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. 2025 Aug 27;15(9):992–999. doi: 10.1038/s41558-025-02411-0

Tropical deforestation is associated with considerable heat-related mortality

C L Reddington 1,, C Smith 1, E W Butt 1, J C A Baker 1, B F A Oliveira 2, E I Yamba 3, D V Spracklen 1
PMCID: PMC12417208  PMID: 40933509

Abstract

Tropical deforestation induces local warming and is a potential human health risk, having been linked to elevated human heat stress and reduced safe outdoor working hours. Here we show deforestation-induced local warming is associated with 28,000 (95% confidence interval: 23,610–33,560) heat-related deaths per year using a pan-tropical assessment. Analysis of satellite data shows tropical deforestation during 2001–2020 exposed 345 million people to local warming with population-weighted daytime land surface warming of 0.27 °C. Estimated heat-related mortality rates are greatest in Southeast Asia (8–11 deaths for every 100,000 people living in deforested areas) followed by tropical regions of Africa and the Americas. In regions of forest loss, local warming from deforestation could account for over one third of total climate heat-related mortality, highlighting the important contribution of tropical deforestation to ongoing warming and heat-related health risks within the context of climate change.

Subject terms: Environmental health, Environmental impact


The authors assess the impacts of tropical deforestation and its subsequent local warming on human heat-related mortality. They estimate that deforestation-related warming (+0.27 °C) is associated with approximately 28,000 heat-related deaths per year.

Main

Over recent decades, tropical forests have faced extensive deforestation and degradation1,2, driven primarily by agricultural expansion and logging3. The impacts of tropical forest loss are profound, affecting biodiversity4, global climate5,6 the hydrological cycle7 and human communities812. Previous studies have demonstrated a strong association between tropical forest loss and increases in surface temperature on both local6,1219 and regional20,21 scales. The local warming associated with deforestation can be immediate and of substantial magnitude22, equivalent to or larger than that projected from a century of global climate change under a high emissions scenario12,20.

Human exposure to elevated temperatures presents a major potential health risk. Heat stress can negatively affect mood and mental health23, impair physical performance24 and reduce labour productivity25,26. Furthermore, exposure to heat is associated with an increased risk of morbidity and mortality from cardiovascular diseases and other causes27,28. Considerable heat-related mortality has been attributed to recent climate change29.

The effects of climate change on human health are compounded by socioeconomic and demographic factors30. Population vulnerability to climate change is linked to health expenditure and proportions of obese and elderly populations31. Along with these factors, heat-related human health effects can be modulated by the degree of technological adaptation32, which can be strongly linked to socioeconomic status33. In lower-income countries with limited adaptive capacity, including many countries in the tropics, heat-stress-related labour capacity losses may have substantial economic consequences34 and increase poverty35.

Tropical deforestation is associated with increases in human heat exposure12,22,36. In field experiments, deforestation-induced heat exposure has been demonstrated to reduce cognitive performance37 and labour productivity26. Across the tropics, local warming from deforestation between 2003 and 2018 was associated with losses in safe thermal working conditions for 2.8 million outdoor workers12. Little is known about the potential for deforestation-induced warming to lead to additional deaths at the pan-tropical scale. Wolff et al.10 showed that in Berau Regency in Indonesia, the combination of global climate change and deforestation between 2002 and 2018 increased population-weighted mean temperatures by 0.86 °C, accounting for an estimated 7.3–8.5% of all-cause mortality (or 101–118 additional deaths per year). Wider assessments of the population-weighted warming due to deforestation or the potential impacts on health and mortality are lacking but are urgently needed to inform land use policy and climate adaptation strategies.

Here, we make the first pan-tropical assessment of the population-weighted warming due to tropical deforestation and the associated heat-related mortality burden. We focus our analysis on tropical deforestation that occurred from 2001 to 2020. We use spatially explicit satellite datasets of annual tree cover change1 to identify forest loss at a ~1 km2 spatial scale. We use satellite datasets of land surface temperature38 to quantify surface warming that has occurred over this period. Through comparing land surface temperature change over locations of forest loss to neighbouring locations without forest loss, we isolate the warming due to deforestation. We then use human population distribution data39 to map population-weighted exposure to this warming. Finally, we use data on non-accidental mortality40 combined with relationships between heat exposure and excess mortality from the literature31 to estimate the heat-attributable excess mortality due to nearby tropical deforestation. Our analysis provides important evidence of the negative potential human health impacts of tropical deforestation at local, regional and national scales.

Forest cover loss and local temperature changes

During 2001–2020, a total of 1.6 million km2 of forest area (with greater than 10% forest canopy cover) was lost across the tropics. The greatest forest loss occurred across Tropical Central and South America (~760,000 km2), with extensive forest loss also occurring across Southeast Asia (~490,000 km2) and Tropical Africa (~340,000 km2). Surface temperatures in the tropics have generally increased over this time period due to a combination of global climate change and deforestation, with regional annual mean warming (ΔT) of +0.34 °C in Tropical Central and South America, +0.10 °C in Tropical Africa and +0.72 °C in Southeast Asia. Areas of forest loss coincide with areas of strong positive ΔT across many regions of the tropics (Fig. 1). We defined 1 km2 pixels that experienced at least two percentage points of forest loss during 2001–2020 as pixels that experienced deforestation (Methods). A total of 60% of pixels with warming of greater than four standard deviations from the mean (4.4 °C) experienced deforestation during 2001–2020, while deforested pixels make up only 17% of pixels in the tropics. The average ΔT in deforested locations across the tropics (+0.70 °C) exceeds warming that has occurred over areas that have maintained forest cover (+0.20 °C) (Table 1). Regionally, average ΔT in deforested locations (+0.73 °C in Tropical Central and South America, +0.75 °C in Tropical Africa and +0.61 °C in Southeast Asia) are 2–9× the average ΔT in locations that maintained forest cover (+0.30 °C in Tropical Central and South America, +0.08 °C in Tropical Africa and +0.31 °C in Southeast Asia). Similar to previous studies10,12,17, we assess the warming due to deforestation using land surface temperature data because near-surface air temperature data are not available at sufficiently high spatial resolution in the tropics. We compared land surface temperature and near-surface air temperature from the European Centre for Medium-Range Weather Forecasts Reanalysis v5 (ERA5 (ref. 41)) over the same period and find they agree to within 2% (Extended Data Table 1), confirming our approach is justified (Methods).

Fig. 1. Forest loss, surface warming and population distribution across the tropics.

Fig. 1

a, The percentage-point change in forest cover from 2001 to 2020. b, The change in annual mean land surface temperature (ΔT) between the 2001–2003 mean and the 2018–2020 mean. c, The spatial distribution of population count in 2020.

Table 1.

Changes in annual mean land surface temperature (ΔT) in areas of the tropics that maintained (‘non-deforested’) and lost (‘deforested’) forest cover during 2001–2020

Region ΔT in non-deforested locations (°C) ΔT in deforested locations (°C) Deforestation-induced local ΔT (°C)
Area-wgtd Pop-wgtd Area-wgtd Pop-wgtd Area-wgtd Pop-wgtd
Tropical Central and South America 0.30 −0.12 0.73 0.40 0.53 0.22
Tropical Africa 0.08 0.12 0.75 0.97 0.39 0.32
Southeast Asia 0.31 0.36 0.61 0.56 0.37 0.26
Tropics (25° S to 25° N) 0.20 0.19 0.70 0.70 0.45 0.27

The estimated local ΔT due to forest loss between 2001 and 2020 (excluding the contribution of global climate change) is also shown (Methods). The area-weighted mean (‘area-wgtd’) and population-weighted mean (‘pop-wgtd’) ΔTs are shown for each region. All regions are bounded by latitudes of 25° S and 25° N.

Extended Data Table 1.

Comparison of ERA5 2-m air temperature (t2m) with MODIS land surface temperature (LST) and ERA5 LST

Region (25S-25N) ERA5_t2m_daily / MODIS_LST (2001 tropical forest pixels) ERA5_t2m_daily / ERA5_LST_daily ERA5_t2m_daily / ERA5_LST_10–11amLT ERA5_t2m_daily / ERA5_LST_10-11amLT (2001 tropical forest pixels)
Tropical C & S America 0.9835 0.9989 0.9854 0.9887
Tropical Africa 0.9652 0.9960 0.9755 0.9835
Tropical Central Asia 0.9655 0.9974 0.9801 0.9837
Southeast Asia 0.9757 0.9969 0.9840 0.9906

Values shown are ratios between daily-mean ERA5 t2m and either MODIS-Terra LST (at ~10:30am local time (LT)), daily mean ERA5 LST, or hourly ERA5 LST at 10:00–11:00 am LT. Ratios are calculated at the ~1-km-pixel-level between 6-year (2001–2003 and 2018–2020) regional means. Ratios for MODIS LST at ERA5 LST at 10:00–11:00 am LT are calculated over tropical forest pixels only (using 2001 forest cover fraction).

Deforestation-induced ΔT and human heat exposure

To estimate the ΔT due to deforestation only, excluding the contribution of global climate change and regional climate variability, we compared ΔT over locations of forest loss with neighbouring locations without forest loss. Over 2001–2020, deforestation is associated with 0.45 °C of warming on average across deforested areas of the tropics (Table 1). The regional mean deforestation-induced ΔT is greatest in Tropical Central and South America (+0.53 °C), with slightly lower ΔT in Tropical Africa (+0.39 °C) and Southeast Asia (+0.37 °C). This means that deforestation accounts for over half of the regional average warming in deforested areas of the tropics (and ~70% in Tropical Central and South America). In general, the regions with the greatest deforestation-induced warming correspond to the regions with the greatest forest loss (Fig. 2), particularly in the Arc of Deforestation in the southern Amazon and Sumatra and Kalimantan in Indonesia. Strong deforestation-induced warming is also visible in other areas that have experienced extensive forest loss1, including in Central America (Guatemala and Nicaragua), southern West Africa (Cote d’Ivoire, Ghana and Nigeria), Central and Eastern Africa (Democratic Republic of the Congo, Uganda and Tanzania) and Mainland Southeast Asia (Cambodia and Vietnam).

Fig. 2. Change in local annual mean surface temperature (ΔT) due to deforestation during 2001–2020.

Fig. 2

af, The maps show regions of Tropical Central and South America (a and b), Tropical Africa (c and d), and Southeast Asia (e and f). The maps in a, c and e show the deforestation-induced ΔT at the ~1 km2 pixel level. The maps in b, d and f show the population-weighted mean deforestation-induced ΔT for second-level administration divisions for populations located in areas of forest loss. The division boundaries are from GADM (https://gadm.org/index.html). The areas with no data points are shown in white.

This local warming associated with deforestation has important implications for large populations that live across tropical forest regions (Fig. 1c). The tropics (25° S – 25° N) are home to over 3.5 billion people, with 13% (452 million people) living in regions that have experienced forest loss during the 2001–2020 period. We estimate that 345 million people were exposed to warming due to deforestation during 2001–2020 (Table 2), with substantial numbers of people exposed to deforestation-induced ΔT of greater than +1 °C (33 million people), +2 °C (8.0 million people) and +3 °C (2.6 million people). Across the tropics, 76% of people living in regions of tropical forest loss were exposed to deforestation-induced warming, with a similar proportion in the different tropical regions (74–80%). In Tropical Africa, 148 million people were exposed to warming from deforestation, compared with 122 million people in Southeast Asia and 67 million people in Tropical Central and South America.

Table 2.

Population exposure to local warming from deforestation between 2001 and 2020 and the associated heat-related non-accidental mortality burden

Region/ country Population in locations of forest loss Population exposed to deforestation-induced warming Annual deforestation-associated heat-related mortality Annual deforestation-associated heat-related mortality rate (deaths per 100,000 people) Percentage of total heat-related mortality Percentage of total non-accidental mortality
Tropics (25° S to 25° N) 452 million 345 million (76%) 28,330 (23,610–33,560) 6 (5–7) 39.1% 1.06%
Tropical Central and South America 89.8 million 66.9 million (74%) 2,520 (2,160–2,950) 3 (2–3) 43.5% 0.55%
Tropical Africa 185 million 148 million (80%) 9,890 (8,250–11,850) 5 (4–6) 35.2% 0.85%
Southeast Asia 165 million 122 million (74%) 15,680 (13,000–18,470) 10 (8–11) 42.4% 1.60%
Indonesia 62.9 million 48.9 million (78%) 6,730 (5,540–7,930) 14 (11–16) 46.4% 0.41%
Malaysia 17.5 million 15.3 million (88%) 2,100 (1,680–2,550) 14 (11–17) 37.3% 1.26%
Vietnam 10.9 million 6.95 million (64%) 2,020 (1,730–2,310) 29 (25–33) 52.0% 0.35%
Democratic Republic of the Congo 51.0 million 42.0 million (82%) 1,840 (1,530–2,190) 4 (4–5) 34.0% 0.31%
Philippines 16.9 million 13.9 million (82%) 1,740 (1,490–2,010) 13 (11–14) 30.9% 0.31%
Nigeria 21.0 million 17.2 million (82%) 1,310 (1,090–1,570) 8 (6–9) 23.1% 0.09%
Mozambique 8.98 million 8.03 million (89%) 1,020 (870–1,230) 13 (11–14) 50.3% 0.47%
Brazil 30.7 million 21.6 million (70%) 990 (890–1,100) 5 (4–5) 38.6% 0.09%
Tanzania 9.35 million 8.03 million (86%) 800 (670–930) 10 (9–12) 107.0% 0.23%
Uganda 11.5 million 9.17 million (80%) 650 (560–770) 7 (6–8) 37.0% 0.27%

The results are shown for populations located in areas of forest loss only, aggregated for the whole tropics, for the three main tropical forest regions and for the ten countries with the greatest deforestation-associated heat-related mortality burdens. All regions are bounded by latitudes of 25° S and 25° N. Populations are only counted in forest loss pixels with valid ΔT data and a net forest extent increase of <50%-point. Mortality burdens are shown to the nearest ten for the total mortality and nearest whole number for the mortality rate. The uncertainty ranges are shown in parentheses and are estimated using the 95% CI from the non-accidental mortality rates40. Note that deforestation-associated heat-related deaths in a region can exceed the number of total heat-related deaths in that region where surrounding non-deforested areas experience an overall cooling (Methods).

Over 2001–2020, the populations in areas of tropical forest loss were exposed to a mean ΔT of +0.27 °C due to deforestation (Table 1). Regional population-weighted mean ΔT is greatest in Tropical Africa (+0.32 °C), where deforestation-induced warming overlaps with more heavily populated areas, and lowest in Tropical Central and South America (+0.22 °C), where deforested areas with strong warming are more sparsely populated (Fig. 1). Across all regions, population-weighted warming due to deforestation is less than area-weighted warming (Table 1) due to lower population densities in rural areas, which typically experience greater forest loss (Extended Data Figs. 13).

Extended Data Fig. 1. Population as a function of tropical forest loss.

Extended Data Fig. 1

Population count in 2020 versus percentage-point forest cover loss between 2001 and 2020. Green points show data for Tropical Central and South America, red points show data for Tropical Africa, and blue points show data for Southeast Asia.

Extended Data Fig. 3. Deforestation-induced ΔT over 2001 to 2020 as a function of rural and urban populations.

Extended Data Fig. 3

Results are shown for populations in locations of forest loss in a. Tropical Central and South America, b. Tropical Africa, and c. Southeast Asia. Dashed vertical lines show the population-weighted mean deforestation-induced ΔT for each region.

Deforestation-associated heat-attributable mortality

We estimated the heat-related excess mortality burden associated with deforestation by combining our estimates of deforestation-induced ΔT with region-specific heat vulnerability indices31 and non-accidental mortality rates (including mortality from all causes apart from external causes)40. In general, areas with the greatest mortality burden correspond to regions with moderate to high levels of forest loss and deforestation-induced warming (Fig. 3). However, because the mortality estimates also depend on other factors (population count (Fig. 1c), non-accidental mortality rates and population heat vulnerability (Extended Data Table 2)), the spatial pattern differs from that of the deforestation-induced ΔT (Fig. 2). The spatial distribution of the deforestation-associated heat-related mortality rate (that is, deaths per 100,000 people) (Extended Data Fig. 4) is more consistent with deforestation-induced ΔT (Fig. 2), demonstrating that the heat-related mortality burden is strongly dependent on the magnitude of the population within areas of forest loss.

Fig. 3. Heat-related non-accidental mortality associated with deforestation-induced warming.

Fig. 3

ac, The maps show regions of Tropical Central and South America (a), Tropical Africa (b), and Southeast Asia (c). The colours show the number of deaths per year (central estimate) for populations located in areas of forest loss, aggregated by second-level administration divisions (boundaries from GADM, https://gadm.org/index.html). Note that the colour scales are different for each region. The administration divisions containing no data points are shown in white.

Extended Data Table 2.

Heat vulnerability indices estimated by Lee et al.31

Country / continent Data period Number of locations Heat Vulnerability (%p °C−1) Mortality causes
Mexico 1998–2014 10 1.83 All
Central America 10 1.83
Argentina 2005–2015 3 2.07 Non-external
Brazil 1997–2011 18 2.57 Non-external
Chile 2004–2014 2 2.49 All
Colombia 1998–2013 5 1.62 [Not provided]
South America 28 2.34
Iran 2004–2013 1 2.93 Non-external
Central Asia 1 2.93
Philippines 2006–2010 4 9.15 All
Taiwan 1994–2007 3 2.83 Non-external
Thailand 1999–2008 56 4.39 Non-external
Vietnam 2009–2013 2 11.82 Non-external
Southeast Asia 65 5.29
Australia 1988–2009 3 1.02 Non-external
China 1996–2008 16 1.46 Non-external

Data used to estimate the indices were taken from the database collected through the Multi-City Multi-Country (MCC) Collaborative Research Network. Relevant information on the data is included in the table; additional information on the MCC dataset can be found in Gasparrini et al.96. Causes of mortality considered depend on available data (either all-cause or non-external/non-accidental mortality).

Extended Data Fig. 4. Heat-related non-accidental mortality rate associated with deforestation-induced warming.

Extended Data Fig. 4

The maps show regions of Tropical Central and South America (a), Tropical Africa (b), and Southeast Asia (c). Colours show number of deaths per year per 100,000 people located in areas of forest loss (central estimate), aggregated by second-level administration divisions. Boundaries for second-level administration divisions are from GADM (https://gadm.org/index.html).

Overall, we estimate that warming due to deforestation over 2001–2020 is associated with an additional 28,330 (95% confidence interval (CI): 23,610–33,560) non-accidental deaths per year (Table 2). The estimated deforestation-associated heat-related mortality burden is greatest in Southeast Asia (15,680 (95% CI: 13,000–18,470) annual excess deaths) due to a relatively large exposed population, predominantly in Indonesia, with greater heat vulnerability. In Tropical Africa we estimate 9,890 (95% CI: 8,250–11,850) annual excess deaths associated with deforestation. This is lower than in Southeast Asia, despite greater population exposure to deforestation-induced warming and higher underlying non-accidental mortality rates, because of the lower heat vulnerability that we have assumed for populations in this region (Methods). Although areas of forest loss in Tropical Central and South America experience some of the largest deforestation-induced warming in the tropics, populations in these areas are relatively low, leading to lower population exposure and heat-related mortality (2,520 (95% CI: 2,160–2,950) annual excess deaths) than in the other tropical regions.

Discussion

Tropical forest regions have warmed substantially over the last two decades due to a combination of climate change and land-use change. We show that over the period 2001–2020, tropical deforestation has caused annual mean land surface warming of 0.7 °C, in line with previous assessments1218. In our analysis, deforestation-induced warming accounts for 64% of the total warming experienced over regions with tropical forest loss (Table 1), demonstrating that deforestation is a major driver of local warming. Deforestation caused 39% of the population-weighted warming experienced over regions with tropical forest loss (Table 1).

Our findings suggest that warming from tropical deforestation impacts large numbers of people and could result in a substantial health burden. We estimate that 345 million people were exposed to local warming from forest loss during 2001–2020. We estimate this warming is associated with an annual heat-related mortality burden of 28,330 (95% CI: 23,610–33,560), equivalent to 39% of the total heat-related mortality (from global climate change and deforestation combined) over locations of forest loss (Table 2). The Global Burden of Disease (GBD) Study42 estimated annual excess deaths attributable to high temperature in 2019 to be 14,400 (95% CI: 10,800–18,300) in Latin America and the Caribbean, 50,800 (95% CI: 36,400–66,300) in Sub-Saharan Africa and 41,200 (95% CI: 34,600–49,300) in Southeast Asia. We estimate the total annual heat-related excess deaths (associated with warming from both global climate change and deforestation during 2001–2020) for forest loss regions to be 5,800 (95% CI: 5,000–6,700) in Tropical Central and South America, 28,000 (95% CI: 23,300–33,800) in Tropical Africa and 37,000 (95% CI: 30,700–43,600) in Southeast Asia. Calculating these mortality burdens for the total population, our estimates are comparable with those from the GBD for Latin America and the Caribbean and Sub-Saharan Africa but notably higher for Southeast Asia. However, large differences in methodology, timescale, spatial resolution and temperature datasets complicate direct comparison. Notably, GBD estimates rely on ERA5 (ref. 41) near-surface air temperature, which lacks recent and dynamic land cover data (using a monthly climatological vegetation map for the years 2000–200843). Therefore, in regions with sparse weather station coverage, ERA5 does not account for land cover change impacts on local temperature and does not capture increases in temperature with increasing deforestation44.

Heat-related mortality from deforestation accounts for 1.1% of non-accidental mortality over regions of tropical forest loss, increasing to 1.6% over Southeast Asia (Table 2). Wolff et al.10 estimated that warming from the combination of global climate change and deforestation during 2002–2018 accounted for 7.3–8.5% of all-cause mortality in the Berau Regency in East Kalimantan, Indonesia. In comparison, we estimate warming from global climate change and deforestation during 2001–2020 accounts for 6.7% of all-cause mortality in Berau Regency and 8.0% for populations in locations of forest loss (Extended Data Table 3). We estimate greater population-weighted ΔT, due to the inclusion of more years of surface temperature data, but we apply a lower heat vulnerability index to be conservative and to be consistent with the regional average value for Southeast Asia from Lee et al.31. We estimate that warming from deforestation during 2001–2020 accounts for 2.0% of all-cause mortality in areas of forest loss in Berau Regency and 34.5% of the total heat-attributable mortality (from global climate change and deforestation combined).

Extended Data Table 3.

Comparison of results and methods from this study to Wolff et al.10

Reference Wolff et al.10 This study (sensitivity experiments) This study (main results)
LST data Afternoon LST (MODIS-Aqua) Morning LST (MODIS-Terra)
Population data & year (Population of Berau) Berau Census 2018 & LandScan 2017 (232,528) LandScan 2020 (206,331)
LST time period 2002 to 2018 2001–2003 to 2017–2019 2001–2003 to 2018–2020
Forest loss threshold in "kept forest" pixel 0%p 0%p <0.5%p 0%p <0.5%p <0.5%p <0.5%p <0.5%p
Mean ΔT in forest loss pixels (°C) 1.03 0.80 0.80 1.05 1.05 1.05 1.05 1.05
Mean ΔT in kept forest pixels (°C) 0.08 0.10 0.18 0.36 0.43 0.43 0.43 0.43
Δpop-wgtd T (°C) 0.86 1.61 1.61 1.36 1.36 1.36 1.36 1.36
Heat vulnerability index (%p °C−1) 9.15 9.15 9.15 9.15 9.15 9.15 5.29 5.29
Mortality cause (deaths per 100,000 in Berau) All-cause (596) All-cause (532) All-cause (532) All-cause (532) All-cause (532) Non-accidental (495) All-cause (532) Non-accidental (495)
Increase in heat-related deaths in Berau (heat-attributable increase in total mortality) 101 (7.3%) 141 (12.9%) 141 (12.9%) 121 (11.0%) 121 (11.0%) 113 (11.0%) 73 (6.7%) 68 (6.7%)
Pop-wgtd mean ΔTa (°C) 1.53 1.53 1.68 1.68 1.68 1.68 1.68
Increase in heat-related deathsa (heat-attributable increase in total mortalitya) 93 (11.9%) 93 (11.9%) 101 (12.9%) 101 (12.9%) 94 (12.9%) 63 (8.0%) 58 (8.0%)
Deforestation-associated values:
Pop-wgtd mean ΔTa (°C) 0.60 0.54 0.58 0.55 0.55 0.55 0.55
Increase in heat-related deathsa (heat-attributable increase in total mortalitya) 39 (3.6%) 35 (3.2%) 38 (3.5%) 36 (3.3%) 34 (3.3%) 22 (2.0%) 20 (2.0%)
Contribution to total heat-attributable mortalitya 42.3% 38.1% 37.8% 35.7% 35.7% 34.5% 34.5%

Sensitivity tests varied methodological assumptions to more closely match those of Wolff et al.10, including i) the time period of Land Surface Temperature (LST) data used, ii) the ‘kept forest’ (or ‘non-deforested’) pixel definition applied, iii) the heat vulnerability index used, and iv) the mortality cause considered. Differences in some assumptions remain, for example, in the forest cover definition ( >50% in 2000 in Wolff et al.10 and ≥10% in 2001 in this study) and ‘deforested pixel’ definition ( >0%p forest loss in Wolff et al.10 and ≥2%p forest loss in this study). The methods and results in the final column are those presented in the main text of this study.

aIn forest loss pixels only.

We find that 42% of the tropics-wide heat-related mortality burden associated with deforestation occurs in regions which had greater than 50% forest canopy cover in 2001 compared with 58% in regions of intermediate canopy cover (10–50%) (Extended Data Table 4). Most forest loss occurs in regions that have already been partially deforested such as the Arc of Deforestation (Fig. 1a), which also overlap regions with greater population density (Fig. 1c) and heat-related mortality (Fig. 3). In Africa, forest loss in areas of intermediate canopy cover accounts for 70% of the heat-related mortality burden associated with forest loss. This highlights the impact of forest loss within regions of naturally occurring intermediate canopy cover such as the miombo woodlands of Africa and the Cerrado and Chaco in South America. Our work highlights the importance of sustainable management of these biomes to reduce potential negative health impacts on local populations.

Extended Data Table 4.

Comparison of deforestation-associated heat-related mortality results for different time-periods and forest-cover-related thresholds

ΔT data period T data Forest cover fraction (in 2001) Net increase in forest extent threshold Forest cover loss in ‘deforested’ pixels Pop in locations of forest loss (millions) Pop exposed to deforestation-induced warming (millions) Annual deforestation-associated heat-related mortality Annual deforestation-associated heat-related mortality rate (deaths / 100,000 people)
2001–2003 to 2018–2020 MODIS-Terra LST ≥10% >50%p ≥2%p 452 345 (76%) 28,330 (23,610–33,560) 6 (5–7)
2001–2003 to 2018–2020 MODIS-Terra LST ≥10% >50%p ≥10%p 147 119 (84%) 13,830 (8,480–16,400) 9 (6–11)
2001–2003 to 2018–2020 MODIS-Terra LST ≥10% >50%p ≥1%p 602 456 (76%) 30,790 (15,670–36,460) 5 (4–6)
2001–2003 to 2018–2020 MODIS-Terra LST ≥50% >50%p ≥2%p 169 128 (76%) 11,840 (9,820–14,030) 7 (6–8)
2001–2003 to 2018–2020 MODIS-Terra LST ≥10% >20%p ≥2%p 448 341 (76%) 27,570 (22,980–32,650) 6 (5–7)
2001 to 2019 MODIS-Terra LST ≥10% >50%p ≥2%p 446 319 (71%) 32,200 (26,830–38,110) 7 (6–9)
2001 to 2020 MODIS-Terra LST ≥10% >50%p ≥2%p 445 322 (72%) 32,600 (27,170–38,620) 7 (6–9)
2001–2003 to 2018–2020 (LST & forest cover) MODIS-Terra LST ≥10% >50%p ≥2%p 429 331 (76%) 27,670 (23,050–32,770) 6 (5–8)
2001–2005 to 2016–2020 MODIS-Terra LST ≥10% >50%p ≥2%p 453 344 (76%) 24,720 (20,610–29,270) 7 (6–8)
2003–2005 to 2018–2020 MODIS-Terra LST ≥10% >50%p ≥2%p 452 328 (73%) 25,670 (21,390–30,410) 6 (5–7)
2003–2005 to 2018–2020 MODIS-Aqua LST ≥10% >50%p ≥2%p 445 323 (73%) 30,590 (25,520–36,230) 7 (6–8)
2001–2003 to 2018–2020 MODIS-Terra LST scaled by ERA5 ≥10% >50%p ≥2%p 452 345 (76%) 28,000 (23,340–33,170) 6 (5–7)

Changing time-periods and threshold assumptions can change the number of pixels classed as tropical forest and ‘deforested’ in our analysis and therefore the magnitude of the population in pixels of forest loss. Note in this work, populations in forest loss pixels are only counted where the net forest extent increase is below the selected threshold and land surface temperature (LST) data pixels are valid.

To contextualize the heat-related mortality burden, it is important to consider other health risks associated with tropical deforestation. Smoke pollution from deforestation-related fires can degrade regional air quality45,46 leading to adverse health impacts47,48. In 2015, peatland fires in Indonesia resulted in exposure of 69 million people in Equatorial Asia to unhealthy air quality conditions49. Long-term exposure to particulate air pollution from forest and vegetation fires is estimated to cause ~3,000–16,800 premature deaths annually in South America5052, ~6,000–59,000 in Southeast Asia49,53,54 and ~43,000 in Africa55. Our estimates of the heat-related mortality burden associated with deforestation-induced warming are comparable with the lower end of estimates of these fire-related mortality estimates.

Tropical deforestation is also linked to increased malaria risk in some contexts11,56, with evidence suggesting it is an important driver of childhood malaria risk in poor households57. With deforestation-driven malaria incidence estimates only available for the Brazilian Amazon11, we compare our results to national-level malaria mortality estimates from the GBD42, noting that these may underestimate the burden in deforested areas. In 2019, malaria accounted for 0.04% (95% CI: 0.02–0.07%) of total deaths in Latin America and Caribbean, 7.98% (95% CI: 3.24–15.17%) in Sub-Saharan Africa, and 0.04% (95% CI: 0.01–0.16%) in Southeast Asia42. We estimate that heat-related mortality associated with deforestation during 2001–2020 accounts for a smaller proportion of total deaths than malaria in Tropical Africa (0.13%) but greater proportions in Tropical Central and South America (0.08%) and Southeast Asia (0.23%). These results suggest that the deforestation-associated heat-related mortality burden is comparable with other major health burdens linked to tropical deforestation in the Americas and Southeast Asia.

There are no country-specific heat vulnerability indices available for African countries due to lack of data31, and so we have used the continental-average heat vulnerability index for South America. Lee et al.31 report that the heat vulnerability index shows a large negative dependence on the total health expenditure per capita and a large positive dependence on proportions of obese and elderly populations. A comparison of the key factors that affect heat vulnerability31 for Sub-Saharan Africa and other regions and countries (Extended Data Table 5) suggests that using the South American heat vulnerability index for African countries may be conservative. Increasing the heat vulnerability index used for African countries from the South American index (2.34%p °C−1) to the Southeast Asian index (5.29%p °C−1) more than doubles the deforestation-associated heat-attributable mortality burden estimate for Tropical Africa. Our analysis highlights the critical need for increased climate and health data to improve understanding of heat-health relationships in tropical African countries and other understudied tropical regions.

Extended Data Table 5.

Data on key factors affecting the heat vulnerability indices31

Region/country Current health expenditure per capita (current US$) (2020)97 Prevalence of overweight (% of adults) (2016)98 Population ages 65 and above (% of total population) (2020)99
Sub-Saharan Africa 74.6 28.9 3.1
Latin America & Caribbean 598.0 59.4 8.8
Latin America & Caribbean (excluding high income) 584.6 59.1 8.6
East Asia & Pacific 792.8 31.2 12.1
East Asia & Pacific (excluding high income) 448.0 31.0 10.9
Argentina 895.1 62.7 11.7
Australia 5958.8 64.5 16.2
Brazil 705.0 56.5 9.3
Chile 1280.6 63.1 12.4
China 583.4 32.3 12.6
Colombia 462.2 59.0 8.5
Iran, Islamic Rep. 338.2 61.6 7.1
Mexico 538.5 64.9 8.0
Philippines 166.0 27.6 5.2
Thailand 305.1 32.6 13.9
Viet Nam 154.2 18.3 8.4

Values are shown for three broad tropical regions and for the individual countries with heat vulnerability indices available. Values highlighted in bold are those closest to the values for Sub-Saharan Africa.

Our study focused on the local biophysical warming impacts of deforestation (that is, warming within the same 1 km2 pixel as the forest loss). Butt et al.21 demonstrated that deforestation of the Amazon caused strong warming at distances up to 100 km away from the forest loss. We do not include potential health effects of associated regional temperature changes on populations located outside deforested regions, suggesting we may have underestimated the impacts on human health. Tropical deforestation also releases CO2 that contributes to global warming. During 2014–2023, deforestation released 1.7 GtC yr−1, accounting for 15% of total anthropogenic CO2 emissions58. The global warming from release of CO2 is not included in our study, meaning that our estimates of heat-related mortality associated with deforestation are likely to be conservative. We estimate that non-deforested regions of the tropics have warmed by 0.2 °C over 2001–2020 (Table 1). Based on the contribution to global emissions, CO2 from tropical deforestation may have accounted for 0.03 °C (15%) of this warming, which is substantially less than the biophysical warming (0.45 °C) in regions of tropical deforestation. Nevertheless, the warming from CO2 emissions acts globally and the contribution of tropical deforestation to the global burden of heat-related mortality29 may be substantial. This highlights the strong potential for reducing tropical deforestation to contribute to reduced warming at both local and global scales.

Future global climate change is projected to increase heat-related mortality in the tropics31,59 and severely impact outdoor worker wellbeing and health60. Tropical deforestation and its associated local warming are likely to amplify these impacts. Climate model simulations indicate that cropland expansion into tropical forests could elevate local near-surface air temperature and increase heat stress in low-latitude regions61. In deforested areas of the tropics, future global climate change is projected to decrease safe outdoor working hours for millions of people12. In the Amazon region, scenarios of future climate warming and deforestation project substantial increases in heat stress and reductions in work capacity62. Furthermore, compound climate extremes including drought-heatwave episodes, which may be associated with enhanced fire activity and heat-related mortality in Brazil63, are increasing in a warming world64. In 2023 and 2024, critical episodes of prolonged drought occurred in the Brazilian Amazon, illustrating how climate change intensifies health threats through direct impacts, such as heatwaves and water scarcity, and indirect impacts, such as air pollution from fires.

Lower-income populations in the tropics are already experiencing a greater increase in the frequency of extreme temperatures compared with higher income populations65 and are projected to be disproportionately impacted under future global warming66. Tropical nations have particularly high heat vulnerability indices, suggesting their populations may be at higher mortality risk due to climate change31. This higher heat vulnerability is linked to lower per-capita health expenditure31, reflecting persistent socioeconomic disparities in healthcare access67. Vulnerable populations, particularly traditional and indigenous communities, often live near deforested areas and face limited access to resources and infrastructure needed to cope with the combination of rising temperatures and environmental changes caused by deforestation and climate change62. Our findings suggest that for populations in areas of tropical forest loss, deforestation-driven warming may exacerbate the heat-related health effects of global climate change, with critical implications for outdoor labour10,12. Furthermore, these populations may also suffer from disproportionate exposure to other deforestation-related health risks, such as malaria57 and fire-sourced air pollution54.

Our results underscore the role of deforestation in intensifying local warming within the broader context of climate change. Conservation of tropical forests can help mitigate local warming and strengthen the adaptive capacity of vulnerable populations. Future work should explore how protected areas function as buffers against temperature extremes, particularly for surrounding populations. Overall, our findings highlight the urgent need for targeted policy interventions to reduce tropical forest loss, alongside improved adaptation strategies and access to healthcare, to protect vulnerable populations in the tropics from the health risks associated with deforestation.

Methods

Temperature datasets

As in previous work17,21, we used land surface temperature (LST) data from NASA MODIS, specifically the MOD11A2 8-d LST data (here using the latest version 6.1)38 at 0.01° × 0.01° spatial resolution. We excluded data where the estimated emissivity error was greater than 0.02 and where the LST error was greater than 1 K, following Li et al.13. We used MODIS data from the Terra satellite (10:30 local overpass time) because of its longer sampling period compared with the Aqua satellite (February 2000 onwards versus July 2002 onwards) (13:30 overpass time) and due to lower cloud cover in the morning.

We first aggregated the 8-day LST data by month ignoring any 8-day period where data were missing due to clouds or because of the quality screening process. We then calculated 3-year means for two periods at the start (2001–2003) and end (2018–2020) of the study period. Using 3-year averages reduces the influences of climate variability. The LST dataset was regridded using bilinear interpolation (using Python package xESMF68) to match the finer resolution of the population data grid (30 arc-seconds). The ΔT in multiannual mean LST was then calculated by subtracting the 2001–2003 mean LST from the 2018–2020 mean LST. Our final ΔT dataset comprised over 64 million pixels (~1 km2 in extent) over the tropics (25° S to 25° N).

To assess the impacts of using morning LST data in place of daily mean air temperature data (as used by Lee et al.31 to derive the heat vulnerability indices), we used 2-m temperature (t2m) and LST data from the ERA5 (ref. 41) at 0.25° × 0.25° spatial resolution. We downloaded the hourly Analysis-Ready, Cloud Optimized (ARCO) ERA5 data from the Google Cloud Public Dataset Program69 for the years 2001–2003 and 2018–2020. First, we calculated daily mean t2m and extracted the ERA5 LST data at 10:00–11:00 local time. Second, we aggregated both variables by month and calculated 6-year means, regridding to match the population data grid (30 arc-seconds). Third, we calculated the relationship between ERA5 LST and ERA5 t2m over tropical forest pixels (using 2001 forest cover) of the main tropical forest regions (Extended Data Table 1).

Forest cover datasets

Forest cover data were taken from the Global Forest Change (GFC) V1.9 dataset1 at 30 m × 30 m spatial resolution. Annual forest cover for the period 2000–2020 was calculated by taking tree cover in the year 2000, defined as canopy closure for all vegetation taller than 5 m in height, and subjecting it to annual forest loss, defined as a disturbance from a forest to non-forest state. Forest cover was calculated at the native 30 m × 30 m spatial resolution and then converted to match the resolution of the population data by first calculating the forest cover fraction in each larger pixel (0.008° × 0.008°) and then converting to a 30 arc-second resolution using area-weighted regridding (using Python package Iris70). The percentage-point change in forest cover between 2001 and 2020 was calculated as the difference between the annual forest cover fractions (in per cent) in 2001 and 2020.

Forest cover gain can lead to cooling that can offset some of the warming due to forest loss71. To identify and exclude areas where forest regrowth has occurred, we used forest extent data at 30 m × 30 m spatial resolution from the Global Land Analysis and Discovery (GLAD) Global Land Cover and Land Use Change dataset72,73, available for the years 2000 and 2020. In the forest extent dataset, forest presence is indicated for pixels with 5 m or greater forest height. We converted this dataset to match the resolution of the population data using the same method as for the GFC data and calculated the percentage-point difference in forest extent between 2000 and 2020. We then removed any 30-arc-second pixels with greater than a 50%-point net increase in forest extent between 2000 and 2020 from the ΔT data.

Elevation dataset

We used elevation data from the Global Multi-resolution Terrain Elevation Data (GMTED2010)74 at 7.5-arc-second spatial resolution, which was regridded using bilinear interpolation to match the resolution of the population data.

Population and mortality datasets

Spatially explicit population data for the year 2020 was taken from LandScan75,39 at 30-arc-second spatial resolution representing an average population over 24 h (Fig. 1c). We used LandScan data for 2001 to test the sensitivity of our results to changing population density and distribution (‘Methodological limitations and justification’ section). To explore exposure of rural and urban populations, we used the Settlement Model Layers data from the Global Human Settlement Layer (GHSL) 2023 Data Package76,77.

Annual all-cause mortality and non-accidental mortality rates for all ages for the year 2019 were taken from the Global Burden of Disease Study (GBD)40. Non-accidental mortality (or non-external mortality) includes mortality from all causes except external causes such as accidents, suicides and homicides. We used data from 2019 instead of 2020 to exclude possible effects of coronavirus disease 2019 on the mortality rates. We used the highest resolution data available from the GBD40: province/state level data for Brazil and Indonesia and national-level data for all other countries in the tropics. We used GBD non-accidental mortality rates from 2001 to test the sensitivity of our results to changes in the annual mortality rates (‘Methodological limitations and justification’ section).

To estimate total annual all-cause and non-accidental mortality burdens at the pixel level, we multiplied the GBD mortality rates by the gridded total population data (pop)

nonacc_morti=popi×nonacc_mortratecountry, 1

where nonacc_mortratecountry is the national (or subnational) non-accidental mortality rate and nonacc_morti is the total annual non-accidental mortality burden per pixel (i).

Heat vulnerability indices

To estimate the heat-related excess mortality burden, we used country- or continent-specific heat vulnerability indices from Lee et al.31 following Wolff et al.10. The heat vulnerability index is the percentage-point increase of regional excess mortality per 1 °C increase of regional temperature (%p °C−1). Lee et al.31 first estimated location-specific temperature-mortality relationships for 459 locations in 28 countries using daily mean temperature, then estimated the projected excess mortality attributable to temperature change over 2010–2099 using a calibrated multimodel mean temperature time-series under different scenarios. The heat vulnerability indices were obtained for each location by applying linear regressions to the projection data31.

The heat vulnerability indices were estimated by Lee et al.31 for 10 continental regions and 28 countries; those used in this study are shown in Extended Data Table 2. Where country-specific indices were not available, we applied a continent-specific value. Following Lee et al.31, for countries located in Central and South Asia, we applied the heat vulnerability index from Iran; for countries located in Central America, we applied the index from Mexico. Lee et al.31 were unable to derive indices for African countries due to a lack of data; therefore, we have applied the lowest continental-average index (from South America) for the whole of the Tropical Africa.

Estimating deforestation-induced temperature change

We estimated the local ΔT due to forest loss between 2001 and 2020 at the 30-arc-second (~1 km2) pixel level across the tropics (25° S to 25° N). To remove the influence of global climate change over the study period on ΔT, we used a moving-window nearest-neighbour approach7,17.

In our analysis we used all 30-arc-second pixels within the tropics (25° S to 25° N) with 10% or greater forest cover fraction in 2001. Pixels with less than 0.5%-point forest cover loss between 2001 and 2020 were classified as ‘non-deforested’ pixels. Pixels with 2%-point or greater forest cover loss between 2001 and 2020 were classified as ‘deforested’ pixels. Our final ΔT dataset comprised ~16.8 million non-deforested pixels and ~11.3 million deforested pixels across the tropics (25° S to 25° N).

For each deforested pixel, we selected all surrounding pixels that maintained forest cover (‘non-deforested’ pixels) within a circle of 0.25° radius (~27 km at the equator) and within an elevation of ±50 m. If no surrounding non-deforested pixels were available within the 0.25° radius circle (3% of pixels), the radius of the circle was extended to 0.50°, with the same elevation constraints of within ±50 m. We used 0.25° and 0.5° radius circles similar to those used in previous work (for example, refs. 13,14,16). These previous studies—and ours—assume the background climate to be uniform over this distance. We calculated the mean ΔT over all selected non-deforested (‘control’) pixels and subtracted this from the ΔT of the central deforested pixel to get the deforestation-induced ΔT. A total of 0.58% of deforested pixels across the tropics were without surrounding non-deforested pixels within the specified spatial circle and elevation range; these pixels were retained in the data array but stored with a missing data indicator. We then divided the resulting deforestation-induced ΔT data array by the percentage-point change in forest cover to calculate the change in temperature per percentage-point forest cover loss.

At low levels of forest cover loss (<10%-point), the variability in ΔT per percentage-point forest cover loss exceeds the range in values found at greater levels of forest cover loss. To reduce this variability, we used a moving average smoothing approach. For each deforested pixel, we calculated the mean ΔT per percentage-point forest cover loss over all surrounding deforested pixels within a 0.10° rolling circle, excluding any pixel with less than 5%-point forest cover loss or with a z-score greater than 3 from the mean. For deforested pixels without surrounding deforested pixels with ≥5%-point forest cover loss within the 0.10° spatial circle (0.4% of all deforested pixels across the tropics), we used a regional mean value for ΔT per percentage-point forest cover loss. Finally, we multiplied the ‘smoothed’ pixel-level ΔT-per-percentage-point-forest-cover-loss values by the pixel-level percentage-point change in forest cover to obtain a more robust estimate of the pixel-level deforestation-induced ΔT.

Estimating deforestation-associated heat-related mortality

To estimate heat-related excess mortality, we followed the approach of Wolff et al.10, using the relationships between heat-attributable excess mortality and temperature estimated by Lee et al.31. Wolff et al.10 estimated heat-related mortality due to global climate change and deforestation combined. In this study, we estimated the heat-related mortality due specifically to local deforestation-induced warming.

First, we calculated the pixel-level deforestation-induced ΔT over 2001–2020 in all deforested pixels across the tropics (as described above). Second, to estimate the percentage-point increase in heat-attributable excess mortality (%pincrease_mort) per deforested pixel (i), we multiplied the country/continent-specific heat vulnerability indices (HVI) by the pixel-level ΔT in all deforested pixels with a positive temperature change (79% of all deforested pixels across the tropics) (ΔTdefor)

%pincrease_morti=ΔTdefori×HVIcountry. 2

The mortality impact of the 2001–2020 deforestation-induced warming will already be included in the non-accidental mortality burden data from 2019 (‘Population and mortality datasets’ section). Thus, following Wolff et al.10, we next calculated the corrected counterfactual mortality burden (CF_mort) (that is, without the excess mortality associated with the deforestation-induced ΔT that would already be included in the total non-accidental mortality burden) per deforested pixel (i)

CF_morti=nonacc_morti1+%pincrease_morti. 3

Lastly, we calculated the mortality attributable to warming from deforestation for each deforested pixel, as the difference between the counterfactual non-accidental mortality and total non-accidental mortality

heat_morti=nonacc_mortiCF_morti. 4

The results are estimated using annual non-accidental mortality rates and therefore represent an annual excess mortality burden associated with exposure to a ~20-year temperature change. Following Wolff et al.10, we refer to the heat-health impact results as an annual excess heat-attributable mortality burden. The uncertainty range in the heat-attributable mortality estimates was calculated based on the uncertainty range (the 95% CI) of the GBD all-cause/non-accidental mortality rates40.

For comparison, we also estimated the total heat-related mortality attributable to warming over 2001–2020 from global climate change and deforestation combined. This was done using the same method as above but replacing the deforestation-induced ΔT with the total ΔT. We note that where a deforested pixel experiences warming but surrounding non-deforested (‘control’) pixels experience an overall cooling, the deforestation-induced ΔT will be greater than the total ΔT, and the number of deforestation-associated heat-related deaths will exceed the number of total heat-related deaths in that pixel.

Methodological limitations and justification

We defined forested locations in the tropics as pixels with 10% forest canopy cover of vegetation taller than 5 m in height, which is consistent with the definition from the Food and Agriculture Organization of the United Nations78. We defined deforestation to be a net loss in forest cover of 2%-points or greater between 2001 and 2020. We accounted for dynamics of forest cover change within the given time period, by using the GLAD forest extent dataset to remove pixels with a >50%-point net increase in forest extent between 2000 and 2020. We tested the sensitivity to these assumptions. Defining deforestation as net forest loss greater than 1%-point, increased the number of data pixels and population included in our analysis, increasing our estimated mortality burden by 9% (Extended Data Table 4), but remains within our cited uncertainty range. Applying a lower threshold to the net increase in forest extent (20%-point) reduced the population exposed to deforestation-associated warming by only 1% (Extended Data Table 4).

We analysed the change in forest cover and LST between 2001 and 2020. The years of data included in the analysis were selected to maximize the study period with the available data, while also avoiding strong ENSO years in our 3-year averages of the LST data (2001–2003 and 2018–2020). We note that our analysis method attempts to remove the impact of climate variability through comparing temperature change over regions of forest loss with nearby regions with no forest loss. For example, during El Nino periods, both regions of forest loss and regions of no forest loss will experience a warming due to the impacts of El Nino. Our analysis pulls out the impact of forest loss during the El Nino by subtracting the temperature of surrounding forested pixels. We tested the sensitivity to the selected years of LST data by recalculating for a different 3-year period (from 2003–2005 to 2018–2020), 5-year periods (from 2001–2005 to 2016–2020) and for single years (2001–2019 and 2001–2020). Estimated deforestation-associated heat-related mortality burdens for these different time periods lie within our 95% CIs (varying by −13% to +15%) (Extended Data Table 4), showing that our method is robust to these assumptions. Averaging the forest loss data to match the same years as the LST data (from 2001–2003 to 2018–2020) reduces the heat-related mortality burden associated with deforestation by only 2% (Extended Data Table 4).

We used LST data to estimate human exposure and heat-related health impacts of deforestation-induced warming rather than near-surface air temperature, because air temperature data are not available at sufficiently high spatial resolution and coverage for the study time period. The use of LST data for exploring fine-scale temperature changes under tropical forest loss has been discussed and justified in previous studies10,12,17. For tropical forest regions, there is a particularly uneven and sparse distribution of ground-based meteorological stations79,80, which means that air temperature measurements from these stations (or datasets that spatially interpolate these measurements) are not appropriate for a tropics-wide assessment of fine-scale deforestation-induced temperature changes. Where meteorological stations exist, previous studies have shown a tight connection between LST and near-surface air temperature14,8183. Estimates of near-surface air temperature from climate reanalyses, such as the ERA5 (ref. 41), have been used extensively to estimate human exposure to extreme heat and the associated health impacts40,8486. While the relatively coarse resolution of ERA5 data make it unsuitable for examining fine-scale temperature changes driven by deforestation, it is reported to well capture changes in air temperature where meteorological station density is high79. To assess the impacts of using LST data in place of air temperature data, we used the relationship between ERA5 daily mean t2m and ERA5 10:00–11:00 local time LST (Extended Data Table 1) to adjust MODIS LST to daily mean 2-m air temperature. We then recalculated the impacts of forest loss using this adjusted ‘air temperature data’, which reduces the deforestation-associated heat-attributable mortality burden by only 1% (Extended Data Table 4).

We used morning measurements of LST from MODIS-Terra for its greater data availability compared with MODIS-Aqua (an overpass of 13:30 local time). Furthermore, MODIS-Terra tends to sense a cooler land surface than MODIS-Aqua and is therefore more representative of the daily mean temperature data used to derive the heat vulnerability indices by Lee et al.31. Using afternoon LST data from MODIS-Aqua (for 2003–2005 mean to 2018–2020 mean) increased the population-weighted warming associated with deforestation to +0.29 °C and increased the estimated deforestation-associated heat-attributable mortality burden to 30,590 (95% CI: 25,520–36,230) (Extended Data Table 4). This mortality burden is 19% greater than with MODIS-Terra LST for the same period and within our stated 95% CI.

In this work, we have not assessed the potential impact of deforestation on humidity. In situ measurements87,88 and reanalysis data89 show a general reduction in humidity in cleared areas of the tropics compared with forested areas, although this difference can be seasonally dependent. Results of a modelling study suggest that changes in humidity under simulated cropland expansion into low-latitude forested areas could moderate combined impacts on moist heat and heat stress61. However, Masuda et al.26 and Parsons et al.12 show that despite potential deforestation-induced changes in humidity, humid heat exposure increases substantially in areas of tropical forest loss compared with nearby forested areas, negatively impacting outdoor workers. There is a strong need for field measurements of humidity in tropical forest areas to enable further research into impacts of deforestation on humidity and the associated health impacts

Following Wolff et al.10, we have not included an estimation of the change in cold-related mortality under higher temperatures. For tropical countries, the reduction in cold-related mortality under increasing temperatures is small and is outweighed by the associated increase in heat-related mortality31.

The heat vulnerability indices were developed by Lee et al.31 using either non-accidental or all-cause mortality rates (Extended Data Table 2), depending on the data available for each country. For simplicity we report results estimated using non-accidental mortality rates. Using all-cause mortality rates in all locations increases the total deforestation-associated heat-attributable mortality burden across the tropics by ~8% (with a 15% increase in Tropical Central and South America where differences between non-accidental and all-cause mortality rates are greatest).

We report heat-related mortality estimates that are relevant for a near-present-day population, using population count and spatial distribution for 2020 and non-accidental (or all-cause) mortality rates for 2019. During 2001–2020, population count has increased across the tropics, while changes in non-accidental mortality rates are mixed. Using population count and spatial distribution and non-accidental mortality rates for the start of the study period (2001) reduces the total deforestation-associated heat-attributable mortality burden across the tropics by ~10%.

Reporting summary

Further information on research design is available in the Nature Portfolio Reporting Summary linked to this article.

Online content

Any methods, additional references, Nature Portfolio reporting summaries, source data, extended data, supplementary information, acknowledgements, peer review information; details of author contributions and competing interests; and statements of data and code availability are available at 10.1038/s41558-025-02411-0.

Supplementary information

Reporting summary (1.4MB, pdf)

Acknowledgements

The research has been supported by funding from the European Research Council under the European Union’s Horizon 2020 research and innovation programme (DECAF project; grant agreement no. 771492) (C.L.R., J.C.A.B., D.V.S.), the International Science Partnerships Fund (ISPF), through the Met Office Climate Science for Service Partnership (CSSP) Brazil (E.W.B., C.S., J.C.A.B., D.V.S.), the Natural Environmental Research Council (NE/Z00005X/1) (E.W.B., D.V.S.), and the UK Research and Innovation Future Leaders Fellowship (MR/X034097/1) (J.C.A.B.).

Extended data

Extended Data Fig. 2. Deforestation-induced ΔT over 2001 to 2020 as a function of area and population.

Extended Data Fig. 2

Results are shown for populations in locations of forest loss (see Methods) in a. Tropical Central and South America, b. Tropical Africa, and c. Southeast Asia. Dashed vertical lines show the area- and population-weighted mean deforestation-induced ΔT for each region.

Author contributions

C.L.R. and D.V.S. developed the concept of the study; C.S., J.C.A.B. and E.W.B. provided data and analysis tools; C.L.R. performed the research and analysed data; B.F.A.O. and E.I.Y. contributed region-specific expertise; and all authors contributed to experimental design, interpretation of results and writing of the paper.

Peer review

Peer review information

Nature Climate Change thanks Jun Ge, Jihoon Jung and the other, anonymous, reviewer for their contribution to the peer review of this work.

Data availability

The datasets used in the analyses for this study are freely available to download from the following locations: MODIS land surface temperature data at https://www.earthdata.nasa.gov/; European Centre for Medium-Range Weather Forecasts Reanalysis v5 (ERA5) Analysis-Ready, Cloud Optimized (ARCO) dataset on GitHub at https://github.com/google-research/arco-era5; Global Forest Change (GFC) dataset at https://storage.googleapis.com/earthenginepartners-hansen/GFC-2023-v1.11/download.html; Global Land Analysis and Discovery (GLAD) Global Land Cover and Land Use Change dataset at https://glad.umd.edu/dataset/GLCLUC2020; Global Multi-resolution Terrain Elevation Data (GMTED2010) at https://earthexplorer.usgs.gov/; LandScan population data at https://landscan.ornl.gov/; Global Human Settlement Layer dataset at https://human-settlement.emergency.copernicus.eu/ghs_smod2023.php; GBD Study cause-specific mortality rates at https://gbd2019.healthdata.org/gbd-results/ or https://vizhub.healthdata.org/gbd-results/; and digital geospatial data for plotting administrative boundaries from Database of Global Administrative Boundaries (GADM) at https://gadm.org/index.html. The processed data files produced and used in the analyses of this study are available through Code Ocean90.

Code availability

The data were analysed using open-source Python packages (including xESMF68, Iris70, xarray91, NumPy92, Matplotlib93, Pandas94 and Cartopy95) that are freely available online. The Python code used to produce the central results of this study is available as a Compute Capsule through Code Ocean90. Any other Python code used is available upon request from the corresponding author.

Competing interests

The authors declare no competing interests.

Footnotes

Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Extended data

is available for this paper at 10.1038/s41558-025-02411-0.

Supplementary information

The online version contains supplementary material available at 10.1038/s41558-025-02411-0.

References

  • 1.Hansen, M. C. et al. High-resolution global maps of 21st-century forest cover change. Science342, 850–853 (2013). [DOI] [PubMed] [Google Scholar]
  • 2.Vancutsem, C. et al. Long-term (1990–2019) monitoring of forest cover changes in the humid tropics. Sci. Adv.7, eabe1603 (2021). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Pendrill, F. et al. Disentangling the numbers behind agriculture-driven tropical deforestation. Science377, eabm9267 (2022). [DOI] [PubMed] [Google Scholar]
  • 4.Giam, X. Global biodiversity loss from tropical deforestation. Proc. Natl Acad. Sci. USA114, 5775–5777 (2017). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Mitchard, E. T. A. The tropical forest carbon cycle and climate change. Nature559, 527–534 (2018). [DOI] [PubMed] [Google Scholar]
  • 6.Lawrence, D., Coe, M., Walker, W., Verchot, L. & Vandecar, K. The unseen effects of deforestation: biophysical effects on climate. Front. For. Glob. Change5, 756115 (2022). [Google Scholar]
  • 7.Smith, C., Baker, J. C. A. & Spracklen, D. V. Tropical deforestation causes large reductions in observed precipitation. Nature615, 270–275 (2023). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Pienkowski, T., Dickens, B. L., Sun, H. & Carrasco, L. R. Empirical evidence of the public health benefits of tropical forest conservation in Cambodia: a generalised linear mixed-effects model analysis. Lancet Planet. Health1, e180–e187 (2017). [DOI] [PubMed] [Google Scholar]
  • 9.Wolff, N. H., Masuda, Y. J., Meijaard, E., Wells, J. A. & Game, E. T. Impacts of tropical deforestation on local temperature and human well-being perceptions. Global Environ. Change52, 181–189 (2018). [Google Scholar]
  • 10.Wolff, N. H. et al. The effect of deforestation and climate change on all-cause mortality and unsafe work conditions due to heat exposure in Berau, Indonesia: a modelling study. Lancet Planet. Health5, e882–e892 (2021). [DOI] [PubMed] [Google Scholar]
  • 11.MacDonald, A. J. & Mordecai, E. A. Amazon deforestation drives malaria transmission, and malaria burden reduces forest clearing. PNAS116, 22212–22218 (2019). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Parsons, L. A. et al. Tropical deforestation accelerates local warming and loss of safe outdoor working hours. One Earth4, 1730–1740 (2021). [Google Scholar]
  • 13.Li, Y. et al. Local cooling and warming effects of forests based on satellite observations. Nat. Commun.6, 1–8 (2015). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Alkama, R. & Cescatti, A. Biophysical climate impacts of recent changes in global forest cover. Science351, 600–604 (2016). [DOI] [PubMed] [Google Scholar]
  • 15.Bright, R. M. et al. Local temperature response to land cover and management change driven by non-radiative processes. Nat. Clim. Change7, 296–302 (2017). [Google Scholar]
  • 16.Duveiller, G. et al. The mark of vegetation change on Earth’s surface energy balance. Nat. Commun.9, 679 (2018). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Baker, J. C. A. & Spracklen, D. V. Climate benefits of intact amazon forests and the biophysical consequences of disturbance. Front. For. Glob. Change2, 443097 (2019). [Google Scholar]
  • 18.Prevedello, J. A., Winck, G. R., Weber, M. M., Nichols, E. & Sinervo, B. Impacts of forestation and deforestation on local temperature across the globe. PLoS ONE14, e0213368 (2019). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Abera, T. A. et al. Deforestation amplifies climate change effects on warming and cloud level rise in African montane forests. Nat. Commun.15, 6992 (2024). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Zeppetello, L. R. V. et al. Large scale tropical deforestation drives extreme warming. Environ. Res. Lett.15, 084012 (2020). [Google Scholar]
  • 21.Butt, E. W. et al. Amazon deforestation causes strong regional warming. Proc. Natl Acad. Sci. USA120, e2309123120 (2023). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Masuda, Y. J. et al. How are healthy, working populations affected by increasing temperatures in the tropics? Implications for climate change adaptation policies. Glob. Environ. Change56, 29–40 (2019). [Google Scholar]
  • 23.Rony, M. K. K. & Alamgir, H. M. High temperatures on mental health: recognizing the association and the need for proactive strategies—a perspective. Health Sci. Rep.6, e1729 (2023). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Périard, J. D., Eijsvogels, T. M. H. & Daanen, H. A. M. Exercise under heat stress: thermoregulation, hydration, performance implications, and mitigation strategies. Physiol. Rev.101, 1873–1979 (2021). [DOI] [PubMed] [Google Scholar]
  • 25.Dasgupta, S. et al. Effects of climate change on combined labour productivity and supply: an empirical, multi-model study. Lancet Planet. Health5, e455–e465 (2021). [DOI] [PubMed] [Google Scholar]
  • 26.Masuda, Y. J. et al. Warming from tropical deforestation reduces worker productivity in rural communities. Nat. Commun.12, 121601 (2021). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Green, H. et al. Impact of heat on mortality and morbidity in low and middle income countries: a review of the epidemiological evidence and considerations for future research. Environ. Res.171, 80–91 (2019). [DOI] [PubMed] [Google Scholar]
  • 28.Silveira, I. H. et al. Heat waves and mortality in the Brazilian Amazon: effect modification by heat wave characteristics, population subgroup, and cause of death. Int. J. Hyg. Environ. Health248, 114109 (2023). [DOI] [PubMed] [Google Scholar]
  • 29.Vicedo-Cabrera, A. M. et al. The burden of heat-related mortality attributable to recent human-induced climate change. Nat. Clim. Chang.11, 492–500 (2021). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Yardley, J., Sigal, R. J. & Kenny, G. P. Heat health planning: the importance of social and community factors. Global Environ. Change21, 670–679 (2011). [Google Scholar]
  • 31.Lee, J. Y. et al. Predicted temperature-increase-induced global health burden and its regional variability. Environ. Int.131, 105027 (2019). [DOI] [PubMed] [Google Scholar]
  • 32.Barreca, A., Clay, K., Deschenes, O., Greenstone, M. & Shapiro, J. S. Adapting to climate change: the remarkable decline in the US temperature-mortality relationship over the twentieth century. J. Political Econ.124, 105–159 (2016). [Google Scholar]
  • 33.Davis, L., Gertler, P., Jarvis, S. & Wolfram, C. Air conditioning and global inequality. Global Environ. Change69, 102299 (2021). [Google Scholar]
  • 34.Parsons, L. A. et al. Global labor loss due to humid heat exposure underestimated for outdoor workers. Environ. Res. Lett.17, 014050 (2022). [Google Scholar]
  • 35.Saeed, W. et al. The poverty impacts of labor heat stress in West Africa under a warming climate. Earth’s Future10, e2022EF002777 (2022). [Google Scholar]
  • 36.Suter, M. K. et al. Association between work in deforested, compared to forested, areas and human heat strain: an experimental study in a rural tropical environment. Environ. Res. Lett.14, 084012 (2019). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Masuda, Y. et al. Heat exposure from tropical deforestation decreases cognitive performance of rural workers: an experimental study. Environ. Res. Lett.15, 124015 (2020). [Google Scholar]
  • 38.Wan, Z., Hook, S. & Hulley, G. MODIS/Terra Land Surface Temperature/Emissivity 8-Day L3 Global 1km SIN Grid V061. NASA Land Processes Distributed Active Archive Center10.5067/MODIS/MOD11A2.061 (2021).
  • 39.Rose, A. et al. LandScan Global 2020 [dataset]. Oak Ridge National Laboratory10.48690/1523378 (2021).
  • 40.Murray, C. J. L. et al. Global burden of 87 risk factors in 204 countries and territories, 1990–2019: a systematic analysis for the global burden of disease study 2019. Lancet396, 1223–1249 (2020). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.Hersbach, H. et al. The ERA5 global reanalysis. Q. J. R. Meteorolog. Soc.146, 1999–2049 (2020). [Google Scholar]
  • 42.Global Burden of Disease Collaborative Network. Global Burden of Disease Study 2021 (GBD 2021) data resources. Institute for Health Metrics and Evaluationhttps://ghdx.healthdata.org/gbd-2021 (2024).
  • 43.Boussetta, S., Balsamo, G., Beljaars, A., Kral, T. & Jarlan, L. Impact of a satellite-derived leaf area index monthly climatology in a global numerical weather prediction model. Int. J. Remote Sens.34, 3520–3542 (2013). [Google Scholar]
  • 44.da Silva, Q. P., Moreira, D. S., de Freitas, H. C. & Domingues, L. M. Discrepancies between observation and ERA5 reanalysis in the Amazon deforestation context: a case study. Dyn. Atmos. Oceans106, 101442 (2024). [Google Scholar]
  • 45.Reddington, C. L. et al. Contribution of vegetation and peat fires to particulate air pollution in South-east Asia. Environ. Res. Lett.9, 094006 (2014). [Google Scholar]
  • 46.de Oliveira, I. N. et al. Air pollution from forest burning as environmental risk for millions of inhabitants of the Brazilian Amazon: an exposure indicator for human health. Cadernos de Saúde Pública39, e00131422 (2023). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 47.Jacobson, L. S. V. et al. Acute effects of particulate matter and black carbon from seasonal fires on peak expiratory flow of school children in the Brazilian Amazon. PLoS ONE9, e104177 (2014). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 48.Xue, T. et al. Associations between exposure to landscape fire smoke and child mortality in low-income and middle-income countries: a matched case-control study. Lancet Planet. Health5, e588–e598 (2021). [DOI] [PubMed] [Google Scholar]
  • 49.Crippa, P. et al. Population exposure to hazardous air quality due to the 2015 fires in Equatorial Asia. Sci. Rep.6, 37074 (2016). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 50.Reddington, C. L. et al. Air quality and human health improvements from reductions in deforestation-related fire in Brazil. Nat. Geosci.8, 768–771 (2015). [Google Scholar]
  • 51.Butt, E. W. et al. Large air quality and human health impacts due to Amazon forest and vegetation fires. Environ. Res. Commun.2, 095001 (2020). [Google Scholar]
  • 52.Butt, E. W., Conibear, L., Knote, C. & Spracklen, D. V. Large air quality and public health impacts due to Amazonian deforestation fires in 2019. GeoHealth5, e2021GH000429 (2021). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 53.Kiely, L. et al. Air quality and health impacts of vegetation and peatfires in Equatorial Asia during 2004–2015. Environ. Res. Lett.15, 094054 (2020). [Google Scholar]
  • 54.Reddington, C. L. et al. Air pollution from forest and vegetation fires in Southeast Asia disproportionately impacts the poor. GeoHealth5, e2021GH000418 (2021). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 55.Bauer, S. E., Im, U., Mezuman, K. & Gao, C. Y. Desert dust, industrialization, and agricultural fires: health impacts of outdoor air pollution in Africa. J. Geophys. Res. Atmos.124, 4104–4120 (2019). [Google Scholar]
  • 56.Fornace, K. M. et al. Association between landscape factors and spatial patterns of Plasmodium knowlesi infections in Sabah, Malaysia. Emerg. Infect. Dis.22, 201–208 (2016). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 57.Estifanos, T. K., Fisher, B., Galford, G. L. & Ricketts, T. H. Impacts of deforestation on childhood malaria depend on wealth and vector biology. GeoHealth8, e2022GH000764 (2024). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 58.Friedlingstein, P. et al. Global carbon budget 2024. Earth Syst. Sci. Data17, 965–1039 (2025). [Google Scholar]
  • 59.Mora, C. et al. Global risk of deadly heat. Nat. Clim. Change7, 501–506 (2017). [Google Scholar]
  • 60.Masuda, Y. J. et al. Impacts of warming on outdoor worker well-being in the tropics and adaptation options. One Earth7, 382–400 (2024). [Google Scholar]
  • 61.Orlov, A. et al. Changes in land cover and management affect heat stress and labor capacity. Earth’s Future11, e2022EF002909 (2023). [Google Scholar]
  • 62.de Oliveira, B. F. A. et al. Deforestation and climate change are projected to increase heat stress risk in the Brazilian Amazon. Commun. Earth Environ.2, 207 (2021). [Google Scholar]
  • 63.Libonati, R. et al. Drought–heatwave nexus in Brazil and related impacts on health and fires: a comprehensive review. Ann. N.Y. Acad. Sci.1517, 44–62 (2022). [DOI] [PubMed] [Google Scholar]
  • 64.Mukherjee, S. & Mishra, A. K. Increase in compound drought and heatwaves in a warming world. Geophys. Res. Lett.48, e2020GL090617 (2021). [Google Scholar]
  • 65.Herold, N., Alexander, L., Green, D. & Donat, M. Greater increases in temperature extremes in low versus high income countries. Environ. Res. Lett.12, 034007 (2017). [Google Scholar]
  • 66.King, A. D. & Harrington, L. J. The inequality of climate change from 1.5 to 2 °C of global warming. Geophys. Res. Lett.45, 5030–5033 (2018). [Google Scholar]
  • 67.Wagstaff, A. & Neelsen, S. A comprehensive assessment of universal health coverage in 111 countries: a retrospective observational study. Lancet Glob. Health8, e39–e49 (2020). [DOI] [PubMed] [Google Scholar]
  • 68.Zhuang, J. et al. pangeo-data/xESMF: v0.8.2 (v0.8.2). Zenodo10.5281/zenodo.8356796 (2023).
  • 69.Carver, R. W., and Merose, A. ARCO-ERA5: an analysis-ready cloud-optimized reanalysis dataset. American Meteorological Societyhttps://ams.confex.com/ams/103ANNUAL/meetingapp.cgi/Paper/415842 (2023).
  • 70.Met Office Iris: a Python package for analysing and visualising meteorological and oceanographic data sets, v3.1.0. GitHubhttps://github.com/SciTools/iris/releases/tag/v3.1.0 (2021).
  • 71.Su, Y. et al. Asymmetric influence of forest cover gain and loss on land surface temperature. Nat. Clim. Chang13, 823–831 (2023). [Google Scholar]
  • 72.Potapov, P. et al. The global 2000–2020 land cover and land use change dataset derived from the Landsat archive: first results. Front. Remote Sens.10.3389/frsen.2022.856903 (2022).
  • 73.Potapov, P. et al. Mapping and monitoring global forest canopy height through integration of GEDI and Landsat data. Remote Sens. Environ.10.1016/j.rse.2020.112165 (2020).
  • 74.Danielson, J. J. & Gesch, D. B. Global Multi-resolution Terrain Elevation Data 2010 (GMTED2010) Open-File Report 2011–1073 (US Geological Survey, 2011).
  • 75.Bhaduri, B. et al. LandScan USA: a high-resolution geospatial and temporal modeling approach for population distribution and dynamics. GeoJournal69, 103–117 (2007). [Google Scholar]
  • 76.Schiavina, M., Melchiorri, M. & Pesaresi, M. GHS-SMOD R2023A—GHS settlement layers, application of the Degree of Urbanisation methodology (stage I) to GHS-POP R2023A and GHS-BUILT-S R2023A, multitemporal (1975–2030). European Commission Joint Research Centre10.2905/A0DF7A6F-49DE-46EA-9BDE-563437A6E2BA (2023).
  • 77.European Commission GHSL Data Package 2023 (Publications Office of the European Union, 2024); https://data.europa.eu/doi/10.2760/098587
  • 78.Global Forest Resources Assessment. Terms and definitions—FRA 2020 Forest Resources Assessment Working Paper 188 (Food and Agriculture Organization of the United Nations, 2020); https://www.fao.org/3/I8661EN/i8661en.pdf
  • 79.Liu, R. et al. Global-scale ERA5 product precipitation and temperature evaluation. Ecol. Indic.166, 112481 (2024). [Google Scholar]
  • 80.Mistry, M. N. et al. Comparison of weather station and climate reanalysis data for modelling temperature-related mortality. Sci. Rep.12, 5178 (2022). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 81.Liu, J., Hagan, D. F. T., Holmes, T. R. & Liu, Y. An analysis of spatio-temporal relationship between satellite-based land surface temperature and station-based near-surface air temperature over Brazil. Remote Sens.14, 4420 (2022). [Google Scholar]
  • 82.Gallo, K., Hale, R., Tarpley, D. & Yu, Y. Evaluation of the relationship between air and land surface temperature under clear- and cloudy-sky conditions. J. Appl. Meteorol. Climatol.50, 767–775 (2011). [Google Scholar]
  • 83.Mildrexler, D. J., Zhao, M. & Running, S. W. A global comparison between station air temperatures and MODIS land surface temperatures reveals the cooling role of forests. J. Geophys. Res.116, G03025 (2011). [Google Scholar]
  • 84.Thompson, V. et al. The most at-risk regions in the world for high-impact heatwaves. Nat. Commun.14, 1–8 (2023). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 85.Brimicombe, C. et al. Effects of ambient heat exposure on risk of all-cause mortality in children younger than 5 years in Africa: a pooled time-series analysis. Lancet Planet. Health8, e640–e646 (2024). [DOI] [PubMed] [Google Scholar]
  • 86.Romanello, M. et al. The 2024 report of the Lancet Countdown on health and climate change: facing record-breaking threats from delayed action. Lancet404, 1847–1896 (2024). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 87.Fisch, G. et al. The convective boundary layer over pasture and forest in Amazonia. Theor. Appl. Climatol.78, 47–59 (2004). [Google Scholar]
  • 88.Dubreuil, V. et al. Impact of land-cover change in the Southern Amazonia climate: a case study for the region of Alta Floresta, Mato Grosso, Brazil. Environ. Monit. Assess.184, 877–891 (2012). [DOI] [PubMed] [Google Scholar]
  • 89.Xu, X. et al. Deforestation triggering irreversible transition in Amazon hydrological cycle. Environ. Res. Lett.17, 034037 (2022). [Google Scholar]
  • 90.Reddington, C. L. et al. Data files and code for manuscript ‘Tropical deforestation is associated with considerable heat-related mortality’. Code Oceanhttps://codeocean.com/capsule/9925363/tree (2025).
  • 91.Hoyer, S. & Hamman, J. xarray: N-D labeled arrays and datasets in Python. J. Open Res. Softw.5, 10 (2017). [Google Scholar]
  • 92.Harris, C. R. et al. Array programming with NumPy. Nature585, 357–362 (2020). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 93.Hunter, J. D. Matplotlib: a 2D graphics environment. Comput. Sci. Eng.9, 90–95 (2007). [Google Scholar]
  • 94.The Pandas development team. pandas-dev/pandas: Pandas (v2.1.3). Zenodo10.5281/zenodo.13819579. (2024).
  • 95.Elson et al. SciTools/cartopy: REL: v0.24.1 (v0.24.1). Zenodo10.5281/zenodo.1182735 (2024).
  • 96.Gasparrini, A. et al. Projections of temperature-related excess mortality under climate change scenarios. Lancet Planet. Health1, e360–e367 (2017). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 97.World Bank World Development Indicators: Current Health Expenditure per Capita (Current US$) (World Bank Group, 2024); https://data.worldbank.org/indicator/SH.XPD.CHEX.PC.CD
  • 98.World Bank Gender Statistics: Prevalence of Overweight (% of Adults) (World Bank DataBank, 2016); https://databank.worldbank.org/source/gender-statistics/Series/SH.STA.OWAD.MA.ZS
  • 99.United Nations World Development Indicators: Population Ages 65 and Above (% of Total Population) World Population Prospects: 2022 Revision (United Nations Population Division, 2022); https://data.worldbank.org/indicator/sp.pop.65up.to.zs

Associated Data

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

Supplementary Materials

Reporting summary (1.4MB, pdf)

Data Availability Statement

The datasets used in the analyses for this study are freely available to download from the following locations: MODIS land surface temperature data at https://www.earthdata.nasa.gov/; European Centre for Medium-Range Weather Forecasts Reanalysis v5 (ERA5) Analysis-Ready, Cloud Optimized (ARCO) dataset on GitHub at https://github.com/google-research/arco-era5; Global Forest Change (GFC) dataset at https://storage.googleapis.com/earthenginepartners-hansen/GFC-2023-v1.11/download.html; Global Land Analysis and Discovery (GLAD) Global Land Cover and Land Use Change dataset at https://glad.umd.edu/dataset/GLCLUC2020; Global Multi-resolution Terrain Elevation Data (GMTED2010) at https://earthexplorer.usgs.gov/; LandScan population data at https://landscan.ornl.gov/; Global Human Settlement Layer dataset at https://human-settlement.emergency.copernicus.eu/ghs_smod2023.php; GBD Study cause-specific mortality rates at https://gbd2019.healthdata.org/gbd-results/ or https://vizhub.healthdata.org/gbd-results/; and digital geospatial data for plotting administrative boundaries from Database of Global Administrative Boundaries (GADM) at https://gadm.org/index.html. The processed data files produced and used in the analyses of this study are available through Code Ocean90.

The data were analysed using open-source Python packages (including xESMF68, Iris70, xarray91, NumPy92, Matplotlib93, Pandas94 and Cartopy95) that are freely available online. The Python code used to produce the central results of this study is available as a Compute Capsule through Code Ocean90. Any other Python code used is available upon request from the corresponding author.


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