Next Article in Journal
Consequences of Oviposition Site Choice for Geckos in Changing Environments
Previous Article in Journal
Comparative Chloroplast Genomes of Six Magnoliaceae Species Provide New Insights into Intergeneric Relationships and Phylogeny
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Biology
Volume 11
Issue 9
10.3390/biology11091280
biology-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

A Fuzzy-Based Model to Predict the Spatio-Temporal Performance of the Dolichogenidea gelechiidivoris Natural Enemy against Tuta absoluta under Climate Change

by
Komi Mensah Agboka
1,2,
Henri E. Z. Tonnang
1,*,
Elfatih M. Abdel-Rahman
1,
John Odindi
2,
Onisimo Mutanga
2 and
Samira A. Mohamed
1
1
International Centre of Insect Physiology and Ecology (ICIPE), Nairobi P.O. Box 30772-00100, Kenya
2
School of Agricultural, Earth, and Environmental Sciences, University of KwaZulu-Natal, Pietermaritzburg 3209, South Africa
*
Author to whom correspondence should be addressed.
Biology 2022, 11(9), 1280; https://doi.org/10.3390/biology11091280
Submission received: 15 July 2022 / Revised: 24 August 2022 / Accepted: 25 August 2022 / Published: 28 August 2022
Browse Figures
Versions Notes

Abstract

Simple Summary

Tuta absoluta is an invasive pest threatening the productivity of the tomato crop. Dolichogenidea gelechiidivoris was imported and released as a natural enemy of Tuta absoluta. Mapping the efficacy of Dolichogenidea gelechiidivoris can improve its use as a control agent against Tuta absoluta. The Dolichogenidea gelechiidivoris efficacy map provides a tool for its targeted deployment as a Tuta absoluta natural enemy.

Abstract

The South American tomato pinworm, Tuta absoluta, causes up to 100% tomato crop losses. As Tuta absoluta is non-native to African agroecologies and lacks efficient resident natural enemies, the microgastrine koinobiont solitary oligophagous larval endoparasitoid, Dolichogenidea gelechiidivoris (Marsh) (Syn.: Apanteles gelechiidivoris Marsh) (Hymenoptera: Braconidae) was released for classical biological control. This study elucidates the current and future spatio-temporal performance of D. gelechiidivoris against T. absoluta in tomato cropping systems using a fuzzy logic modelling approach. Specifically, the study considers the presence of the host and the host crop, as well as the parasitoid reproductive capacity, as key variables. Results show that the fuzzy algorithm predicted the performance of the parasitoid (in terms of net reproductive rate (R0)), with a low root mean square error (RMSE) value (<0.90) and a considerably high R2 coefficient (=0.98), accurately predicting the parasitoid performance over time and space. Under the current climatic scenario, the parasitoid is predicted to perform well in all regions throughout the year, except for the coastal region. Under the future climatic scenario, the performance of the parasitoid is projected to improve in all regions throughout the year. Overall, the model sheds light on the varying performance of the parasitoid across different regions of Kenya, and in different seasons, under both current and future climatic scenarios.

1. Introduction

In the last two decades, Africa has become the hotspot for many crop pest invasions. These include the Bactrocera dorsalis (Hendel) (Diptera: Tephritidae) in 2003 [1], Tuta absoluta (Meyrick) (Lepidoptera: Gelechiidae) in 2007 [2], Spodoptera frugiperda (J.E. Smith) (Lepidoptera: Noctuidae) in 2016 [3], and Drosophila suzukii Matsumura (Diptera: Drosophilidae) in 2019 [4]. The invasion by these devastating pests and the damage to their respective host plants have far-reaching economic and ecological implications. For example, following the detection and spread of the South American tomato pinworm, Tuta absoluta, up to 100% crop losses have been reported [5,6]. In addition to yield and monetary losses, environmental damage arises due to the heavy use of insecticides as a mitigation measure.
Significant crop loss caused by T. absoluta can be attributed to several factors that include the pest’s high dispersal capacity [7], wide thermal tolerance [8], high reproduction rate [8], lack of efficient co-evolved natural enemy to suppress its exploding population [9], and ability to adapt to the new ecosystems [10,11]. Due to enormous yield losses attributable to T. absoluta and its fast spread, farmers have generally adopted synthetic chemical insecticides as a primary mitigation measure [12]. However, this approach has diverse negative impacts on human, animal, and environmental health [13,14,15]. Furthermore, the approach is often ineffective in the management of the pest due to resistance to several classes of insecticides [15,16] and the cryptic nature of most of its developmental stages [17,18,19]. Therefore, an integrated management strategy in harmony with the environment is necessary for the sustainable management of T. absoluta. Being non-native to African agroecologies and lacking efficient resident natural enemies, classical biological control presents an ideal option for the suppression of the pest.
The International Centre of Insect Physiology and Ecology (ICIPE) in Nairobi, Kenya, jointly with the International Potato Center (CIP) in Lima, Peru, introduced the microgastrine koinobiont solitary oligophagous larval endoparasitoid, Dolichogenidea gelechiidivoris (Marsh) (Syn.: Apanteles gelechiidivoris Marsh) (Hymenoptera: Braconidae). The parasitoid was first imported from Peru to Kenya in 2017 for testing under quarantine conditions and final field release for classical biological control [9], based on its efficiency against T. absoluta in its aboriginal home range. For example, in Peru and Colombia, parasitism rates of about 57% [20] and 77% [21], respectively, have been reported.
Following its introduction in Kenya, and based on its outstanding performance against the African population of the target pest [9], the parasitoid was first released in Kirinyaga County, Kenya, in October 2020, as the first attempt for classical control of T. absoluta since its transatlantic invasion in 2006. However, its successful establishment and subsequent impact on the pest is determined by, among other things, environmental variables, particularly temperature [22] and the availability of the host insect [23,24,25] and host plants [26].
Using temperature and other climatic variables, several models have been proposed to project the habitat suitability for the establishment of natural enemies in Africa [8]. Indeed, these models have generated an important body of knowledge with regard to the potential parasitoid establishment. However, few of these models have investigated the natural enemy’s temperature-dependent performance at scale and linked it to the presence of the host and the host crop under present and future climatic conditions. Furthermore, the limitation of such models includes the uncertainties surrounding the complexity of the mechanism underpinning the establishment of parasitoids in different agroecologies, hence the need for more flexible and robust modelling approaches.
The use of the fuzzy set theory holds great potential in dealing with such uncertainties. Unlike other Artificial Intelligence approaches that include machine learning algorithms (maximum entropy and the genetic algorithm for ruleset prediction (GARP)), fuzzy sets allow for a representation of the inherent uncertainty in the data, as well as a linguistic description of the pattern under study, allowing for more accurate conclusions [27,28]. Furthermore, fuzzy sets are flexible and can be combined with other domain knowledge such as a geographic information system (GIS). Such combinations have been successfully used to provide insight into biological control agents’ mechanisms in managing insect pests at scale. For example, Bone et al. [29] used a combination of these approaches to identify areas vulnerable to the mountain pine beetle, Dendroctonus ponderosae Hopkins. Furthermore, Garcia et al. [30] augmented the work of Bone et al. [29] by developing an index to identify the most optimal areas to release Tamarixia radiata for the biological control of Diaphorina citri. This study exploits a fuzzy logic algorithm to determine the current and future spatio-temporal performance of D. gelechiidivoris against T. absoluta in tomato cropping systems, with a focus on the presence of the host and the host crop and the parasitoid reproductive capacity as key variables.

2. Materials and Methods

2.1. Study Area

The study was conducted in Kenya’s major tomato growing regions, i.e., 38 counties stretching through the Western, Nyanza, Eastern, Coast, Rift valley, and Central regions (Figure 1). The study sites represent all the agroecological zones, i.e., the humid, sub-humid, semi-humid, arid, and semi-arid zones. The regions exhibit two tomato cropping seasons dependent on rainfall patterns, with the long rainy season from March to July and the short rainy season from October to December. The temperature varies across the different tomato-growing regions (Table 1). Generally, most regions support various cropping systems, such as mono-cropping, mixed farming, and rotational farming systems, throughout the cropping calendar [31].

2.2. Assumption and Modelling Procedure

The fuzzy logic modelling approach used in this study integrates predefined rules and assumptions derived from the bioecology of the parasitoid and its host. The implementation and computation of the multiscale modelling approach were carried out in R statistical software [32]. The primary assumptions were (1) the parasitoid, D. gelechiidivoris, would survive within the same habitats where T. absoluta can survive; (2) the cropland contained T. absoluta’s primary (i.e., tomato) and secondary (other solanaceous) crops; (3) areas with a probability of greater than 0.2 were assumed to be suitable for T. absoluta, as the pest has been reported to be very resilient to a wide range of temperatures [9]; and (4) the parasitoid efficacy primarily depended on temperature; therefore, other climatic variables were set at optimal levels [33,34].

2.3. Data

The data used in modelling were related to the presence of the parasitoid host crop (tomato), the presence of the parasitoid host, T. absoluta, and the performance indicator of the parasitoid, i.e., the net reproductive rate (R0). For the presence of tomato in the study sites, Landsat 8 images (2020) were downloaded from the USGS portal https://earthexplorer.usgs.gov (accessed on 20 January 2022) and used to classify the study area’s land use/land covers (LULCs). The ground truth data for training and accuracy assessment were obtained in the Google Earth Engine (GEE) platform, while the presence of T. absoluta was confirmed using the MaxEnt ecological niche model. The georeferenced records used in the study were obtained from Kinyanjui et al. [35] and the 19 bioclimatic variables were sourced from the WorldClim platform www.worldclim.org (accessed on 20 January 2022) at an approximate 1 km2 spatial resolution [36,37]. The net reproductive rate (R0) was obtained from Aigbedion-Atalor et al. [38] and used as an indicator for parasitoid performance. In this regard, we defined the R0 as the average number of daughters that an adult female produces during her lifetime, which is one of the indicators of parasitoid performance on its host. For extrapolation over the study area under future scenarios, the Model Intercomparison Project of the Max Planck Institute Earth System Model Lower-Resolved version (MPI-ESM1.2-LR) projection was used due to its popularity [39]. The future scenario of the shared socioeconomic pathways version (SSP2-4.5) was hypothesized as the more realistic case scenario under the Coupled Model Intercomparison Project Phase 6 (CMIP6).

2.4. Land Use/Land Cover Characterization

Satellite image pre-processing, classification and accuracy assessment, and post-classification processing were used to determine the study area’s LULC. Firstly, cloud-free Landsat imagery was pre-processed to correct for atmospheric anomalies [40,41]. The images were then projected to Google Mercator (EPSG: 3857) and clipped according to the study area boundary. The individual bands were stacked and displayed as standard false colors (4-3-2 for TM and for 5-4-3 for OLI) for vegetation analysis.
Secondly, training samples were automatically selected in the GEE platform for classification and accuracy assessment. The selected samples were then used to extract Landsat 8 spectral and temporal features to train the random forest classifier. Details of the nine delineated LULC classes are given in Table S1 (supplementary). Furthermore, image validation was carried out using high resolution Google Earth images. The digitized polygons were then converted to raster format using the rasterize tool in QGIS, and the r.kappa tool in QGIS was used to compare classified outputs and rasterized referenced data. Finally, the classified outputs were filtered using a majority filter to remove noise and enhance cartographic appearance for post-classification processing. The LULC statistics were obtained for each class value using the raster layer unique value statistics tool in QGIS. The result was then imported into Excel and converted to square kilometres (km2) (Table S2 in supplementary). The error matrix, accompanied by statistical measures such as overall accuracy (OA) and kappa (K) coefficient (Table S3 in supplementary), was generated and assessed.

2.5. Presence of the Parasitoid Host, T. absoluta

MaxEnt software version 3.4.1 [42] was used to predict the habitat suitability of the parasitoid host, T. absoluta, for the classified LULCs in the study area. The georeferenced records of T. absoluta were obtained from Kinyanjui et al. [35] and the 19 bioclimatic variables were sourced from the WorldClim platform www.worldclim.org (accessed on 20 January 2022) [36,37], in addition to the classified LULCs used as variables. Prior to running MaxEnt, the variables were clipped to Kenya country boundaries and converted to American Standard Code for Information Interchange (ASCII) format using the ‘raster’ package [43] in R statistical software [32]. Then, the ‘virtual species’ package [44] in R statistical software [32] was used to explore the spatial correlation of the 19 bioclimatic variables using the Pearson’s correlation coefficient and the cluster tree. A 0.7 threshold cutoff of the Pearson’s correlation coefficient was used to select the variables (Figure S1 in supplementary). The least-correlated bioclimatic variables were then consolidated with other predictor variables in the MaxEnt model (Table S4 in supplementary). The predictor variables had different spatial resolutions, and hence, they were resampled to the highest resolution in the dataset (30 m pixel size). The MaxEnt model was run in 5000 iterations and five replicates for better accuracy, and the performance of the MaxEnt model was assessed using the area under the curve (AUC).

2.6. Predicting the Spatio-Temporal Performance of D. gelechiidivoris

The spatio-temporal performance of D. gelechiidivoris at scale was predicted for each month of the year to include pre- and post-tomato cropping for current and future projection. To predict the spatio-temporal, temperature-based performance of D. Gelechiidivoris on its host, T. absoluta, we automated deduction through computation using the rules described in Table 2 as the main component. The Mamdani inference fuzzy algorithm theory was preferred due to its simplicity and popularity [45]. These rules were obtained by expert knowledge [46] using laboratory findings on the temperature-based performance of the parasitoid, i.e., the parasitoid net reproductive rate (R0) (Table S5 in supplementary). The algorithm entails the following fundamental rules: IF x is M THEN y is N [45]. For the semantical interpretation extended to the set [0,1] of truth values [47] of IF x is M THEN y is N in the Generalized Modus Ponens (GMP), we chose a fuzzy relation ( M   →   N ) ( x ,   y ) = m i n ( M ( x ) , N ( y ) ) and we computed N ′ in the GMP as follows [48]:
N ′ ( y ) = ( M ′ ∘ ( M → N ) ) ( y ) = ∨ x ∈ X ( M ′ ( x ) ∧ N (   y ) ) ,   y ∈ Y .  
where M ′ and N ′ denote restrictions related to M and N .
Overall, we considered and extended the conditional premise of the Mandani GMP to be valid for each i = 1 , … , n [48] rule defined for the parasitoid performance, as follows:
r u l e s i = I F   x   i s   M i   T H E N   y   i s   N i ,   i = 1 ,   … n
where M i represents fuzzy sets (the parasitoid temperature-based performance), x is the premise variable (temperature in °C), and y is the consequence variable, i.e., the performance of the parasitoid (R0). To assess the performance of the Fuzzy logic algorithm, the root mean square error (RMSE) and the coefficient of determination (R2) were used as the accuracy metrics.

3. Results

The error matrix showed very high classification accuracy (i.e., overall accuracy of 0.9, with a kappa coefficient (K) of 0.92), suggesting a reliable LULC classification. The classification output revealed that a significant (50.28%) proportion of the study area is dominated by grass cover, followed by cropland (37.61%), and barren class (0.05%) (Table S2 in supplementary). Furthermore, the mapping of the LULC revealed that croplands are primarily located in the key tomato production counties (Figure S2 in supplementary).
The MaxEnt modelling algorithm showed an average AUC of greater than 0.85, indicating that the model accurately predicted the distribution of T. absoluta. The results confirmed a high risk of infestation of T. absoluta in the selected study sites (Figure S3 in supplementary).
The fuzzy algorithm predicted the performance of the parasitoid (R0) with a low RMSE value (<0.90) and a considerably high R2 (=0.98) coefficient, accurately predicting the parasitoid’s spatio-temporal performance. Under the current climatic scenario, the parasitoid is predicted to perform fairly well in all regions throughout the year, except for the coastal region (Figure 2). The outcome of the fuzzy algorithms in predicting the parasitoid spatio-temporal distribution is further substantiated by the number of pixels of each class extracted using QGIS [49]. In two regions (i.e., Nyanza and Western), where the parasitoid was projected to perform optimally, the performance did not vary considerably across the seasons (Figure 3). On the other hand, the parasitoid performance was predicted to be worse in the Rift valley and very poor in the coastal regions. Interestingly, the parasitoid exhibited an erratic yet fairly good performance in the Central region across the seasons, with July and August being the least conducive for a parasitoid (Figure 3).
Under the future climatic scenario, overall, the performance of D. gelechiidivoris was projected to improve (Figure 4). Nevertheless, the parasitoid performance in the Nyanza and Western regions was predicted to be good, rather than optimal, across the year. Conversely, in the Rift valley and coastal regions, the parasitoid performance was predicted to improve considerably as compared to the current scenario, being optimal for the entire year. Notably, the parasitoid performance remained erratic in the Central region, but with an overall noticeable enhancement. In particular, the parasitoid performance was projected to be enhanced considerably in June and December. On the other hand, the parasitoid performance was projected to slightly decline in February and March compared to the current scenario (Figure 5).

4. Discussion

Alien invasive insect pests commonly arrive at their new invasive range without their efficient, co-evolved natural enemies; hence, they tend to multiply exponentially, with far-reaching socioeconomical and ecological consequences. This is similar to the South American tomato leafminer, T. absoluta, in its Afro-Eurasian invasion. In Kenya, although several indigenous parasitoid species have been reported to be associated with the pest, their performance in terms of percent parasitism is quite low [35]. On the other hand, the laboratory performance of the introduced D. gelechiidivoris’s percent parasitism [9] and density-dependent response [50] makes it a promising biocontrol approach for T. absoluta.
Although the laboratory experiments provide vital information on parasitoid performance, the findings may not necessarily mirror its performance under natural field conditions. Indeed, in nature, the parasitoid performance against its target host is governed by an array of complex and intertwining biotic and abiotic factors, which can impact negatively or positively on the outcome of biological control (e.g., [51,52,53]). These factors include parasitoid reproductive rate and dispersal ability, inter- and intra-specific competition, predation and availability of host insect, and the associated host plants [33,34]. Other factors include parasitoid thermal tolerance [33,34] and farmers’ management practices such as the use of pesticides and soil health management within the landscape matrix [54].
Various ecological and phenological models have recently been used to predict the establishment of different parasitoid species under current and/or future scenarios in Africa [8]. Using Insect Life Cycle Modelling (ILCYM) software, the thermal thresholds and demographics parameters of D. gelechidivoris have been investigated based on the thermal response curves [38]. Indeed, these models have generated substantial knowledge regarding the potential parasitoid establishment. Nevertheless, none of these models has addressed the aspects related to parasitoid spatio-temporal distribution. Additionally, none of these models has considered parameters such as LULC and the host insect availability. Furthermore, these models have some limitations which include the uncertainties surrounding the complexity of the mechanism underpinning the establishment of parasitoids in different agroecologies; hence, there is a necessity for more flexible modelling approaches.
In the current study, using a more robust yet flexible modelling approach that combined the fuzzy logic model and the species distribution model, we incorporated three key variables, namely, the availability of the host insect and its associated host plants as mapped by LULC and the temperature-based performance of the parasitoid in terms of the parasitoid net reproductive rate (R0), as reported by Aigbedion-Atalor et al. [38]. The approach was used to model the spatio-temporal performance of the T. absoluta parasitoid, D. gelechiidivoris, in vulnerable regions of Kenya. The outcome of the fuzzy logic model predicted the performance of D. gelechiidivoris with very high accuracy (R2 = 0.98). The spatio-temporal differential performance of the parasitoid across the various regions could be explained by the different climatic conditions that characterize these regions, with the Rift valley and coastal regions being too cold and too hot, respectively, for D. gelechiidivoris (Table 1). Similar findings for varying performance with season across the different regions in Kenya were reported for other parasitoid species. For example, Diglyphus isaea (Walker) (Hymenoptera: Eulophidae) was reported to be more abundant at the high and middle elevations throughout the year, while Phaedrotoma scabriventris (Nixon) (Hymenoptera: Braconidae) and Opius dissitus Muesebeck (both (Hymenoptera: Braconidae) had better performances at low elevations during the long rainy season [55].
With the expected temperature increase of 2 °C by the year 2050, the parasitoid performance against the target pest, T. absoluta, is generally predicted to improve, notably in the Rift valley and coastal regions. In the Rift valley region, this enhancement in performance could be attributed to an increase in temperature to an optimal range of 20–25 °C. However, in the coastal region, the reason for enhanced performance is unclear. We speculate that the reason for enhanced performance could be attributed to the fact that the target pest population may be reduced considerably due to potential stressors.
Nevertheless, we recognize the importance of incorporating additional information pertaining to farmers’ practices. For instance, a model incorporating the frequency of pesticide usage and its effect on parasitoid performance should lead to a more refined prediction. It was reported that farmers in Kirinyaga county are spraying up to 16 times per tomato growing season, which reduces the abundance of natural enemies [56]. In addition, a layer’s resolution impacts the output accuracy when using a geospatial algorithm [57]; therefore, since the study targeted small-scale farmers, using higher-resolution bioclimatic data, the same as the classified LULC (i.e., a 30 m resolution), will increase the accuracy of the results. Nevertheless, the outcome of our model provides a solid ground and essential information to guide the parasitoid release and augmentation at both temporal and spatial scales within T. absoluta’s framework of the Integrated Pest Management (IPM). A similar conclusion was drawn by Bone et al. [29], who confirmed that the fuzzy sets theory could satisfactorily be used as a tool for decision support regarding insect pest management. Furthermore, Garcia et al. [30] acknowledge the use of fuzzy sets to develop realistic models regarding biological systems at a landscape level.
Despite the fuzzy algorithm’s high accuracy in the present study, it is important to highlight that this algorithm suffers from a few limitations and drawbacks, as does any other Artificial Intelligence algorithm. For instance, fuzzy logic is a bit generic, and its inputs are somewhat not precisely defined in most study cases [46]. In other words, the fuzzy logic inputs are largely defined by expert knowledge. Hence, these inputs might not be exactly the same (i.e., they could vary considerably according to the expert understanding of the system). For example, in this study experiment, we defined the presence of the parasitoid at a 0.2 level of probability. However, for another case study, such a parasitoid presence could be defined at a 0.4 probability score. Therefore, special care should be taken before extrapolating the model developed in this study to other points in space and time, as the choice of a model usually depends on the study’s purpose and available information [58,59]. However, there are advantages that fuzzy logic offers in terms of flexibility and simplicity, which reduce the model’s vulnerability to uncertainty as no exact information on the system is needed [46]. Given these advantages, the fuzzy logic model is one of the most useful Artificial Intelligence algorithms in many agricultural applications, and its importance is growing considerably in ecology with successful applications in insect pest management (e.g., [29,60]) and biological control [30]. For example, Center and Verma [61] described the applications of fuzzy logic in biological and agricultural systems. They concluded that fuzzy logic provides a methodology for describing complex systems and performs better than the conventional (parametric) methods for time-varying, nonlinear, adaptive systems, such as those found in biological and agricultural processes. Such advantages make it suitable for this study, as demonstrated by the high accuracy obtained.

5. Conclusions

This study predicted the spatio-temporal performance of D. gelechiidivoris as a biocontrol agent for T. absoluta using fuzzy sets through a multilevel modelling approach, with high accuracy. The fuzzy logic modelling approach used in this study integrates predefined rules and assumptions derived from the bioecology of the parasitoid and its host. The data used in modelling were related to the presence of the parasitoid host crop (tomato), the parasitoid host, T. absoluta, and the performance indicator of the parasitoid. The outcome of the fuzzy logic model predicted the performance of D. gelechiidivoris with very high accuracy (R2 = 0.98). Under the current climatic scenario, the parasitoid is predicted to perform fairly well in all regions throughout the year, except for the coastal region. Under the future climatic scenario, the performance of D. gelechiidivoris is projected to improve. Overall, the model sheds light on the varying performance of the parasitoid across different regions of Kenya and in different seasons under both current and future climatic scenarios. The outcome of our model provides solid ground and the essential information to guide the parasitoid release and augmentation at both temporal and spatial scales within T. absoluta’s IPM framework.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/biology11091280/s1, Figure S1: The least-correlated bioclimatic variables’ spatial correlation with the selected variables highlighted with red; Figure S2: Classified LULC map for different years based on the nine classes extracted from the study area with a proportionate coverage area; Figure S3: Map of suitability areas of T. absoluta for the classified LULC in the strategic tomato production areas; Table S1: Description of the LULC classes of the study; Table S2: Landcover statistics; Table S3: Accuracy assessment; Table S4: Selected non-colinear variables used to predict the habitat suitability for Tuta absoluta using the MaxEnt model; Table S5: Temperature-based performance of the parasitoid Dolichogenidea gelechiidivoris.

Author Contributions

Conceptualization, K.M.A. and H.E.Z.T.; methodology, K.M.A. and H.E.Z.T.; formal analysis, K.M.A.; resources, S.A.M. and H.E.Z.T.; data curation, K.M.A.; writing—original draft preparation, K.M.A.; writing—review and editing, K.M.A., H.E.Z.T., S.A.M., O.M., E.M.A.-R. and J.O.; supervision, O.M., E.M.A.-R. and J.O.; funding acquisition, S.A.M. and H.E.Z.T. All authors have read and agreed to the published version of the manuscript.

Funding

This work received financial support from the German Federal Ministry for Economic Cooperation and Development (BMZ), commissioned by the Deutsche Gesellschaft für Internationale Zusammenarbeit (GIZ) through the Fund International Agricultural Research (FIA) (grant number: 81250394); the Biovision foundation Tuta IPM project (project ID: BV DPP-012/2019–2021); and the Norwegian Agency for Development Cooperation, the section for research, innovation and higher education grant number RAF-3058 KEN-18/0005. In addition, the authors gratefully acknowledge the financial support for this research from the following organizations and agencies: the Swedish International Development Cooperation Agency (Sida); the Swiss Agency for Development and Cooperation (SDC); the Federal Democratic Republic of Ethiopia; and the Government of the Republic of Kenya. The first author of this study is supported by the German Academic Exchange Service’s In-Region Postgraduate Scholarship (DAAD). The views expressed herein do not necessarily reflect the official opinions of the donors.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

All data generated or analyzed during this study are included in this published article (and its supplementary information files). The codes that support the findings of this study are available permanently and freely online at the International Centre of Insect Physiology and Ecology (ICIPE) data warehouse through the following link: https://dmmg.icipe.org/dataportal/dataset/a-fuzzy-based-modelling-approach-to-predict-the-spatio-temporal-performance (accessed on 10 August 2022).

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Lux, S.A.; Copeland, R.S.; White, I.M.; Manrakhan, A.; Billah, M.K. A new invasive fruit fly species from the Bactrocera dorsalis (Hendel) group detected in East Africa. Int. J. Trop. Insect Sci. 2003, 23, 355–361. [Google Scholar] [CrossRef]
  2. Mohamed, E.S.I.; Mohamed, M.E.; Gamiel, S.A. First record of the tomato leafminer, Tuta absoluta (Meyrick)(L epidoptera: Gelechiidae) in Sudan. EPPO Bull. 2012, 42, 325–327. [Google Scholar] [CrossRef]
  3. Goergen, G.; Kumar, P.L.; Sankung, S.B.; Togola, A.; Tamò, M. First report of outbreaks of the fall Armyworm Spodoptera frugiperda (J E Smith) (Lepidoptera, Noctuidae), a new alien invasive pest in West and Central Africa. PLoS ONE 2016, 11, e0165632. [Google Scholar] [CrossRef] [PubMed]
  4. Kwadha, C.A.; Okwaro, L.A.; Kleman, I.; Rehermann, G.; Revadi, S.; Ndela, S.; Khamis, F.M.; Nderitu, P.W.; Kasina, M.; George, M.K.; et al. Detection of the spotted wing drosophila, Drosophila suzukii, in continental sub-Saharan Africa. J. Pest Sci. 2021, 94, 251–259. [Google Scholar] [CrossRef]
  5. Giorgini, M.; Guerrieri, E.; Cascone, P.; Gontijo, L. Current strategies and future outlook for managing the neotropical tomato pest Tuta absoluta (Meyrick) in the Mediterranean Basin. Neotrop. Entomol. 2019, 48, 1–17. [Google Scholar] [CrossRef]
  6. Illakwahhi, D.T.; Srivastava, P.B.B.L. Control and management of tomato leafminer -Tuta Absoluta (Meyrick) (Lepidotera, Gelechiidae).A Review. IOSR J. Appl. Chem. 2017, 10, 14–22. [Google Scholar] [CrossRef]
  7. Machekano, H.; Mutamiswa, R.; Nyamukondiwa, C. Evidence of rapid spread and establishment of Tuta absoluta (Meyrick)(Lepidoptera: Gelechiidae) in semi-arid Botswana. Agric. Food Secur. 2018, 7, 1–12. [Google Scholar] [CrossRef]
  8. Mohamed, S.A.; Wamalwa, M.; Obala, F.; Tonnang, H.E.Z.; Tefera, T.; Calatayud, P.-A.; Subramanian, S.; Ekesi, S. A deadly encounter: Alien invasive Spodoptera frugiperda in Africa and indigenous natural enemy, Cotesia icipe (Hymenoptera, Braconidae). PLoS ONE 2021, 16, e0253122. [Google Scholar] [CrossRef]
  9. Aigbedion-Atalor, P.O.; Mohamed, S.A.; Hill, M.P.; Zalucki, M.P.; Azrag, A.G.A.; Srinivasan, R.; Ekesi, S. Host stage preference and performance of Dolichogenidea gelechiidivoris (Hymenoptera: Braconidae), a candidate for classical biological control of Tuta absoluta in Africa. Biol. Control 2020, 144, 104215. [Google Scholar] [CrossRef]
  10. Guimapi, R.Y.A.; Mohamed, S.A.; Okeyo, G.O.; Ndjomatchoua, F.T.; Ekesi, S.; Tonnang, H.E.Z. Modeling the risk of invasion and spread of Tuta absoluta in Africa. Ecol. Complex. 2016, 28, 77–93. [Google Scholar] [CrossRef]
  11. Fiaboe, K.R.; Agboka, K.; Agboyi, L.K.; Koffi, D.; Ofoe, R.; Kpadonou, G.E.; Agnamba, A.O.; Assogba, K.; Adjevi, M.K.A.; Zanou, K.T.; et al. First report and distribution of the South American tomato pinworm, Tuta absoluta (Meyrick)(Lepidoptera: Gelechiidae) in Togo. Phytoparasitica 2021, 49, 167–177. [Google Scholar] [CrossRef]
  12. Mansour, R.; Brévault, T.; Chailleux, A.; Cherif, A.; Grissa-Lebdi, K.; Haddi, K.; Mohamed, S.A.; Nofemela, R.S.; Oke, A.; Sylla, S.; et al. Occurrence, biology, natural enemies and management of Tuta absoluta in Africa. Entomol. Gen. 2018, 38, 83–112. [Google Scholar] [CrossRef]
  13. Yalcin, M.; Mermer, S.; Kozaci, L.D.; Turgut, C. Insecticide resistance in two populations of Tuta absoluta (Meyrick, 1917)(Lepidoptera: Gelechiidae) from Turkey. Türkiye Entomol. Derg. 2015, 39, 137–145. [Google Scholar]
  14. Sridhar, V.; Onkara naik, S.; Nitin, K.S.; Ashokan, R.; Swathi, P.; Gadad, H. Efficacy of integrated pest management tools evaluated against Tuta absoluta (Meyrick) on tomato in India. J. Biol. Control 2019, 33, 264–270. [Google Scholar] [CrossRef]
  15. Guedes, R.N.C.; Roditakis, E.; Campos, M.R.; Haddi, K.; Bielza, P.; Siqueira, H.A.A.; Tsagkarakou, A.; Vontas, J.; Nauen, R. Insecticide resistance in the tomato pinworm Tuta absoluta: Patterns, spread, mechanisms, management and outlook. J. Pest Sci. 2019, 92, 1329–1342. [Google Scholar] [CrossRef]
  16. Santana, P.A.; Kumar, L.; Da Silva, R.S.; Picanço, M.C. Global geographic distribution of Tuta absoluta as affected by climate change. J. Pest Sci. 2019, 92, 1373–1385. [Google Scholar] [CrossRef]
  17. Silva, G.A.; Picanço, M.C.; Bacci, L.; Crespo, A.L.B.; Rosado, J.F.; Guedes, R.N.C. Control failure likelihood and spatial dependence of insecticide resistance in the tomato pinworm, Tuta absoluta. Pest Manag. Sci. 2011, 67, 913–920. [Google Scholar] [CrossRef]
  18. Cocco, A.; Deliperi, S.; Delrio, G. Control of Tuta absoluta (Meyrick)(Lepidoptera: Gelechiidae) in greenhouse tomato crops using the mating disruption technique. J. Appl. Entomol. 2013, 137, 16–28. [Google Scholar] [CrossRef]
  19. Bawin, T.; Dujeu, D.; De Backer, L.; Francis, F.; Verheggen, F.J. Ability of Tuta absoluta (Lepidoptera: Gelechiidae) to develop on alternative host plant species. Can. Entomol. 2016, 148, 434–442. [Google Scholar] [CrossRef]
  20. Palacios, M.; Cisneros, F. Management of the potato tuber moth. Program 4. In Integrated Pest Management; Program Report; International Potato Center: Lima, Peru, 1995; pp. 87–91. [Google Scholar]
  21. Vallejo Cabrera, F.A. Mejoramiento Genético y Producción de Tomate en Colombia; Universidad Nacional de Colombia: Bogotá, Colombia, 1999. [Google Scholar]
  22. Moore, M.E.; Hill, C.A.; Kingsolver, J.G. Differing thermal sensitivities in a host–parasitoid interaction: High, fluctuating developmental temperatures produce dead wasps and giant caterpillars. Funct. Ecol. 2021, 35, 675–685. [Google Scholar] [CrossRef]
  23. Bai, B.; Smith, S.M. Effect of host availability on reproduction and survival of the parasitoid wasp Trichogramma minutum. J. Ecol. Antomol. 1993, 18, 279–286. [Google Scholar] [CrossRef]
  24. Hohmann, C.L.; Luck, R.F. Effect of host availability and egg load in Trichogramma platneri Nagarkatti (Hymenoptera: Trichogrammatidae) and its consequences on progeny quality. Braz. Arch. Biol. Technol. 2004, 47, 413–422. [Google Scholar] [CrossRef]
  25. Iverson, A.L.; Gonthier, D.J.; Pak, D.; Ennis, K.K.; Burnham, R.J.; Perfecto, I.; Rodriguez, M.R.; Vandermeer, J.H. A multifunctional approach for achieving simultaneous biodiversity conservation and farmer livelihood in coffee agroecosystems. Biol. Conserv. 2019, 238, 108179. [Google Scholar] [CrossRef]
  26. Agboka, K.M.; Tonnang, H.; Abdel-Rahman, E.; Kimathi, E.; Mutanga, O.; Odindi, J.; Niassy, S.; Mohamed, S.; Ekesi, S. A systematic methodological approach to estimate the impacts of a classical biological control agents dispersal at landscape: Application to fruit fly Bactrocera dorsalis and its endoparasitoid Fopius arisanus. Authorea, 2022; Preprint. Available online: https://europepmc.org/article/ppr/ppr475970 (accessed on 10 April 2022).
  27. Jamielniak, J.A. A mathematical approach to study stress-related behaviors in captive golden-bellied capuchins (Sapajus xanthosthernos). Comput. Ecol. Softw. 2016, 6, 83. [Google Scholar]
  28. Zadeh, L.A. Fuzzy sets. Inf. Control 1965, 8, 338–353. [Google Scholar] [CrossRef]
  29. Bone, C.; Dragicevic, S.; Roberts, A. Integrating high resolution remote sensing, GIS and fuzzy set theory for identifying susceptibility areas of forest insect infestations. Int. J. Remote Sens. 2005, 26, 4809–4828. [Google Scholar] [CrossRef]
  30. Garcia, A.G.; Diniz, A.J.F.; Parra, J.R.P. A fuzzy-based index to identify suitable areas for host-parasitoid interactions: Case study of the Asian citrus psyllid Diaphorina citri and its natural enemy Tamarixia radiata. Biol. Control 2019, 135, 135–140. [Google Scholar] [CrossRef]
  31. Louis, G.N.; Aloo, F.; Were, K.; Kebeney, J.K.; Kibwage, J.; Sikei, G.; Wokabi, S.; Paul, M.N. Land, agriculture and livestock. no. GoK 2007. 2011; pp. 108–123. Available online: https://www.nema.go.ke/images/Docs/Regulations/KenyaSoECh6.pdf (accessed on 10 January 2022).
  32. R Core Team. A Language and Environment for Statistical Computing; R Foundation for Statistical Computing: Vienna, Austria, 2020. [Google Scholar]
  33. Bajonero, J.; Córdoba, N.; Cantor, F.; Rodríguez, D.; Cure, J.R. Biología y ciclo reproductivo de Apanteles gelechiidivoris (Hymenoptera: Braconidae), parasitoide de Tuta absoluta (Lepidoptera: Gelechiidae). Agron. Colomb. 2008, 26, 417–426. [Google Scholar]
  34. Cely Pardo, N.L. Determinación de Niveles de daño Ocasionados por Diferentes Densidades de Población de Tuta Absoluta (Lepidoptera: Gelechiidae) en Tomate Bajo Invernadero; CO-BAC: Bogotá, Colombia, 2006. [Google Scholar]
  35. Kinyanjui, G.; Khamis, F.M.; Ombura, F.L.O.; Kenya, E.U.; Ekesi, S.; Mohamed, S.A. Distribution, abundance and natural enemies of the invasive tomato leafminer, Tuta absoluta (Meyrick) in Kenya. Bull. Entomol. Res. 2021, 111, 658–673. [Google Scholar] [CrossRef] [PubMed]
  36. Fick, S.E.; Hijmans, R.J. WorldClim 2: New 1-km spatial resolution climate surfaces for global land areas. Int. J. Climatol. 2017, 37, 4302–4315. [Google Scholar] [CrossRef]
  37. Booth, T.H. Why understanding the pioneering and continuing contributions of BIOCLIM to species distribution modelling is important. Austral Ecol. 2018, 43, 852–860. [Google Scholar] [CrossRef]
  38. Aigbedion-Atalor, P.; Hill, M.P.; Azrag, A.G.A.; Zalucki, M.P.; Mohamed, S.A. Disentangling thermal effects using life cycle simulation modelling on the biology and demographic parameters of Dolichogenidea gelechiidivoris, a Parasitoid of Tuta Absoluta. J. Therm. Biol. 2022, 107, 103260. [Google Scholar] [CrossRef] [PubMed]
  39. Salehie, O.; Hamed, M.M.; bin Ismail, T.; Shahid, S. Projection of droughts in Amu Darya River Basin for shared socioeconomic pathways. Res. Sq. 2021; preprint. Available online: https://www.researchsquare.com/article/rs-1088081/v1 (accessed on 10 April 2022).
  40. Hemati, M.; Hasanlou, M.; Mahdianpari, M.; Mohammadimanesh, F. A systematic review of landsat data for change detection applications: 50 years of monitoring the earth. Remote Sens. 2021, 13, 2869. [Google Scholar] [CrossRef]
  41. Young, N.E.; Anderson, R.S.; Chignell, S.M.; Vorster, A.G.; Lawrence, R.; Evangelista, P.H. A survival guide to Landsat preprocessing. Ecology 2017, 98, 920–932. [Google Scholar] [CrossRef] [PubMed]
  42. Phillips, S.J.; Anderson, R.P.; Schapire, R.E. Maximum entropy modeling of species geographic distributions. Ecol. Modell. 2006, 190, 231–259. [Google Scholar] [CrossRef]
  43. Hijmans, R.J. Raster: Geographic Data Analysis and Modeling. R Package Version 3.3–7. 2020. Available online: https://cran.r-project.org/package=raster (accessed on 10 January 2022).
  44. Leroy, B.; Meynard, C.N.; Bellard, C.; Courchamp, F. virtualspecies, an R package to generate virtual species distributions. Ecography 2016, 39, 599–607. [Google Scholar] [CrossRef]
  45. Perfilieva, I. Fuzzy IF-THEN rules from logical point of view. In Computational Intelligence, Theory and Applications; Springer: Berlin/Heidelberg, Germany, 2006; pp. 691–697. [Google Scholar]
  46. Keshwani, D.R.; Jones, D.D.; Meyer, G.E.; Brand, R.M. Rule-based Mamdani-type fuzzy modeling of skin permeability. Appl. Soft Comput. 2008, 8, 285–294. [Google Scholar] [CrossRef]
  47. Zadeh, L.A. Outline of a new approach to the analysis of complex systems and decision processes. IEEE Trans. Syst. Man. Cybern. 1973, 1, 28–44. [Google Scholar] [CrossRef]
  48. Perfilieva, I. Analytical theory of fuzzy if-then rules with compositional rule of inference. In Fuzzy Logic; Springer: Berlin/Heidelberg, Germany, 2007; pp. 174–191. [Google Scholar]
  49. QGIS Development Team. QGIS Geographic Information System; Open Source Geospatial Foundation: Chicago, IL, USA, 2009. [Google Scholar]
  50. Mama Sambo, S.; Ndlela, S.; du Plessis, H.; Obala, F.; Mohamed, S.A. Ratio dependence effects of the parasitoid Dolichogenidea gelechiidivoris on its associated host Tuta absoluta. Biocontrol Sci. Technol. 2022, 32, 497–510. [Google Scholar] [CrossRef]
  51. Groth, M.Z.; Loeck, A.E.; Nornberg, S.D.; Bernardi, D.; Nava, D.E. Biology and thermal requirements of Fopius arisanus (Sonan, 1932) (Hymenoptera: Braconidae) reared on Ceratitis capitata eggs (Wiedemann) (Diptera: Tephritidae). Neotrop. Entomol. 2017, 46, 554–560. [Google Scholar] [CrossRef] [PubMed][Green Version]
  52. Silva-Torres, C.S.A.; Matthews, R.W. Development of Melittobia australica Girault and M. digitata Dahms (Parker) (Hymenoptera: Eulophidae) parasitizing Neobellieria bullata (Parker) (Diptera: Sarcophagidae) puparia. Neotrop. Entomol. 2003, 32, 645–651. [Google Scholar] [CrossRef]
  53. Sow, G.; Arvanitakis, L.; Niassy, S.; Diarra, K.; Bordat, D. Performance of the parasitoid Oomyzus sokolowskii (Hymenoptera: Eulophidae) on its host Plutella xylostella (Lepidoptera: Plutellidae) under laboratory conditions. Int. J. Trop. Insect Sci. 2013, 33, 38–45. [Google Scholar] [CrossRef]
  54. Le Provost, G.; Thiele, J.; Westphal, C.; Penone, C.; Allan, E.; Neyret, M.; van der Plas, F.; Ayasse, M.; Bardgett, R.D.; Birkhofer, K.; et al. Contrasting responses of above-and belowground diversity to multiple components of land-use intensity. Nat. Commun. 2021, 12, 1–13. [Google Scholar] [CrossRef]
  55. Foba, C.N.; Akutse, K.S.; Fiaboe, K.K.M.; Lagat, Z.O.; Gitonga, L.M. Interaction between Phaedrotoma scabriventris Nixon and Opius dissitus Muesebeck (Hymenoptera: Braconidae): Endoparasitoids of Liriomyza leafminer. Afr. Entomol. 2015, 23, 120–131. [Google Scholar] [CrossRef]
  56. Nderitu, P.W.; Muturi, J.; Otieno, M.; Arunga, E.E.; Mattias, J. Tomato leafminer (Tuta absoluta) (Meyrick 1917) (Lepidoptera: Gelechiidae) prevalence and farmer management practices in Kirinyanga County, Kenya. J. Entomol. Nematol. 2018, 10, 43–49. [Google Scholar] [CrossRef]
  57. Usery, E.L.; Finn, M.P.; Scheidt, D.J.; Ruhl, S.; Beard, T.; Bearden, M. Geospatial data resampling and resolution effects on watershed modeling: A case study using the agricultural non-point source pollution model. J. Geogr. Syst. 2004, 6, 289–306. [Google Scholar] [CrossRef]
  58. Bell, J.R.; Aralimarad, P.; Lim, K.-S.; Chapman, J.W. Predicting insect migration density and speed in the daytime convective boundary layer. PLoS ONE 2013, 8, e54202. [Google Scholar] [CrossRef]
  59. Liebhold, A.M.; Tobin, P.C. Population ecology of insect invasions and their management. Annu. Rev. Entomol. 2008, 53, 387–408. [Google Scholar] [CrossRef]
  60. Ibrahim, E.A.; Salifu, D.; Mwalili, S.; Dubois, T.; Collins, R.; Tonnang, H.E.Z. An expert system for insect pest population dynamics prediction. Comput. Electron. Agric. 2022, 198, 107124. [Google Scholar] [CrossRef]
  61. Center, B.; Verma, B.P. Fuzzy logic for biological and agricultural systems. In Artificial Intelligence for Biology and Agriculture; Springer: Berlin/Heidelberg, Germany, 1998; pp. 213–225. [Google Scholar]
Biology 11 01280 g001
Figure 1. The study site showing the occurrence of the parasitoid host, T. absoluta.
Figure 1. The study site showing the occurrence of the parasitoid host, T. absoluta.
Biology 11 01280 g001
Biology 11 01280 g002
Figure 2. Spatio-temporal performance of D. gelechiidivoris in the strategic tomato production areas under the current climate conditions.
Figure 2. Spatio-temporal performance of D. gelechiidivoris in the strategic tomato production areas under the current climate conditions.
Biology 11 01280 g002
Biology 11 01280 g003
Figure 3. Current projection of the performance of D. gelechiidivoris in selected regions in Kenya using pixels counts (the number of pixels in each class per month).
Figure 3. Current projection of the performance of D. gelechiidivoris in selected regions in Kenya using pixels counts (the number of pixels in each class per month).
Biology 11 01280 g003
Biology 11 01280 g004
Figure 4. Spatio-temporal performance of D. gelechiidivoris in the strategic tomato production areas under the future climate projection (2050).
Figure 4. Spatio-temporal performance of D. gelechiidivoris in the strategic tomato production areas under the future climate projection (2050).
Biology 11 01280 g004
Biology 11 01280 g005
Figure 5. Future (2050) projection of the performance of D. gelechiidivoris in selected regions in Kenya using pixels counts (the number of pixels in each class per month).
Figure 5. Future (2050) projection of the performance of D. gelechiidivoris in selected regions in Kenya using pixels counts (the number of pixels in each class per month).
Biology 11 01280 g005
Table 1. Monthly long-term average temperatures (1991–2021) per tomato cropping region.
Table 1. Monthly long-term average temperatures (1991–2021) per tomato cropping region.
Months 1WesternNyanzaRift ValleyCentralEasternCoast
January21.023.618.919.319.627.9
February21.924.619.520.020.528.1
March21.623.919.319.820.428.7
April20.522.818.118.619.528.1
May19.522.517.217.718.726.6
June18.622.416.416.817.825.9
July18.222.516.116.317.225.4
August18.322.716.516.717.625.5
September19.023.217.517.918.826.2
October19.723.218.318.619.626.8
November19.822.717.717.818.727.2
December20.222.918.118.218.727.7
1 Source: Climate-data.org https://en.climate-data.org/ (accessed on 20 February 2022).
Table 2. Net reproduction rate (R0) of D. gelechiidivoris based on temperature variability.
Table 2. Net reproduction rate (R0) of D. gelechiidivoris based on temperature variability.
Temperature ThresholdNet Reproduction Rate (R0)Fuzzy Partition Variable Names
10–15 °C0.13–1.55Suboptimal lower temperature threshold
20 and 25 °C15–14Optimal
30–35 °C2.18–0.06Suboptimal higher temperature threshold
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Agboka, K.M.; Tonnang, H.E.Z.; Abdel-Rahman, E.M.; Odindi, J.; Mutanga, O.; Mohamed, S.A. A Fuzzy-Based Model to Predict the Spatio-Temporal Performance of the Dolichogenidea gelechiidivoris Natural Enemy against Tuta absoluta under Climate Change. Biology 2022, 11, 1280. https://doi.org/10.3390/biology11091280

AMA Style

Agboka KM, Tonnang HEZ, Abdel-Rahman EM, Odindi J, Mutanga O, Mohamed SA. A Fuzzy-Based Model to Predict the Spatio-Temporal Performance of the Dolichogenidea gelechiidivoris Natural Enemy against Tuta absoluta under Climate Change. Biology. 2022; 11(9):1280. https://doi.org/10.3390/biology11091280

Chicago/Turabian Style

Agboka, Komi Mensah, Henri E. Z. Tonnang, Elfatih M. Abdel-Rahman, John Odindi, Onisimo Mutanga, and Samira A. Mohamed. 2022. "A Fuzzy-Based Model to Predict the Spatio-Temporal Performance of the Dolichogenidea gelechiidivoris Natural Enemy against Tuta absoluta under Climate Change" Biology 11, no. 9: 1280. https://doi.org/10.3390/biology11091280

APA Style

Agboka, K. M., Tonnang, H. E. Z., Abdel-Rahman, E. M., Odindi, J., Mutanga, O., & Mohamed, S. A. (2022). A Fuzzy-Based Model to Predict the Spatio-Temporal Performance of the Dolichogenidea gelechiidivoris Natural Enemy against Tuta absoluta under Climate Change. Biology, 11(9), 1280. https://doi.org/10.3390/biology11091280

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop