLC in 97 maize kernel samples. Fumonisins were the most common toxins found in all samples (67%), followed by aflatoxins (55.7%) and zearalenone (27.8%). The incidence of aflatoxin positive samples (61.7%) in the Southeastern provinces was higher than in the Central Highlands (50%), while fumonisins and zearalenone incidences were higher in the Central Highlands. The mean level of fumonisin B1 in samples from the Central Highlands provinces (1757 µg/kg) was significantly greater (p < 0.05) than in the Southeastern provinces (740 µg/kg). Importantly, the percentage of positive samples (about 70%) that had over 20 µg/kg (ppb) aflatoxin was very high. Moreover, many samples (53%) contained more than one mycotoxin and this result highlights the difficulty of diagnosing mycotoxicoses in the field and the need for ongoing research to reduce the occurrence of mycotoxins in Vietnamese maize.

1. Introduction

The significance of the effects of mycotoxins on animal production and human health has been known since the 1960s [1]. Mycotoxins are fungal metabolites which have low molecular weights that are not recognized by the body’s immune system and are insidious poisons [2]. Moreover, many mycotoxin-producing fungi are also plant pathogens, leading to economic crop losses. These toxins can be formed in many stages of plant production, from growing to harvest, drying, and storage [2,3]. Among the many different mycotoxins, aflatoxins, fumonisins and zearalenone are well known owing to their occurrence and toxicities, especially in animals [4]. Aflatoxins are produced by Aspergillus spp. including A. flavus, A. parasiticus, A. nomius, and A. pseudotamarii, and there are four major aflatoxins: B1, B2, G1 and G2 [3,5]. Maize and peanuts are important crops that are often contaminated with aflatoxins [6]. The aflatoxins are considered the most important mycotoxin because of its toxicity and designation as a carcinogen [1,2,3]. The disease resulting from aflatoxin ingestion is aflatoxicosis and in livestock it may result in reduced growth performance, changes in some liver enzymes, liver damage, decreased milk and egg production and reduced immune response [2,3,4]. Fumonisins are mycotoxins, produced predominantly by Fusarium verticillioides (previously F. moniliforme) and F. proliferatum with four main types, B1, B2, A1, A2, of which fumonisin B1 is produced in the largest amount and has the highest toxicity [7]. The fumonisins cause equine leukoencephalomalacia, and pulmonary edema in pigs and may induce esophageal cancer and neural tube defects in humans [7,8,9]. Fumonisin B1 is commonly found in maize and maize-based food and feed in Africa, China, France, Indonesia, Italy, the Philippines, South America, Thailand, and the USA [7,10,11]. In Southeast Asia, fumonisins are the most prevalent mycotoxin detected, with 58% positive samples, and maize is the most contaminated feed, with 71% positive samples [12]. Zearalenone is also produced by many species of the Fusarium genus and is a mycotoxin with estrogenic characteristics [13]. In this genus, Fusarium graminearum is the most widely distributed species that produces zearalenone in wheat and maize world-wide [14]. Zearalenone toxicity mostly affects the reproductive function of animals, especially pigs, by inducing feminization, decreasing the number of fetuses per sow and reducing sow fertility [13,15].
Of the cereal grains, maize is the crop most affected by mycotoxin contamination [16]. In Vietnam, maize is the second most important human food staple after rice, particularly in the rural and mountainous areas. It is also the main energy feed source for Vietnam’s livestock industries. The Southeast region—Mekong Delta Upland is an agro-ecological zone with the second largest maize growing area in Vietnam, followed by the Central Highlands-Central Coast Upland [17]. The Southeastern and Central Highlands provinces are in the tropical monsoon region where weather conditions are favorable for the production of many mycotoxins. However, the mycotoxin contamination of maize grown in these regions has not been examined in detail. Therefore, a survey on the occurrence of fumonisins, aflatoxins and zearalenone in maize obtained from four provinces in the Southeastern Mekong Delta Uplands and Central Highlands of Vietnam was conducted.

2. Results and Discussion

The occurrence of mycotoxins in the two study areas is shown in Table 1, and was different among the toxins. The Southeastern provinces had about a 10% higher incidence of aflatoxin contaminated samples than in the Central Highlands. In contrast, the incidence of zearalenone and fumonisins positive samples was higher in the Highlands provinces than in the Southeast. Overall, the highest percentage of samples was contaminated with fumonisins (67%), followed by aflatoxins (55.7%) and zearalenone (27.8%). Two worldwide surveys of the occurrence of mycotoxins have been published for the periods 2003–2005 [12] and 2009–2011 [18]. Both surveys included data from Southeast Asia (Malaysia, Philippines, Thailand, Indonesia and Vietnam). The results in the present study are in accordance with the occurrence of the toxins found in Southeast Asia, where fumonisins were also the most commonly found mycotoxin, followed by aflatoxins. A similar result was found in a preliminary survey of maize samples from Vietnam [19]. In contrast, Trung et al. [20] conducted a survey by collecting samples from North, Central and South Vietnam that showed 68% of tested samples were contaminated with AFB1, while the percentage of fumonisin B1 positive samples was only 32%.
Table 1. Occurrence of aflatoxins, fumonisins and zearalenone in samples of maize from the Southeastern Mekong Delta Uplands and Central Highlands of Vietnam.
Table 1. Occurrence of aflatoxins, fumonisins and zearalenone in samples of maize from the Southeastern Mekong Delta Uplands and Central Highlands of Vietnam.
SamplesAflatoxinsFumonisinsZearalenone
DN + BP aDN + DL aTotalDN + BP aDN + DL aTotalDN + BP aDN + DL aTotal
Analyzed (n)475097475097475097
Positive (n)29255426396552227
Positive (%)61.750.055.755.378.067.010.644.027.8
a DN + BP: Dong Nai + Binh Phuoc; DN + DL: Dak Nong + Dak Lak provinces.
The distribution of aflatoxins, fumonisins and zearalenone were different between the Southeast Mekong Delta uplands and Central Highlands (Table 2). The aflatoxins tend to be more common in Dong Nai and Binh Phuoc provinces. These provinces have higher mean temperatures than Dak Nong and Dak Lak, which provides good conditions for the production of aflatoxins [2]. Moreover, most of the samples collected in Binh Phuoc were not dried well and were stored in poor conditions in the houses of small farmers. Both factors may have contributed to the high percentage of AF positive samples in both the Southeastern provinces and the Central Highlands. Fumonisins and zearalenone on the other hand were more common in samples from the Central Highlands. The fusarium toxins develop more rapidly in fields under condition of high air humidity and moderate temperatures, which are more prevalent in Central Highlands than in the Southeastern provinces [14].
The results in Table 2 show very clearly that the mean FB1 level in DN + DL was significantly higher than in DN + BP (p < 0.05). Moreover, the median and concentration range of FB1 in DN + DL were also much higher and wider than in DN + BP. Although aflatoxin B1 concentration in DN + DL samples was not significantly higher than in DN + BP, the aflatoxin B2 mean value in DN + DL tended to be higher than in DN + BP (p = 0.071), and one sample from Dak Lak had 810 ppb of AFG1. The mean concentrations of aflatoxin B1 in these two areas were much higher than the maximum tolerated level mandated by the European Union (EU, 5 µg/kg) and U.S. Food and Drug Administration Compliance Policy Guides for maize (FDA, 20 µg/kg). Furthermore, the concentrations of toxins in DN + DL had wider ranges than in DN + BP. These ranges were also wider than the fumonisin B1 range in samples from North, Central and South Vietnam (400–3300 ppb), and aflatoxin B1 range (7–126.5 ppb) reported in the survey conducted by Trung et al. [20]. Although there was no significant difference between zearalenone contents in samples from the Southeast Upland and Central Highlands, the mean and range of this toxin in DN + DL was higher than in DN + BP.
Table 2. Aflatoxins, fumonisins and zearalenone levels (μg/kg) in maize from the Southeast Mekong Delta Uplands and Central Highlands of Vietnam.
Table 2. Aflatoxins, fumonisins and zearalenone levels (μg/kg) in maize from the Southeast Mekong Delta Uplands and Central Highlands of Vietnam.
Mycotoxins RegionDN + BP aDN + DL aProb.
AFB1 bn 2925
Mean 104.7170.20.221
Median 8128
Range 1–4502–844
AFB2 bn 2515
Mean 10.520.70.071
Median 5.511
Range 1–332–86
AFG1 bn 54
Mean 12.82080.306
Median 29.5
Range 2–543–810
FB1 bn 2639
Mean 74017570.042 *
Median 390.5871
Range 102–2747160–10799
FB2 bn 2035
Mean 357.97510.102
Median 229.5367
Range 108–834102–5051
ZEA bn 522
Mean 48.8299.50.367
Median 4498
Range 35–8036–2409
a DN+BP: Dong Nai + Binh Phuoc; DN+DL: Dak Nong + Dak Lak; b AFB1: Aflatoxin B1; AFB2: Aflatoxin B2; AFG1: Aflatoxin G1; FB1: Fumonisin B1; FB2: Fumonisin B2; ZEA: Zearalenone; * p < 0.05.
The number of toxins in a contaminated sample is shown in Figure 1. Only 16% of samples had no detectable toxins, whilst 31% contained one mycotoxin and the remaining 53% were contaminated with more than one toxin. This result is similar to the results for Southeast Asia which appeared in the two world surveys [12,18].
Figure 1. The co-occurrence of mycotoxins in maize kernels sampled in Vietnam.
Figure 1. The co-occurrence of mycotoxins in maize kernels sampled in Vietnam.
Agriculture 05 01195 g001
The distribution of aflatoxin concentrations in the samples is shown in Table 3. The percentage of positive samples that had over 20 ppb aflatoxin was very high (about 70%). Moreover, the occurrence of samples with over 300 µg/kg (ppb) was higher than the occurrence of samples with from 98.4 to 126.5 ppb in the survey of Trung et al. [20] (14.8% > 11.8%).
Table 3. Distribution of total aflatoxin levels in maize kernel samples.
Table 3. Distribution of total aflatoxin levels in maize kernel samples.
Aflatoxins (μg/kg)Frequency% of Samples
0 ≤ 201731.5
21–1001425.9
101–3001527.8
>300814.8
The distribution of fumonisin concentrations in the samples is shown in Table 4. The majority (90%) of samples analysed had fumonisin concentrations of less than 4000 ppb (4 ppm). The occurrence of positive samples with over 12,000 ppb was low (3.1%).
Table 4. Distribution of total fumonisins levels in maize kernel samples.
Table 4. Distribution of total fumonisins levels in maize kernel samples.
Fumonisins (μg/kg)Frequency% of Samples
0 ≤ 40005990.8
4001–800034.6
8001–12,00011.5
>12,00023.1
The distribution of zearalenone concentrations in the samples is shown in Table 5. Zearalenone positive samples that contained less than 100 ppb (0.1 ppm) was high (63%) and about 11% of samples contained over 500 ppb. In comparison, a Brazillian survey showed only about 17% positive samples with less than 100 ppb, and 6.7% samples with over 500 ppb [21].
Table 5. Distribution of zearalenone levels in maize kernel samples.
Table 5. Distribution of zearalenone levels in maize kernel samples.
Zearalenone (µg/kg)Frequency% of Samples
0 ≤ 1001763.0
<100–500725.9
500–100013.7
>100027.4

3. Experimental Section

3.1. Site Description

Two provinces in the Southeastern Mekong Delta Uplands, Binh Phuoc and Dong Nai, and two in the Central Highlands, Dak Lak and Dak Nong, were chosen for the survey, since their maize production is well developed and is used for livestock in the area.

3.1.1. Dong Nai and Binh Phuoc—Warm Region

These provinces are located in the tropical monsoon area; the climate is hot and humid, with two seasons, a rainy season from May to November and a dry season from December to April. The average rainfall is from 1800 to 2000 mm per year, relative humidity is 80% to 90%, and average temperature is about 27 °C. This area has an elevation ranging from 100 to 200 m above sea level. This region has the second largest planted maize area in Vietnam with two rain-fed maize crops per year; the summer-autumn and autumn-winter. Maize grown in these provinces is mainly for commercial production, owing to the good transportation system and the proximity to feed mills. In these provinces, the maize area is usually around 1.0 ha, and it is an important source of income for the farmers [17].

3.1.2. Dak Lak and Dak Nong—Cool Region

These provinces are located in the Central Highlands region, at 500 to 800 m above sea level, in the tropical monsoon area, with two seasons, a rainy season from May to November and a dry season (from December to April). The average temperature is from 18 to 25 °C, so it is relatively cool throughout the year. The average rainfall is from 1750 mm to 3150 mm per year and relative humidity is around 85% to 87%. There is one rain-fed maize crop per year, grown in the summer-autumn season. Maize is mainly grown in semi-commercial production systems on sloping land. The infrastructure in many places is poor and although the farmers own on average 1.3 ha for maize cultivation, there are still many poor families in the rural areas [17].

3.2. Sampling Method

A total of 97 maize kernel samples (about 1 kg per sample) was purchased from local retail traders and small farmers in the four provinces of Southeastern and Central highlands of Vietnam from the end of August to the beginning of October 2009, the maize harvesting season. The number of samples was 22, 25, 20 and 30 from Dong Nai, Binh Phuoc, Dak Nong and Dak Lak, respectively. Samples were dried in an oven at 60 °C for 8 h then stored in plastic bags with a desiccator (silica gel in small bags to stop mould activity) at room temperature before analysis.

3.3. Mycotoxin Analysis Methods

The methods used for aflatoxins, fumonisins and zearalenone analyses, including sample preparation, clean-up and HPLC analysis have been detailed by Binder et al. [12]. The procedures were completed by Romer Labs, Singapore.
Briefly, aflatoxins and zearalenone were extracted from 25 g milled samples using 100 mL acetonitrile/water (84:16) and 4 mL filtrate was cleaned-up on a Mycosep #226 AflaZon cartridge. The fumonisins were extracted separately from another 25 g sample using 100 mL acetonitrile/water (50:50). Filtrate was adjusted to pH 6–9 and 3 mL was diluted in 8 mL methanol/water (3:1) and passed through a Multisep 211 column, washed with 8 mL methanol/water (3:1) and eluted with 10 mL methanol/acetic (99:1).
The aflatoxins were analyzed using HPLC with separation on a Zorbax SB-Aq column (4.6 × 150 mm, 5 μm) at 30 °C with mobile phase water/acetonitrile/methanol (5:1:1), flow rate 2 mL/min and post-column derivatization using a Kobra cell and fluorescence detection (excitation wavelenght at 360 nm and emission wavelenght at 440 nm).
Zearalenone was also analyzed by HPLC on a Hypersil ODS column (2.1 × 100 mm, 5 µm) using an isocratic mobile phase water/acetonitrile (64:36), column temperature 30 °C and fluorescence detection (excitation wavelenght at 235 and emission wave length at 460 nm).
Fumonisins were precolumn derivatized with naphthalene 2,3-dicarboxaldehyde before HPLC separation on a Hypersil ODS (Octadecylsilan) column (2.1 × 200 mm, 5 µm) using mobile phase acetonitrile/water/methanol/acetic acid (48/46/5/1) at a flow rate of 0.5 mL/min and fluorescence detection (excitation wavelength at 420 nm and emission wavelenght at 500 nm).
Normal recovery from spiked samples was 80% for AFB1, 100% for zearalenone and 75% for fumonisins. The limit of quantification was 1 μg/kg for AFB1, 25–32 µg/kg for zearalenone and 100 μg/kg for fumonisins. Control samples were used for quality control of the routine analyses.

3.4. Data Analysis

The data were calculated and analysed using the Excel program, with the incidence of positive aflatoxin, fumonisin and zearalenone samples in the total, range, mean and median values. The distribution of aflatoxin, fumonisin and zearalenone levels in maize kernels was also calculated by Excel. The differences in aflatoxin, fumonisin and zearalenone concentration in maize between the Southeastern provinces and Central Highlands were compared by ANOVA in Minitab 13 (Minitab Inc., Pennsylvania, PA, USA). Sources of variance were geographical areas and error.

4. Conclusions

Maize kernel samples from the Southeastern and Central Highlands of Vietnam were frequently contaminated with aflatoxins and fumonisins at high concentrations. Aflatoxin B1 levels were much higher than the maximum tolerated AFB1 level of both the European Union and the Food and Drug Aministration. Therefore, maize from these regions can be considered as a major health problem for the consumers. In the Central Highlands, the incidence of positive maize samples contaminated with fumonisins and zearalenone was higher than in the Southeastern provinces. Although fumonisins or zearalenone contamination incidences were higher than aflatoxins, their levels of contamination were mostly within acceptable range. On the other hand, aflatoxins seem to be a major problem due to their high levels of contamination. Many samples contained more than one mycotoxin and this result highlights the difficulty of diagnosing mycotoxicoses in the field due to the synergistic effects of mycotoxins on animals. These results emphasize the need for ongoing research to reduce the occurrence of mycotoxins in Vietnamese maize.

Acknowledgments

We would like to thank Preston for his valuable advice and helpful corrections and Romer Labs, Singapore for analyses. This work was financially supported by the Swedish International Development Cooperation Agency (SIDA) and Biomin Holding GmbH.

Author Contributions

P.N.H. and T.N.Q. conceived and designed the survey; P.N.H. performed the survey; P.N.H. and T.N.Q. analyzed the data; B.O. and H.P. gave advice and contributed to the preparation of the paper.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Richard, J.L. Some major mycotoxins and their mycotoxicoses—An overview. Int. J. Food Microbiol. 2007, 119, 3–10. [Google Scholar] [CrossRef] [PubMed]
  2. Bryden, W.L. Mycotoxins and mycotoxicoses: Significance, occurrence and mitigation in the food chain. In General and, Applied Toxicology, 3rd ed.; John Wiley & Sons, Ltd.: Chichester, UK, 2009; pp. 3529–3553. [Google Scholar]
  3. CAST. Mycotoxins: Risks in Plant, Animal, and Human Systems; Council for Agricultural Science and Technology: Ames, IA, USA, 2003. [Google Scholar]
  4. Pettersson, H. Controlling mycotoxins in animal feed. In Mycotoxins in Food; Magan, N., Olsen, M., Eds.; Woodhead Publishing: Cambridge, UK, 2004; pp. 262–304. [Google Scholar]
  5. Abbas, H.K. (Ed.) Aflatoxin and Food Safety; CRC Press: Boca Raton, FL, USA, 2005; pp. 13–28.
  6. Reddy, K.R.N.; Abbas, H.K.; Abel, C.A.; Shier, W.T.; Oliveira, C.A.F.; Raghavender, C.R. Mycotoxin contamination of commercially important agricultural commodities. Toxin Rev. 2009, 28, 154–168. [Google Scholar] [CrossRef]
  7. Voss, K.A.; Smith, G.W.; Haschek, W.M. Fumonisins: Toxicokinetics, mechanism of action and toxicity. Anim. Feed Sci. Tech. 2007, 137, 299–325. [Google Scholar] [CrossRef]
  8. Gelineau-van Waes, J.; Starr, L.; Maddox, J.; Aleman, F.; Voss, K.A.; Wilberding, J.; Riley, R.T. Maternal fumonisin exposure and risk for neural tube defects: Mechanisms in an in vivo mouse model. Birth Defects Res. A Clin. Mol. Teratol. 2005, 73, 487–497. [Google Scholar] [CrossRef] [PubMed]
  9. Marasas, W.O. Fumonisins: History, world-wide occurrence and impact. In Fumonisins in Food; Jackson, L., DeVries, J., Bullerman, L., Eds.; Springer US: New York, NY, USA, 1996; Volume 392, pp. 1–17. [Google Scholar]
  10. CTA. Mycotoxins in Grain; CTA: Wageningen, The Netherlands, 1997. [Google Scholar]
  11. Soriano, J.M.; Dragacci, S. Occurrence of fumonisins in food. Food Res. Int. 2004, 37, 985–1000. [Google Scholar] [CrossRef]
  12. Binder, E.M.; Tan, L.M.; Chin, L.J.; Handl, J.; Richard, J. Worldwide occurrence of mycotoxins in commodities, feeds and feed ingredients. Anim. Feed Sci. Tech. 2007, 137, 265–282. [Google Scholar] [CrossRef]
  13. Summerell, B.A.; Leslie, J.F.; Backhouse, D.; Bryden, W.L.; Burgess, L.W. (Eds.) Fursarium: Paul E. Nelson Memorial Symposium; APS Press: St Paul, MN, USA.
  14. Desjardins, A.E. Fusarium Mycotoxins: Chemistry Genetics and Biology; APS Press: St Paul, MN, USA, 2005. [Google Scholar]
  15. Fink-Gremmels, J.; Malekinejad, H. Clinical effects and biochemical mechanisms associated with exposure to the mycoestrogen zearalenone. Anim. Feed Sci. Tech. 2007, 137, 326–341. [Google Scholar] [CrossRef]
  16. Miller, J.D. Mycotoxins in small grains and maize: Old problems, new challenges. Food Add. Contam. A 2008, 25, 219–230. [Google Scholar] [CrossRef] [PubMed]
  17. Dinh Thao, T.; Tri Khiem, N.; Xuan Trieu, M.; Gerpacio, R.V.; Pingali, P.L. Maize in Vietnam: Production Systems, Constraints, and Research Priorities; CIMMYT: Mexico, D.F., Mexico, 2004. [Google Scholar]
  18. Rodrigues, I.; Naehrer, K. A three-year survey on the worldwide occurrence of mycotoxins in feedstuffs and feed. Toxins 2012, 4, 663–675. [Google Scholar] [CrossRef] [PubMed]
  19. Miraglia, M.; van Egmond, H.P.; Brera, C.; Gilbert, J. Mycotoxins and Phytotoxins. In IX International Iupac Symposium on Mycotoxins and Phycotoxins; Alaken, Inc.: Fort Collins, CO, USA, 1998. [Google Scholar]
  20. Trung, T.; Tabuc, C.; Bailly, S.; Querin, A.; Guerre, P.; Bailly, J. Fungal mycoflora and contamination of maize from Vietnam with aflatoxin B1 and fumonisin B1. World Mycotoxin J. 2008, 1, 87–94. [Google Scholar] [CrossRef]
  21. Silva, C.M.G.; Vargas, E.A. A survey of zearalenone in corn using Romer Mycosep™ 224 column and high performance liquid chromatography. Food Add. Contam. 2001, 18, 39–45. [Google Scholar] [CrossRef] [PubMed]

Share and Cite

MDPI and ACS Style

Phuong, N.H.; Thieu, N.Q.; Ogle, B.; Pettersson, H. Aflatoxins, Fumonisins and Zearalenone Contamination of Maize in the Southeastern and Central Highlands Provinces of Vietnam. Agriculture 2015, 5, 1195-1203. https://0-doi-org.brum.beds.ac.uk/10.3390/agriculture5041195

AMA Style

Phuong NH, Thieu NQ, Ogle B, Pettersson H. Aflatoxins, Fumonisins and Zearalenone Contamination of Maize in the Southeastern and Central Highlands Provinces of Vietnam. Agriculture. 2015; 5(4):1195-1203. https://0-doi-org.brum.beds.ac.uk/10.3390/agriculture5041195

Chicago/Turabian Style

Phuong, Nguyen Hieu, Nguyen Quang Thieu, Brian Ogle, and Hans Pettersson. 2015. "Aflatoxins, Fumonisins and Zearalenone Contamination of Maize in the Southeastern and Central Highlands Provinces of Vietnam" Agriculture 5, no. 4: 1195-1203. https://0-doi-org.brum.beds.ac.uk/10.3390/agriculture5041195

Article Metrics

Back to TopTop