Atmospheric aerosol particles that can nucleate ice are referred to as ice-nucleating particles (INPs). Recent studies have confirmed that aerosol particles emitted by the oceans can act as INPs. This very relevant information can be included in climate and weather models to predict the formation of ice in clouds, given that most of them do not consider oceans as a source of INPs. Very few studies that sample INPs have been carried out in tropical latitudes, and there is a need to evaluate their availability to understand the potential role that marine aerosol may play in the hydrological cycle of tropical regions. This study presents results from the first measurements obtained during a field campaign conducted in the tropical village of Sisal, located on the coast of the Gulf of Mexico of the Yucatan Peninsula in Mexico in January–February 2017, and one of the few data sets currently available at such latitudes (i.e., 21^∘ N). Aerosol particles sampled in Sisal are shown to be very efficient INPs in the immersion freezing mode, with onset freezing temperatures in some cases as high as −3 ^∘C, similarly to the onset temperature from Pseudomonas syringae. The results show that the INP concentration in Sisal was higher than at other locations sampled with the same type of INP counter. Air masses arriving in Sisal after the passage of cold fronts have surprisingly higher INP concentrations than the campaign average, despite their lower total aerosol concentration. The high concentrations of INPs at warmer ice nucleation temperatures ($T>-\mathrm{15}$ ^∘C) and the supermicron size of the INPs suggest that biological particles may have been a significant contributor to the INP population in Sisal during this study. However, our observations also suggest that at temperatures ranging between −20 and −30 ^∘C mineral dust particles are the likely source of the measured INPs.

Most precipitation from deep clouds over the continents and in the intertropical convergence zone is strongly influenced by the presence of ice crystals whose formation requires the presence of ice nucleating particles (INPs). Although there are a large number of INP sources, the ice nucleating abilities of aerosol particles originating from oceans, deserts, and wildfires are poorly described at tropical latitudes. To fill this gap in knowledge, the National Autonomous University of Mexico micro-orifice uniform deposit impactor droplet freezing technique (UNAM-MOUDI-DFT) was constructed to measure the ice nucleating activity of aerosol samples that were collected in Sisal and Mérida, Yucatán (Mexico) under the influence of cold fronts, biomass burning (BB), and African dust (AD) intrusions during five short-term field campaigns between January 2017 and July 2018. The three different aerosol types were distinguished by their physicochemical properties. Marine aerosol (MA), BB, and AD air masses were found to contain INPs; the highest concentrations were in AD (from 0.071 to 36.07 L⁻¹ at temperatures between −18 and −27 ^∘C), followed by MA (from 0.068 to 18.90 L⁻¹ at temperatures between −15 and −28 ^∘C) and BB (from 0.063 to 10.21 L⁻¹ at temperatures between −20 and −27 ^∘C). However, MA had the highest surface active site densities (n_s) between −15 and −30 ^∘C. Additionally, supermicron particles contributed more than 72 % of the total INP concentration independent of aerosol type.

On a global scale, African dust is known to be one of the major sources of mineral dust particles, as these particles can be efficiently transported to different parts of the planet. Several studies have suggested that the Yucatán Peninsula could be influenced by such particles, especially in July, associated with the strengthening of the Caribbean low-level jet. Although these particles have the potential to significantly impact the local air quality, as shown elsewhere (especially with respect to particulate matter, PM), the arrival and impact of African dust in Mexican territory has not been quantitatively reported to date. Two short-term field campaigns were conducted to confirm the arrival of African dust on the Yucatán Peninsula in July 2017 and July 2018 at the Mérida atmospheric observatory (20.98^∘ N, 89.64^∘ W). Aerosol particles were monitored at ground level using different online and off-line sensors. Several PM_2.5 and PM₁₀ peaks were observed during both sampling periods, with a relative increase in the PM levels ranging between 200 % and 500 % with respect to the normal background conditions. Given that these peaks were found to be highly correlated with supermicron particles and chemical elements typically found in mineral dust particles, such as Al, Fe, Si, and K, they are linked with African dust. This conclusion is supported by combining back trajectories with vertical profiles from radiosondes, reanalysis, and satellite images to show that the origin of the air masses arriving at Mérida was the Saharan Air Layer (SAL). The good agreement found between the measured PM₁₀ concentrations and the estimated dust mixing ratio content from MERRA-2 (Version 2 of the Modern-Era Retrospective analysis for Research and Applications) corroborates the conclusion that the degradation of the local (and likely regional) air quality in Mérida is a result of the arrival of African dust.