Pascal Viville

Analysis of Pollen and Nectar of Arbutus unedo as a Food Source for Bombus terrestris (Hymenoptera : Apidae)

Abstract The mineral, total amino acid, and sterol compositions of pollen collected by Apis mellifera L. were compared with the pollen of a plant consumed by Bombus terrestris (L.): Arbutus unedo L. This plant provides the predominant food resource for the main autumn generation of B. terrestris in southern France. Honey bees also forage on this plant, although only for nectar. The mineral composition of 30 pollen samples collected by honey bees is close to the presently known requirements of A. mellifera, except for Cu and Mn, which are substantially lower. The total amino acid mean composition of a set of 54 pollen samples fits the basic requirements of honey bees except for valine, isoleucine, and methionine, which are present in lower concentrations in all the samples. For pollen of A. unedo, the amino acid balance is not very different from that of the survey. The main sterolic component in pollen of A. unedo, β-sitosterol, is known to have antifeedant effects on A. mellifera. Honey bees cannot dealkylate C29 sterols like β-sitosterol or δ5-avenasterol to obtain C27 cholesterol and ecdysteroids. Because these phytosterols as well as cholesterol are nearly absent from pollen of A. unedo, the metabolic capabilities of Apis seem unadapted to this plant. On the contrary, pollen of A. unedo is freely consumed by B. terrestris, which develops huge autumn populations solely on this food. These data indicate that the sterolic metabolisms of B. terrestris and A. mellifera differ, allowing separation in foraging activity.

Design and Use of Organic Nanoparticles Prepared from Star-Shaped Polymers with Reactive End Groups

Star-shaped poly(isobornyl acrylate) (PiBA) was prepared by atom transfer radical polymerization (ATRP) using multifunctional initiators. The optimal ATRP conditions were determined to minimize star-star coupling and to preserve high end group functionality (>90%). Star-shaped PiBA with a narrow polydispersity index was synthesized with 4, 6, and 12 arms and of varying molecular weight (10,000 to 100,000 g x mol(-1)) using 4 equiv of a Cu(I)Br/PMDETA catalyst system in acetone. Matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) analysis, NMR spectroscopy, and size exclusion chromatography (SEC) confirmed their controlled synthesis. The bromine end group of each arm was then transformed to a reactive end group by a nucleophilic substitution with methacrylic acid or cinnamic acid (conversion >90%). These reactive star polymers were used to prepare PiBA nanoparticles by intramolecular polymerization of the end groups. The successful preparation of this new type of organic nanoparticles on a multigram scale was proven by NMR spectroscopy and SEC. Subsequently, they have been used as additives for linear, rubbery poly(n-butyl acrylate). Rheology measurements indicated that the viscoelastic properties of the resulting materials can be fine-tuned by changing the amount of incorporated nanoparticles (1-20 wt %), as a result of the entanglements between the nanoparticles and the linear polymers.

Micro- and nanostructure of the adhesive material secreted by the tube feet of the sea star Asterias rubens

To attach to underwater surfaces, sea stars rely on adhesive secretions produced by specialised organs, the tube feet. Adhesion is temporary and tube feet can also voluntarily become detached. The adhesive material is produced by two types of adhesive secretory cells located in the epidermis of the tube foot disc, and is deposited between the disc surface and the substratum. After detachment, this material remains on the substratum as a footprint. Using LM, SEM, and AFM, we described the fine structure of footprints deposited on various substrata by individuals of Asterias rubens. Ultrastructure of the adhesive layer of attached tube feet was also investigated using TEM. Whatever the method used, the adhesive material appeared as made up of globular nanostructures forming a meshwork deposited on a thin homogeneous film. This appearance did not differ according to whether the footprints were fixed or not, and whether they were observed hydrated or dry. TEM observations suggest that type 2 adhesive cells would be responsible for the release of the material constituting the homogeneous film whereas type 1 adhesive cells would produce the material forming the meshwork. This reticulated pattern would originate from the arrangement of the adhesive cell secretory pores on the disc surface.

Morphology and roughness of high-vacuum sublimed oligomer thin films

Abstract We present an atomic force microscopy study on the morphology and roughness of sexithienyl (T6) thin films evaporated on mica in high vacuum. The effects of two thermal processes are investigated: (i) temperature of the substrate during evaporation, and (ii) annealing temperature in high vacuum. The former yields a good control on the extension of grain boundaries and the aggregate ordering, but does not affect surface roughness. The latter is characterized by a threshold temperature (~ 175 °C) above which a smooth continuous surface is formed. The roughness scaling behaviour is analysed by the power spectrum of the topographical profiles. T6 surface is self-affine over 1–2 orders of magnitude of the spatial frequencies. However, films prepared at substrate temperatures above 200 °C or annealed above the critical temperature exhibit an extended self-affine behaviour. The roughness scaling factor suggests a growth process of the Kardar-Parisi-Zhang universality class.

Miscibility between differently shaped mesogens: Structural and morphological study of a phthalocyanine-perylene binary system.

The thermotropic, structural, and morphological properties of blends of a disk-like liquid crystalline phthalocyanine derivative and a lath-shaped perylenetetracarboxidiimide mesogen derivative have been studied by combining differential scanning calorimetry, thermal polarized optical microscopy, X-ray diffraction, solid-state nuclear magnetic resonance, and atomic force microscopy. The two compounds are fully miscible for blends containing at least 60 mol % of the disk-like molecule. In such composition range, the homogeneous blends form a columnar hexagonal (Col(h)) mesophase for which the thermal stability is enhanced compared to that of the corresponding mesophase of the pure phthalocyanine. The miscible blends self-align homeotropically between two glass slides. For blends containing between 55 and 40 mol % of the disk-shaped molecule, the two components are fully miscible at high temperature but the perylene derivative forms a separate crystalline phase when the temperature is decreased. Phase separation is systematically observed in blends containing less than 40 mol % of the discotic molecule. In this case, the resulting Col(h) mesophase is less stabilized compared to the blends containing a larger amount of the phthalocyanine derivative. These phase-separated blends do not show any homeotropic alignment. AFM investigations confirm the formation of a single columnar morphology in the phthalocyanine-rich blends, consistent with the full miscibility between the two compounds. Solid-state NMR measurements on the mixed phase show the influence of the presence of the perylene molecules on the molecular dynamics of the molecules; remarkably, the presence of the host molecules improves the local order parameter in the phthalocyanine columnar phase.

PTFE Surface Etching in the Post-discharge of a Scanning RF Plasma Torch: Evidence of Ejected Fluorinated Species

The texturization of poly(tetrafluoroethylene) (PTFE) surfaces is achieved at atmospheric pressure by using the post-discharge of a radio-frequency plasma torch supplied in helium and oxygen gases. The surface properties are characterized by contact angle measurement, X-ray photoelectron spectroscopy and atomic force microscopy. We show that the plasma treatment increases the surface hydrophobicity (with water contact angles increasing from 115 to 1558) only by modifying the PTFE surface morphology and not the stoichiometry. Measurements of sample mass losses correlated to the ejection of CF2 fragments from the PTFE surface evidenced an etching mechanism at atmospheric pressure.

Substrate‐Induced Crystal Plastic Phase of a Discotic Liquid Crystal

A new phase of a known discotic liquid crystal is observed at the interface with a rigid substrate. The structure of the substrate-induced phase has been characterized by atomic force microscopy, specular X-ray diffraction, and small-angle and wide-angle grazing incidence X-ray diffraction. The substrate-induced phase, which has a thickness of ∼30 nm and a tetragonal symmetry, differs notably from the bulk phase. The occurrence of such phase casts a new light on alignment of discotic liquid crystals.

Evidence of the Synergetic Role of Charged Species and Atomic Oxygen in the Molecular Etching of PTFE Surfaces for Hydrophobic Surface Synthesis

The transformation of a poly(tetrafluoroethylene) (PTFE) hydrophobic surface into a superhydrophobic one using a low pressure RF plasma is explored using optical emission spectrometry (OES), X-ray photoelectron spectroscopy (XPS), water contact angle (WCA) measurements, mass measurements, and atomic force microscopy (AFM). It is shown that the increase in contact angle is due to an increase of roughness provoked by a chemical etching of the surface. We propose a molecular mechanism for etching that requires the simultaneous presence of atomic oxygen and negatively charged species (electrons) at the PTFE surface.

Synthesis and texturization processes of (super)-hydrophobic fluorinated surfaces by atmospheric plasma

The atmospheric pressure PECVD deposition and texturization of hydrophobic coatings using liquid fluorinated C6F12 and C6F14 precursors are investigated. The effect of the carrier gas (argon and helium) is discussed in terms of the behavior of the gas phase and of the characteristics of the deposited film. Mass spectrom-etry measurements indicate that the fragmentation is higher with argon while helium reacts very easily with oxygen impurities leading to the formation of CxFyOz compounds. These observations are consistent with the chemical composition of the films determined by XPS and the variation in the deposition rate. Moreover, the streamers present in the argon discharge affect the morphology of the surface by increasing the roughness, which leads to the increase in the hydrophobicity of the coatings.

Surface and Fouling-Release Properties of Silicone/Organomodified Montmorillonite Coatings

Poly(dimethylsiloxane) (PDMS)/organomodified montmorillonite (OMMT) nanocomposites have been prepared, characterised and the fouling-release properties of these materials have been studied through laboratory assays involving a representative soft-fouling species, the green alga, Ulva. The bulk mechanical properties of the polymer matrix have been slightly changed by the addition of OMMT, i.e., to a higher Youngs modulus value. The surface properties of the nanocomposites were modified after immersion in water. Indeed, it appears that the surface topography, as observed with AFM, is affected by the presence of OMMT after immersion in water. The data indicate that the modified surface affects the fouling release behaviour of sporelings (young plants) of Ulva; percentage removal by hydrodynamic shear stress increases from 28% for the unfilled PDMS control to 78% for the 2 wt% filled coating.