Impact of North America on the aerosol composition in the North Atlantic free troposphere
In the AEROATLAN project we study the composition of aerosols collected over ∼ 5 years at Izaña Observatory (located at ∼ 2400 m a.s.l. in Tenerife, the Canary Islands) under the prevailing westerly airflows typical of the North Atlantic free troposphere at subtropical latitudes and midlatitudes. Ma...
| Published in: | Atmospheric Chemistry and Physics |
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| Main Authors: | , , |
| Format: | Text |
| Language: | English |
| Published: |
2018
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| Subjects: | |
| Online Access: | https://doi.org/10.5194/acp-17-7387-2017 https://www.atmos-chem-phys.net/17/7387/2017/ |
| Summary: | In the AEROATLAN project we study the composition of aerosols collected over ∼ 5 years at Izaña Observatory (located at ∼ 2400 m a.s.l. in Tenerife, the Canary Islands) under the prevailing westerly airflows typical of the North Atlantic free troposphere at subtropical latitudes and midlatitudes. Mass concentrations of sub-10 µm aerosols (PM 10 ) carried by westerly winds to Izaña, after transatlantic transport, are typically within the range 1.2 and 4.2 µg m −3 (20th and 80th percentiles). The main contributors to background levels of aerosols (PM 10 within the 1st–50th percentiles = 0.15–2.54 µg m −3 ) are North American dust (53 %), non-sea-salt sulfate (14 %) and organic matter (18 %). High PM 10 events (75th–95th percentiles ≈ 4.0–9.0 µg m −3 ) are prompted by dust (56 %), organic matter (24 %) and non-sea-salt sulfate (9 %). These aerosol components experience a seasonal evolution explained by (i) their spatial distribution in North America and (ii) the seasonal shift of the North American outflow, which migrates from low latitudes in winter (∼ 32° N, January–March) to high latitudes in summer (∼ 52° N, August–September). The westerlies carry maximum loads of non-sea-salt sulfate, ammonium and organic matter in spring (March–May), of North American dust from midwinter to mid-spring (February–May) and of elemental carbon in summer (August–September). Our results suggest that a significant fraction of organic aerosols may be linked to sources other than combustion (e.g. biogenic); further studies are necessary for this topic. The present study suggests that long-term evolution of the aerosol composition in the North Atlantic free troposphere will be influenced by air quality policies and the use of soils (potential dust emitter) in North America. |
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