Harmonia axyridis (Pallas) secondary metabolites quantification in relation with aposematism : Part I : Harmonine quantificationFischer, Christophe ; Heuskin, Stéphanie ; Laurent, Pascal et alPoster (2010, January) These last few years, the multicoloured Asian ladybird, Harmonia axyridis Pallas (Insects: Coleoptera: Coccinellidae), an invasive species, has swiftly spread out in Europe. This aposematic and highly ... [more ▼] These last few years, the multicoloured Asian ladybird, Harmonia axyridis Pallas (Insects: Coleoptera: Coccinellidae), an invasive species, has swiftly spread out in Europe. This aposematic and highly polymorphic insect is problematic in several ways. It seems to outcompete native coccinellid species; they can group on fruits in vineyards and spoil wine when crushed with grapes; they can aggregate by hundreds in houses to winter. This study aims to investigate the relations between the chemical defences of H. axyridis and warning signals expressed by this bug. To achieve this goal, two original quantification methods of H. axyridis secondary metabolites have been undertaken. The first one allows Fast-GC quantifying harmonine, its main defence alkaloid. The other one permits to determine its emission rate of 2-isopropyl-3-methoxypyrazine, a highly odorous compound probably involved in the communication between individuals and in the aposematism of this insect. This last point will be detailed in another poster. Firstly, a method of extraction, acetylation and purification of harmonine from H. axyridis has been devised to obtain a calibration standard because this molecule is not commercially available. The identity of the extracted compound has been confirmed by mass spectrometry and multidimensional NMR. The GC purity of this N,N-diacetylharmonine is of 100%. During the experiments, its stability in acetone solution at 4°C has been verified. Using this purified molecule, an original method of harmonine quantification has been developed by fast gas chromatography and validated using accuracy profile. The method has been validated for concentrations ranging from 28µg/ml to more than 264µg/ml, with a maximal error risk of 20%. From about 100µg/ml, peaks symmetry decreased, but did not influence the quantification. That accuracy profile validation has been compared with a more classical validation using AOAC (2006) norm, which confirmed the first validation. This method allows quantifying harmonine in one single insect. Harmonine has been quantified in 80 H. axyridis divided into four groups of at least 15 individuals on basis of the morph type and the elytra hue. Males and females harmonine contents did not significantly differ. The mean harmonine content was of 106.6µg/individual with a standard deviation of 80.2µg/individual. The results distribution obtained was not normal and a strong variability between individuals was observed, which explains the high standard deviation. These results and those of the pyrazine and colour analysis have been statistically analyzed in order to show potential correlations between these factors. It would appear that elytra colour is linked with the insect harmonine content. Individuals with a non-melanic orange colour presented harmonine content significantly higher than other studied colours. The harmonine content does not seem linked to the pyrazine emission rate. [less ▲] Detailed reference viewed: 149 (23 ULg) Harmonia axyridis (Pallas) secondary metabolites quantification in relation with aposematism : Part II : Pyrazine quantificationFischer, Christophe ; Heuskin, Stéphanie ; Marlet, Christelle et alPoster (2010, January) The main objective of this study is to investigate the presence of links between chemical defences and warning signals presented by Harmonia axyridis (Pallas), the multicoloured Asian ladybird (Insects ... [more ▼] The main objective of this study is to investigate the presence of links between chemical defences and warning signals presented by Harmonia axyridis (Pallas), the multicoloured Asian ladybird (Insects: Coleoptera: Coccinellidae). This second part describes an original quantification method for 2-isopropyl-3-methoxypyrazine (IPMP) by active sampling on thermally desorbed adsorbent (TD) coupled with GC-MS analysis. This highly odorous compound is supposed to be implicated in intra- and interspecific communication. In order to allow harmonine quantification (a defence alkaloid, see Part 1), this method avoid any hemolymph loses by the ladybird (Coccinellids can emit hemolymph when stressed). This method is non-lethal and applicable on one single insect. The quantification method has been validated from 37,5pg to 10 000 pg per adsorbent cartridge. On this range, there is no breakthrough and desorption is complete (>99.4%). At the LOQ (37.5pg/cartridge), the bias is of 20%, but rapidly decreased to less than 5% on the rest of the validated range (100 to 10 000 pg/cartridge). According to AOAC (2006) norm, this method is repeatable but not reproducible. The IPMP emission rate following a stress has been quantified on 80 H. axyridis grouped in four classes on basis of the morph type and the elytra hue. Males and females emission rates did not significantly differ. The mean emission rate is of 707 pg/4h with an extremely high standard deviation of 1766pg/4h due to a great individual variability and a strongly asymmetric distribution of the results. These results and those of the harmonine and colour analysis have been statistically analyzed in order to show potential correlations between these factors. It seems that elytra colour is linked with the insect IPMP emission rate. Individuals with a melanic red colour presented IPMP emission rate significantly lower than other studied colours. The harmonine content does not seem linked to the pyrazine emission rate. [less ▲] Detailed reference viewed: 76 (7 ULg) Harmonic analysis of tidal elevations and currents, improvements and statistical study of the resultsMouchet, Anne ![]() Poster (1991, August) Detailed reference viewed: 1 (0 ULg) Harmonic Trusses : the Search for Minimum Weight; Latteur, Pierre ![]() (1998, February) Detailed reference viewed: 16 (0 ULg) Harmonic-Balance Finite-Element Modelling of Electromagnetic Devices: A Novel Approach; Dular, Patrick ; Geuzaine, Christophe et alin IEEE Transactions on Magnetics (2002), 38(2), 521--524 Detailed reference viewed: 13 (2 ULg) L'harmonisation des conditions individuelles de travail en cas de transfert conventionnel d'entrepriseKefer, Fabienne ![]() in La cession d'entreprise: les aspects sociaux (2011) Detailed reference viewed: 6 (0 ULg) L’harmonisation des conditions individuelles de travail en cas de transfert conventionnel d’entrepriseKefer, Fabienne ![]() in La cession d’entreprise : les aspects sociaux (2011, April 07) Detailed reference viewed: 19 (2 ULg) Harmonisation des démarches de validation, est-elle possible ?Hubert, Philippe ; Chiap, Patrice ; et alConference (2003) Detailed reference viewed: 19 (1 ULg) Harmonisation des strategies de validation et estimation de l'incertitude associee dans le cadre de l'accreditation des laboratoires d'essaisHubert, Philippe ; Rozet, Eric ; Boulanger, Bruno et alin Acta Clinica Belgica. Supplementum (2006), S1(1), 53-55 In order to achieve the harmonization of validation strategies, the interpretation of several validation criteria is proposed. Furthermore, a simple and visual decision tool to assess the validity of an ... [more ▼] In order to achieve the harmonization of validation strategies, the interpretation of several validation criteria is proposed. Furthermore, a simple and visual decision tool to assess the validity of an analytical procedure is described: the accuracy profile based on the estimation of the total error of the measurements. This profile build with beta-expectation tolerance intervals can also compute with efficiency the uncertainty related to the results of a laboratory, which is an essential parameter for the accreditation of laboratories under ISO 17025. [less ▲] Detailed reference viewed: 58 (14 ULg) Harmonisation des stratégies de validation, utopie ou réalité ?Hubert, Philippe ; Boulanger, Bruno ; Dewé, Walthère et alConference (2004) Detailed reference viewed: 7 (2 ULg) Harmonisation du droit de la construction et protection du consommateurKohl, Benoît ![]() Scientific conference (2008, May 08) Detailed reference viewed: 9 (0 ULg) Harmonisation et constructionKohl, Benoît ![]() Article for general public (2009) Detailed reference viewed: 32 (14 ULg) Harmonisation européenne des critères d'interprétation de l'Antibiogramme: Pourquoi, Quand, Difficultés et solutionsMELIN, Pierrette ![]() Conference (2009, June 18) Detailed reference viewed: 5 (0 ULg) Harmonisation européenne des critères d'interprétation de l'Antibiogramme: Pourquoi, Quand, Difficultés et solutionsMELIN, Pierrette ![]() Scientific conference (2009, June 09) Detailed reference viewed: 8 (0 ULg) Harmonisation européenne des critères d'interprétation de l'Antibiogramme: Pourquoi, Quand, Difficultés et solutionsMELIN, Pierrette ![]() Conference (2009, November 20) Detailed reference viewed: 12 (1 ULg) Harmonisation européenne des critères d'interprétation de l'Antibiogramme: Pourquoi, Quand, Difficultés et solutionsMelin, Pierrette ![]() Conference (2009, May 06) Detailed reference viewed: 2 (0 ULg) Harmonisation of European Construction Law : Consumers FirstKohl, Benoît ![]() Conference (2008, September 04) Detailed reference viewed: 13 (0 ULg) Harmoniser le prix du livre importé de France. Impact d’un mark-up sur le consommateur, le secteur de la librairie et la diversité culturelleHabrand, Tanguy ![]() Report (2010) Detailed reference viewed: 49 (7 ULg) Harmonization of clinical practice guidelines for the prevention and treatment of osteoporosis and osteopenia in Europe : a difficult challengeReginster, Jean-Yves ![]() in Calcified Tissue International (1996), 59(S1), 24-29 Detailed reference viewed: 3 (1 ULg) Harmonization of strategies for the validation of quantitative analytical procedures - A SFSTP proposal - part IHubert, Philippe ; ; Boulanger, Bruno et alin Journal of Pharmaceutical & Biomedical Analysis (2004), 36(3), 579-586 This paper is the first part of a summary report of a new commission of the Societe Francaise des Sciences et Techniques Pharmaceutiques (SFSTP). The main objective of this commission was the ... [more ▼] This paper is the first part of a summary report of a new commission of the Societe Francaise des Sciences et Techniques Pharmaceutiques (SFSTP). The main objective of this commission was the harmonization of approaches for the validation of quantitative analytical procedures. Indeed, the principle of the validation of theses procedures is today widely spread in all the domains of activities where measurements are made. Nevertheless. this simple question of acceptability or not of an analytical procedure for a given application, remains incompletely determined in several cases despite the various regulations relating to the good practices (GLP, GMP,...) and other documents of normative character (ISO, ICH. FDA,...). There are many official documents describing the criteria of validation to be tested, but they do not propose any experimental protocol and limit themselves most often to the general concepts. For those reasons, two previous SFSTP commissions elaborated validation guides to concretely help the industrial scientists in charge of drug development to apply those regulatory recommendations. If these two first guides widely contributed to the use and progress of analytical validations, they present, nevertheless, weaknesses regarding the conclusions of the performed statistical tests and the decisions to be made with respect to the acceptance limits defined by the use of an analytical procedure. The present paper proposes to review even the bases of the analytical validation for developing harmonized approach, by distinguishing notably the diagnosis rules and the decision rules. This latter rule is based on the use of the accuracy profile, uses the notion of total error and allows to simplify the approach of the validation of an analytical procedure while checking the associated risk to its usage. Thanks to this novel validation approach, it is possible to unambiguously demonstrate the fitness for purpose of a new method as stated in all regulatory documents. (C) 2004 Elsevier B.V. All rights reserved. [less ▲] Detailed reference viewed: 183 (30 ULg) |
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