4.8 Article

Aerosol Toxins Emitted by Harmful Algal Blooms Susceptible to Complex Air-Sea Interactions

期刊

ENVIRONMENTAL SCIENCE & TECHNOLOGY
卷 55, 期 1, 页码 468-477

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.est.0c05795

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资金

  1. Spanish Ministry of Science, Innovation and Universities [PGC2018095013-B400]
  2. Agency for Administration of University and Research Grants (Government of Catalonia, Spain) [2017SGR-310]
  3. Water Research Institute (IdRA) of the University of Barcelona
  4. CoCliME project, an ERA4CS Network (ERA-NET) by JPI Climate
  5. EPA (IE)
  6. ANR (FR)
  7. BMBF (DE)
  8. UEFISCDI (RO)
  9. RCN (NO)
  10. FORMAS (SE)
  11. European Union [690462]
  12. Agencia Estatal de Investigacion (AEI)
  13. Fondo Europeo de Desarrollo Regional (FEDER) [CTM2017-89117-R]
  14. Ramon y Cajal fellowship [RYC-2012-11922]

向作者/读者索取更多资源

Critical research is needed to study harmful algal blooms threatening ecosystems and human health, particularly through respiratory routes. This study used a marine aerosol generation tank to investigate the concentrations of toxins synthesized by a natural bloom in both water and air. The results suggest that the production and diffusion of marine toxins in the atmosphere are regulated by complex interactions between biological processes and air-sea aerosol production dynamics.
Critical research is needed regarding harmful algal blooms threatening ecosystem and human health, especially through respiratory routes. Additional complexity comes from the poorly understood factors involved in the physical production of marine aerosols coupled with complex biogeochemical processes at ocean surfaces. Here-by using a marine aerosol generation tank-five bubble-bursting experiments (with contrasting incubation times and, likely, physiological microalgal states) were run to investigate simultaneously the concentrations of the toxins, synthesized by a natural Ostreopsis cf. ovata bloom, in suspension in the water and in the atmosphere. The first two experiments (EXP1-2) were run with moderate levels of O. cf. ovata cell numbers (ca. 10(5) cells.L-1) and total toxin in suspension (4 x 10(6) pg.L-water(-1)) obtained at an early phase of the bloom. After 0.75-4 h incubation, toxin concentration in the aerosols accounted for 49-69 pg.L-air(-1). By striking contrast, three experiments (EXP3-5)-conducted with samples collected two weeks later with higher cell abundances and higher toxin concentration in the seston (respectively, about 1 x 10(6) cells.L-1 and 2 x 10(8) pg.L-water(-1)) and incubated for 21 h-showed about 15-fold lower atmospheric concentrations (3-4 pg.L-air(-1)), while important foam accumulation was observed in the water surface in the tank. Offline spectroscopic analysis performed by proton-nuclear magnetic resonance spectroscopy showed that the particulate organic carbon in the water was drastically different from that of bubble-bursting aerosols from the tank experiments-suggesting a selective transfer of organic compounds from seawater into the atmosphere. Overall, the results suggest that aerosol production and diffusion of marine toxins in the atmosphere are regulated by complex interactions between biological processes and air-sea aerosol production dynamics.

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