Le platane est un arbre de la famille des Platanaceae très commun en ville en particulier en Europe et dans toutes les zones tempérées. Les espèces du genre Platanus et plus particulièrement l’espèce Platanus orientalis, très répandue en Grèce, sont sévèrement attaquées par des agents phytopathogènes provoquant le chancre coloré du platane, l’anthracnose ou l’oïdium. En revanche, Platanus acerifolia, un hybride obtenu entre P. occidentalis and P. orientalis, très commun en France, se montre plus résistant vis-à-vis de ces pathogènes. L’étude par HPLC d’extraits de deux espèces de Platanaceae européennes P. acerifolia et P. orientalis a montré des différences selon le solvant d’extraction. L’extrait dichlorométhanique de P. acerifolia s’est montré plus riche en composés que l’espèce P. orientalis. Par contre, les chromatogrammes obtenus à partir des extraits méthanoliques sont très similaires et dominés par les deux composés majoritaires (tiliroside et platanoside). Des techniques préparatives comme la chromatographie de partage centrifuge (CPC), la moyenne pression (MPLC), la chromatographie sur colonne de Sephadex ou sur résine XAD-7 ont été utilisées afin d’isoler les différents constituants majoritaires et d’identifier les composés qui diffèrent d’une espèce à l’autre. L’élucidation structurale est réalisée grâce à des techniques telles que HR-EIS-MS et RMN 1D & 2D. L’étude de l’extrait dichlorométhanique nous a permis de compléter la connaissance phytochimique de ces deux plantes européennes et a conduit à l’isolement et à la détermination structurale de 38 molécules dont 7 composés nouveaux (1 coumarine, 3 flavonols prenylés, 2 dihydrochalcones, un terpénoïde. Par ailleurs, l’extrait méthanolique a conduit d’une part à l’isolement du tiliroside et du platanoside majoritaires et d’autre part à l’isolement de composés minoritaires, trente-trois autres molécules dont 5 nouveaux composés (1 flavonol glucosylé, 3 coumarines, 1 dihydrochalcone). Enfin, l’évaluation biologique des composés isolés in vitro ou in vivo a été réalisée sur différentes cibles : activités antifongiques, anti-âge, antioestrogéniques. Les activités cytotoxiques sur les cellules de cancer du sein MCF-7 et sur les cellules de cancer de l’endomètre (ISHIKAWA). / Platanus is a small genus of trees belonging to Platanaceae family, very common in Europe and temperate zones. Platanus species, and especially Platanus orientalis (Oriental plane), wide-spread in Greece are known to be severely attacked by phytopathogens such as Ceratocystis fimbriata f. sp. platani for canker stain, Apiognomonia veneta for anthracnose and Microsphaera platini for powdery mildew. However Platanus acerifolia (London plane), a hybrid between the P. occidentalis and P. orientalis, which is very common in France, have been found to be resistant to these pathogenic fungi. The HPLC profile of the dichloromethane extracts of the two species P. orientalis and P. acerifolia revealed a qualititative difference whereas, the methanol extracts were found to be similar with two predominant phenolic constituents (tiliroside and platanoside) present in both species. Further isolation and purification of their secondary metabolites were performed using various chromatographic techniques (CPC, MPLC, CC, XAD-7, Sephadex LH20, prep-TLC) and their identification was performed by HRMS and NMR (1 & 2D) spectroscopy. The studies of dichloromethane extract allowed us to deal with phytochemical knowledge of these two European plants in depth and led to isolation and structural elucidation of 38 compounds including 7 news constituents (1 coumarin, 3 flavonols, 2 dihydrochalcones and 1 terpenoid). Moreover, the methanol extract led to the isolation of their major constituents (tiliroside and platanoside) in one step. Furthermore, 33 minors compounds were isolated including 5 news compounds (one flavonol glycoside 3 coumarins and 1 dihydrochalcone). In addition, the isolated compounds have been subjected to in vitro or in vivo evaluation on different targets: antifungal, anti-ageing, anti-oestrogenic properties. Finally, the cytotoxic activity was studied on breast cancer cells (MCF-7) and endometrial cancer (Ishikawa).

In urban areas, trees are often planted in bare soil sidewalk openings (tree pits) which recently are being covered with permeable pavements. Pavements are known to alter soil moisture and temperature, and may have implications for tree growth, root development and depth, drought resilience, and sidewalk lifting. Furthermore, tree pits are often the only unsealed soil surface and are important for water exchange between soil and atmosphere. Therefore, covering tree pits with pavement, even permeable, may have implications for the urban water balance and stormwater management. A better understanding of permeable pavement on tree pavement soil system functioning can inform improved tree pit and street design for greater sustainability of urban environments. We conducted experiments at two sites in Virginia, USA (Mountains and Coastal Plain) with different climate and soil. At each location, we constructed 24 tree pits in a completely randomized experiment with two factors: paved with resin-bound porous-permeable pavement versus unpaved, and planted with Platanus x acerifolia 'Bloodgood' versus unplanted (n = 6). We measured tree stem diameter, root growth and depth, and soil water content and temperature over two growing seasons. We also monitored tree sap flow one week in June 2017 at the Mountains. In addition, we calibrated and validated a soil water flow model, HYDRUS-1D, to predict soil water distribution for different rooting depths, soil textures and pavement thicknesses. Trees in paved tree pits grew larger, with stem diameters 29% (Mountains) and 51% (Coastal Plain) greater. Roots developed faster under pavement, possibly due to the increased soil water content and the extended root growing season (14 more days). Tree transpiration was 33% of unpaved and planted pit water outputs, while it was 64% for paved and planted pits. In June 2016, planted pits had decreased root-zone water storage, while unplanted pits showed increased storage. A water balance of the entire experimental site showed overall decreased soil water storage due to tree water extraction becoming the dominant factor. HYDRUS-1D provided overall best results for model validation at 10 cm depth from soil surface (NSE = 0.447 for planted and paved tree pits), compared to 30- and 60 cm depths. HYDRUS-1D simulations with greater pavement thickness resulted in changes in predicted soil water content at the Coastal Plain, with higher values at 10- and 30-cm depths, but lower values at 60-cm depth. At the Mountains, virtually no difference was observed, possibly due to different soil texture (sandy vs clayey). Tree pits with permeable pavement accelerated tree establishment, but promoted shallower roots, possibly increasing root-pavement conflicts and tree drought susceptibility. Paved tree pits resulted in larger trees, increasing tree transpiration, but reduced soil evaporation compared to unpaved pits. Larger bare soil pits surrounded by permeable pavement might yield the best results to improve urban stormwater retention. Also, HYDRUS 1D was successful at simulating soil water content at 10-cm depth and may be valuable to inform streetscape design and planning. / PHD / Trees in cities are often planted in pavement cutouts (tree pits) that are usually the only available area for water exchange between soil and atmosphere. Tree pits are typically covered with a variety of materials, including permeable pavement. Pavements are known to modify soil water distribution and temperature, affecting tree growth, rooting depth, drought resilience, and sidewalk lifting. A better understanding of this system can inform tree pit and street design for greater sustainability. We constructed 24 tree pits at each of two regions in Virginia, USA (Mountains and Coastal Plain). These tree pits were paved with permeable pavement or unpaved, and planted with London Plane or unplanted. We measured stem diameter, root growth, and soil water content and temperature over two years and tree sap flow for one week in summer (Mountains only). We also used a soil water flow model, HYDRUS-1D, to predict water distribution for different rooting depths, soil textures and pavement thicknesses. After the first growing season trees in pavement were larger, with stem diameters 29% (Mountains) and 51% (Coastal Plain) greater. Roots developed faster under pavement, possibly due to increased soil water content and a 14-day increase in root growing season. Also, in June 2017, tree transpiration was 33% of unpaved-and-planted pit water outputs, and 64% of paved-and-planted pits. In June 2016, root-zone water storage decreased in planted pits but increased in unplanted pits. When considering the entire experimental site, soil water storage decreased, with tree water extraction being the dominant factor. HYDRUS-1D performed better at 10-cm soil depth than at 30- and 60-cm depths. At the Coastal Plain, HYDRUS-1D predicted higher soil water content at 10- and 30-cm depths with increased pavement thickness, but lower values at 60-cm depth. At the Mountains, there was no effect, possibly due to higher clay content. Permeable pavement accelerated tree establishment, but promoted shallower roots, increasing drought susceptibility and risk for root-pavement conflicts. Pavement resulted in larger trees and greater transpiration, but reduced soil evaporation. Larger bare-soil pits surrounded by permeable pavement might optimize stormwater retention.