The exceptionally violent eruption of the Hunga Tonga‐Hunga Ha'apai volcano (HTHH) of 15 January 2022, in the South Pacific, was associated with a powerful blast that injected gases, steam and aerosol to unprecedentedly high altitudes. This article details unique observations of the young volcanic plume from ground‐based lidars at Reunion (21°S, 55°E). Two lidars, operating at wavelengths of 355 and 532 nm, recorded the plume overhead from 19 January until 28 January providing the vertical structure and the optical properties of the plume. A series of thick stratospheric plumes between 36 and 18 km altitude have been characterized along time, with aerosol optical depth as high as 0.84 at 532 nm and negative Angström exponents for the main layers down to −0.8 ± 0.8. The diversity of plumes properties is explained by the injection heights of the volcanic material as well as stratospheric dynamics and chemistry.

The Forests gAses aeRosols Clouds Exploratory (FARCE) campaign was conducted in March–April 2015 on the tropical island of La Réunion. For the first time, several scientific teams from different disciplines collaborated to provide reference measurements and characterization of La Réunion vegetation, volatile organic compounds (VOCs), biogenic VOCs (BVOCs), (bio)aerosols and composition of clouds, with a strong focus on the Maïdo mountain slope area. The main observations obtained during this 2-month intensive field campaign are summarized. They include characterizations of forest structure, concentrations of VOCs and precursors emitted by forests, aerosol loading and optical properties in the planetary boundary layer (PBL), formation of new particles by nucleation of gas-phase precursors, ice-nucleating particles concentrations, and biological loading in both cloud-free and cloudy conditions. Simulations and measurements confirm that the Maïdo Observatory lies within the PBL from late morning to late evening and that, when in the PBL, the main primary sources impacting the Maïdo Observatory are of marine origin via the Indian Ocean and of biogenic origin through the dense forest cover. They also show that (i) the marine source prevails less and less while reaching the observatory; (ii) when in the PBL, depending on the localization of a horizontal wind shear, the Maïdo Observatory can be affected by air masses coming directly from the ocean and passing over the Maïdo mountain slope, or coming from inland; (iii) bio-aerosols can be observed in both cloud-free and cloudy conditions at the Maïdo Observatory; (iv) BVOC emissions by the forest covering the Maïdo mountain slope can be transported upslope within clouds and are a potential cause of secondary organic aerosol formation in the aqueous phase at the Maïdo Observatory; and (v) the simulation of dynamics parameters, emitted BVOCs and cloud life cycle in the Meso-NH model are realistic, and more advanced Meso-NH simulations should use an increased horizontal resolution (100 m) to better take into account the orography and improve the simulation of the wind shear front zone within which lies the Maïdo Observatory. Using various observations and simulations, this work draws up an inventory of the in situ studies that could be performed in La Réunion and at the Maïdo Observatory. It also aims to develop scientific collaborations and to support future scientific projects in order to better understand the forest–gas–aerosol–cloud system in an insular tropical environment.

Aerosols are essential climate variables that need to be observed at a global scale to monitor the evolution of the atmospheric composition and potential climate impacts. We used the measurements performed over the May 2007–December 2019 period by a ground-based sun photometer installed at the island of La Réunion (21°S, 55°E), together with a linear regression fitting model, to assess the climatology and types of aerosols reaching this observation site located in a sparsely documented pristine area, and the forcings responsible for the variability of the observed aerosol optical depth (AOD) and related trend. The climatology of the aerosol optical depth (AOD) at 440 nm (AOD₄₄₀) and Ångström exponent between 500 and 870 nm (α) revealed that sea salts could be considered as the La Réunion AOD₄₄₀ and α baselines (0.06 ± 0.03 and 0.61 ± 0.40, respectively, from December to August), which were mainly modulated by biomass burning (BB) plumes passing over La Réunion (causing a doubling of AOD₄₄₀ and α up to 0.13 ± 0.07 and 1.06 ± 0.34, respectively, in October). This was confirmed by the retrieved aerosol volume size distributions showing that the coarse-mode (fine-mode) dominated the total volume concentration for AOD₄₄₀ lower (higher) than 0.2 with a mean radius equal to 3 μm (0.15 μm). The main contribution to the AOD₄₄₀ variability over La Réunion was evaluated to be the BB activity (67.4 ± 28.1%), followed by marine aerosols (16.3 ± 4.2%) and large-scale atmospheric structures (5.5 ± 1.7%). The calculated trend for AOD₄₄₀ equaled 0.02 ± 0.01 per decade (2.6 ± 1.3% per year). These results provide a scientific reference base for upcoming studies dedicated to the quantification of the impact of wildfire emissions on the southwestern Indian Ocean’s atmospheric composition and radiative balance.

The Oxygenated Compounds in the Tropical Atmosphere: Variability and Exchanges (OCTAVE) campaign aimed to improve the assessment of the budget and role of oxygenated volatile organic compounds (OVOCs) in tropical regions, and especially over oceans, relying on an integrated approach combining in situ measurements, satellite retrievals, and modeling. As part of OCTAVE, volatile organic compounds (VOCs) were measured using a comprehensive suite of instruments on Reunion Island (21.07° S, 55.38° E) from 7 March to 2 May 2018. VOCs were measured at a receptor site at the Maïdo observatory during the entire campaign and at two source sites: Le Port from 19 to 24 April 2018 (source of anthropogenic emissions) and Bélouve from 25 April to 2 May 2018 (source of biogenic emissions) within a mobile lab. The Maïdo observatory is a remote background site located at an altitude of 2200 m, whereas Bélouve is located in a tropical forest to the east of Maïdo and Le Port is an urban area located northwest of Maïdo. The major objective of this study was to understand the sources and distributions of atmospheric formaldehyde (HCHO) in the Maïdo observatory on Reunion Island. To address this objective, two different approaches were used to quantify and determine the main drivers of HCHO at Maïdo. First, a chemical-kinetics-based (CKB) calculation method was used to determine the sources and sinks (biogenic, anthropogenic/primary, or secondary) of HCHO at the Maïdo site. The CKB method shows that 9% of the formaldehyde formed from biogenic emissions and 89% of HCHO had an unknown source; that is, the sources cannot be explicitly described by this method. Next, a positive matrix factorization (PMF) model was applied to characterize the VOC source contributions at Maïdo. The PMF analysis including VOCs measured at the Maïdo observatory shows that the most robust solution was obtained with five factors: secondary biogenic accounting for 17%, primary anthropogenic/solvents (24%), primary biogenic (14%), primary anthropogenic/combustion (22%), and background (23%). The main contributions to formaldehyde sources as described by the PMF model are secondary biogenic (oxidation of biogenic VOCs with 37%) and background (32%). Some assumptions were necessary concerning the high percentage of unknown HCHO sources of the CKB calculation method such as the biogenic emission factor resulting in large discrepancies between the two methods.

Fires occur seasonally in Southern Africa, from June to November, increasing tropospheric aerosol loading and triggering harmful consequences for the environment and human health. This study aims to examine 13 years of aerosol optical characteristics and types over Southern Africa and Reunion Island. Using AERONET sun photometers and MODIS observations, we found that a high aerosol optical depth and Angström exponent are associated with two predominant types of aerosols (biomass burning/urban industrial and mixed type) throughout the spring season. According to CALIOP observations, the major aerosol types with occurrence frequencies above 10% are polluted continental/smoke, polluted dust, and elevated smoke, whereas dust, clean continental, and dusty marine have occurrence frequencies below 1%. In comparison to other seasons, the vertical profiles of elevated smoke have different shapes in spring, with a seasonal shift in the peak altitude (from 3–4 km), when fire activity is at its maximum. At these altitudes, the northern regions presented occurrence frequencies of 32% on average, while lower values were found for the southern or farthest regions (<10–20% on average). The Lagrangian HYSPLIT model back-trajectories demonstrated eastward transport, with air masses from South America and the Atlantic Ocean that recirculate around the study sites. The aerosols are mainly derived from active biomass burning areas near the study sites and, to a lesser extent, from remote sources such as South America.