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. 2021 Nov 4;16(11):e0257736. doi: 10.1371/journal.pone.0257736

Socioeconomic and health impacts of fall armyworm in Ethiopia

Zewdu Abro 1, Emily Kimathi 2, Hugo De Groote 3, Tadele Tefera 1, Subramanian Sevgan 2, Saliou Niassy 2, Menale Kassie 2,*
Editor: Rodney N Nagoshi4
PMCID: PMC8568106  PMID: 34735485

Abstract

Since 2016, fall armyworm (FAW) has threatened sub-Saharan ‘Africa’s fragile food systems and economic performance. Yet, there is limited evidence on this transboundary pest’s economic and food security impacts in the region. Additionally, the health and environmental consequences of the insecticides being used to control FAW have not been studied. This paper presents evidence on the impacts of FAW on maize production, food security, and human and environmental health. We use a combination of an agroecology-based community survey and nationally representative data from an agricultural household survey to achieve our objectives. The results indicate that the pest causes an average annual loss of 36% in maize production, reducing 0.67 million tonnes of maize (0.225 million tonnes per year) between 2017 and 2019. The total economic loss is US$ 200 million, or 0.08% of the gross domestic product. The lost production could have met the per capita maize consumption of 4 million people. We also find that insecticides to control FAW have more significant toxic effects on the environment than on humans. This paper highlights governments and development partners need to invest in sustainable FAW control strategies to reduce maize production loss, improve food security, and protect human and environmental health.

Introduction

Maize is a staple food for more than 300 million Africans [1,2]. Despite the importance of maize, its production is constrained by several biotic and abiotic factors that contribute to sub-Saharan ‘Africa’s (SSA) pervasive food insecurity. For a long time, stemborers and Striga weed were the main maize pests in SSA, a combination known to cause complete maize production failure [3]. The recent invasion (since 2016) of maize by fall armyworm (FAW), Spodoptera frugiperda, hereafter referred to as FAW, has exacerbated the already fragile food systems and food security in the region [48]. Farm-level estimates in some SSA countries showed that FAW causes maize production losses of between 11% and 67% [6,914].

Infestation by invasive transboundary pests such as FAW also causes additional costs due to insecticide use and labor to control the pest [10,1517]. The application of insecticides is the primary FAW control strategy in SSA countries [18]. This inevitably has impacts beyond abating maize production losses; insecticide pollution can adversely affect the environment, biodiversity, and health of the producers and consumers [12,1922]. Furthermore, FAW invasions can affect trade, income, and food consumption due to reductions in maize supply. FAW invasions can also increase health expenditure arising from exposure to insecticides and affect the performance of businesses along the maize value chain, such as maize input suppliers and contributors to the livestock feed sector [2325]. Unless effective control strategies are implemented, the pest will continue to cause massive destruction to maize and affect the livelihoods of millions of people in SSA. Implementing such control strategies requires updates on the current impact of FAW on the economy, food security, and health (human and environmental).

Despite FAW’s economic importance, there are limited studies on its impact on production, the cost of control, including insecticides, and the unintended negative consequences of insecticide use on human and environmental health. Using survey data from Ghana and Zambia, Day, Rwomushana and colleagues extrapolated production losses due to FAW for twelve SSA countries [12,26]. Country-specific studies are crucial because the effects of FAW vary across and within countries due to differences in agro-ecology, farming practices, and farm and farmer characteristics. De Groote and colleagues showed that losses caused by FAW vary by agro-ecological zones [6]. Many of the existing studies did not capture the large degree of agro-ecological and socioeconomic heterogeneity of smallholder farmers in SSA because the studies rely on limited geographical areas [9,10,13,27]. Many of these studies also use data collected at the early stages of FAW invasion. The real impacts of FAW infestation may take time to become evident as the infestation varies from season to season. The arrival of FAW has changed the dynamics of existing farming system constraints to maize production, leading to a new status quo [28].

Invasion by FAW has significantly increased insecticide use in most invaded regions [10,17]. The majority of studies have focused on the efficacy of insecticide for the management of FAW in the invaded regions [29,30], but the increased use of insecticides for FAW control is affecting the health of farmers. For instance, farmers have reported sickness in Ghana and Zambia after applying insecticides recommended for controlling FAW [12]. However, no systematic study has been conducted so far to document the health and environmental effects of insecticides.

In this paper, we present evidence on the economic and health cost of FAW. Particularly, we estimated the pest’s effect on maize production, food security, and the effects of insecticide use on public and environmental health. The evidence will help prioritize investment in FAW management strategies that simultaneously reduce losses and maintain ecological balance. As secondary objectives, we endeavor to understand farmers’ current FAW control measures, effectiveness, and support that communities receive in combating the pest. Since the accuracy of production loss estimates depends on farmers’ knowledge of the pest [31], we examined farmers’ awareness and knowledge about FAW.

To measure FAW’s effects on maize production and achieve the secondary objectives, we combined agroecology-based community surveys using focus groups discussion (FGD) with nationally representative datasets collected by Ethiopia’s Central Statistical Agency (CSA). We covered 150 villages/communities and 1,100 farmers distributed across 30 districts of maize-growing agro-ecological zones. We also collected data from 180 agricultural development agents (DAs) and their supervisors in these communities to validate the results from the community survey data. The DAs live and work in the villages, have extensive knowledge of the farming system in the study communities, and conduct campaigns and scouting exercises, distribute insecticides and provide advisory services to farmers to manage FAW. Supervisors visit and provide technical support to DAs. We recorded yield and yield losses agreed by each member of the FGD, often after a hot debate. This can help to minimize recall bias and avoid too high or too low estimates. The datasets from the CSA’s Agricultural Sample Survey showed a good picture of maize production in Ethiopia. On average, the data covers 17,833 maize-growing farmers across the country. We developed a simple arithmetic formula to quantify maize production losses at the national level. Using secondary data obtained from the Ministry of Agriculture (Ethiopia), we applied the environmental impact quotient (EIQ) approach to quantify adverse health risks and the environmental effects of insecticides used to manage FAW [32,33].

We report three key results. First, 97% and 88% of the farmers interviewed were aware of and correctly identified FAW, respectively. Knowledge of farmer’s awareness of FAW is vital to estimating its effects accurately. Second, FAW has a considerable socioeconomic impact in Ethiopia that varies by agro-ecology. From 2017 to 2019, the country lost 0.67 million tonnes of maize production, worth US$ 200 million (0.08% of the Gross Domestic Product). This lost maize could have met the maize consumption requirement of 4 million food-insecure households. Third, FAW has a negative spillover effect on biodiversity and the human population. In the short term, the application of insecticides to control FAW has greater potential toxic effects on the environment than on humans. It also aggravates food insecurity by killing beneficial insects and contaminating other essential natural resources in the long term.

Overall, our findings present a cautionary note about the impacts of FAW. Lack of appropriate control measures against FAW combined with other production constraints can lead to high economic losses to society and monetary expenditures associated with managing this pest. Although the food security cost is not high at the household level (60 kg per year per affected farmer), the economic and biodiversity losses are high at the national level. For example, from 2017 and 2019, the country lost US$ 204 million worth of income due to maize production losses and insecticides purchases. However, if the pest persists, it can cause food security and poverty problems in the long run by reducing marketed surplus and income [10].

Context and responses to FAW occurrence in Ethiopia

Since FAW first occurrence in West Africa in 2016, it has spread quickly throughout SSA, including Ethiopia [12,26]. In Ethiopia, FAW is a threat to over 9 million maize-growing farm households. It was first observed in 2017 [34] and is currently one of the most destructive maize pests in the country. Maize is an economically important and strategic food security crop covering 20% of cultivated land and accounting for 30% of cereal production [35]. It provides the largest share of calories (22%) for most Ethiopians [36]. It is also the most productive cereal crop in the country, with an average yield of 4 tonnes/ha [35].

The sudden invasion of FAW has forced the government of Ethiopia and stakeholders to use insecticides as an emergency measure in FAW-affected maize fields. Over the study period, the Ministry of Agriculture of Ethiopia (MOA), through the Regional and District Bureaus of Agriculture, distributed 457,427 liters of insecticides, sprayed on 1.5 million ha of maize [37]. The direct cost of insecticides to the government was about US$ 4 million [37]. This does not include the insecticides that farmers purchased themselves through other means or the costs of surveillance and management, on which no data are available. While insecticides were used to reduce losses due to FAW, they have unintended consequences on human and environmental health [12,26].

Materials and methods

Study areas

This study covers the major maize-producing districts and agro-ecological zones of Ethiopia. We used the sampling frame prepared by the Sustainable Intensification of Maize-Legume Cropping Systems in Eastern and Southern Africa (SIMLESA) project of the International Wheat and Maize Improvement Center (CIMMYT) [38]. The SIMLESA survey was designed to represent the key maize-producing agro-ecological zones of Ethiopia. It covered 225 maize-producing villages in 39 districts in Amhara, Benishangul Gumuz, Oromia, Southern Nations and Nationalities (SNNP), and the Tigray Regional States. In our study, we cover 30 districts and 150 villages. We dropped seven districts in the Oromia Regional State due to security reasons and excluded the Benishangul Gumuz and the Tigray Regional States for logistical reasons. The three remaining Regional States (Amhara, Oromia, and SNNPR) jointly produce more than 86% of the country’s maize, as reported in Table 1 [35].

Table 1. Area under maize cultivation and production by agro-ecological zones in Ethiopia.

Agro-ecological zones Cultivated land (millions of ha) Production (millions of tonnes)
2017 2018 2019 2017 2018 2019
Wet upper mid-altitudes 0.85 0.97 0.85 3.74 4.27 3.78
Wet lower mid-altitudes 0.05 0.03 0.03 0.14 0.09 0.09
Dry mid-altitudes 0.34 0.29 0.34 1.00 0.88 1.37
Wet lowlands 0.01 0.03 0.03 0.04 0.11 0.13
Dry lowlands 0.04 0.04 0.02 0.08 0.05 0.07
Highlands 0.69 0.85 0.82 2.95 3.59 3.59
Total 1.98 2.20 2.08 7.95 8.98 9.03

Source: CSA’s agricultural sample survey (2017–2019).

The study villages and their corresponding agro-ecological zones are represented in Fig 1. The agroecological zone classifications are from the CIMMYT’s maize mega-environments (MMEs). An MME is a homogenous production environment with similar agro-climatic conditions defined using rainfall and temperature [39,40]. Rainfall and temperature are key parameters that affect maize production and the biology and spread of FAW [41,42].

Fig 1. The study areas and the location of sample communities within maize mega-environments.

Fig 1

Among the communities we surveyed, 71 villages are classified as wet upper mid-altitudes, 48 are in the highlands, 28 are in the dry mid-altitudes, two are found in the wet lower mid-altitudes, and one is in the dry lowlands. Over the study period, nearly 96% of the maize production in the country came from three major MMEs: the wet upper mid-altitudes (45%), the highlands (39%), and the dry mid-altitudes (12%). The remainder of the country’s maize production came from the wet lower mid-altitudes, wet lowlands, and dry lowlands, each contributing nearly 1% (Table 1).

Data sources and collection

We used data from three sources: first, we used primary community survey data collected using FGD and expert opinion data collected through individual interview. These datasets collected between June and July 2020 from 150 communities. On average, seven farmers participated per FGD, making 1,100 (10% women) farmers in total. The expert opinion survey involved 180 agricultural experts, of whom 150 were development agents (DAs) who worked closely with the farmers, and 30 were DAs supervisors who worked in the districts’ agriculture offices. These experts have direct knowledge and expertise on agricultural production and districts and villages’ farming systems. They coordinated FAW awareness campaigns and management, conduct scouting exercises, and distributed insecticides. The DAs are also responsible for reporting production and related data to the district agricultural office, including areas affected by FAW and the numbers of farmers affected in their respective command areas. We used a structured questionnaire covering various topics, including farmers’ awareness and knowledge of FAW, the percentage of farmers affected by FAW, control strategies, attainable yield, actual yield, and yield losses due to FAW. We collected data on the percentage of farmers affected by FAW in their respective villages and the yield losses due to FAW in the 2017, 2018, and 2019 production seasons.

Self-report data, especially when collected over time, might be prone to recall bias. Although we cannot entirely rule out recall bias, we developed confidence in farmers’ yield and yield losses estimates for the following reasons: (1). we recorded yield and yield losses data agreed by each member of the FGD, often after a hot debate. This can help to minimize recall bias and avoid too high or too low estimates. This helps to minimize recall bias and avoid too high or too low estimates. A recent study [43] in Ethiopia also shows that difference in self-reported and objectively measured yield is not big. Even in some cases, farmer’s reported yield is better than yield objectively measured by W-walk and Transect methods [44]; (2) because of the community-level campaigns and intensive information exchange through extension and other local communication channels to control FAW, farmers provided attention to the pest, and its impact, which can help them provide reasonable estimates of yields and yield losses data; (3) Farmers cultivate maize on same plot year after year, and production variation across years is limited-implying recalling recent years’ data might not be difficult; and (4) the data were collected after well-trained enumerators and supervisors carefully explained until the FGD participants understand the questions.

To understand farmers’ FAW awareness and knowledge levels, we asked each FGD participant two questions: (1) Are you aware of FAW? and (2) Can you identify FAW from these pictures? (Fig 2). Awareness implies that the farmers have heard about FAW through fellow farmers and development agents, but they may not experience the pest in their fields. Knowledge is much more than awareness, and farmers must identify or know FAW from the pictures, and we asked question (2) if the farmers said yes to question (1). The questionnaire had an introductory statement to obtain verbal consent from respondents and agricultural experts. We have also got approval from icipe’s science committee.

Fig 2. Pictures of lepidopterous insect pests shown to farmers.

Fig 2

A) stemborers (either Chilo partellus (A1), or Busseola Fusca (A2); B) Spodoptera exempta; and C) Spodoptera frugiperda, obtained from [6] with permission.

The second dataset comes from the agricultural sample survey datasets for 2017, 2018, and 2019 main seasons. These datasets are nationally representative household survey data collected by Ethiopia’s Central Statistical Agency [35]. The agency obtained verbal consent from respondents. The third datasets consist of insecticide data collected by the authors from the Ministry of Agriculture [37].

To measure the effect of FAW, we combined the community survey data with the CSA data, from which we obtained the total maize area and the number of maize-growing farmers in the country CSA datasets. We identified the agro-ecological zones for each survey community by overlaying their coordinates with the global maize mega-environments’ shapefile. Because we did not have access to the farmers’ coordinates in the CSA survey, we used the centroids of the CSA’s survey areas to identify the key MMEs. Finally, we used region, zone, district, and MMEs as unique identifiers to combine the two datasets.

Measuring maize production losses

Maize yield loss is the difference between attainable yield without FAW and actual yield in FAW presence [6]. However, FAW is not the only cause of yield loss. Several other factors contribute to yield loss, including abiotic factors (e.g., drought and soil fertility) and other biotic factors (e.g., diseases, stemborers, and locusts). Results may be biased if farmers are asked directly to estimate yield loss due to FAW alone without considering the potential yield loss attributable to other production constraints. To mitigate this problem, we first asked farmers to compute the actual maize yield in the community in the presence of all production constraints, including FAW. Second, we asked them to estimate the attainable yield in the absence of production constraints. Third, we asked farmers to quantify FAW’s contribution and other production constraints to the yield gap, the difference between the attainable and actual yields.

We calculated the total production loss (PLi) due to FAW using Eq (1) as follows:

PLi=ikAi×[(Ya-Y)×Li]×(Nhi×Fai) (1)

where the index i represents agro-ecological zones; k denotes the number of agro-ecological zones; Ai is the average land size (ha) devoted to maize in that zone; Ya is the attainable yield without production stresses, including FAW (tonnes/ha); and Y is the actual yield in the presence of FAW and other production stresses (tonnes/ha). Li is the proportion of the average yield losses attributed to FAW (%); Nh is the number of maize-growing households; and Fai is the proportion of farmers affected by FAW. We obtained the values for Ya, Y, Li and Fai from the community survey data, while the values of Ai and Nhi were from the CSA datasets (Table 2).

Table 2. Attainable yield, actual yield, and average land size in Ethiopia (2017–2019).

Agro-ecological zones Attainable yield (tonnes/ha)-(Ya) Actual yield (tonnes/ha)-(Y) Yield losses due to FAW and other stresses (tonnes/ha)-(YaY) Average land size (ha)-(Ai) Number of farmers (millions) (Nhi)
A B C = A-B D E
Wet upper mid-altitudes 4.02 2.76 1.26 0.12 3.41
(0.10) (0.08) (0.05) (0.08) (0.02)
Wet lower mid-altitudes 5.08 3.73 1.35 0.08 0.32
(0.90) (0.82) (0.15) (0.01) (0.01)
Dry mid-altitudes 4.40 2.86 1.54 0.14 1.29
(0.13) (0.13) (0.07) (0.01) (0.01)
Dry lowlands 3.10 2.47 0.63 0.10 0.33
(0.12) (0.16) (0.11) (0.02) (0.01)
Highlands 4.13 2.88 1.25 0.11 3.80
(0.14) (0.11) (0.06) (0.06) (0.01)
Average 4.11 2.82 1.29 0.12 9.28
(0.07) (0.06) (0.03) (0.04) (0.01)

Note: Standard errors in parenthesis.

Sources: Columns A and B are from the community survey data; columns D and E are from the CSA’s agricultural sample survey.

Although farmers and government incur management costs, we focused on production losses (PLi) because we did not have full management cost data. However, as discussed in the next section, we report the insecticides costs and measure the impacts of insecticides spraying on human health and the environment.

Measuring the impacts of insecticides on environmental and human health

While insecticides were used to boost crop productivity, they have unintended consequences on human and environmental health. The use of insecticides poses a risk to human health, water quality, food safety, aquatic species, and beneficial insects [21,4551]. The objective of measuring the health and environmental impacts of insecticides used to control FAW was to account for the indirect cost of the pest, regardless of who used the insecticides and their impact on individual farmers. In developing countries, insecticides spraying is often conducted manually, without adequate measures to prevent negative effects on human health and the environment [12,52].

To measure the potential risks to human health and the environment caused by insecticides used to control FAW, we used the environmental impact quotient (EIQ) [32,33]. For the empirical application of this method in the agriculture sector, see [21,48,53]. Although the EIQ uses arbitrary weights to measure the effects of the insecticides, it has been used in other studies as there is no readily available alternative to EIQ at present [21,48,54,55]. In any event, it is vital to consider the health and environmental effects [21]. We calculate the EIQ for each active insecticides ingredient as follows:

EIQ=CDT×5+DT×P+C×S+P2×SY+L+[F×R+D×S+P2×3+Z×P×3+B×P×5]}/3 (2)

where C is chronic toxicity; DT is dermal toxicity; SY is systemicity; F is fish toxicity; L is leaching potential; R is surface loss potential; D is bird toxicity; S is soil residues half-life; Z is bee toxicity; B is beneficial arthropod toxicity; P is plant surface residues half-life. The first, the second, and the third part of the Eq (2) within the square brackets are the producer, consumer, and environmental effects of the pesticides, respectively. We used the EIQ Field Use [33]. We obtain the EIQ Field Use by multiplying the EIQ value with the active ingredient of the pesticides used and its application rate [32]. From Eq (2), the average of the producer, consumer, and environmental effects provide the EIQ. The environmental effects of insecticides include the threat to birds, bees, and other beneficial insects. It may also contaminate groundwater and soil due to the potential leaching of the insecticides [46]. Low EIQ values indicate the negative impacts of insecticides are low and vice versa. EIQ relies on published toxicology and environmental fate data [32,33].

Results and discussion

FAW awareness and knowledge of farmers

We found that 97% of the FGD participants were aware of FAW. Moreover, 88% of the farmers in the FGDs correctly identified FAW (Table 3), slightly more than those in Kenya (82%) [6]. Fewer farmers in the wet upper mid-altitude and highland MMEs correctly identified FAW than farmers in other agro-ecological zones. These two agro-ecological zones contribute more than 80% of the country’s maize production, suggesting that the extension system may need additional capacity-building activities for farmers.

Table 3. Farmers’ awareness and knowledge of FAW in the study areas (%).

Agro-ecological zones Awareness of FAW (%) Correctly identified FAW (%)
Wet upper mid-altitudes 92.00 70.00
Wet lower mid-altitudes 100.00 100.00
Dry mid-altitudes 99.00 88.00
Dry lowlands 100.00 100.00
Highlands 92.00 80.00
Average 97.00 88.00

Source: Community survey.

FAW control strategies used by farmers

It seems the effectiveness of FAW control strategies varied by agro-ecology (Fig 3). Farmers in the wet lower mid-latitude and dry lowland agro-ecological zones named a few control methods. We asked farmers to score their effectiveness on a scale from zero (none) to ten (maximum). Insecticides received an average score of six (Fig 3 Panel A). The effectiveness of chemicals remained the highest (Fig 3, Panels B-F). Cultural (e.g., rotation and fallow) and biological (e.g., caring for the striped earwig species during field management) pest control techniques received a score of five. The effectiveness of botanical extracts (e.g., neem-based products) and mechanical control (e.g., killing larvae of the pest) received below-average scores. The FGD participants gave a low effectiveness score (two) for agro-ecological approaches (e.g., cropping systems such as intercropping), which were promoted to control FAW in Ethiopia and elsewhere [2,7,18,56]. This result is in line with a study in southern Ethiopia that found that intercropping (maize-legume) had little impact on controlling maize production losses due to FAW in southern Ethiopia [10]. However, an experimental study in Uganda showed that intercropping was more effective than monocropping in controlling FAW and stemborers [57].

Fig 3. Farmers’ FAW control strategies by agro-ecological zones.

Fig 3

External support for FAW control

The impact of the pest may depend on the type of support the community receives to manage the pest. We asked the FGD participants to assess if the community they belonged to had received external support (e.g., training and funding) for controlling FAW. We also asked whether the support had increased, decreased, or remained the same. The support included training in FAW management, provision of credit, free insecticides, and spraying equipment. Farmers receive support from the regional and federal governments, Agricultural Research Systems, and development organizations. More than half of the communities (61%) had not received any support (Table 4). For 6% of the communities, support had remained the same, suggesting that farmers had received continuous support since the first occurrence of FAW in their respective communities. About 21% of the communities reported that external support for FAW control had increased. On the other hand, 11% of the studied communities reported that they had received external support, but it had decreased over time. The absence or low level of support may have contributed to higher production losses.

Table 4. FAW control support to the study communities.

External support: Wet Upper Mid-altitudes Wet Lower Mid-altitudes Dry Mid-altitudes Dry Lowlands Highlands Average
Not at all 61.00 100.00 63.00 0.00 61.00 61.00
Increased 21.00 0.00 30.00 0.00 18.00 21.00
Same 7.00 0.00 0.00 100.00 5.00 6.00
Decreased 10.00 0.00 5.00 0.00 15.00 11.00
Do not know 2.00 0.00 1.00 0.00 0.00 1.00
Total 100.00 100 100.00 100.00 100.00 100.00

Source: Community survey.

Farmers affected by fall armyworm

The map in Fig 4 shows the distribution of the affected farmers by agro-ecology. The FGD results indicated that FAW affected 40% of maize farmers (Table 5), while the expert opinion interviews estimated that 51% of the farmers were affected (Table A1 in S3 File). In the wet lower mid-altitudes containing 3% of all maize farmers (Table A2 in S3 File), farmers were the most affected (59%). In the dry lowlands, where 4% of maize farmers are located, FAW affected 17% of farmers. For the other agro-ecological zones, the proportion of farmers affected by FAW was close to the country’s average at 40%. The total number of farmers affected by FAW over the study period was 3.7 million per annum.

Fig 4. Geographic distribution of average farmers affected (%) by FAW (2017–2019).

Fig 4

Table 5. Proportion of farmers affected by FAW (%).

Agro-ecological zones 2017 2018 2019 Average
Wet upper mid-altitudes 36.40 39.64 39.71 38.60
(2.51) (2.49) (2.28) (1.40)
Wet lower mid-altitudes 55.00 55.00 67.50 59.17
(20.00) (25.00) (27.50) (11.21)
Dry mid-altitudes 44.02 41.71 45.27 43.68
(4.73) (5.07) (4.96) (2.82)
Dry lowlands 20.00 12.50 17.50 16.67
(0.00) a (2.50) (2.50) (1.67)
Highlands 37.95 42.39 44.75 41.67
(3.58) (4.06) (4.07) (2.25)
Average 38.07 40.68 42.13 40.30
(1.86) (1.97) (1.89) (1.10)

Note: Standard errors of the mean are reported in parenthesis;

a the standard errors are zero because FGD participants provided 20% loss for all data points.

Source: Community survey.

Maize yield losses due to FAW

We estimated that, on average, FAW causes an annual loss of 36% in maize production (Table 6), despite the use of control measures. This estimate was close to the agricultural experts’ estimate of 32% (Table A1 in S3 File). The map in Fig 5 shows the distribution of the yield losses by agro-ecology. In the wet mid-altitudes and highland agro-ecological zones, losses were close to the country’s average of 36%. However, yield losses in the dry lowlands were higher than the country’s average. This was perhaps because of the limited support farmers had received for FAW control in this zone (Table 4), the resulting limited use of control strategies (Fig 3), and the absence of hosts other than maize. The variability in yield loss could be due to several factors, including farming practices, natural enemies’ availability, and climatic factors [18]. Several studies have established the role of climatic factors in FAW incidence. The combined effect of natural enemies, including predators and parasitoids, could be up to 60% effective in controlling FAW if these natural enemies were conserved [29,58]. Heavy downpours can reduce FAW by washing away neonates and affecting the flight capability of adult moths. Soil health in terms of soil moisture and fertility enhance plant vigor, which, in turn, protects crops against heavy damage [59,60]. The yield loss estimates are lower than those reported in Kenya [6]. However, this comparison should be interpreted with caution as yield losses depend on several factors (agro-ecology, farm management, years of data collection, estimation approach, etc.).

Table 6. Yield losses due to FAW (%).

Agro-ecological zones 2017 2018 2019 Average
Wet upper mid-altitudes 34.37 34.71 35.82 34.97
(2.14) (1.96) (2.05) (1.18)
Wet lower mid-altitudes 35.00 32.50 35.00 34.17
(5.00) (2.50) (5.00) (2.01)
Dry mid-altitudes 38.78 41.21 43.46 41.17
(3.78) (3.47) (3.15) (1.99)
Dry lowlands 80.00 80.00 80.00 80.00
(0.00) a (0.00) a (0.00) a (0.00) a
Highlands 33.20 36.43 34.20 34.61
(3.13) (2.69) (2.75) (1.65)
Average 35.13 36.64 36.96 36.25
(1.61) (1.45) (1.48) (0.87)

Note: Standard errors in parenthesis;

a the standard errors are zero because FGD participants provided 80% loss for all data points.

Source: Community survey.

Fig 5. Geographic distribution of average yield loss (%) due to FAW (2017–2019).

Fig 5

Production losses: Economic and food security implications

This sub-section reports the total maize production losses computed using Eq (1), presented by agro-ecological zones (Table 7) and administrative regions (Table A4 in S3 File). For 2017, we estimated Ethiopia lost 0.18 million tonnes of maize to FAW (Table 7). The production loss increased from 0.22 million tonnes in 2018 to 0.25 million tonnes in 2019. The increase in loss over time could be attributable to changes in the proportion of farmers affected (Table 5), the percentage yield losses (Table 6), the number of maize farmers (Table A2 in S3 File), and maize land size (Table A3 in S3 File). The highest production losses are in the wet upper mid-altitude, highland, and dry mid-altitude agro-ecological zones. The production losses are small compared to the first estimates by Day and colleagues [12,26]. For 2017, our estimate was 7% of the 2.74 million tonnes of maize production loss in Ethiopia, estimated by Day and colleagues [26]. Similarly, our estimated losses were 13% of the 1.67 million tonnes of maize loss in 2018 estimated by Rwomushana and colleagues [12].

Table 7. Estimated total maize production losses.

MMEs Loss (millions of tonnes) Loss (millions of US$) ¥
2017 2018 2019 2017 2018 2019
Wet upper mid-altitudes 0.064 0.080 0.084 15.21 22.35 28.53
Wet lower mid-altitudes 0.007 0.004 0.006 1.52 0.89 1.73
Dry mid-altitudes 0.049 0.047 0.073 13.33 14.94 24.87
Wet lowlands 0.002 0.005 0.005 0.55 1.37 1.53
Dry lowlands 0.002 0.002 0.002 0.75 0.58 0.46
Highlands 0.057 0.089 0.095 14.22 25.24 32.28
Total 0.182 0.228 0.265 45.59 65.38 89.40

¥ We use producer prices to estimate the value of production losses.

The exchange rate was 26.87 ETB/US$ in 2017, 27.43 ETB/US$ in 2018, and 29.23 ETB/US$ in 2019.

Source: Authors’ computation based on community survey and CSA’s agricultural sample survey.

Over the study period, the total production loss was 0.67 million tonnes of maize, generating an economic loss of US$ 200 million to the Ethiopian economy (Table 7). The economic loss is equivalent to 0.08% of the country’s Gross Domestic Product (US$ 262 billion) from 2017 to 2019 [61]. Alternatively, the losses were equivalent to 3% of the total foreign direct investment (US$ 7,327 million) in 2017 and 2018 alone [4]. Using the 152 kg per capita consumption of maize in Ethiopia [62], the quantity of maize lost could have met the per capita maize consumption of over 50% (4.3 million) of the country’s chronically food-insecure (8.5 million people) [63].

Although the economic and food security costs are high at the national level, the food security impact does not seem to be high at the household level-the per capita maize production loss is 60 kg per year (0.22 million tonnes divided by 3.7 million affected framers). A study in southern Ethiopia finds no significant effect of FAW on per capita maize consumption at the household level [10]. However, if the pest persists, it can have food security and poverty implication at the household level by reducing marketed surplus and income [10].

Human and environmental effects of insecticides used for FAW control

Four insecticides were used in Ethiopia to reduce the impact of the pest (Table 8). According to the World Health Organization (WHO), malathion is slightly hazardous while the other chemicals are moderately hazardous [64]. All these insecticides have a high toxicity impact on the environment (e.g., by killing beneficial insects). Malathion, diazinon, and dimethoate carry considerable risk for the environment [51], as shown by the high EIQ values (Table 8). Synthetic insecticides are important management options for FAW control, but repeated application increases the accumulation of insecticides in the environment and raises major concern, as demonstrated by the high EIQ values. Furthermore, resistance to major classes of synthetic insecticides in the native regions of this pest is another problem. The efficacy of a synthetic insecticide-based management strategy is not guaranteed, as FAW has developed resistance to many active ingredients from different classes of insecticides [8,6567]. This suggests an urgent need for resistance management as a vital component of integrated pest management. The risk impact on human health is relatively low, given the relatively low value of EIQ for consumers and producers. However, repeated exposure to small doses of insecticides can lead to long-term effects in humans. This calls for judicious and appropriate use of synthetic insecticides to successfully manage FAW and sustain the increased productivity of maize in Ethiopia and elsewhere in Africa. Previous reports show that Ethiopia is home to many natural enemies of FAW [68]. The adverse impacts of these insecticides on non-target and beneficial organisms and the environment might also explain pest incidence variations and yield losses because of the negative impact of insecticides on biological control agents. Our results suggest the importance of control strategies that effectively suppress the pest without compromising the natural environment. These may include biopesticides [69], predators, parasitoids, and pathogens [68,70], and push-pull strategies [18,71].

Table 8. Human health and environmental impacts of insecticides used to control FAW.

Insecticides Active ingredient (%) Application rate (liter/ha) Quantity (liters) Components of field use EIQ
Average EIQ Consumer effects Producer effects Ecological effects
Malathion 50 2 114,529 23.80 3.80 7.70 49.60
Diazinon 60 1 256,914 22.60 1.30 3.50 63.00
Dimethoate 40 1 25,488 11.50 3.90 3.50 26.90
Chlorpyrifos 48 0.5 60,496 5.50 0.40 1.20 14.90

Source: Authors’ computation based on MoA’s pesticides data [37].

Conclusions

Data on production losses are crucial for informed management of pests and evaluating the effectiveness of pest control measures. In this paper, we present the first comprehensive estimate of the impact of FAW on maize production, food security, and health in Ethiopia, contributing to the few existing studies in SSA. We used primary community survey data combined with a nationally representative agricultural household survey to achieve our objectives.

The pest caused significant economic and food losses at the country level. About 0.67 million tonnes of maize were lost, equivalent to 2.54% of the maize production (25.96 million tonnes) over the study period. This generates US$ 200 million (0.08% of the country’s GDP) economic loss. These results vary by agro-ecology, which is vital for prioritizing investment. At the country’s current 152 kg per capita consumption of maize, the maize lost to FAW could have met the maize consumption requirement of over 4 million food-insecure people. In the long run, together with other co-existing production constraints, FAW can put the livelihoods of many poor people at risk and may reverse the gains already made in productivity and poverty reduction that the country has achieved over the last three decades. Apart from the direct economic and food security losses, controlling FAW using pesticides contributes to environmental damage, threatening sustainable food production.

A key implication of these findings is that developing and promoting affordable, accessible, ecologically friendly control strategies must be facilitated to control the pest sustainably and effectively. Our analysis has the following caveats. First, we did not capture the total management costs, such as insecticides and labor costs, in controlling the pest. Second, although we indicate the toxicity of insecticides for the environment and human health, the insecticides application’s health, and environmental costs (monetary costs to the society) are not factored into the analysis. Third, we cannot entirely rule out recall bias, although we recorded the yield and yield losses data agreed by each member of the FGD that can help minimize recall bias and avoid too high or too low estimates. We recommend future studies to (1) consider both the direct and total indirect costs of the pest to reflect its overall cost, and (2) introduce effective, healthy, and environmentally friendly management strategies for FAW control and conduct comprehensive agroecological zone-specific evaluations of their effectiveness.

Supporting information

S1 File. Data processing approach: Stata do file.

(PDF)

S2 File. The community survey data: Stata dataset file.

(ZIP)

S3 File. Appendix Tables A1-A4.

(DOCX)

Acknowledgments

We thank Zebdewos Selato and Hulubanchi Abera of the Ministry of Agriculture for their support and data on insecticides for FAW control in Ethiopia. We also thank Solomon Balew for supporting the research by designing the CSPro program during data collection, the enumerators, and supervisors for their dedication in conducting the survey, and the farmers and experts who participated in the study. We thank Rahel Solomon for processing the letters and bringing the Ethiopia’s Central Statistical Agency datasets. Finally, we thank the anonymous reviewers for this insightful feedback that further improves the paper’s quality.

Data Availability

The community survey data are available in the Supporting information of this submission. The household survey are available upon request of the Central Statistics Agency of Ethiopia (https://www.statsethiopia.gov.et/); The names of the datasets are Agriculture Sample Survey 2017/2018 (2010 E.C.), Agriculture Sample Survey 2018/2019 (2011 E.C.), and Agriculture Sample Survey 2019/2020 (2012 E.C.).

Funding Statement

This study was supported by the USAID Feed the Future IPM Innovation Lab, Virginia Tech (Grant No. AID-OAA-L-15-00001); the Norwegian Agency for Development Cooperation (NORAD, Grant No. RAF-3058 KEN-18/0005); and the European Commission (Grant No. DCI-FOOD/2018/402-634). We also acknowledge the International Centre of Insect Physiology and Ecology (icipe) core support provided by the Foreign, Commonwealth and Development Office (FCDO), UK; the Swedish International Development Cooperation Agency (Sida); the Swiss Agency for Development and Cooperation (SDC); Germany’s Federal Ministry for Economic Cooperation and Development (BMZ); the Federal Democratic Republic of Ethiopia; and the Kenyan Government. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

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The socioeconomic and health impacts of Fall Armyworm in Ethiopia

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Reviewer #1: Yes

Reviewer #2: Partly

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2. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: Yes

Reviewer #2: Yes

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Reviewer #1: Yes

Reviewer #2: Yes

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Reviewer #1: Yes

Reviewer #2: Yes

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5. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: Introduction, hypothesis, objectives, methodology, results and conclusions are clearly explained. References section needs revision based on the journal's guidelines. Also, some sections need to be moved to introduction and conclusion sections.

My comments and suggestions are provided in the attached file.

Reviewer #2: The study purported to investigate the socio-economic, environmental and health impacts of fall armyworm, an invasive pest that is causing devastating effects on maize production in Africa. The authors used data from focus group discussions (FGDs), combined with secondary household survey data covering three production seasons (2017-2019) in Ethiopia. They found that FAW infestation leads to average maize yield loss of 36%, as well as negative effects on the environment than on human health. Below are a few comments that could be considered when improving the paper.

1. It is questionable if the FGD participants were able to remember the actual and attainable yields in 2017 and 2018 when the FGDs were conducted in June-July 2020. Moreover, in lines 202-204, the authors wrote “Secondly, we asked them to estimate the attainable yield in the absence of production constraints. Thirdly, we asked farmers to quantify FAW’s contribution and other production constraints to the yield gap….”. Are you really sure that the farmers could reliably indicate how much yield they would have obtained in the absence of production constraints and the contribution of FAW? Thus, the yield loss estimates of 36% or 0.67 million tonnes of maize and the total economic loss to Ethiopia are based on data that are likely to be fraught with recall bias and measurement errors, raising questions about their reliability. The authors need to reflect on these concerns. I would have thought that a more reliable method would have been to compare the yield estimates of FAW-affected and non-affected households, as was done by a previous related study in Ethiopia, i.e., Kassie et al. 2020.

2. The authors found that while 97% of the FGD participants were aware of FAW, only 88% were able to correctly identify FAW. One may wonder how a farmer can be aware of FAW when they cannot identify it? In this context, it would be helpful to explain what is considered to be awareness of FAW. Does awareness imply that a farmer has at least heard about FAW?

3. In lines 248-250, the authors stated “Moreover, 88% of the 249 farmers in the FGDs correctly identified the FAW from the pictures shown (Table 3), slightly more than those in Kenya (82%) (De Groote et al., 2020).” Out of curiosity, I went to look at the De Groote et al. (2020) paper and found that the four pictures of insect pests labelled A1, A2, B and C in your manuscript are exactly as those presented in the De Groote et al. (2020) paper. Surprisingly, you did not attribute the source of the pictures to De Groote et al. (2020) or indicate the original source, if any. Wouldn’t this give rise to an issue of copyright infringement?

4. In lines 297-298, the authors wrote “…while the expert opinion interviews estimated that 51% of the farmers were affected (Table A1, Appendix)”. This percentage and others in Table A1 seem to be unreliable and based on expert guesstimates because there is no indication that the 180 experts sought the opinions of farmers on FAW or observed farmers’ fields for FAW attack. How did the experts know how many farmers were affected by FAW? Same applies to the expert estimates of yield loss due to FAW.

5. Finally, I have reservations that you were actually able to estimate the effect of FAW on human health and the environment, based on the data used. For example, it is indicated in the abstract that “We also find that the application of insecticides to control FAW has more significant toxic effects on the environment than on humans”. However, you did not provide any evidence on insecticides used by the sampled farmers for FAW control. Your EIQ estimations were based on MoA’s pesticides data (government distributed pesticides) and application rates that may not reflect the farmers’ actual pesticide application practices against FAW. Moreover, the use of these pesticides may not have an effect on human health if the farmers use the appropriate personal protective equipment and observe the necessary safe pesticide practices, and vice versa. It appears your results may rather be reflective of the potential health and environmental effects of the listed pesticides in Ethiopia, regardless of whether or not they are used for FAW control.

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Reviewer #1: No

Reviewer #2: No

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Attachment

Submitted filename: PONE-D-21-14461_reviewer M1.1.pdf

PLoS One. 2021 Nov 4;16(11):e0257736. doi: 10.1371/journal.pone.0257736.r002

Author response to Decision Letter 0


1 Sep 2021

Responses to the two reviewers and the Academic Editor feedback uploaded or attached along with other files.

Attachment

Submitted filename: Responses_to_Reviewer#2_feedback.docx

Decision Letter 1

Rodney N Nagoshi

9 Sep 2021

The socioeconomic and health impacts of Fall Armyworm in Ethiopia

PONE-D-21-14461R1

Dear Dr. Kassie,

We’re pleased to inform you that your manuscript has been judged scientifically suitable for publication and will be formally accepted for publication once it meets all outstanding technical requirements.

Within one week, you’ll receive an e-mail detailing the required amendments. When these have been addressed, you’ll receive a formal acceptance letter and your manuscript will be scheduled for publication.

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Kind regards,

Rodney N. Nagoshi, Ph.D.

Academic Editor

PLOS ONE

Additional Editor Comments (optional):

Reviewers' comments:

Acceptance letter

Rodney N Nagoshi

28 Oct 2021

PONE-D-21-14461R1

Socioeconomic and health impacts of Fall Armyworm in Ethiopia

Dear Dr. Kassie:

I'm pleased to inform you that your manuscript has been deemed suitable for publication in PLOS ONE. Congratulations! Your manuscript is now with our production department.

If your institution or institutions have a press office, please let them know about your upcoming paper now to help maximize its impact. If they'll be preparing press materials, please inform our press team within the next 48 hours. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information please contact onepress@plos.org.

If we can help with anything else, please email us at plosone@plos.org.

Thank you for submitting your work to PLOS ONE and supporting open access.

Kind regards,

PLOS ONE Editorial Office Staff

on behalf of

Dr. Rodney N. Nagoshi

Academic Editor

PLOS ONE

Associated Data

    This section collects any data citations, data availability statements, or supplementary materials included in this article.

    Supplementary Materials

    S1 File. Data processing approach: Stata do file.

    (PDF)

    S2 File. The community survey data: Stata dataset file.

    (ZIP)

    S3 File. Appendix Tables A1-A4.

    (DOCX)

    Attachment

    Submitted filename: PONE-D-21-14461_reviewer M1.1.pdf

    Attachment

    Submitted filename: Responses_to_Reviewer#2_feedback.docx

    Data Availability Statement

    The community survey data are available in the Supporting information of this submission. The household survey are available upon request of the Central Statistics Agency of Ethiopia (https://www.statsethiopia.gov.et/); The names of the datasets are Agriculture Sample Survey 2017/2018 (2010 E.C.), Agriculture Sample Survey 2018/2019 (2011 E.C.), and Agriculture Sample Survey 2019/2020 (2012 E.C.).


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