Climate Variability Modulates the Impact of Price Spikes on Food Insecurity
Organizations: Image Processing Laboratory, Universitat de València, València, Spain. · Artificial Intelligence Group, Wageningen University & Research, Wageningen, The Netherlands. · Joint Research Centre, European Commission, Ispra, Italy.
Abstract
Climate variability influences whether a market disruption escalates into a food crisis, yet broad climate patterns like El Niño, tracked months before they alter hydro-climatic conditions, are still not incorporated as an early-warning component in food-security responses. We address this gap by introducing sensitivity regimes, a stratification of regions by the direction and strength of their vegetation response to the El Niño Southern Oscillation, and using them to estimate how food price spikes affect acute food insecurity across sub-Saharan Africa. Integrating remote sensing, socioeconomic data, and causal machine learning, we find that in regions where ENSO systematically suppresses vegetation, a price spike raises the share of the population at acute risk by 5.4 percentage points in the following month. In regions where vegetation is unaffected by or positively linked to ENSO, the estimated effect is smaller (around 2 percentage points) and statistically insignificant. These results demonstrate that climate context is critical for understanding food security vulnerabilities. Sensitivity regimes can be combined with operational price-spike triggers to stage anticipatory action: the ENSO state flags vulnerable regions months ahead, and a pre-positioned response in those regions to a price spike would avert the largest jump in acute food insecurity.
Figures & tables
| Model | Regime | CATE (p.p.) | C.I. | p-value |
| Negative | 6.00 | (2.57, 8.73) | 0.020 | |
| Linear DML | Weak | 1.94 | (-0.47, 4.99) | 0.098 |
| Positive | 2.16 | (-3.92, 4.21) | 0.784 | |
| Negative | 5.35 | (2.16, 8.08) | 0.020 | |
| Causal Forest DML | Weak | 1.80 | (-0.47, 4.75) | 0.137 |
| Positive | 1.70 | (-3.70, 4.15) | 0.922 |
Appendix figures & tables17 assets
Supplementary material from the paper’s appendix.
Appendix
| Domain | Variable | Description | Source |
| Outcome | rCSI | Reduced Coping Strategy Index crisis prevalence, monthly mean. | WFP |
| Treatment | ALPS | Alert for Price Spikes averaged for staple food commodities. | WFP Prices |
| Mean Temperature (Crop) | Spatial mean of the monthly average temperature over crop-covered areas. | ASAP | |
| Mean FPAR (Crop) | Spatial mean of the monthly average fraction of absorbed photosynthetically active radiation (FPAR) over crop-covered areas. | ASAP | |
| From | To | Justification and references |
| ENSO | NDVI, Crop Drivers | ENSO alters regional rainfall and temperature patterns, which drive vegetation greenness and define crop growing conditions (Anyamba et al., 2018; Ropelewski and Halpert, 1987; FAO et al., 2023). |
| ENSO | GDP | Climate shocks associated with ENSO influence aggregate output and growth, particularly in agriculture-dependent economies (Dell et al., 2012; Burke et al., 2015). |
| NDVI | Crop Drivers | Vegetation condition indices are closely tied to local biophysical crop conditions such as canopy development and water stress (Anyamba et al., 2018; FAO et al., 2023). |
| Crop Drivers | GDP | Weather- and climate-sensitive crop conditions affect yields and agricultural value added, which is a key component of GDP in many low- and middle-income countries (Dell et al., 2012; Burke et al., 2015; FAO et al., 2023). |
| Crop Drivers | Conflicts | Agricultural prod. failures can exacerbate income loss, rural hardship, and competition over resources, recognized as structural and proximate drivers of conflict and instability (Burke et al., 2015; FSIN and Global Network Against Food Crises, 2024). |
| Crop Drivers | IDPs | Agroclimatic shocks contribute to livelihood collapse and displacement, especially in agriculture-dependent settings (FSIN and Global Network Against Food Crises, 2024; IDMC, 2024). |
| From | To | Justification and references |
| GDP, Food Prices | rCSI | Household income and employment prospects modulated by GDP growth influence the need to adopt negative coping strategies (FAO et al., 2023; World Bank, 2020). |
| Conflicts | IDPs | Violent conflict is the leading global driver of internal displacement (IDMC, 2024; FSIN and Global Network Against Food Crises, 2024). |
| Conflicts | ALPS | Conflict disrupts markets, transport, and production, constraining supply and raising transaction costs (FAO et al., 2023; FSIN and Global Network Against Food Crises, 2024). |
| Conflicts | rCSI | Conflicts reduce incomes, destroy assets and constrain humanitarian access, all of which raise the prevalence of acute food insecurity and severe coping captured by rCSI (FSIN and Global Network Against Food Crises, 2024; FAO et al., 2023). |
| IDPs | ALPS | Inflows of displaced populations can increase local demand, strain markets and infrastructure, and contribute to localised food price spikes (FSIN and Global Network Against Food Crises, 2024; IDMC, 2024). |
| IDPs | rCSI | IDPs face greater exposure to shocks, have constrained access to livelihoods and services, and are consistently among the most food-insecure groups (FSIN and Global Network Against Food Crises, 2024; IDMC, 2024). |
| Strong-pixel q | Min. Dominance | Min. Coverage | Unchanged | Pos Neg | #Neg | #Weak/#Pos | |
| 0.20 | 0.20 | 0.10 | 1.000 | 1.000 | 0 | 158 | 204/203 |
| 0.20 | 0.20 | 0.20 | 1.000 | 1.000 | 0 | 158 | 204/203 |
| 0.10 | 0.15 | 0.10 | 0.993 | 0.989 | 0 | 159 | 200/206 |
| 0.10 | 0.15 | 0.20 | 0.993 | 0.989 | 0 | 159 | 200/206 |
| Metric | Value | Notes |
| # ADM1 units | 222 | Study countries only |
| Baseline counts (Neg/Weak/Pos) | 71 / 64 / 87 | |
| Mean stability | 0.941 | |
| Share stability | 0.794 | |
| Share stability | 0.622 | |
| Mean Pos Neg switch prob. | Median = 0, 75th pct = 0 |
| GID_0 | Country | ADM1 | Baseline | Stability | |||
| MOZ | Mozambique | Maputo | Negative | 0.575 | 0.575 | 0.425 | 0.000 |
| NGA | Nigeria | Sokoto | Weak | 0.585 | 0.000 | 0.585 | 0.415 |
| KEN | Kenya | Kericho | Negative | 0.585 | 0.585 | 0.380 | 0.035 |
| NGA | Nigeria | Nasarawa | Weak | 0.590 | 0.410 | 0.590 | 0.000 |
| NGA | Nigeria | Rivers | Positive | 0.600 | 0.005 | 0.395 | 0.600 |
| KEN | Kenya | Turkana | Negative | 0.615 | 0.615 | 0.385 | 0.000 |
| Regime | Before trimming | After trimming | ||
| Control | Treated | Control | Treated | |
| Overall | 829 | 845 | 483 | 455 |
| Negative | 318 | 238 | 227 | 130 |
| Weak | 271 | 378 | 158 | 220 |
| Positive | 240 | 229 | 98 | 105 |
| Confounder | SMD (Before) | SMD (After) |
| Conflict Stock Displacement | 0.080 | 0.240 |
| Mean Temperature (Crop) | 0.115 | 0.118 |
| Mean Soil Moisture (Crop) | 0.202 | 0.064 |
| Mean FPAR (Crop) | 0.232 | 0.156 |
| ACLED Fatalities | 0.199 | 0.182 |
| Rural Population | 0.035 | 0.085 |
| Confounder | SMD (Before) | SMD (After) |
| Conflict Stock Displacement | 0.441 | 0.274 |
| Mean Temperature (Crop) | 0.137 | 0.118 |
| Mean Soil Moisture (Crop) | 0.408 | 0.333 |
| Mean FPAR (Crop) | 0.406 | 0.325 |
| ACLED Fatalities | 0.302 | 0.165 |
| Rural Population | 0.183 | 0.102 |
| Confounder | SMD (Before) | SMD (After) |
| Conflict Stock Displacement | 0.518 | 0.309 |
| Mean Temperature (Crop) | 0.177 | 0.061 |
| Mean Soil Moisture (Crop) | 0.123 | 0.336 |
| Mean FPAR (Crop) | 0.220 | 0.065 |
| ACLED Fatalities | 0.291 | 0.299 |
| Rural Population | 0.034 | 0.088 |
| Confounder | SMD (Before) | SMD (After) |
| Conflict Stock Displacement | 0.248 | 0.089 |
| Mean Temperature (Crop) | 0.212 | 0.336 |
| Mean Soil Moisture (Crop) | 0.028 | 0.003 |
| Mean FPAR (Crop) | 0.213 | 0.018 |
| ACLED Fatalities | 0.086 | 0.083 |
| Rural Population | 0.071 | 0.049 |
| Model family | CV for ( ) (Regressor) | CV ROC–AUC for ( ) (Classifier) |
| Random Forest | 0.214 | 0.613 |
| Gradient Boosting | 0.394 | 0.633 |
| XGBoost | 0.352 | 0.637 |
| In-sample (selected models) | 0.786 | 0.982 |
| Model | Regime | CATE (p.p.) | C.I. | p-value |
| Negative | 6.065 | (3.257, 8.124) | 0.020 | |
| Diff. in Means | Weak | -0.040 | (-3.596, 3.114) | 0.922 |
| Positive | 0.423 | (-4.807, 5.344) | 0.765 | |
| Negative | 4.135 | (2.051, 5.633) | 0.020 | |
| Linear Regression | Weak | 1.084 | (-0.881, 4.204) | 0.157 |
| Positive | 3.312 | (-1.014, 5.671) | 0.216 |
| Method | Regime | Placebo eff. | Placebo | RCC eff. | RCC | RSR eff. | RSR |
| Negative | 0.008 | 0.385 | 0.000 | 0.885 | 0.000 | 0.938 | |
| LinearDML | Weak | -0.004 | 0.807 | 0.002 | 0.808 | 0.002 | 0.500 |
| Positive | 0.012 | 0.615 | -0.005 | 0.769 | 0.002 | 0.688 | |
| Negative | 0.010 | 0.269 | 0.002 | 0.769 | 0.001 | 0.750 | |
| CausalForestDML | Weak | -0.004 | 0.731 | 0.002 | 0.731 | 0.002 | 0.500 |
| Positive | 0.012 | 0.615 | -0.004 | 0.769 | 0.003 | 0.688 |
| Method | Lead | N (T/C) | Negative | Weak | Positive |
| 0 | 823 (423/400) | 0.0514 (0.0255, 0.0795) | 0.0206 (-0.0030, 0.0558) | -0.0070 (-0.0475, 0.0317) | |
| 1 | 938 (455/483) | 0.0599 (0.0257, 0.0873) | 0.0194 (-0.0047, 0.0499) | 0.0216 (-0.0392, 0.0421) | |
| LinearDML | 2 | 845 (430/415) | 0.0550 (0.0328, 0.0814) | 0.0024 (-0.0179, 0.0472) | -0.0472 (-0.0772, 0.0049) |
| 3 | 840 (419/421) | 0.0675 (0.0294, 0.0894) | 0.0151 (-0.0112, 0.0370) | -0.0496 (-0.0908, -0.0056) | |
| 4 | 777 (414/363) | 0.0638 (0.0412, 0.0923) | 0.0193 (-0.0145, 0.0679) | -0.0738 (-0.1054, -0.0209) | |
| 0 | 823 (423/400) | 0.0524 (0.0256, 0.0805) | 0.0199 (-0.0060, 0.0510) | -0.0125 (-0.0465, 0.0398) |
| Method | Contrast | (p.p.) | C.I. | -value |
| Linear DML | Neg – Pos | 3.844 | (0.909, 11.738) | 0.039 |
| Neg – Weak | 4.061 | ( , 6.809) | 0.098 | |
| Causal Forest DML | Neg – Pos | 3.650 | ( , 10.678) | 0.078 |
| Neg – Weak | 3.549 | ( , 6.572) | 0.137 |