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ORIGINAL RESEARCH article

Front. Microbiol., 01 November 2023
Sec. Food Microbiology

Dynamic geospatial modeling of mycotoxin contamination of corn in Illinois: unveiling critical factors and predictive insights with machine learning

  • 1Food and Feed Safety Research Unit, Southern Regional Research Center, Agriculture Research Service, United States Department of Agriculture, New Orleans, LA, United States
  • 2Dale Bumpers Small Farms Research Center, Agriculture Research Service, United States Department of Agriculture, Booneville, AR, United States
  • 3Microbiology and Agrochains Wageningen Food Safety Research, Wageningen, Netherlands
  • 4Atmospheric and Ocean Science Program, Princeton University, Princeton, NJ, United States
  • 5Agricultural Products Inspection, Illinois Department of Agriculture, Springfield, IL, United States
  • 6Mycotoxin Prevention and Applied Microbiology Research Unit, United States Department of Agriculture, Agricultural Research Service, National Center for Agricultural Utilization Research, Peoria, IL, United States

Mycotoxin contamination of corn is a pervasive problem that negatively impacts human and animal health and causes economic losses to the agricultural industry worldwide. Historical aflatoxin (AFL) and fumonisin (FUM) mycotoxin contamination data of corn, daily weather data, satellite data, dynamic geospatial soil properties, and land usage parameters were modeled to identify factors significantly contributing to the outbreaks of mycotoxin contamination of corn grown in Illinois (IL), AFL >20 ppb, and FUM >5 ppm. Two methods were used: a gradient boosting machine (GBM) and a neural network (NN). Both the GBM and NN models were dynamic at a state-county geospatial level because they used GPS coordinates of the counties linked to soil properties. GBM identified temperature and precipitation prior to sowing as significant influential factors contributing to high AFL and FUM contamination. AFL-GBM showed that a higher aflatoxin risk index (ARI) in January, March, July, and November led to higher AFL contamination in the southern regions of IL. Higher values of corn-specific normalized difference vegetation index (NDVI) in July led to lower AFL contamination in Central and Southern IL, while higher wheat-specific NDVI values in February led to higher AFL. FUM-GBM showed that temperature in July and October, precipitation in February, and NDVI values in March are positively correlated with high contamination throughout IL. Furthermore, the dynamic geospatial models showed that soil characteristics were correlated with AFL and FUM contamination. Greater calcium carbonate content in soil was negatively correlated with AFL contamination, which was noticeable in Southern IL. Greater soil moisture and available water-holding capacity throughout Southern IL were positively correlated with high FUM contamination. The higher clay percentage in the northeastern areas of IL negatively correlated with FUM contamination. NN models showed high class-specific performance for 1-year predictive validation for AFL (73%) and FUM (85%), highlighting their accuracy for annual mycotoxin prediction. Our models revealed that soil, NDVI, year-specific weekly average precipitation, and temperature were the most important factors that correlated with mycotoxin contamination. These findings serve as reliable guidelines for future modeling efforts to identify novel data inputs for the prediction of AFL and FUM outbreaks and potential farm-level management practices.

1. Introduction

Mycotoxin contamination of food and feed crops, such as corn, in the United States (US) leads to annual losses estimated in the range of $418 million to $1.66 billion (Vardon et al., 2003; Wu, 2006; Mitchell et al., 2016; Johns et al., 2022). These toxins are produced by distinct fungal species of Aspergillus and Fusarium (Proctor et al., 2018; Munkvold et al., 2019) and are well characterized by their severe health impacts on humans, livestock, and animals (Vardon et al., 2003). In corn, aflatoxins (AFL) are primarily caused by A. flavus and A. parasiticus, and fumonisins (FUM) are produced by F. verticillioides and F. proliferatum (Woloshuk and Shim, 2013). The severity of disease epidemics and associated mycotoxin contamination is driven by environmental and agronomical conditions, with the former being the most relevant. Each fungal species has optimal conditions that favor inoculum formation and dispersal, disease development, and mycotoxin production. For example, for A. flavus, the optimal growth temperatures are 30 to 35°C (Abdel-Hadi et al., 2012), while for F. verticillioides, temperature ranges between 20 and 25°C (Medina et al., 2014) are ideal for growth. These temperature optima tend to favor the growth of aflatoxin-producing fungal species such as Aspergillus spp. in southern latitudes (Klich, 2002; Kerry et al., 2021), whereas these optima favor the growth of Fusarium spp. in northern latitudes (Zingales et al., 2022). The geographical distribution of these fungi in the US will most likely change due to climate change leading to an expansion of the temporal and latitudinal temperature growth optima of these mycotoxigenic fungi (Nnadi and Carter, 2021; Yu et al., 2022; Zingales et al., 2022). Additionally, in general, hot conditions favor A. flavus conidiation and dispersal and Fusarium infection of corn (McMillian et al., 1985; Payne et al., 1986, 1988; Diener et al., 1987; Widstrom et al., 1990; Payne and Widstrom, 1992; Guo et al., 1996; Sétamou et al., 1997; Scheidegger and Payne, 2003; Cotty and Jaime-Garcia, 2007). Furthermore, kernel water activity (0.92–0.97 aw) and insect injury contribute to mycotoxin production (Warfield Colleen and Gilchrist David, 1999; Miller, 2001; Munkvold, 2003; Bush et al., 2004).

The agroecosystem and production of fungal mycotoxins involve soil biogeochemical characteristics that impact both crops and fungi. For example, carbonate content, saturated hydraulic conductivity, pH, bulk density, and texture, among others, influence soil microbial communities, and which species of fungi, including pathogens, might dominate in a given soil environment (Weil and Brady, 2002). Soil property variability is related to factors such as geologic deposition, age of material, climate, duration of soil development, land use history, and other factors. Much of the soils in Northern IL were formed in glacial and periglacial deposits from the Wisconsin glacial episode of the late Pleistocene associated with various advances and retreats of the continental Laurentide ice sheet, while soils in the more southern portion of the state developed from older parent materials with a difference in soil age of approximately 100,000 years or more (Bergstrom et al., 1976). The soil in Northern IL is richer in clay and carbonate materials. Previous studies in IL have shown a north–south difference in historical mycotoxin contamination (Castano-Duque et al., 2022). The 40° latitude in IL marks a geographical and meteorological boundary in the state that leads to differences in weather from mixed humid to wintry conditions (Köppen, 2011; Beck et al., 2018). Correspondingly, warmer, more humid conditions in Southern IL, provide relatively more favorable conditions for the fungi to infect corn and produce mycotoxins at lower latitudes compared to higher latitudes.

Integrated pest and disease management strategies that aim to minimize economic losses associated with mycotoxin contamination need to account for spatial and temporal-specific factors as well as weather, crop health and genetics, past agronomic practices, and soil characteristics. Mycotoxin contamination assessment tools are key for growers and stakeholders to be informed of the potential probabilities of mycotoxin outbreaks and facilitate the deployment of strategies aimed at controlling disease and grain contamination (Focker et al., 2020). Satellite-acquired databases, including the normalized difference vegetation index (NDVI), have been previously used in studies evaluating mycotoxins in European wheat and led to higher mycotoxin model accuracy (Wang et al., 2022). Several studies have shown significant correlations among climate, soil properties, NDVI, and agricultural management practices with AFL contamination in Africa, as reviewed by Keller et al. (2022). AFL studies conducted in Eastern and Western Kenya (Mutiga et al., 2014) support the utility of remote-sensing data such as NDVI, rainfall, and soil properties (such as organic carbon content, pH, total exchangeable bases, salinity, texture, and soil type) to accurately predict AFL contamination (Smith et al., 2016). Soils and their interactions with hydroclimate are highly variable (Smith et al., 2019; Vergopolan et al., 2022) and influence fungal and microbial populations in soils.

Predicting mycotoxin contamination through models has benefited corn production in other countries, but US corn growers, which produce the most corn in the world, have yet to realize such benefits. Published models assess mycotoxin contamination of milk in Eastern Europe (Van der Fels-Klerx et al., 2019) and mycotoxin risk in small grains, corn, and other cereal crops in Italy (Leggieri et al., 2021), Serbia (Liu et al., 2021), Europe (Wang et al., 2022), and Korea (Lee et al., 2018). Machine learning (ML) technologies such as artificial neural networks have been developed in Europe to identify mycotoxin contamination in corn kernels post-harvest using electronic nose technology in northern Italy (Leggieri et al., 2021). Mycotoxin contamination prediction modeling involves other factors, such as fungal development and dispersal. Spore dispersal modeling is an actively developing field of research worldwide, as reviewed by González-Domínguez et al. (2023). Furthermore, the impact of AFL predictive risk models in sub-Saharan Africa has been reviewed by Keller et al. (2022), showing the economic impact of these technologies. The basis of these models served as a general roadmap to model the prediction of AFL and FUM contamination in IL-US. In the US, modeling of fungal diseases has been done by the Fusarium head blight (FHB) risk assessment tool from the US Wheat and Barley Scab Initiative (https://www.wheatscab.psu.edu/) that uses modeling approaches to alert wheat and barley growers of FHB risk (Shah et al., 2018). A US-based predictive model based on insurance claims used as a proxy for mycotoxin contamination values is available for corn (Yu et al., 2020, 2022). However, insurance claims are not necessarily equivalent to actual mycotoxin values. Previous US models targeted the prediction of multinomial levels of AFL and FUM contamination and showed that ML approaches can detect weather factors pre-harvest that significantly impact mycotoxin accumulation in IL (Castano-Duque et al., 2022).

The need for US-focused models is even more important when considering that mycotoxin contamination is predicted to increase in the years to come due to climate change (Van der Fels-Klerx et al., 2016, 2019). Climate change models predict increased fungal growth and subsequent toxin production (Battilani et al., 2016) due to negative effects on crop host health and the interaction of multiple abiotic factors such as drought, leading to losses in corn production (Long Stephen et al., 2006; Battilani et al., 2016; Peng et al., 2020). Increasing temperatures, longer drought periods, and rising carbon dioxide levels (Vaughan et al., 2014, 2016) as the effects of climate change are expected to continue leading to increased crop vulnerability combined with favorable conditions for fungi such as Aspergillus spp. to grow and produce toxins. These conditions will lead to an increase in plant stress hormones that have been shown to alter plant defense responses (Guo et al., 2008), making the crop more vulnerable to fungal infection and mycotoxin contamination. Therefore, it is predicted that climate change has the potential to negatively impact northern corn-producing states (Corn Belt), as projected weather conditions will increase AFL-related risk (Wu et al., 2011). Risk assessment analysis using 16 climatic models from 2031 to 2040 in the US has shown that 89.5% of corn-growing counties will experience an increase in AFL prevalence, and this projection includes corn in the northern states, suggesting the spread of fungal infection and mycotoxin contamination from southern regions toward the northern Corn Belt (Yu et al., 2022), where it has the potential to be even more devastating to corn production. Models developed by using mycotoxin data from major US corn-growing states and trained using weather, satellite, and geographically dynamic features for US-focused areas are critically needed. They will benefit corn growers by mitigating losses projected to occur in extreme weather events associated with climate change.

We developed a mycotoxin model that is geospatial dynamic and IL-focused to identify novel risk factors correlated with mycotoxin contamination, we applied machine learning predictive models. We provided new information about the influence of soil properties and remote-sense data (NDVI) on the prediction of AFL and FUM contamination in corn. Understanding the correlations of these factors with mycotoxin contamination can lead to region time-specific targeted integrated pest management practices to prevent AFL and FUM outbreaks, thus serving as guidelines to identify factors that contribute to the contamination risk.

2. Materials and methods

2.1. Mycotoxin data

We used 14 years of historical contamination data, daily county-specific weather data, remotely sensed satellite reflectance data, and data on soil-specific features. Feature engineering (Battilani et al., 2013; Van der Fels-Klerx et al., 2019) was used in combination with gradient boosting models (GBMs) (Friedman, 2001) and neural networks (NNs) to predict (Torgo, 2016) AFL and FUM. In this study, we used 1,772 observations of mycotoxin concentrations, AFL, and FUM from IL-grown corn. Data on the response variable were obtained from historic yearly survey summaries for 2003–2004 and 2008–2021 (data for 2020 were not available due to the COVID-19 pandemic) published by the IL Department of Agriculture. The years used for model validation were selected from these data based on the percentage of incidence of high contamination events. AFL was measured in 2010 (960 data points, 4% incidence of high contamination levels) and FUM was measured in 2016 (960 data points, 8.1% incidence of high contamination levels). The sample collection was done as described by Castano-Duque et al. (2022); briefly, the kernel sample collection was performed at harvest by randomly collecting 2.3–4.5 kg of whole kernels from four corn producers from each county. While mycotoxin analyses were conducted as soon as possible after collection, to minimize post-harvest mycotoxin accumulation, the samples were dried and stored at 4°C. This mycotoxin data set was zero-inflated, with high contamination levels being rare events (Castano-Duque et al., 2022). This issue was considered during data preparation for ML analysis by using the synthetic minority oversampling technique (Torgo, 2016) that allowed us to generate a balanced data set of the high and low contamination events.

2.2. Output variables and correlation analysis

We categorized into discrete variables the AFL and FUM contamination values by following the US Food and Drug Administration's legal threshold limits for mycotoxins in feed (https://www.fda.gov/food/natural-toxins-food/mycotoxins). For AFL, a high category was considered for concentrations >20 ppb (20 ng/g) and low for levels 20 ppb or lower (Supplementary material 1). For FUM, a high contamination level was for concentrations >5 ppm (5,000 ng/g), and the rest of the observations were low (Supplementary material 1). The FUM threshold used is the FDA guidance for equids and rabbits, which is lower than for other classes of livestock. A correlation analysis was performed among all the predictors and output variables using a confidence level of 0.95 for the correlation and clustering method in R (Team, 2017).

2.3. Weather, satellite, and soil data

Soil physical and chemical properties, satellite reflectance data, and soil moisture were analyzed to account for geographic, geomorphic, and surficial geological heterogeneity relating to crop health and soil habitat suitability for mycotoxin-producing fungi. All the satellite data were extracted and summarized by the county after refining them to reflect only land uses for corn and wheat (Boryan et al., 2011). For the extraction of crop specificity of satellite data, a data mask layer was generated for corn acreage for each year of study from the National Agricultural Statistics Service Cropland Data layer (NASS CDL—https://nassgeodata.gmu.edu/CropScape/) data set (Boryan et al., 2011). NASS CDL provides 30-meter grid cell estimates of crop type grown for the Conterminous United States for each year starting in 2005 to the present. Each grid cell represents a best estimate of crop type for a 30-meter by 30-meter division of land. To make the data mask, in each year of study, for each grid cell classed as corn in Illinois, a value of 1 was assigned, while a value of 0 was assigned for all other land uses. Each time-series normalized difference vegetation index (NDVI) layer from the MODIS satellite data was multiplied by the mask so that only pixels of MODIS with their centroids falling within corn acreage were tabulated for the county-level NDVI averages (Didan, 2021). The same process was repeated for wheat, with a separate mask file produced from the NASS CDL and separate NDVI county-level averages produced.

Soil properties were similarly aggregated to the county level by using the NASS CDL data mask. In this case, values of 1 were assigned to cropland, and values of 0 were assigned to other land uses such as forest or urban (Boryan et al., 2011). Soil properties were then queried for all pixels with a value >0 in the Soil Properties data layer from UC Davis and USDA NRCS (Walkinshaw et al., 2022). Mean values for all soil properties for cropland were tabulated to represent cropland soil properties by county. Climatological soil moisture estimates were obtained for the top 5 cm of the soil in IL from SMAP-HydroBlocks at 30 m resolution, developed by combining microwave satellite remote sensing, radiative transfer modeling, machine learning, and a high-resolution land surface model (Vergopolan et al., 2020, 2021).

The physical soil properties available for examination within the mycotoxin model context were water-holding capacity, hydraulic conductivity, bulk density, and soil texture (sand, silt, and clay content). Soil chemical properties include calcium carbonate content, cation exchange capacity, electrical conductivity, pH, and organic matter content. Estimates were determined for the 800 × 800 m pixels for various soil depth increments using measured values and interpolation techniques (Walkinshaw et al., 2022). The soil data were queried for soil properties by examining the intersection of each pixel with the cropland reported in the national cropland data layer of the National Agricultural Statistics Service of the USDA (Boryan et al., 2011). This national cropland data layer (CropScape—https://nassgeodata.gmu.edu/CropScape/) provides estimates of cropping land use for 30 m × 30 m land units (pixels) throughout the contiguous continental US for a 5-year summary period prior to the publication date (the summary period used was 2017–2021). For each county, the cropland was characterized for the final 5 years of the study. Only the land area that was planted in crops for the period of study was summarized for its soil properties, which were aggregated to the county-wide level as mean soil property estimates. These estimates excluded urban, forested, and other land uses not pertaining to crop production.

Soil moisture estimates (m3 H2O/m3-soil) were extracted from the SMAP-HydroBlocks (Vergopolan et al., 2021) 2015 to 2019 soil moisture average. SMAP-HydroBlocks is a satellite-based surface soil moisture product available at 30 m resolution over the conterminous United States. SMAP-HydroBlocks is derived from NASA's Soil Moisture Active-Passive product and the HydroBlocks-Radiative Transfer Model using a “cluster-based merging scheme” (Vergopolan et al., 2020) that is parameterized using machine learning-guided refinements based on relations among other in situ, satellite-based observation, and land use-land cover characteristics (Vergopolan et al., 2020). The data product provides soil moisture estimates for the top 5 cm of the soil surface at 6-h intervals. In turn, SMAP-HydroBlocks is sensitive to rainfall, drought, and evapotranspiration dynamics relevant to the microenvironment of mycotoxin-producing fungi.

Historical daily average air temperature, precipitation, and general vegetation index data were obtained from GRO-Intelligence (https://gro-intelligence.com/). A non–crop-specific vegetative index from GRO-intelligence was calculated from satellite data by taking into consideration multiple light spectra to enhance the presence of green vegetation by calculating the normalized difference vegetation index (NDVI), and this NDVI will be called veg_index to differentiate it from crop-specific NDVI. Crop-specific NDVI was calculated for each pixel of reported corn production for each year studied and for each pixel of reported winter wheat production for each year studied. The NDVI values, which were identical to the pixels of soil property estimates, were also summarized with a county-wide mean to characterize NDVI for corn and wheat-cropped land over time. NDVI was calculated from the MODIS satellite data (Didan, 2021) by obtaining the difference between the near-infrared reflectance and the red reflectance divided by the sum of the near-infrared and the red reflectance given in the MODIS data set. Higher values of NDVI are given when vegetation is healthy and green, as it absorbs red light and reflects near-infrared light. These NDVI values are available every 16 days from the MODIS satellite from February 2000 to 2023 and are reported in a 250-m resolution. We extracted these time-series values from MODIS data for the pixels determined to be growing either corn or wheat for each 16-day period available using Google Earth Engine. The crop-specific NDVI and veg_index (general NDVI) data were then interpolated into weekly summaries for the periods of study.

Historic meteorological data, soil properties data, and NDVI data were linked to the county-level mycotoxin data by using the county and the year as common information. After linking toxin data with weather, NDVI, and soil data, there were 1,772 data points across 99 counties.

2.4. Features engineering and data imputation for the AFL modeling

Daily average precipitation (mm) and air temperature (°C) data, averaged per county for the 14 years of historical data, were acquired from GRO-Intelligence. Furthermore, we used the geographical centroids of each county (latitude and longitude) and the climate zones (Friedman, 2001). For AFL models, we engineered a weekly aflatoxin risk index (ARI) as the cumulative sum per week of daily ARI. The monthly ARI was previously described (Castano-Duque et al., 2022); herein, we modified it to calculate a daily ARI (Eq. 1). These ARI equations have been applied to data from Eastern Europe in particular from Ukraine, which has a climate equivalent to IL (Van der Fels-Klerx et al., 2019).

ARI = growth or weighted_growth × afla or weighted_afla ×dispersal × (1 + ECB_damage)    (1)

In the daily ARI, fungal growth was calculated on a daily basis (Battilani et al., 2013) as described by Castano-Duque et al. (2022). Weighted fungal growth (10% of original growth) was generated for days of the month throughout the year when there was no corn in the field. The distribution of mycotoxin levels in relation to the thermal climate zone in IL (Friedman, 2001) has been examined and linked to differences in mycotoxin contamination distribution (Castano-Duque et al., 2022). In IL, there are two climate zones: a mixed-humid climate zone with a monthly outdoor temperature below 7°C during the winter and a cold climate zone with 5,900 heating degree days per year (18.3°C basis) (Baechler and Love, 2004). These climatological differences were considered in the model by assuming that the planting date in the mixed-humid zone started about 15th May and in the cold zone in April. This was assumed to be different in the cold and mixed-humid counties due to differences in no-corn in the field times in northern and southern states (January to April, 15th May, and December for cold and January to April and December for mixed-humid). These dates were included by calculating the ARI (Eq. 1). One of the assumptions in our model is that during days of the year when there is no corn in the field, the fungal growth was 90% less. The daily AFL production index was calculated (Battilani et al., 2013) as described by Castano-Duque and Vaughan (Castano-Duque et al., 2022). The spore dispersal was set as an ON/OFF switch (Van der Fels-Klerx et al., 2019; Castano-Duque et al., 2022). The assumption in our model is that if there is any daily precipitation, the dispersal is OFF, and if there is no daily precipitation, the dispersal is ON. Wind and other variables are involved in the spore dispersal of Aspergillus (Segers et al., 2023) and Fusarium (Hoffmann et al., 2021) species; nevertheless, only precipitation was used in this model due to the consistency of daily historical records throughout the geographical region studied in this case study. Insect damage was calculated for European corn borer damage by using growing degree days (Tbase = 6C and Tcut = 30°C) and the logistic equation (Maiorano et al., 2009) (Eq. 2).

A = 7.3

Um = 0.013

Lambda = 1,236.913

R2 = 0.718

e = exp(1)

ECB_damage = A × exp{exp[(μm x e/A) ×(lambda  cumGDD + 1]}    (2)

where ECB (European corn borer) represents damage to the ear by insects, A represents the asymptotic maximum damage level observed in the field approximated to the higher first decimal, μm represents the maximum specific damage rate, λ represents the intersection of the tangent in the inflection point with the x-axis, and accGDD represents the accumulated GDD. Both μm and λ are estimated parameters in Maiorano and Reyneri (Maiorano et al., 2009).

For any missing values in the weekly ARI or vegetative index features, we performed imputation using multivariate imputation by chained equations; in specific, the predictive mean matching (PMM) method was used in R (van Buuren and Groothuis-Oudshoorn, 2011; Team, 2017). This imputation method allowed us to determine plausible data values by adding a data point from the original data whose regression-predicted values are closest to the regression-predicted value for the missing data point from the simulated regression model (van Buuren and Groothuis-Oudshoorn, 2011). Due to the high number of missing data for ARI in weeks 8, 16, 24, 32, 40, and 48, we decided to remove these input features from the model. Finally, we linked the AFL data to the feature data set to create a set of 1,772 data points and 153 features or predictors. The inputs for the AFL model were weekly ARI for each county (Supplementary Table 1). We also added to our input features an average bi-weekly NDVI per county during the weeks of the month when corn might not be in the field (below week 13 and above week 45); an average corn and wheat NDVI; soil properties, latitude, and longitude.

2.5. Weather data and imputation for the FUM modeling

For FUM modeling, we could not use feature engineering functions such as the ARI calculated for AFL produced by Aspergillus because these equations were generated using Aspergillus spp growth curves. The inputs for the FUM model were weekly average temperature and precipitation. We also added to our input features an average bi-weekly veg_index per county during the days of the month when there is no corn in the fields; an average corn and wheat-specific NDVI; soil properties; latitude; and longitude. The daily precipitation and daily average temperature data were averaged weekly per county; each calendar year of weather data was kept separate and linked to mycotoxin yearly data for the 14 years of historical data per year and county (Supplementary Table 1). Average temperatures were expressed in degrees Celsius, and each county was assigned its geographical centroids (latitude and longitude), climate zones (Beck et al., 2018), crop-specific NDVI, and veg_index. For any missing values in our weekly weather data, crop-specific NDVI, and veg_index features, we performed imputation using multivariate imputation by chained equations, specifically the predictive mean matching (PMM) method in R (van Buuren and Groothuis-Oudshoorn, 2011; Team, 2017). Due to the high number of missing data for weather variables in weeks 8, 16, 24, 32, 40, and 48, we decided to remove these input features from the model. Finally, we linked the FUM data to the feature data set to create a set of 1,772 data points and 199 features or predictors.

2.6. Gradient boosting machine learning

GBM was used to perform the prediction of mycotoxin contamination, as GBM allows for the determination of the relative influence of input features on the output variable. The GBM software package in R was used. This software provided extensions to Freund and Schapire's AdaBoost algorithm and Friedman's gradient boosting machine (Friedman, 2001). For performing GBM, we first removed the IL county identifier from the data set and the data for the year that was used for validation, as these would lead to overfitting the model. Next, data were balanced by using the synthetic minority oversampling technique (SMOTE) from the DMwr package in R (Team, 2017), which created a new balanced data set by oversampling observations from the high contamination level class. Finally, the balanced data were partitioned to generate training and testing sets by using a 70 to 30 ratio (Supplementary material 1). We performed GBM for AFL and FUM separately, using the following flags on the training data: a threshold of 500 trees, an interaction depth of 1, a shrinkage of 0.01, and 10 cross-validation folds with the distribution selected as multinomial (Supplementary material 1).

The GBM R package (Ridgeway, 2006) was used to perform prediction analysis using the testing data set and the best fit generated from the training data. GBM uses decision trees in an iterative process to determine the best number of trees leading to the lowest error based on the decline of the loss function. Finally, the GBM package was used to compute the effect values (variable relative influence) for each predictor in the model. The relative influence of each predictor from the tree ensemble is determined as the reduction in the sum of squared error due to the splits on that predictor, then averaging the improvement made by each variable across all the trees to determine the relative effect (Friedman, 2001). Thus, the variables with the largest average decrease in the sum of squared error are considered the most important, expressed as the percentage of the total reduction in the error given by all the predictors. A confusion matrix was developed using the caret package in R that computed the overall statistics, the specific statistics by class, the receiver operating characteristic curve (ROC), and the area under the ROC curve (AUC) values for the multi-class classification to measure the quality of the model's predictions.

For the FUM model, we used the following flags on the training data set: a threshold of 500 trees, interaction depth of 1, shrinkage of 0.01, 10 cross-validation folds, and the distribution was selected as multinomial (Supplementary material 1). The remaining analysis was performed as described for AFL.

2.7. Neural network analysis

NN was selected as a second modeling method because of its high performance in the prediction of rare events (Zamani and Kremer, 2013; Gibson and Kroese, 2022). For performing NN training, we first removed the IL county identifier and the year from the data set to reduce potential overfitting. Then, we selected only the input variables that show a relative influence higher than zero in the GBM and then removed the data for the year that was used for validation. Data without the validation set were balanced using the SMOTE method described for GBM. Data were partitioned to create training and testing sets using a 70-to-30 ratio (Supplementary material 1). The same mean and standard deviation scaling was applied to the testing and validation data sets. We trained the NN model in AFL and FUM separately. The best number of hidden layers and neurons was determined by an exhaustive iterative process that aimed to find the combination of NN parameters with the highest accuracy.

2.8. Validation analysis using GBM and NN

To perform prediction analysis using the GBM and NN models, we used a single year: 2010 for AFL and 2016 for FUM. These years were selected because their incidence of high contamination events was higher than 3% (more than three high contamination events), and the incidence of high contamination events was 4 and 8.1%, respectively. Validation was performed by using the best fit of GBM and the best number of hidden layers (2 layers) and neurons (65 neurons in layer 1 and 15 neurons in layer 2) for AFL and FUM (65 neurons in layer 1 and 30 neurons in layer 2) determined from the training data (Supplementary material 1). All the input features for the validation years were prepared as previously described in the Methods section for the training data. The mycotoxin data for the years 2010 and 2016 included 99 counties and a total of 99 observations.

R code: Available in Supplementary material 1.

3. Results

3.1. AFL and FUM contamination in IL

The AFL data showed that only 3.1% of the samples had concentrations >20 ppb, and only 5.4% of the samples had FUM concentrations >5 ppm (Table 1).

TABLE 1
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Table 1. Incidence of AFL and FUM contamination (high or low) in corn in Illinois from 2003 to 2021.

3.2. Weather variables and feature engineering

AFL risk indexes (ARIs) were the main features engineered by linking fungal growth (Battilani et al., 2013; Van der Fels-Klerx et al., 2019; Liu et al., 2021; Castano-Duque et al., 2022) with the weather. Using ARI instead of temperature and precipitation led to a lower number of input variables incorporated into the AFL model, which also decreased the correlation levels among meteorological variables (Figures 1A, C). For the FUM modeling, we could not use feature engineering functions such as the ARI calculated for AFL produced by Aspergillus. FUM output variables showed a significant correlation with general veg_index, corn-specific NDVI, temperature, and several of the soil properties (Figure 1C). Using GBM and only the relative influential variables for the NN led to the inclusion of a lower number of input variables in the models, decreasing the autocorrelation among variables. Furthermore, GBM allows for the control of overfitting caused by high correlation levels among variables by sequentially generating model ensembles that can learn from the errors of previous ensembles (Cooper, 1990; Friedman, 2001).

FIGURE 1
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Figure 1. Pair-wise correlation analysis of the significant input variables influencing GBM and summary of the GBM model using multinomial mycotoxin outcome. (A) Correlation analysis of the features used for AFL modeling; (B) top 20 influential input features and their relative influence over the model in the prediction of AFL; (C) correlation analysis of the features used for FUM modeling; (D) top 20 influential input features and their relative influence over the model in the prediction of FUM. The correlation is depicted from positive (blue) to negative (red), with blank squares representing non-significant p-values of correlation between variables. For the correlation analysis, the p-value cutoff was 0.05, and the confidence level was 0.95. The blue hue in GBM plots represents the relative influence of the input variables, with light blue high and dark blue low influence levels. The green line is the testing set multinomial deviance loss, the black line is the training set multinomial deviance loss, and the blue dotted vertical line is the number of iterations used.

3.3. GBM analysis for AFL and FUM

We used GBM to model AFL and FUM contamination levels (factorial output variable) with our engineered features for AFL and without engineered features for FUM. The models were used to make predictions for the samples in the testing data set (Table 2, Supplementary Table 1). The optimal number of trees for GBM-AFL and GBM-FUM used was 500, which represents the number of trees at which the cross-validation error is minimized (Figures 1B, D). The McNemar P-value for the GBM-AFL was 0.4862 and for the GBM-FUM was 0.052 (Supplementary Table 1), which indicated that the proportion of type I and type II errors is the same, meaning that there is homogeneity in the proportion of misclassification. This was expected because the training and testing data sets were balanced by using SMOTE. The overall accuracy of the GBM-AFL model in the test data set (30% of data) was 96%, with a balanced accuracy for high contamination of 96%. For GBM-FUM, the overall accuracy of the test data set was 92%, with a balanced accuracy of 92% (Table 3, Supplementary Table 1). Balanced accuracy or performance is a metric that uses the average of the sensitivity and specificity of the model by considering the predicted classes (high and low contamination). The model performance was the same for the prediction of high and low contamination events. Thus, the balanced accuracy is equal to the overall accuracy. The multi-class area under the curve for GBM-AFL in the testing data set was 0.97 and for GBM-FUM was 0.92, which represents the classifier in its ability to distinguish among classes.

TABLE 2
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Table 2. Contingency tables for GBM-AFL, GBM-FUM, NN-AFL, and NN-FUM from the test (30% of the data) and validation (single year) data sets.

TABLE 3
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Table 3. Summary statistics of GBM and NN for AFL and FUM.

The GBM-AFL model showed that of the 153 input features (predictors), only 46 had non-zero influence (Supplementary Table 1). The GBM-FUM showed that of the 199 input features, only 85 had non-zero influence (Supplementary Table 1). For the GBM-AFL model, the top 20 influential features were: ARI in January (Weeks 1, 2, 3, and 4), in February (Weeks 5 and 7), in March (Weeks 11 and 12), in April (Week 18), in May (Week 20), in July (Weeks 27 and 30), in September (Week 37), in October (Week 43), in November (Weeks 45 and 47), and in December (Week 49), soil calcium carbonate (CaCO3), soil electrical conductivity (ec) and soil sodium absorption ratio (sar) (Figure 2, Supplementary Table 1).

FIGURE 2
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Figure 2. ARI relationship with AFL contamination levels and their geospatial distribution in IL from 2003 to 2021. (A) Average ARI in week 4 (January); (B) average ARI in week 11 (March); (C) average ARI in week 27 (July); (D) average ARI 45 (November). Box–Whiskers plot depicts the maximum (25th – 1.5 * interquartile range “IQR”) and minimum [75th percentile + 1.5 * interquartile range (IQR)], and the Box–Whisker plot depicts median, first (25th percentile) and third (75th percentile) quantiles distribution; For AFL, high is >20 ppb and low ≤20 ppb. The violin plot is shaded in red and depicts the density distribution of the soil property in low and high levels of mycotoxin contamination; and the gray dots depict each data point. Maps are shaded in red in relation to the ARI value for a specific week in each year; and the y-axis is latitude and the x-axis is longitude.

In the GBM-AFL, ARI showed a positive correlation with AFL contamination, meaning that high ARI led to high toxin contamination (Figures 1A, 2). At a geospatial level, the ARI throughout IL tends to be higher in the southern region except during 2012, the year with the highest incidence of AFL contamination in the historical data set evaluated (35.4%, Table 1), when the ARI levels were the highest throughout the state in March (week 11) and July (week 27) (Figures 1A, 2). Corn NDVI showed a negative correlation with AFL contamination levels in July (week 30) (Figure 3A) and a positive correlation with wheat NDVI values in February (week 5) (Figure 3B). At a geospatial historical scale, corn NDVI values in week 30 were lower in the southern part of IL in 2012 compared to other years (Figure 3A), and PRCP between weeks 28 and 31 was lower in 2012 compared to other years throughout IL. Calcium carbonate levels in the soil had a negative correlation with AFL levels, meaning that low calcium carbonate tends to be associated with high AFL at harvest (Figure 4A). Lower deposits of calcium carbonate were observed in the southern regions of IL compared to the northeast (Figure 4B). To summarize, the GBM-AFL model showed that ARI pre-planting months (January, February, March, and April) had a strong influence over predictions for AFL contamination at harvest time, and calcium carbonate levels in the soil influence aflatoxin levels.

FIGURE 3
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Figure 3. Crop-specific NDVI relationship with AFL contamination levels and their spatial distribution in Illinois from 2003 to 2021. (A) Corn NDVI in week 30 (July); (B) wheat NDVI in week 5 (February). Box–Whisker plot depicts the maximum (25th – 1.5 * interquartile range “IQR”) and minimum [75th percentile + 1.5 * interquartile range (IQR)], and the Box–Whisker plot depicts median, first (25th percentile), and third (75th percentile) quantiles distribution. For AFL, high is >20 ppb and low ≤20 ppb. The violin plot is shaded in red and depicts the density distribution of the soil property in low and high levels of mycotoxin contamination. The gray dots depict each data point. Maps show the average NDVI values for corn (green) and wheat (yellow) for specific weeks each year.

FIGURE 4
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Figure 4. Calcium carbonate (CaCO3 Kg/m2) relationship with (A) AFL contamination levels from 2003 to 2021 and its (B) spatial distribution in IL. Box–Whisker plot depicts the maximum (25th – 1.5 * interquartile range “IQR”) and minimum [75th percentile + 1.5 * interquartile range (IQR)], and the Box–Whisker plot depicts median, first (25th percentile), and third (75th percentile) quantiles distribution. For AFL, high is >20 ppb and low ≤20 ppb. The violin plot is shaded in red and depicts the density distribution of calcium carbonate in low and elevated levels of mycotoxin contamination; and the gray dots depict each data point. Maps show the weight percentage of calcium carbonate values. For color legend, a non-linear ramp was used.

The GBM-FUM showed that of the 199 input features (predictors), only 85 had non-zero influence (Table 2, Supplementary Table 1). Among the 85 features, the top 20 were: latitude; temperature in January (week 2), February (week 5), April (week 14), July (weeks 30 and 31), August (week 34), November/December (week 44), and December (week 52); precipitation in February (week 7), March (week 12), September (weeks 36 and 39), and October (weeks 41 and 42); veg_index February (week 5) and March (week 11); corn-specific NDVI January (week 1), May (week 19), July (week 28), and October (week 42); wheat-specific NDVI in June/July (week 26); clay percentage 25–50 cm depth; water storage and soil water capacity (Supplementary Table 1). In the GBM-FUM, temperature in July (Week 31) and October (Week 44) had a positive relationship with FUM contamination levels (Figures 5A, B), similarly for PRCP in February (Week 7), higher precipitation led to higher FUM contamination levels (Figure 5C) at a geospatial historical level, and high PCRP in March throughout IL in 2008 was linked to the highest incidence of FUM (25.6%, Table 1). To summarize, weather patterns such as precipitation levels in week 7 (February) above 2.5 mm and week 11 (March) above 0.3 mm can lead to higher FUM levels (Figure 5). Furthermore, temperatures in week 31 (July) above 24°C and week 44 (October) above 10°C correlated with high levels of FUM contamination in corn (Figure 5).

FIGURE 5
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Figure 5. Temperature, precipitation, and veg. index relationships with FUM contamination levels and their geospatial distribution in IL from 2003 to 2021. (A) Average temperature in week 31, July, (B) average temperature in week 44, October, (C) average precipitation in week 7, February, (D) average veg. index in week 11, March. Box–Whisker plot depicts the maximum (25th – 1.5 * interquartile range “IQR”) and minimum [75th percentile + 1.5 * interquartile range (IQR)], and the Box–Whisker plot depicts median, first (25th percentile) and third (75th percentile) quantiles distribution; For FUM, high is >5 ppm, and low ≤5 ppm. The violin plot is shaded in blue and depicts the density distribution of the temperature, precipitation, or veg. index in low and high levels of mycotoxin contamination; and the gray dots depict each data point. Maps of geography are shaded in relation to temperature (red), precipitation (blue), or vegetation index (green) values for specific weeks each year, the y-axis is latitude and the x-axis is longitude.

General vegetation index in March (Week 11) and corn-specific NDVI in February (week 5), May (week 19), and October (week 42) were positively linked to high FUM contamination, which tends to be observed in the southern parts of IL (Figure 6). While the wheat-specific NDVI showed a negative relationship with FUM contamination levels in June (week 26) (Figure 6D). Soil moisture and available water-holding capacity showed a positive correlation with FUM contamination levels, while clay at 0–5 and 25–50 cm showed a negative correlation (Figure 7). At a geospatial scale, both soil moisture and water-holding capacity tend to be higher in the southwest areas of IL, while the clay content tends to be higher in the northeast regions of the state (Figure 7). GBM-FUM showed that pre-planting precipitation and temperature influence the prediction of FUM contamination levels. Furthermore, crop-specific NDVI is a high influencer, as are several soil characteristics linked to water present in the soil.

FIGURE 6
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Figure 6. Crop-specific NDVI relationship with FUM contamination levels and their geospatial distribution in IL from 2003 to 2021. (A) Corn NDVI in week 5, February, (B) corn NDVI in week 19, May, (C) corn NDVI in week 42, October, (D) wheat NDVI in week 26, June. Box–Whisker plot depicts the maximum (25th – 1.5 * interquartile range “IQR”) and minimum [75th percentile + 1.5 * interquartile range (IQR)], and the Box–Whisker plot depicts median, first (25th percentile) and third (75th percentile) quantiles distribution; For FUM, high is >5 ppm, and low ≤5 ppm. The violin plot is shaded in blue and depicts the density distribution of the corn or wheat NDVI in low and high levels of mycotoxin contamination; and gray dots depict each data point. Maps of geography are shaded in relation to corn NDVI (green) or wheat NDVI (yellow) values for specific weeks in each year.

FIGURE 7
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Figure 7. Soil properties relationship with FUM contamination levels and their geospatial distribution in IL. (A) soil moisture (m3 H2O/m3 soil), (B) available water-holding capacity (cm). Box–Whisker plot depicts the maximum (25th – 1.5 * interquartile range “IQR”) and minimum [75th percentile + 1.5 * interquartile range (IQR)], and the Box–Whisker plot depicts median, first (25th percentile) and third (75th percentile) quantiles distribution; (C) percentage of clay content from 0 to 5 cm below surface, (D) percentage of clay content from 25 to 50 cm below surface; For FUM, high is >5 ppm, and low ≤5 ppm. The violin plot is shaded in blue and depicts the density distribution of the soil properties in low and elevated levels of mycotoxin contamination; and the gray dots depict each data point. Maps of geographical shaded red in relation to soil properties values, scale is in miles. For color, legend of soil moisture, a linear ramp was used, and for available water-holding capacity, and clay content, and a non-linear ramp was used.

3.4. NN analysis for AFL and FUM

We used NN to model AFL and FUM contamination levels (factorial output variable) by using the input features with non-zero relative influence values from the GBM results (Supplementary Table 1). The McNemar P-value for testing NN-AFL was 0.007 and for testing NN-FUM was 0.035 (Supplementary Table 1), which indicated that the proportion of type I and type II errors is not the same, meaning that there is a disproportion of misclassification. This misclassification disproportionality can be seen in the NN-AFL model, which classified 14 data points of 486 as low when they were high and 2 data points of 474 as high when they were low contamination levels (Table 2, Supplementary Table 1). Similarly, the NN-FUM classified 26 data points as low when they were high and 12 as high when they were low (Table 2, Supplementary Table 1). The overall accuracy of the NN-AFL model was 98%, with a balanced accuracy for high contamination of 98%. For NN-FUM, the overall accuracy was 96% and the balanced accuracy was 96% (Table 3, Supplementary Table 1). The multi-class area under the curve for NN-AFL in the testing data set was 0.9835, and for NN-FUM, it was 0.96.

3.5. GBM and NN model validation

Model validation was performed by using mycotoxin data from 2010 for AFL (4% incidence) and 2016 for FUM (8.1% incidence) (Table 1). The data included 99 counties and a total of 99 observations in each year (except 2021 with 386 observations). The GBM-AFL model successfully explained low contamination levels of AFL with an accuracy of 96% (Table 3, Supplementary Table 1). The model was not able to correctly predict high contamination events of AFL from the validation data set, which had four observations labeled as high AFL. The overall accuracy of GBM-FUM was 78%, with a specificity of 75% and a balanced accuracy for high levels of 76% (Table 3, Supplementary Table 1). The NN models showed higher balanced accuracy for both AFL and FUM. The NN-AFL model explained high contamination levels with an overall accuracy of 94% and a balanced accuracy of 73% (Table 3, Supplementary Table 1). The NN-AFL model correctly classified 2 out of 4 high contamination events in the validation data set, and only 4 out of 95 data points were misclassified as high when they were low. The McNemar P-value for validating NN-AFL was 0.68 (Supplementary Table 1). The NN-FUM model explained high contamination levels with an overall accuracy of 73% and a balanced accuracy of 85% (Table 3, Supplementary Table 1). The NN-FUM model successfully classified all the high contamination events in the validation data set, but it had 27 data points misclassified as high when they were low. The McNemar P-value for validating NN-FUM was close to zero (0.0000005, Supplementary Table 1).

4. Discussion

Mycotoxin contamination in the US is a pervasive problem that negatively impacts human and animal health and causes losses in the agriculture industry (Vardon et al., 2003; Wu, 2006; Mitchell et al., 2016; Winter and Pereg, 2019). AFL and FUM predictive modeling has been recently studied in the US using machine learning tools (Castano-Duque et al., 2022) that linked weather parameters and latitudinal location in the IL state with historical contamination events of these two mycotoxins. This study builds upon this initial model (Castano-Duque et al., 2022), which provided an IL state case study to account for daily changes in historical weather data (instead of monthly). We also added geospatial soil mineralogical chemical/physical properties and land usage parameters to the models for AFL and FUM. Similarly, predictive mycotoxin models have been developed for northern Italy, linking cropping system factors, and weather variables with deep neural network (DNN) models (Leggieri et al., 2021). Our NN models are unique because we included geospatial dynamic soil and land features linked to the GPS center coordinates of the IL counties. Land usage and soil mineralogical physical/chemical properties are variable for the specific geospatial locations in the US, at both state and county specificity levels (Smith et al., 2019). Using dynamic geospatial data in our models led to the identification of new insights into factors that influence mycotoxin contamination. These factors could be used for risk assessment and to implement timely and region-specific mycotoxin control management practices.

GBM-AFL identified that higher ARI in January, March, July, and November corresponds to higher AFL contamination, meaning that pre-sowing and post-harvest environmental conditions have a strong influence on AFL levels at harvest time. Given that the harvest takes place prior to November, our model assumes that post-harvest input features will influence next year's mycotoxin contamination. Similar correlations were previously proposed by research conducted in the US (Castano-Duque et al., 2022), Africa (Keller et al., 2022), and Serbia (Liu et al., 2021). GBM-FUM showed that high precipitation events during February and March (pre-sowing time), as well as elevated temperatures in July (flowering time) and October (harvest time), influence FUM contamination. Consistently, previous model reports have shown that warmer temperatures early in the planting season (January–April) lead to higher AFL contamination levels in the US (Yu et al., 2022). GBM-AFL showed that corn-specific NDVI at week 30 (July—within flowering time) also influenced AFL contamination; this feature is linked to plant health as NDVI represents a composite satellite measurement of plant greenness. Lower NDVI translates into less green, unhealthy and/or lower density plants, and lower NDVI in week 30 would suggest that the plants were stressed possibly due to abiotic and/or biotic factors.

Previous studies have suggested that crop stress in general also correlates with mycotoxin contamination (Kebede et al., 2012). In 2012, when corn NDVI at week 30 was lower than in other years, the corn crops suffered from extreme drought conditions (NOAA, 2013), which were reflected in lower NDVI values and likely contributed to AFL (contamination levels at harvest time). Studies conducted in Kenya found that AFL contamination is positively associated with high rainfall and NDVI during pre-flowering time while negatively associated during post-flowering time and at harvest (Smith et al., 2016). Our findings agree with published logistic regression models that show that drought stress in corn during flowering time (prior to and beyond mid-silk) is critical for higher contamination at harvest (Damianidis et al., 2018). US-IL models have shown that weather and ARI between corn-growing seasons significantly influence the contamination at the end (Castano-Duque et al., 2022). It is possible that environmental conditions (weather conditions or other agricultural practices) during the spring favor fungal growth (Borràs-Vallverdú et al., 2022), leading to higher corn contamination at the end of the growing season. The development of pest management strategies that take into consideration climate change, such as warmer and wetter spring seasons and drought during the flowering time, is relevant for the management of mycotoxins.

AFL and FUM-GBMs showed that soil properties are also influential factors contributing to the mycotoxin contamination of corn across spatiotemporal scales. Higher calcium carbonate content patterns throughout IL soil were negatively correlated with historical AFL contamination levels. It has been demonstrated that the calcium carbonate content in soils influences soil pH (Weil and Brady, 2002), whereby greater dissolved calcium increases buffering capacity and generates more alkaline soils. Geospatial differences in calcium carbonate in IL soils are due to the advance and retreat of the Laurentide glacier which deposits carbonate-rich materials in the northern half of the state. The negative correlation between AFL levels and calcium carbonate suggests that regions with lower calcium carbonate are associated with higher AFL contamination (Chang and Lynd, 1970), and therefore, calcium carbonate is an important factor in AFL contamination risk.

The abundance of calcium is modulated by both abiotic and biotic factors. In terms of abiotic processes, soils with greater concentrations of CaCO3, such as Northern Illinois, typically exhibit greater Ca2+ concentrations through the dissolution of parent CaCO3 and other Ca-bearing mineralogy via infiltrating rainwater (Smith et al., 2019). In terms of biotic factors, such as soil bacteria, they can also modulate the calcium carbonate content of soil by dissolving calcium carbonate into Ca2+ ions and other carbonate species. Some of these “Calcite Dissolving Bacteria” are Serratia marcescens, Sphingomonas changbaiensis, or Novosphingobium panipatense (Peper et al., 2022). Furthermore, the soil microbiome can become dominated by microbial assemblages that suppress the growth of AFL-producing fungi with increasing Ca2+ (Zhang et al., 2021), FUM-producing fungi (Srinivasan et al., 2009), and suppression of mycotoxin-producing fungi strains by non-toxin-producing fungi (Mehl et al., 2012; Ehrlich, 2014). The presence of both growth-suppressive bacteria and fungi that dissolve calcium carbonate would potentially lead to positive feedback in a calcium carbonate-rich soil. Fungi are involved in carbonate rock destruction, dissolution, precipitation (Verrecchia et al., 2003), and biomineralization (Bindschedler et al., 2016) in laboratory environments. Other environmental factors, such as wet and dry periods, affect the precipitation and accumulation of calcium carbonate in soil (Birkeland, 1974). It is possible that fungal communities and weather parameters co-influence levels of calcium carbonate and calcium ions in the soil, and these compounds can act as a feedback loop that modulates the fungal communities present in the soil. Understanding the native microbial communities and mycotoxin fungi/contamination could aid in understanding the interaction of soil microbiome, calcium carbonate, and AFL contamination. This knowledge of microbiome diversity could be useful for the development of region-specific biocontrol strategies.

The addition of calcium carbonate in the form of limestone to soils is a major agricultural practice in humid climates worldwide, used to directly change the chemical makeup of the rooting zone and improve soil fertility (Weil and Brady, 2002). Greenhouse experiments with peanut plants (Arachis hypogaea L.) showed that adding calcium to the soil leads to a significant reduction in AFL contamination of seeds (Uppala, 2011). Calcium-deficient soils cause calcium deficiency in the corn plant, which can lead to the failure of the upper leaves to unwrap at tasseling time (Melsted, 1953), shorter roots, chlorosis, and necrosis of leaves (do Moraes Gatti et al., 2023). These calcium-deficient symptoms might increase the propensity of fungal infections to thrive, as calcium is an important component of pathogen-associated molecular-triggered immunity (Fountain et al., 2016) and maize defense responses to pathogens (Jiang and Zhang, 2003; Hu et al., 2007; Ma and Berkowitz, 2011). We hypothesize that Northern IL soils, which are richer in CaCO3 and Ca, are conducive to healthier plants capable of greater resistance to fungal disease and supporting microbiomes that also suppress AFL growth. The characterization of IL native microbiome and fungi soil populations linked to their geospatial location in calcium carbonate-rich or poor zones is not known, although this could aid in understanding the interaction of soil microbiome, calcium carbonate, and AFL contamination. This knowledge of microbiome diversity could be useful for the development of region-specific biocontrol strategies and mycotoxin management alongside external limestone application in areas such as Southern IL or other areas with elevated AFL risks, e.g., a corn-growing season with a hot/wet spring followed by drought during flowering time.

GBM-FUM showed that FUM contamination is correlated with soil moisture, available water-holding capacity, and a high percentage of clay. These soil hydropedology properties vary across IL (Smith et al., 2019). Southern IL tends to have higher soil moisture levels compared to the north, with the southern area of the state having historically higher percentages of FUM contamination (Castano-Duque et al., 2022). Correspondingly, a positive correlation was observed between soil moisture and FUM contamination. Other soil properties, such as the percentage of clay, tend to be higher in the northeastern areas of IL (Smith et al., 2019), which historically tend to have lower FUM contamination (Castano-Duque et al., 2022) as demonstrated by the negative correlation between these two variables.

Clay is the smallest mineral component of soil with the highest surface area per unit mass, in general, it has a high water-holding capacity and low hydraulic conductivity compared to other soil textures, making it prone to becoming waterlogged in moist conditions (Libohova et al., 2018), such as heavy rains. Clay's high water-holding capacity and poor permeability to water and gases (Weil and Brady, 2002) can lead to flood stress and waterlogging of plants during high precipitation events. While the relationship between flood-stressed corn and Fusarium spp. is not fully understood, it has been established that Fusarium is a strongly aerobic fungus (Stover, 1953), and it has been shown that among sandy loam, silt loam, or clay soil types, Fusarium solani and Fusarium tricinctum have higher disease severity on soybeans grown in sandy and silt loam soil (Yan and Nelson, 2022). Clay soils have high infiltration capacities as water moves into the shrinkage cracks, but when cracks are not present, their infiltration rate is characteristically slow. The small pores of clay solids when filled with water (saturated and under waterlogging conditions) could also influence Fusarium spp by limiting oxygen availability. It would be key to predict FUM outbreaks to understand the biological effect of clay-rich soils and high precipitation events on Fusarium growth and the diversity of species in different geospatial locations in the US.

Soils in IL with prominent levels of clay, low soil moisture, and low water-holding capacity offer conditions that historically might lead to lower FUM contamination. Clay-rich soils bind strongly to organic matter, contributing to soil aggregation, soil fertility, and cation exchange. Therefore, clay influences soil fertility by modulating cation exchange capacity and soil physical properties (Weil and Brady, 2002). The capacity of clay to hold water and bind to organic matter affects water in the soil and nutrients available for crops. High precipitation events early in the year (February), when there is no corn in the field, could lead to higher FUM contamination. We hypothesize that there must be some biological and chemical interaction between clay-rich soils early in the season and snow and rain events that influence fungal growth in the fields.

The primary abiotic factors contributing to the presence of FUM are water activity and temperature (Sanchis et al., 2006; Picot et al., 2010), but the nature of this relation is complex in the context of soil, hydroclimate variability, and plant water use. In optimal temperatures, increased water activity promotes FUM production, but at temperatures above the thermal optimum of 25°C, decreased water activity also promotes greater FUM production (Marin et al., 2004; Samapundo et al., 2005; Sanchis et al., 2006; Picot et al., 2010). Furthermore, F. verticillioides growth has been shown to be limited by low water activity; however, the FUM1 gene expression was significantly greater with lower water activity (Jurado et al., 2008). Therefore, favorable conditions for FUM production may occur under two different hydroclimate conditions: (1) a wet, i.e., high water activity, period with temperatures in the thermal optimum range; and (2) temperatures above the thermal optimum but dry, i.e., low water activity. Some field-based evidence corroborates the latter, where Roucou et al. (2021) noted increased FUM risk with greater water stress, but only when temperatures were elevated. In this study, the greater historical occurrence of FUM in Southern IL, where soils have less water and a propensity for water stress, would support the second condition. Another biophysical feedback between crop and soil may also drive greater water stress as starches are produced during kernel ripening (Jurado et al., 2008; Picot et al., 2010). As such, positive feedback driving greater risk for FUM production into the latter part of a growing season may develop when: (1) temperatures are elevated; (2) kernel ripening begins and plant water use increases; (3) water stress is persistent, e.g., drought-like conditions; and (4) crops are grown in soils that exasperate water-holding capacity.

Depending on the soil type, complex plant–water interactions can affect plant health positively or negatively. Soils conducive to drought or flooding stress can result in crops with a lower ability to fight fungal infections and increased susceptibility to AFL (Kebede et al., 2012) and FUM (Parsons and Munkvold, 2010; Vaughan et al., 2016) contamination. Furthermore, relative humidity affects fungal sporulation and growth (Foister, 1946); therefore, both soil–fungi–water interactions and plant–fungi–water interactions will affect mycotoxin outbreaks. Further research that includes field trials from different regions of the US that have variable soil types and includes year-round time frames to account for the variation of precipitation and temperature would aid in understanding the causality that these spatial-temporal variables have on fungal load and mycotoxin contamination.

The AFL and FUM-GBM models showed better accuracy values than previously reported in the monthly-based models that did not include geospatial soil dynamic features (Castano-Duque et al., 2022). NN models showed high class-specific performance for 1-year predictive validation for AFL (73%) and FUM (85%), thus the NN models are recommended for annual mycotoxin prediction. The observed overall and specific accuracy levels are at par when compared to other mycotoxin non-US models that showed ranges from 90 to 99% general accuracy for wheat models in Europe (Wang et al., 2022), 75% general accuracy for corn using AFL-maize models in Italy (Battilani et al., 2013) and >75% general accuracy using machine learning models for toxin prediction in corn in northern Italy (Leggieri et al., 2021). Because GBM and NN models showed high-performance levels (Table 3), both can be used for annual mycotoxin prediction. To be implemented, these models would need to use input features for the months of October–December from the previous year's post-harvest and projected weather and NDVI values for a maximum of a month prior to harvest.

Our dynamic geospatial models offer additional information about soil properties and remote-sensed data (NDVI) that influence AFL and FUM contamination in corn. Aspergillus growth begins in the soil, which is the habitat for the fungus; thus, the production of AFL by fungi will be influenced by agricultural practices, environmental conditions, and fungal interaction with soil and plants (Winter and Pereg, 2019). Several studies have shown a significant correlation between climate, soil properties, NDVI, and agricultural management practices and AFL contamination in several countries in sub-Saharan Africa, such as Kenya, Zambia, and others, as reviewed by Keller et al. (2022). AFL surveys and studies conducted in Eastern and Western Kenya (Köppen, 2011) support the utility of remote-sensed data such as NDVI, rainfall, and soil properties to predict aflatoxin contamination (Smith et al., 2016). Satellite-generated databases have been previously used in wheat studies in Europe and led to higher model accuracy (Wang et al., 2022). Previous studies in Africa found that soil organic carbon content, pH, total exchangeable bases, salinity, texture, and soil type were significantly associated with AFL (Smith et al., 2016). Soil data throughout IL embody important geographic variability related to geologic deposition, age of material, climate, duration of pedogenesis, natural history, and other factors. Soil conditions strongly influence which species of fungi dominate in a given soil environment (Weil and Brady, 2002). Our research shows that in the US, specific properties available from geospatial data such as calcium carbonate, pH, clay content, and soil moisture are key factors correlated with historical AFL and FUM outbreaks. Our dynamic geospatial models can guide research and identify multiple factors contributing to the risk of AFL or FUM contamination in a geographical region and within weekly time frames.

Some agronomic practices take place between corn-growing seasons, such as tilling and drilling (Borràs-Vallverdú et al., 2022), while other factors are constant throughout the year, such as soil properties (Smith et al., 2016) and other socio-economical parameters such as training farmers on the detection of contaminated crops in the field and mitigation strategies, and the involvement of the private sector to provide incentives for farmers to adopt aflatoxin management techniques (Titilayo, 2018) that influence mycotoxin contamination. Several of these factors, such as soil properties, were included in our models, although much information on other agronomic practices is not available at the historical geospatial scale needed for this mycotoxin data set. Nevertheless, our models were able to determine that input features linked to weekly temporal zones between corn-growing seasons have a significant influence on the end-of-year mycotoxin contamination. Among these input features, soil properties were a novel addition to the IL models. It remains to be evaluated if there are differences between the diverse fungi Aspergillus (AFL producer) and Fusarium (FUM producer) (Samapundo et al., 2005) in relation to growth, development, and toxin production associated with environmental factors in the field, such as crop rotation using winter wheat. For future applications, quarterly historical data should be used to create a quarterly predictive model. These models would be beneficial for farmers as they will be alerted by the prediction of impending contamination several months in advance before harvest, thus providing ample time to deploy mitigation measures such as biocontrol, irrigation, and/or fungicide application to avoid contamination of their crops.

Data availability statement

The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found below: https://www.gro-intelligence.com/, https://doi.org/10.5067/MODIS/MOD13A2.061, Cropscape: https://nassgeodata.gmu.edu/CropScape/.

Author contributions

LC-D: Conceptualization, Data curation, Formal analysis, Investigation, Methodology, Supervision, Validation, Visualization, Writing—original draft, Writing—review & editing. EW: Data curation, Methodology, Software, Visualization, Writing—review & editing. JB: Data curation, Methodology, Software, Visualization, Writing—review & editing. CL: Conceptualization, Resources, Software, Supervision, Writing—review & editing. NV: Data curation, Methodology, Writing—review & editing. MF: Conceptualization, Methodology, Resources, Software, Writing—review & editing. KB: Data curation, Investigation, Resources, Writing—review & editing. PO: Project administration, Resources, Supervision, Writing—review & editing. HF-K: Conceptualization, Project administration, Resources, Supervision, Writing—review & editing. MV: Conceptualization, Investigation, Project administration, Resources, Supervision, Writing—review & editing. KR: Conceptualization, Investigation, Project administration, Resources, Supervision, Writing—review & editing.

Funding

The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.

Acknowledgments

The authors thank Christine Poppe and Jennifer Teresi at USDA-ARS in Peoria for their help in mining available soil data. USDA is an equal opportunity provider and employer.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

The author(s) declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision.

Publisher's note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Supplementary material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fmicb.2023.1283127/full#supplementary-material

Abbreviations

AFL, Aflatoxins; FUM, Fumonisins; ARI, Aflatoxin risk index; GBM, Gradient boosting machine; NN, Neural network; FHB, Fusarium head blight; BIC, Bayesian information criterion; NDVI, Normalized difference vegetation index; Veg. Index, Vegetative index; PCRP, Precipitation; TAVG, Average temperature; ML, Machine learning; H, High level; L, Low level.

References

Abdel-Hadi, A., Schmidt-Heydt, M., Parra, R., Geisen, R., and Magan, N. (2012). A. systems approach to model the relationship between aflatoxin gene cluster expression, environmental factors, growth and toxin production by Aspergillus flavus. J. R. Soc. Interface 9, 757–767. doi: 10.1098/rsif.2011.0482

PubMed Abstract | CrossRef Full Text | Google Scholar

Baechler, M. C., and Love, P. M. (2004). Building America Best Practices Series: Volume 1; Builders and Buyers Handbook for Improving New Home Efficiency, Comfort, and Durability in the Hot and Humid Climate. Golden, CO, USA: National Renewable Energy Lab (NREL). doi: 10.2172/15011705

CrossRef Full Text | Google Scholar

Battilani, P., Leggieri, M. C., Rossi, V., and Giorni, P. (2013). AFLA-maize, a mechanistic model for Aspergillus flavus infection and aflatoxin B1 contamination in maize. Comput. Electr. Agric. 94, 38–46. doi: 10.1016/j.compag.2013.03.005

CrossRef Full Text | Google Scholar

Battilani, P., Toscano, P., Van der Fels-Klerx, H. J., Moretti, A., Leggieri, M., Brera, C., et al. (2016). Aflatoxin B1 contamination in maize in Europe increases due to climate change. Sci. Rep. 6, 24328. doi: 10.1038/srep24328

PubMed Abstract | CrossRef Full Text | Google Scholar

Beck, H. E., Zimmermann, N. E., McVicar, T. R., Vergopolan, N., Berg, A., Wood, E. F., et al. (2018). Present and future Köppen-Geiger climate classification maps at 1-km resolution. Scient. Data 5, 180214. doi: 10.1038/sdata.2018.214

PubMed Abstract | CrossRef Full Text | Google Scholar

Bergstrom, R. E., Piskin, K., and Follmer, L. R. (1976). Geology for Planning in the Springfield-Decatur Region. Champaign, IL: Illinois State Geological Survey, Prairie Research Institute.

Google Scholar

Bindschedler, S., Cailleau, G., and Verrecchia, E. (2016). Role of fungi in the biomineralization of calcite. Minerals 6, 41. doi: 10.3390/min6020041

CrossRef Full Text | Google Scholar

Birkeland, P. W. (1974). Pedology, Weathering, and Geomorphological Research. Oxford: Oxford University Press.

Google Scholar

Borràs-Vallverdú, B., Ramos, A. J., Cantero-Martínez, C., Marín, S., Sanchis, V., Fernández-Ortega, J., et al. (2022). Influence of agronomic factors on mycotoxin contamination in maize and changes during a 10-day harvest-till-drying simulation period: a different perspective. Toxins 14, 620. doi: 10.3390/toxins14090620

PubMed Abstract | CrossRef Full Text | Google Scholar

Boryan, C., Yang, Z., Mueller, R., and Craig, M. (2011). Monitoring US agriculture: the US Department of Agriculture, National Agricultural Statistics Service, cropland data layer program. Geocarto Int. 26, 341–58. doi: 10.1080/10106049.2011.562309

CrossRef Full Text | Google Scholar

Bush, B. J., Carson, M. L., Cubeta, M. A., Hagler, W. M., and Payne, G. A. (2004). Infection and fumonisin production by Fusarium verticillioides in developing maize kernels. Phytopathology 94, 88–93. doi: 10.1094/PHYTO.2004.94.1.88

PubMed Abstract | CrossRef Full Text | Google Scholar

Castano-Duque, L., Vaughan, M., Lindsay, J., Barnett, K., and Rajasekaran, K. (2022). Gradient boosting and bayesian network machine learning models predict aflatoxin and fumonisin contamination of maize in Illinois – First USA case study. Front Microbiol. 13, 1039947. doi: 10.3389/fmicb.2022.1039947

PubMed Abstract | CrossRef Full Text | Google Scholar

Chang, C. M., and Lynd, J. Q. (1970). Soil microfloral interactions with aflatoxin synthesis and degradation. Mycologia 62, 978–986. doi: 10.1080/00275514.1970.12019039

PubMed Abstract | CrossRef Full Text | Google Scholar

Cooper, G. F. (1990). The computational complexity of probabilistic inference using bayesian belief networks. Artif. Intell. 42, 393–405. doi: 10.1016/0004-3702(90)90060-D

CrossRef Full Text | Google Scholar

Cotty, P. J., and Jaime-Garcia, R. (2007). Influences of climate on aflatoxin producing fungi and aflatoxin contamination. Int. J. Food Microbiol. 119, 109–115. doi: 10.1016/j.ijfoodmicro.2007.07.060

PubMed Abstract | CrossRef Full Text | Google Scholar

Damianidis, D., Ortiz, B. V., Windham, G. L., Bowen, K. L., Hoogenboom, G., Scully, B. T., et al. (2018). Evaluating a generic drought index as a predictive tool for aflatoxin contamination of corn: From plot to regional level. Crop. Prot. 113, 64–74. doi: 10.1016/j.cropro.2018.07.013

CrossRef Full Text | Google Scholar

Didan, K. (2021). MODIS/Terra Vegetation Indices 16-Day L3 Global 1km SIN Grid V061: distributed by NASA EOSDIS Land Processes DAAC. Available online at: https://lpdaac.usgs.gov/products/mod13a2v061/ (accessed November 15, 2022).

Google Scholar

Diener, U. L., Cole, R. J., Sanders, T. H., Payne, G. A., Lee, L. S., Klich, M. A., et al. (1987). Epidemiology of aflatoxin formation by aspergillus flavus*. Annu. Rev. Phytopathol. 25, 249–270. doi: 10.1146/annurev.py.25.090187.001341

CrossRef Full Text | Google Scholar

do Moraes Gatti, V. C., da Silva Barata, H., Silva, V. F., da Cunha, F. F., de Oliveira, R. A., de Oliveira, J. T., et al. (2023). Influence of calcium on the development of corn plants grown in hydroponics. AgriEngineering 5, 623–630. doi: 10.3390/agriengineering5010039

CrossRef Full Text | Google Scholar

Ehrlich, K. C. (2014). Non-aflatoxigenic Aspergillus flavus to prevent aflatoxin contamination in crops: advantages and limitations. Front. Microbiol. 5, 50. doi: 10.3389/fmicb.2014.00050

PubMed Abstract | CrossRef Full Text | Google Scholar

Focker, M., van der Fels-Klerx, H. J., Magan, S. G. E. N., Grahovac, F. B., Budakov, M. D., Suman, M., et al. (2020). The impact of management practices to prevent and control mycotoxins in the European food supply chain: MyToolBox project results. World Mycotoxin J. 14, 139–154. doi: 10.3920/WMJ2020.2588

CrossRef Full Text | Google Scholar

Foister, C. E. (1946). The relation of weather to fungus diseases of plants. II Botan. Rev. 12, 548–591. doi: 10.1007/BF02861806

CrossRef Full Text | Google Scholar

Fountain, J. C., Bajaj, P., Nayak, S. N., Yang, L., Pandey, M. K., Kumar, V., et al. (2016). Responses of Aspergillus flavus to oxidative stress are related to fungal development regulator, antioxidant enzyme, and secondary metabolite biosynthetic gene expression. Front. Microbiol. 7, 2048. doi: 10.3389/fmicb.2016.02048

PubMed Abstract | CrossRef Full Text | Google Scholar

Friedman, J. H. (2001). Greedy function approximation: A gradient boosting machine. Ann. Stat. 29, 1189–1232. doi: 10.1214/aos/1013203451

CrossRef Full Text | Google Scholar

Gibson, L. J., and Kroese, D. P. (2022). “Rare-Event Simulation via Neural Networks,” in Advances in Modeling and Simulation: Festschrift for Pierre L'Ecuyer, eds. Z. Botev, A. Keller, C. Lemieux, B. Tuffin (Cham: Springer International Publishing), 151–68. doi: 10.1007/978-3-031-10193-9_8

CrossRef Full Text | Google Scholar

González-Domínguez, E., Caffi, T., Rossi, V., Salotti, I., and Fedele, G. (2023). Plant disease models and forecasting: changes in principles and applications over the last 50 years. Phytopathology 113, 678–693. doi: 10.1094/PHYTO-10-22-0362-KD

PubMed Abstract | CrossRef Full Text | Google Scholar

Guo, B., Chen, Z. Y., Lee, R. D., and Scully, B. T. (2008). Drought stress and preharvest aflatoxin contamination in agricultural commodity: genetics, genomics and proteomics. J. Integr. Plant Biol. 50, 1281–1291. doi: 10.1111/j.1744-7909.2008.00739.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Guo, B. Z., Russin, J. S., Brown, R. L., Cleveland, T. E., and Widstrom, N. W. (1996). Resistance to aflatoxin contamination in corn as influenced by relative humidity and kernel germination. J. Food Prot. 59, 276–281. doi: 10.4315/0362-028X-59.3.276

PubMed Abstract | CrossRef Full Text | Google Scholar

Hoffmann, A., Funk, R., and Müller, M. E. H. (2021). Blowin' in the wind: wind dispersal ability of phytopathogenic Fusarium in a wind tunnel experiment. Atmosphere 12, 1653. doi: 10.3390/atmos12121653

CrossRef Full Text | Google Scholar

Hu, X., Jiang, M., Zhang, J., Zhang, A., Lin, F., Tan, M., et al. (2007). Calcium–calmodulin is required for abscisic acid-induced antioxidant defense and functions both upstream and downstream of H2O2 production in leaves of maize (Zea mays) plants. New Phytol. 173, 27–38. doi: 10.1111/j.1469-8137.2006.01888.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Jiang, M., and Zhang, J. (2003). Cross-talk between calcium and reactive oxygen species originated from NADPH oxidase in abscisic acid-induced antioxidant defence in leaves of maize seedlings. Plant Cell Environ. 26, 929–939. doi: 10.1046/j.1365-3040.2003.01025.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Johns, L. E., Bebber, D. P., Gurr, S. J., and Brown, N. A. (2022). Emerging health threat and cost of Fusarium mycotoxins in European wheat. Nat. Food 3, 1014–1019. doi: 10.1038/s43016-022-00655-z

PubMed Abstract | CrossRef Full Text | Google Scholar

Jurado, M., Marín, P., Magan, N., and González-Jaén Maria, T. (2008). Relationship between solute and matric potential stress, temperature, growth, and FUM1 gene expression in two Fusarium verticillioides strains from Spain. Appl. Environ. Microbiol. 74, 2032–2036. doi: 10.1128/AEM.02337-07

PubMed Abstract | CrossRef Full Text | Google Scholar

Kebede, H., Abbas, H. K., Fisher, D. K., and Bellaloui, N. (2012). Relationship between aflatoxin contamination and physiological responses of corn plants under drought and heat stress. Toxins 4, 1385–1403. doi: 10.3390/toxins4111385

PubMed Abstract | CrossRef Full Text | Google Scholar

Keller, B., Russo, T., Rembold, F., Chauhan, Y., Battilani, P., Wenndt, A., et al. (2022). The potential for aflatoxin predictive risk modelling in sub-Saharan Africa: a review. World Mycotoxin J. 15, 101–118. doi: 10.3920/WMJ2021.2683

CrossRef Full Text | Google Scholar

Kerry, R., Ingram, B., Garcia-Cela, E., Magan, N., Ortiz, B. V., Scully, B., et al. (2021). Determining future aflatoxin contamination risk scenarios for corn in Southern Georgia, USA using spatio-temporal modelling and future climate simulations. Sci. Rep. 11, 13522. doi: 10.1038/s41598-021-92557-6

PubMed Abstract | CrossRef Full Text | Google Scholar

Klich, M. (2002). Biogeography of Aspergillus species in soil and litter. Mycologia 94, 21–27. doi: 10.1080/15572536.2003.11833245

PubMed Abstract | CrossRef Full Text | Google Scholar

Köppen, W. (2011). The thermal zones of the Earth according to the duration of hot, moderate and cold periods and to the impact of heat on the organic world. Meteorol. Zeitschrift 20, 351–360. doi: 10.1127/0941-2948/2011/105

CrossRef Full Text | Google Scholar

Lee, H.-S., Kwon, N. J., Kim, Y., and Lee, H. (2018). Prediction of mycotoxin risks due to climate change in Korea. Appl. Biol. Chem. 61, 389–396. doi: 10.1007/s13765-018-0370-8

CrossRef Full Text | Google Scholar

Leggieri, M. C., Mazzoni, M., and Battilani, P. (2021). Machine learning for predicting mycotoxin occurrence in maize. Front. Microbiol. 12, 661132. doi: 10.3389/fmicb.2021.661132

PubMed Abstract | CrossRef Full Text | Google Scholar

Libohova, Z., Schoeneberger, P., Bowling, L. C., Owens, P. R., Wysocki, D., Wills, S., et al. (2018). Soil systems for upscaling saturated hydraulic conductivity for hydrological modeling in the critical zone. Vadose Zone J. 17, 170051. doi: 10.2136/vzj2017.03.0051

CrossRef Full Text | Google Scholar

Liu, N., Liu, C., Dudaš, T. N., Loc, M. C., Bagi, F. F., van der Fels-Klerx, H. J., et al. (2021). Improved aflatoxins and fumonisins forecasting models for maize (PREMA and PREFUM), using combined mechanistic and bayesian network modeling—serbia as a case study. Front. Microbiol. 12, 643604. doi: 10.3389/fmicb.2021.643604

PubMed Abstract | CrossRef Full Text | Google Scholar

Long Stephen, P., Ainsworth Elizabeth, A., Leakey Andrew, D. B., Nösberger, J., and Ort Donald, R. (2006). Food for thought: lower-than-expected crop yield stimulation with rising CO2 concentrations. Science 312, 1918–1921. doi: 10.1126/science.1114722

PubMed Abstract | CrossRef Full Text | Google Scholar

Ma, W., and Berkowitz, G. A. (2011). Ca2+ conduction by plant cyclic nucleotide gated channels and associated signaling components in pathogen defense signal transduction cascades. New Phytol. 190, 566–572. doi: 10.1111/j.1469-8137.2010.03577.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Maiorano, A., Reyneri, A., Sacco, D., Magni, A., and Ramponi, C. (2009). A dynamic risk assessment model (FUMAgrain) of fumonisin synthesis by Fusarium verticillioides in maize grain in Italy. Crop. Prot. 28, 243–256. doi: 10.1016/j.cropro.2008.10.012

CrossRef Full Text | Google Scholar

Marin, S., Magan, N., Ramos, A. J., and Sanchis, V. (2004). Fumonisin-producing strains of Fusarium: a review of their ecophysiology. J. Food Prot. 67, 1792–1805. doi: 10.4315/0362-028X-67.8.1792

PubMed Abstract | CrossRef Full Text | Google Scholar

McMillian, W. W., Widstrom, N. W., and Wilson, D. M. (1985). Insect damage and aflatoxin contamination in preharvest corn: Influence of genotype and ear wetting. J. Entomol. Sci. 20, 66–68. doi: 10.18474/0749-8004-20.1.66

CrossRef Full Text | Google Scholar

Medina, A., Rodriguez, A., and Magan, N. (2014). Effect of climate change on Aspergillus flavus and aflatoxin B1 production. Front. Microbiol. 5, 348. doi: 10.3389/fmicb.2014.00348

PubMed Abstract | CrossRef Full Text | Google Scholar

Mehl, H. L., Jaime, R., Callicott, K. A., Probst, C., Garber, N. P., Ortega-Beltran, A., et al. (2012). Aspergillus flavus diversity on crops and in the environment can be exploited to reduce aflatoxin exposure and improve health. Ann. N Y. Acad. Sci. 1273, 7–17. doi: 10.1111/j.1749-6632.2012.06800.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Melsted, S. W. (1953). Some observed calcium deficiencies in corn under field conditions. Soil Sci. Soc. Am. J. 17, 52–54. doi: 10.2136/sssaj1953.03615995001700010013x

CrossRef Full Text | Google Scholar

Miller, J. D. (2001). Factors that affect the occurrence of fumonisin. Environ. Health Perspect. 109, 321–324. doi: 10.1289/ehp.01109s2321

PubMed Abstract | CrossRef Full Text | Google Scholar

Mitchell, N. J., Bowers, E., Hurburgh, C., and Wu, F. (2016). Potential economic losses to the US corn industry from aflatoxin contamination. Food Addit. Contam. Part A Chem. Anal. Control Expo. Risk Assess. 33, 540–550. doi: 10.1080/19440049.2016.1138545

PubMed Abstract | CrossRef Full Text | Google Scholar

Munkvold, G. (2003). Epidemiology of Fusarium diseases and their mycotoxins in maize ears. Eur. J. Plant Pathol. 109, 705–713. doi: 10.1023/A:1026078324268

CrossRef Full Text | Google Scholar

Munkvold, G. P., Arias, S., Taschl, I., and Gruber-Dorninger, C. (2019). “Chapter 9 - Mycotoxins in Corn: Occurrence, Impacts, and Management,” in Corn (Third Edition), ed. S. O. Serna-Saldivar (Oxford: AACC International Press), 235–87. doi: 10.1016/B978-0-12-811971-6.00009-7

CrossRef Full Text | Google Scholar

Mutiga, S. K., Were, V., Hoffmann, V., Harvey, J. W., Milgroom, M. G., Nelson, R. J., et al. (2014). Extent and drivers of mycotoxin contamination: inferences from a survey of kenyan maize mills. Phytopathology 104, 1221–1231. doi: 10.1094/PHYTO-01-14-0006-R

PubMed Abstract | CrossRef Full Text | Google Scholar

Nnadi, N. E., and Carter, D. A. (2021). Climate change and the emergence of fungal pathogens. PLoS Pathog. 17, e1009503. doi: 10.1371/journal.ppat.1009503

PubMed Abstract | CrossRef Full Text | Google Scholar

NOAA (2013). National Centers for Environmental Information, Monthly Drought Report for Annual 2012. Available online at: https://www.ncei.noaa.gov/access/monitoring/monthly-report/drought/201213 (accessed August 2023).

Google Scholar

Parsons, M. W., and Munkvold, G. P. (2010). Associations of planting date, drought stress, and insects with Fusarium ear rot and fumonisin B1 contamination in California maize. Food Addit. Contam. Part A. 27, 591–607. doi: 10.1080/19440040903456337

PubMed Abstract | CrossRef Full Text | Google Scholar

Payne, G. A., Cassel, D. K., and Adkins, C. R. (1986). Reduction of aflatoxin contamination in corn by irrigation and tillage. Phytopathology 76, 679–684. doi: 10.1094/Phyto-76-679

CrossRef Full Text | Google Scholar

Payne, G. A., Thompson, D. L., Lillehoj, E. B., and Zuber, M. S. (1988). Effect of temperature on the preharvest infection of maize kernels by Aspergillus flavus. Phytopathology 78, 1376–1380. doi: 10.1094/Phyto-78-1376

CrossRef Full Text | Google Scholar

Payne, G. A., and Widstrom, N. W. (1992). Aflatoxin in maize. Crit. Rev. Plant Sci. 10, 423–440. doi: 10.1080/07352689209382320

CrossRef Full Text | Google Scholar

Peng, B., Guan, K., Tang, J., Ainsworth, E. A., Asseng, S., Bernacchi, C. J., et al. (2020). Towards a multiscale crop modelling framework for climate change adaptation assessment. Nat. Plants. 6, 338–348. doi: 10.1038/s41477-020-0625-3

PubMed Abstract | CrossRef Full Text | Google Scholar

Peper, A., Brenneman, T., and Yang, L. (2022). Calcite dissolving bacteria from peanut (Arachis hypogaea) pegging zone influences soil calcium level. Front. Microb. 1, 1019134. doi: 10.3389/frmbi.2022.1019134

CrossRef Full Text | Google Scholar

Picot, A., Barreau, C., Pinson-Gadais, L., Caron, D., Lannou, C., Richard-Forget, F., et al. (2010). Factors of the Fusarium verticillioides-maize environment modulating fumonisin production. Crit. Rev. Microbiol. 36, 221–231. doi: 10.3109/10408411003720209

PubMed Abstract | CrossRef Full Text | Google Scholar

Proctor, R. H., McCormick, S. P., Kim, H.-S., Cardoza, R. E., Stanley, A. M., Lindo, L., et al. (2018). Evolution of structural diversity of trichothecenes, a family of toxins produced by plant pathogenic and entomopathogenic fungi. PLoS Pathog. 14, e1006946. doi: 10.1371/journal.ppat.1006946

PubMed Abstract | CrossRef Full Text | Google Scholar

Ridgeway, G. (2006). Generalized boosted models: A guide to the GBM package. Available online at: https://cran.r-project.org/web/packages/gbm/vignettes/gbm.pdf (accessed January 2023).

Google Scholar

Roucou, A., Bergez, C., Méléard, B., and Orlando, B. A. (2021). Fumonisin prevention tool for targeting and ranking agroclimatic conditions favoring exposure in french maize-growing areas. Toxins 13, 214. doi: 10.3390/toxins13030214

PubMed Abstract | CrossRef Full Text | Google Scholar

Samapundo, S., Devliehgere, F., De Meulenaer, B., and Debevere, J. (2005). Effect of water activity and temperature on growth and the relationship between fumonisin production and the radial growth of Fusarium verticillioides and Fusarium proliferatum on corn. J. Food Prot. 68, 1054–1059. doi: 10.4315/0362-028X-68.5.1054

PubMed Abstract | CrossRef Full Text | Google Scholar

Sanchis, V., Marín, S., Magan, N., and Ramos, A. J. (2006). “Ecophysiology of fumonisin producers in Fusarium section Liseola,” in Advances in Food Mycology (Boston, MA: Springer US), 115–122. doi: 10.1007/0-387-28391-9_6

PubMed Abstract | CrossRef Full Text | Google Scholar

Scheidegger, K. A., and Payne, G. A. (2003). Unlocking the secrets behind secondary metabolism: a review of Aspergillus flavus from pathogenicity to functional genomics. J. Toxicol. 22, 423–459. doi: 10.1081/TXR-120024100

CrossRef Full Text | Google Scholar

Segers, F. J. J., Dijksterhuis, J., Giesbers, M., and Debets, A. J. M. (2023). Natural folding of airborne fungal spores: a mechanism for dispersal and long-term survival? Fungal Biol. Rev. 44, 100292. doi: 10.1016/j.fbr.2022.10.005

CrossRef Full Text | Google Scholar

Sétamou, M., Cardwell, K. F., Schulthess, F., and Hell, K. (1997). Aspergillus flavus infection and aflatoxin contamination of preharvest maize in benin. Plant Dis. 81, 1323–1327. doi: 10.1094/PDIS.1997.81.11.1323

PubMed Abstract | CrossRef Full Text | Google Scholar

Shah, D. A., De Wolf, E. D., Paul, P. A., and Madden, L. V. (2018). Functional data analysis of weather variables linked to Fusarium head blight epidemics in the United States. Phytopathology 109, 96–110. doi: 10.1094/PHYTO-11-17-0386-R

PubMed Abstract | CrossRef Full Text | Google Scholar

Smith, D. B., Solano, F., Woodruff, L. G., Cannon, W. F., and Ellefsen, K. J. (2019). Geochemical and mineralogical maps, with interpretation, for soils of the conterminous United States. Report. Reston, VA; Report No.: 2017–5118. doi: 10.3133/sir20175118

CrossRef Full Text | Google Scholar

Smith, L. E., Stasiewicz, M., Hestrin, R., Morales, L., Mutiga, S., Nelson, R. J., et al. (2016). Examining environmental drivers of spatial variability in aflatoxin accumulation in Kenyan maize: Potential utility in risk prediction models. Afr. J. Food, Agric. Nutr. Dev. 16, 11086–11105. doi: 10.18697/ajfand.75.ILRI09

CrossRef Full Text | Google Scholar

Srinivasan, K., Gilardi, G., Garibaldi, A., and Gullino, M. L. (2009). Efficacy of bacterial antagonists and different commercial products against Fusarium wilt on rocket. Phytoparasitica 37, 179–188. doi: 10.1007/s12600-009-0024-9

CrossRef Full Text | Google Scholar

Stover, R. H. (1953). The effect of soil moisture on Fusarium species. Canad. J. Botany. 31, 693–697. doi: 10.1139/b53-050

CrossRef Full Text | Google Scholar

Team, R. C. (2017). R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. Available online at: http://www.R-project.org (accessed July 2023).

Google Scholar

Titilayo, F. (2018). “Aflatoxin management strategies in sub-saharan Africa,” in Mycotoxins, eds. N. Patrick Berka, S. Francois (Rijeka: IntechOpen), 6.

Google Scholar

Torgo, L. (2016). Data Mining with R: Learning with Case Studies. 2 ed. New York, NY: Chapman and Hall/CRC.

Google Scholar

Uppala, L. (2011). Factors Affecting Pre-Harvest Aflatoxin Contamination of Peanut (Arachis hypogaea L.). Auburn, AL: Auburn University.

Google Scholar

van Buuren, S., and Groothuis-Oudshoorn, K. (2011). Mice: multivariate imputation by chained equations in R. J. Stat. Softw. 45, 1–67. doi: 10.18637/jss.v045.i03

CrossRef Full Text | Google Scholar

Van der Fels-Klerx, H., Liu, C., and Battilani, P. (2016). Modelling climate change impacts on mycotoxin contamination. World Mycotox. J. 9, 717–726. doi: 10.3920/WMJ2016.2066

CrossRef Full Text | Google Scholar

Van der Fels-Klerx, H. J., Vermeulen, L. C., Gavai, A. K., and Liu, C. (2019). Climate change impacts on aflatoxin B1 in maize and aflatoxin M1 in milk: A case study of maize grown in Eastern Europe and imported to the Netherlands. PLoS ONE 14, e0218956. doi: 10.1371/journal.pone.0218956

PubMed Abstract | CrossRef Full Text | Google Scholar

Vardon, P., McLaughlin, C., and Nardinelli, C. (2003). “Mycotoxins: Risks in plant, animal, and human systems,” in Potential economic costs of mycotoxins in the United States (Ames, Iowa, USA: Council for Agricultural Science and Technology), 136–42.

Google Scholar

Vaughan, M. M., Huffaker, A., Schmelz, E. A., Dafoe, N. J., Christensen, S., Sims, J., et al. (2014). Effects of elevated [CO2] on maize defence against mycotoxigenic Fusarium verticillioides. Plant Cell Environ. 37, 2691–2706. doi: 10.1111/pce.12337

PubMed Abstract | CrossRef Full Text | Google Scholar

Vaughan, M. M., Huffaker, A., Schmelz, E. A., Dafoe, N. J., Christensen, S. A., McAuslane, H. J., et al. (2016). Interactive effects of elevated [CO2] and drought on the maize phytochemical defense response against mycotoxigenic Fusarium verticillioides. PLoS ONE 11, e0159270. doi: 10.1371/journal.pone.0159270

PubMed Abstract | CrossRef Full Text | Google Scholar

Vergopolan, N., Chaney, N. W., Beck, H. E., Pan, M., Sheffield, J., Chan, S., et al. (2020). Combining hyper-resolution land surface modeling with SMAP brightness temperatures to obtain 30-m soil moisture estimates. Rem. Sens. Environ. 242, 111740. doi: 10.1016/j.rse.2020.111740

CrossRef Full Text | Google Scholar

Vergopolan, N., Chaney, N. W., Pan, M., Sheffield, J., Beck, H. E., Ferguson, C. R., et al. (2021). SMAP-HydroBlocks, a 30-m satellite-based soil moisture dataset for the conterminous US. Scient. Data 8, 264. doi: 10.1038/s41597-021-01050-2

PubMed Abstract | CrossRef Full Text | Google Scholar

Vergopolan, N., Sheffield, J., Chaney, N. W., Pan, M., Beck, H. E., Ferguson, C. R., et al. (2022). High-resolution soil moisture data reveal complex multi-scale spatial variability across the United States. Geophys. Res. Lett. 49, eGL098586. doi: 10.1029/2022GL098586

CrossRef Full Text | Google Scholar

Verrecchia, E. P., Loisy, C., Braissant, O., and Gorbushina, A. A. (2003) “The Role of Fungal Biofilm and Networks in the Terrestrial Calcium Carbonate Cycle,” in Fossil Recent Biofilms: A Natural History of Life on Earth, eds. W. E. Krumbein, D. M. Paterson, G. A. Zavarzin (Dordrecht: Springer Netherlands), 363–9. doi: 10.1007/978-94-017-0193-8_25

CrossRef Full Text | Google Scholar

Walkinshaw, M., O'Geen, A. T., and Beaudette, D. E. (2022). Cartographers. California: California Soil Resources Lab.

Google Scholar

Wang, X., Liu, C., and van der Fels-Klerx, H. J. (2022). Regional prediction of multi-mycotoxin contamination of wheat in Europe using machine learning. Food Res. Int. 159, 111588. doi: 10.1016/j.foodres.2022.111588

PubMed Abstract | CrossRef Full Text | Google Scholar

Warfield Colleen, Y., and Gilchrist David, G. (1999). Influence of kernel age on fumonisin B1production in maize by Fusarium moniliforme. Appl Environ Microbiol. 65, 2853–2856. doi: 10.1128/AEM.65.7.2853-2856.1999

PubMed Abstract | CrossRef Full Text | Google Scholar

Weil, R. R., and Brady, N. C. (2002). The Nature and Properties of Soils. 13 ed Upper Saddle River, New Jersey: Prentice Hall.

Google Scholar

Widstrom, N. W., McMillian, W. W., Beaver, R. W., and Wilson, D. M. (1990). Weather-associated changes in aflatoxin contamination of preharvest maize. J. Prod. Agric. 3, 196–199. doi: 10.2134/jpa1990.0196

CrossRef Full Text | Google Scholar

Winter, G., and Pereg, L. (2019). A review on the relation between soil and mycotoxins: Effect of aflatoxin on field, food and finance. Eur. J. Soil Sci. 70, 882–897. doi: 10.1111/ejss.12813

CrossRef Full Text | Google Scholar

Woloshuk, C. P., and Shim, W. B. (2013). Aflatoxins, fumonisins, and trichothecenes: a convergence of knowledge. FEMS Microbiol. Rev. 37, 94–109. doi: 10.1111/1574-6976.12009

PubMed Abstract | CrossRef Full Text | Google Scholar

Wu, F. (2006). Mycotoxin reduction in Bt corn: potential economic, health, and regulatory impacts. Transg. Res. 15, 277–289. doi: 10.1007/s11248-005-5237-1

PubMed Abstract | CrossRef Full Text | Google Scholar

Wu, F., Bhatnagar, D., Bui-Klimke, T., Carbone, I., Hellmich, R., Munkvold, G., et al. (2011). Climate change impacts on mycotoxin risks in US maize. World Mycotox. J. 4, 79–93. doi: 10.3920/WMJ2010.1246

CrossRef Full Text | Google Scholar

Yan, H., and Nelson, B. (2022). Effects of soil type, temperature, and moisture on development of Fusarium root rot of soybean by Fusarium solani (FSSC 11) and Fusarium tricinctum. Plant Dis. 106, 2974–2983. doi: 10.1094/PDIS-12-21-2738-RE

PubMed Abstract | CrossRef Full Text | Google Scholar

Yu, J., Hennessy, D. A., Tack, J., and Wu, F. (2022). Climate change will increase aflatoxin presence in US Corn. Environ. Res. Lett. 17, 054017. doi: 10.1088/1748-9326/ac6435

CrossRef Full Text | Google Scholar

Yu, J., Hennessy, D. A., and Wu, F. (2020). The impact of Bt corn on aflatoxin-related insurance claims in the United States. Sci. Rep. 10, 10046. doi: 10.1038/s41598-020-66955-1

PubMed Abstract | CrossRef Full Text | Google Scholar

Zamani, M., and Kremer, S. C. (2013). “Neural networks in bioinformatics,” in Handbook on Neural Information Processing, eds. M. Bianchini, M. Maggini, L. C. Jain (Berlin, Heidelberg: Springer Berlin Heidelberg), 505–25. doi: 10.1007/978-3-642-36657-4_15

CrossRef Full Text | Google Scholar

Zhang, W., Zhang, B-w., Deng, J-f., Li, L., Yi, T-y., and Hong, Y-y. (2021). The resistance of peanut to soil-borne pathogens improved by rhizosphere probiotics under calcium treatment. BMC Microbiol. 21, 299. doi: 10.1186/s12866-021-02355-3

PubMed Abstract | CrossRef Full Text | Google Scholar

Zingales, V., Taroncher, M., Martino, P. A., Ruiz, M-J., and Caloni, F. (2022). Climate change and effects on molds and mycotoxins. Toxins 14, 445. doi: 10.3390/toxins14070445

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: Aspergillus, Fusarium, machine learning, gradient boosting, neural network, aflatoxin, fumonisin, soil

Citation: Castano-Duque L, Winzeler E, Blackstock JM, Liu C, Vergopolan N, Focker M, Barnett K, Owens PR, van der Fels-Klerx HJ, Vaughan MM and Rajasekaran K (2023) Dynamic geospatial modeling of mycotoxin contamination of corn in Illinois: unveiling critical factors and predictive insights with machine learning. Front. Microbiol. 14:1283127. doi: 10.3389/fmicb.2023.1283127

Received: 25 August 2023; Accepted: 26 September 2023;
Published: 01 November 2023.

Edited by:

Alicia Rodríguez, University of Extremadura, Spain

Reviewed by:

Alejandro Ortega-Beltran, International Institute of Tropical Agriculture (IITA), Nigeria
Esther Garcia-Cela, University of Hertfordshire, United Kingdom
María Micaela Álvarez Rubio, Complutense University of Madrid, Spain

Copyright © 2023 Castano-Duque, Winzeler, Blackstock, Liu, Vergopolan, Focker, Barnett, Owens, van der Fels-Klerx, Vaughan and Rajasekaran. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Lina Castano-Duque, lina.castano.duque@usda.gov

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