2016
DOI: 10.1016/j.scitotenv.2016.01.193
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Modeling olive pollen intensity in the Mediterranean region through analysis of emission sources

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Cited by 52 publications
(21 citation statements)
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“…To identify the origin and the dispersion processes of airborne pollen grains, the most wide-spread approach is to use dispersion models [30][31][32][33]. To date, only few studies have focused on airborne pollen grains origins and point sources using local meteorological data associated with multiple observation sites [34][35][36]. The current work is based on a 4-years dataset of daily monitoring of airborne pollen at Saclay, a peri-urban site in the Paris region which represents 20% of the French population on only 2% of the French territory surface.…”
Section: Introductionmentioning
confidence: 99%
“…To identify the origin and the dispersion processes of airborne pollen grains, the most wide-spread approach is to use dispersion models [30][31][32][33]. To date, only few studies have focused on airborne pollen grains origins and point sources using local meteorological data associated with multiple observation sites [34][35][36]. The current work is based on a 4-years dataset of daily monitoring of airborne pollen at Saclay, a peri-urban site in the Paris region which represents 20% of the French population on only 2% of the French territory surface.…”
Section: Introductionmentioning
confidence: 99%
“…For example, in fragmented populations of Fraxinus excelsior pollen immigration was between 43 and 68 % (Bacles and Ennos, 2008). The possibility of LDD by pollen in wild and cultivated olive has been observed in different studies (Alba et al, 2006;Pinillos and Cuevas, 2009;Fern andez-Rodr ıguez et al, 2014;Rojo et al, 2016). In particular, studying the potential sources of airborne Olea pollen in the south-west Iberian Peninsula, Fern andezRodr ıguez et al (2014) showed that olive pollen can spread even at the regional scale (up to 200-300 km).…”
Section: Contemporary Pollen Flowmentioning
confidence: 96%
“…A Neubauer chamber (Brand™ 717820, Fisher Scientific SL, Madrid, Spain) was used for pollen counting [42,43]. The resulting value was divided by 2 due to the number of anthers used [43,44]. It was then multiplied by 5, corresponding to the number of anthers per flower [45], and by the total number of flowers on each vine.…”
Section: In Vitro Assays and Laboratory Analysismentioning
confidence: 99%