<?xml version="1.0" encoding="ISO-8859-1"?><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
<front>
<journal-meta>
<journal-id>0718-221X</journal-id>
<journal-title><![CDATA[Maderas. Ciencia y tecnología]]></journal-title>
<abbrev-journal-title><![CDATA[Maderas, Cienc. tecnol.]]></abbrev-journal-title>
<issn>0718-221X</issn>
<publisher>
<publisher-name><![CDATA[Universidad del Bío-Bío]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0718-221X2012000300008</article-id>
<article-id pub-id-type="doi">10.4067/S0718-221X2012005000008</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Valorization of Moroccan olive stones by using it in particleboard panels]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Elbir]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Moubarik]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Rakib]]></surname>
<given-names><![CDATA[E.M]]></given-names>
</name>
<xref ref-type="aff" rid="A03"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Grimi]]></surname>
<given-names><![CDATA[N]]></given-names>
</name>
<xref ref-type="aff" rid="A04"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Amhoud]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Miguel]]></surname>
<given-names><![CDATA[G]]></given-names>
</name>
<xref ref-type="aff" rid="A05"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Hanine]]></surname>
<given-names><![CDATA[H]]></given-names>
</name>
<xref ref-type="aff" rid="A06"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Artaud]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
<xref ref-type="aff" rid="A07"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Vanloot]]></surname>
<given-names><![CDATA[P]]></given-names>
</name>
<xref ref-type="aff" rid="A07"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Mbarki]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,University Sultan Moulay Slimane Faculty of Science and Technology Equipe Systèmes Chimiques Complexes]]></institution>
<addr-line><![CDATA[Beni Mellal ]]></addr-line>
<country>Morocco</country>
</aff>
<aff id="A02">
<institution><![CDATA[,ENSET MAScIR-NANOTECH ]]></institution>
<addr-line><![CDATA[Rabat ]]></addr-line>
<country>Morocco</country>
</aff>
<aff id="A03">
<institution><![CDATA[,University Sultan Moulay Slimane Faculty of Sciences and Technology Laboratory of Organic and Analytical Chemistry]]></institution>
<addr-line><![CDATA[Beni-Mellal ]]></addr-line>
<country>Morocco</country>
</aff>
<aff id="A04">
<institution><![CDATA[,Université de Technologie de Compiègne Centre de Recherche de Royallieu ]]></institution>
<addr-line><![CDATA[Compiègne ]]></addr-line>
<country>France</country>
</aff>
<aff id="A05">
<institution><![CDATA[,University of Algarve Department of Biotechnology ]]></institution>
<addr-line><![CDATA[Faro ]]></addr-line>
<country>Portugal</country>
</aff>
<aff id="A06">
<institution><![CDATA[,Université Sultan Moulay Slimane Faculté des Sciences et Techniques Laboratoire de Valorisation et Sécurité des Produits Agro-alimentaires]]></institution>
<addr-line><![CDATA[Beni-Mellal ]]></addr-line>
<country>Morocco</country>
</aff>
<aff id="A07">
<institution><![CDATA[,Université Paul Cézanne Equipe AD2EM ]]></institution>
<addr-line><![CDATA[Marseille ]]></addr-line>
<country>France</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>11</month>
<year>2012</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>11</month>
<year>2012</year>
</pub-date>
<volume>14</volume>
<numero>3</numero>
<fpage>361</fpage>
<lpage>371</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.cl/scielo.php?script=sci_arttext&amp;pid=S0718-221X2012000300008&amp;lng=en&amp;nrm=iso&amp;tlng=en"></self-uri><self-uri xlink:href="http://www.scielo.cl/scielo.php?script=sci_abstract&amp;pid=S0718-221X2012000300008&amp;lng=en&amp;nrm=iso&amp;tlng=en"></self-uri><self-uri xlink:href="http://www.scielo.cl/scielo.php?script=sci_pdf&amp;pid=S0718-221X2012000300008&amp;lng=en&amp;nrm=iso&amp;tlng=en"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[The main objective of this work was to find new applications to valorize olive stones (endocarp and seed). In order to improve knowledge on olive stones, the phenolic compounds concentration of three varieties of Moroccan olive trees: Moroccan Picholine, Menara and Haouzian were studied. Olive stones of three varieties were characterized by Fourier Transform Mid Infrared Spectroscopy (FT-MIR). Total phenolic compounds are quantified after solid-liquid extraction by an assay of Folin-Ciocalteu. Moroccan Picholine stones (11.32 mg GAE/g DM) have a higher content of total phenolic compounds than Haouzia stones (4.55 mg GAE/g DM) and Menara stones (3.56 mg GAE/g DM). Thermogravimetric analysis indicates that up to 195°C; there is no degradation of the stones. The biocide performance on agar-agar was tested with decay fungi. Biodegradation studies show that the most interesting results are obtained with Moroccan Picholine stones. The presence of Moroccan Picholine in a particleboard panels improves the total resistance of the particleboard panels against both Coriolus versicolor and Coniophora puteana rot fungi.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[Decay resistance]]></kwd>
<kwd lng="en"><![CDATA[olive stone]]></kwd>
<kwd lng="en"><![CDATA[particleboard]]></kwd>
<kwd lng="en"><![CDATA[phenolic compounds]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[ <p align="justify"><font face="verdana" size="2">Maderas. Ciencia y tecnolog&iacute;a    2012; 14 (3):361-371</font></p>  	    <p></p>     <p align="right"><font face="verdana" size="2"><strong><font size="2" face="Verdana, Arial, Helvetica, sans-serif"><strong>ART&Iacute;CULO</strong></font></strong></font></p>     <p align="center"><font face="verdana" size="4"><strong>Valorization of Moroccan    olive stones by using it in particleboard panels    <br>   </strong></font></p>     <p align="justify"><font face="verdana" size="2"><strong>M. Elbir<sup>1</sup>,    A. Moubarik<sup>2&#9824;</sup>, E.M. Rakib<sup>3</sup>, N. Grimi<sup>4</sup>,    A. Amhoud<sup>1</sup>, G. Miguel<sup>5</sup>, H. Hanine<sup>6</sup>, J. Artaud<sup>7</sup>,    P. Vanloot<sup>7</sup>, M. Mbarki<sup>1    <br>   </sup></strong><sup>1</sup>Equipe Syst&egrave;mes Chimiques Complexes, Faculty    of Science and Technology, University Sultan Moulay Slimane. PB 523, Beni Mellal,    Morocco.    <br>   <sup>2</sup>MAScIR-NANOTECH, ENSET, Avenue de l'Arm&eacute;e Royale, Madinat    El Irfane, 10100 Rabat, Morocco.    <br>   <sup>3</sup> Laboratory of Organic and Analytical Chemistry, Faculty of Sciences    and Technology, University Sultan Moulay Slimane., B.P 523, Beni-Mellal, Morocco.    <br>   <sup>4</sup> Universit&eacute; de Technologie de Compi&egrave;gne EA 4297 TIMR,    UTC/ESCOM, Centre de Recherche de Royallieu, B.P. 20529, 60205 Compi&egrave;gne,    France.    ]]></body>
<body><![CDATA[<br>   <sup>5</sup>Department of Biotechnology, University of Algarve, Faro, Portugal.    <br>   <sup>6</sup>Laboratoire de Valorisation et S&eacute;curit&eacute; des Produits    Agro-alimentaires, Facult&eacute; des Sciences et Techniques, Universit&eacute;    Sultan Moulay Slimane, B.P 523, Beni-Mellal, Morocco    <br>   <sup>7</sup>ISM2, UMR 6263, Equipe AD2EM, Universit&eacute; Paul C&eacute;zanne,    case 451, 13397 Marseille Cedex 20, France.</font> </p>  	    <p align="left"><font size="2" face="Verdana, Arial, Helvetica, sans-serif"><a href="#back">Corresponding    author</a> </font></p> <hr align="center" size="1" noshade> <font face="verdana" size="2"><b>ABSTRACT</b></font>    <p></p>     <p align="justify"><font face="verdana" size="2"> The main objective of this work    was to find new applications to valorize olive stones (endocarp and seed). In    order to improve knowledge on olive stones, the phenolic compounds concentration    of three varieties of Moroccan olive trees: Moroccan Picholine, Menara and Haouzian    were studied. Olive stones of three varieties were characterized by Fourier    Transform Mid Infrared Spectroscopy (FT&#45;MIR). Total phenolic compounds are    quantified after solid&#45;liquid extraction by an assay of Folin&#45;Ciocalteu.    Moroccan Picholine stones (11.32 mg GAE/g DM) have a higher content of total    phenolic compounds than Haouzia stones (4.55 mg GAE/g DM) and Menara stones    (3.56 mg GAE/g DM). Thermogravimetric analysis indicates that up to 195&deg;C;    there is no degradation of the stones. The biocide performance on agar&#45;agar    was tested with decay fungi. Biodegradation studies show that the most interesting    results are obtained with Moroccan Picholine stones. The presence of Moroccan    Picholine in a particleboard panels improves the total resistance of the particleboard    panels against both <i>Coriolus versicolor</i> and <i>Coniophora puteana</i>    rot fungi.</font> </p>     <p align="justify"><font face="verdana" size="2"><b>Keywords:</b> Decay resistance,    olive stone, particleboard, phenolic compounds</font><font face="verdana" size="2"><b>&nbsp;</b></font></p>  	 <hr align="center" size="1" noshade> <font face="verdana" size="3"><strong>INTRODUCTION</strong></font>    <p></p>     <p align="justify"><font face="verdana" size="2">Oleaceae is a family comprising    600 species in 25 genera. Many of the genera are economically important such    as the olive (<i>Olea europaea</i>) which is cultivated for its fruit and oil    (Wallander and Albert 2000). The olive tree is among the oldest woody crops    and is particularly widespread throughout the Mediterranean region and plays    an important role in its rural economy, local heritage, and environment protection.    The largest producing countries are located in the Mediterranean and Middle    East regions providing 98% of the total cultivated surface area, and 99% of    the total olive fruit production (Niaounakis and Halvadakis 2006, Besnard <i>et    al</i>. 2011).</font></p>     <p align="justify"><font face="verdana" size="2"><i>Olea europaea</i> dried fruit    has pharmacological properties, such as anti&#45;bacterial, anti&#45;viral,    anti&#45;inflammatory activities and detoxification (Ding 1999). Such properties    have been attributed to the presence of many compounds including phenols. Olive    fruits are rich in phenolic compounds that represent 1 to 14% weight of dry    pulp. The phenolic composition in the various parts of the fruit is complex    depending on the variety, collection season, growing conditions, and time of    ripening (Solinas <i>et al.</i> 1975, Vlahov 1992, Esti <i>et al.</i> 1998,    Romani <i>et al</i>. 1999). Very few studies have focused upon the phenolic    composition of olive seeds, nevertheless some phenolic compounds have been identified    including salidroside, nuzhenide, hydroxytyrosol, nuzhenide 11&#45;methyl oleoside,    oleuropein, tyrosol, and demethyloleuropein (<a href="#F1">Figure 1</a>) at    all stages of maturation (Maestro&#45;Dur&aacute;n <i>et al.</i> 1994, Servili    <i>et al</i>.1999, Silva <i>et al.</i> 2010).</font></p>     ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2">The olive stones and seeds are    an important by&#45;product generated in the olive oil extraction. Generally,    this material is used as combustible to produce electric energy or heat. A large    number of research articles have been published dealing with the chemical composition    of olives and olive oil. However, only a few studies have been dedicated to    analyzing the components and uses of the olive stone (Rodr&iacute;guez <i>et    al</i>. 2008).</font></p>     <p align="justify"><font face="verdana" size="2">The main objectives of this work    are the extraction of phenolic compounds, the characterization (chemical, thermal    and biological) and the valorization of Moroccan olive stones in particleboard    panels.</font></p>     <p align="center">&nbsp;</p>  	 <table width="75%" border="0" align="center">   <tr>      <td>    <p align="center"><a name="F1"></a><img src="/fbpe/img/maderas/2012nahead/fig1_aop0812.jpg" width="450" height="547"></p></td>   </tr>   <tr>      <td>    
<p align="center"><font face="verdana" size="2"><b>Figure 1.</b> Some          components found in stone and seed olives</font></p></td>   </tr> </table>     <p align="justify">&nbsp;</p>  	    <p align="justify"><font face="verdana" size="2"><b>&nbsp;</b></font></p>  	     <p align="justify"><font face="verdana" size="3"><b>EXPERIMENTAL METHODS</b></font></p>  	    <p align="justify"><font face="verdana" size="2"><b>Plant materials</b></font></p>     <p align="justify"><font face="verdana" size="2">Mature olive fruits were obtained    from the Moroccan Picholine variety, which grows widely in the province of Beni    Mellal and from Menara and Haouzia varieties growing in the province of Marrakech    of Middle Atlas and Marrakech&#45;Tensift&#45;Al Haouz (Morocco), respectively.    Olive fruits were boiled (between 70 and 80&deg;C) in water for 8 minutes, and    pulped by crushing them manually. Olive stones were then air dried on paper    towels (2&#45;4 days). After drying, the olive stones were ground (particle    less than 0.5 mm) in a knife mill "Retsch SK1".</font></p>  	    ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2">Maritime pine (<i>Pinus pinaster</i>) particles was provided by the sawmill Ets. Labadie (Roquefort, France) Sd (moisture content around 8&#150;10%).</font></p>  	    <p align="justify"><font face="verdana" size="2"></font></p>  	     <p align="justify"><font face="verdana" size="2"><strong>Extraction and estimation    of total phenolic compounds</strong></font></p>     <p align="justify"><font face="verdana" size="2">The solid&#45;liquid extraction    of total phenolic compounds was performed with a Soxhlet apparatus. Olive stone    powder (60 g) was extracted in a Soxhlet apparatus, first with hexane (500 ml)    for 5 hours to remove lipids, then with acetone (500 ml) for 5 hours and finally    with ethanol (500 ml) for 5 hours to remove total phenolic compounds (Rakib    <i>et al</i>. 2010).</font></p>     <p align="justify"><font face="verdana" size="2">Total phenols are estimated by    Folin&#45;Ciocalteu method (Singleton and Rossi 1965, Scalbert <i>et al.</i>    1989). A 2.5 ml portion of Folin&#45;Ciocalteu reagent and 2 ml of a sodium    carbonate solution (75 g/l) are added to 0.5 ml of the diluted extract. The    assay tubes are kept 15 min in a water bath at 50&deg;C and then transferred    to cold water. The absorbance read was 760 nm. A calibration curve with equation:    y = 0.0021x + 0.0015 (r<sup>2</sup> = 0.99) was constructed using gallic acid    solutions within the range 10&#150;100 mg/l. Contents of total phenolic compound    in olive stones were expressed as gallic acid equivalents in milligrams per    gram dry matter (mg GAE/g, DM). The results were averages of triplicate analyses.</font></p>     <p align="justify">&nbsp;</p>  	    <p align="justify"><font face="verdana" size="2"><b>Fourier Transform Middle&#45;Infrared Spectroscopy (FT&#45;MIR)</b></font></p>  	     <p align="justify"><font face="verdana" size="2">Analyses were performed with    FT&#45;MIR. The spectra of the samples were recorded with a Perkin Elmer's FTIR    (Spectrum One). Samples were deposited without preparation on attenuated total    reflection (ATR) cell that is equipped by a diamond crystal. The crystal was    cleaned between measurements by deionized water and dried by lint&#45;free tissue.    Spectra were recorded between 4000 and 600 cm<sup>&#45;1</sup>, at 0.5 cm<sup>&#45;1</sup>    nominal resolution.</font></p>  	     <p align="justify">&nbsp;</p>     <p align="justify"><font face="verdana" size="2"><b>Thermogravimetric analysis    (TGA)</b></font></p>  	     ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2">Thermogravimetric analysis (TGA)    was used to determine the thermal stability and degradation of olive stones    using a TGA Q50 thermogravimetric apparatus. Ten milligrams of each cured sample    were placed on a balance located in the furnace and heat was applied over the    temperature range from room temperature to 600 &deg;C at a heating rate of 5    &deg;C/min in air. Mass losses versus temperature thermograms were obtained    showing the different decomposition processes.</font></p>  	     <p align="justify">&nbsp;</p>     <p align="justify"><font face="verdana" size="2"><b>Particleboard preparation</b></font></p>  	     <p align="justify"><font face="verdana" size="2">Single layer laboratory particleboards    of dimension 350 mm x 310 mm x 14 mm were prepared from maritime pine (<i>Pinus    pinaster</i>). The addition of the commercial Urea Formaldehyde (UF) resins    to the particles was 7.5 % based on solid mass; press time was 7.5 min at 195&deg;C    press platen temperature with a maximum specific pressure of 25 kg/cm<sup>2</sup>.    The UF resin had a density of 1280&#150;1290 kg/m<sup>3</sup>, a pH of about    8.5&#150;9, and a viscosity of 350&#150;600 mPa.s, all measured at 20 &plusmn;    2&deg;C; the gel time was 40&#45;50 seconds at 100&deg;C. The content of free    formaldehyde is maximum 0.15 % based on the liquid resin. The particles with    size between 1 to 4 mm were dried to approx 2 &plusmn; 0.5 % moisture content    prior to application of the resin. Each olive stone powder was ground and mixed    at different concentrations (from 0 to 15%, w/w) in particles. The target board    density was 710 kg/m<sup>3</sup>. The particleboards were pre&#45;conditioned    at 25&deg;C and 65 % relative humidity in a V&ouml;tsch climate room for one    week before testing.</font></p>  	    <p align="justify"><font face="verdana" size="2"><b>Biological properties</b></font></p>  	    <p align="justify"><font face="verdana" size="2"><b>Decay test of the particleboard composites</b></font></p>  	     <p align="justify"><font face="verdana" size="2">Particleboards composites measuring    20 &times; 20 &times; 14 mm<sup>3</sup> were prepared for decay test, from Maritime    pine (<i>Pinus pinaster</i>). A fungal decay test was done according to an adaptation    of the standard EN 113 (AFNOR 1996) using a brown rot fungus, <i>Coniophora    puteana</i> (BAM Ebw.15) and the white rot fungus, <i>Coriolus versicolor</i>    (CTB 863A). A culture medium was prepared in Roux flasks. In each one, a nutritive    medium, made up of a malt&#45;agar mixture was placed (40 g of malt and 20 g    of agar dissolved in 1000 ml distilled water). After sterilization (121&deg;C    for 20 min at 1 bar), the <i>Coriolus versicolor</i> and <i>Coniophora puteana</i>    were inoculated on culture medium in Petri dishes under sterile conditions.    Then they were placed in constant conditions at 25&deg;C and 65% relative humidity    for 3 weeks to favour fungal development. After being conditioned at 25&deg;C    and 65% air moisture content, the particleboard composite samples were put into    Petri dishes and exposed to <i>Coriolus versicolor</i> and <i>Coniophora puteana</i>    for 16 weeks in darkness. Finally, test results were expressed as percentage    of weight loss of composite panels due to fungal attacks after decay test using    equation (1) (the measurement was done after drying of each sample). Ten replicates    were used for each decay fungus. Weight loss was calculated as follows:</font></p>     <p align="justify">&nbsp;</p> <table width="75%" border="0" align="center">   <tr>      <td>    <p align="center"><font face="verdana" size="2">Weight loss (%) =<img src="/fbpe/img/maderas/2012nahead/ec1_aop0812.jpg" width="112" height="52" align="middle"></font></p></td>     <td>    
<p align="center"><font face="verdana" size="2">(1)</font></p></td>   </tr> </table>     ]]></body>
<body><![CDATA[<p align="center">&nbsp;</p>     <p align="justify"><font face="verdana" size="2">Where <em>m<sub>i</sub></em>    and <em>m<sub>f</sub></em> are the oven&#45;dry weights of the sample before    and after the decay test.</font></p>  	    <p align="justify"><font face="verdana" size="2"></font></p>  	    <p align="justify"><font face="verdana" size="2"><b>Decay test of olive stone powders</b></font></p>  	     <p align="justify"><font face="verdana" size="2">In order to confirm the fungicidal    effect, olive stone powder was added to the culture medium. Each olive stone    powder was ground and mixed at different concentrations (from 0 to 7%, p/v)    in malt&#45;agar culture medium. After sterilization, the <i>Coriolus versicolor</i>    and <i>Coniophora puteana</i> fungi were inoculated in the centre of the culture    medium under sterile conditions. Then they were placed in constant conditions    at 25&deg;C and 65% relative humidity for 15 days to favour fungal development.    The mean radius of the fungal development was measured. Test results were expressed    as percentage of fungal development using equation (2). Ten replicates were    used for each fungal development.</font></p>  	    <p align="justify"><font face="verdana" size="2"></font></p>  	 <table width="75%" border="0" align="center">   <tr>      <td>    <p align="center"><font face="verdana" size="2">Percentage of fungal          development (%) = <img src="/fbpe/img/maderas/2012nahead/ec2_aop0812.jpg" width="61" height="48" align="middle"></font></p></td>     <td>    
<p align="center"><font face="verdana" size="2">(2)</font></p></td>   </tr> </table>     <p align="center">&nbsp;</p>  	    <p align="justify"><font face="verdana" size="2">Where</font></p>  	     ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2"><em>R<sub>1</sub></em>: is the    mean radius of the fungal development after 15 days (olive stone powders present    in Petri dishes).</font></p>  	     <p align="justify"><font face="verdana" size="2"> <em>R<sub>o</sub></em>: is the    mean radius of the fungal development after 15 days (control: without presence    of olive stone powder).</font><font face="verdana" size="2">&nbsp;</font></p>  	    <p align="center"><font face="verdana" size="2">&nbsp;</font></p>  	     <p align="justify"><font face="verdana" size="3"><strong>RESULTS AND DISCUSSION</strong></font></p>  	     <p align="justify"><font face="verdana" size="2"><b>Impact of olive stones varieties    on polyphenols extraction</b></font></p>     <p align="justify"><font face="verdana" size="2"><a href="#T1">Table 1</a> shows    the polyphenols concentration in acetone and ethanol extracts. The results showed    that Moroccan Picholine variety growing in the province of Beni Mellal had the    higher contents of total phenolic compounds (11.32 mg/g DM), followed by Haouzia    (4.55 mg/g DM) and Menara (3.56 mg/g DM) variety. The relative amounts of phenols    found in our experiment are in agreement with those already reported by some    authors which described the lower levels of phenols in stones and seeds in comparison    to the remaining tissues (pulp, leaves) of olives (Ryan <i>et al</i>. 2003).    Nevertheless, compared with some other berries, the total phenolics contents    in olive stones (3.56&#45;11.32 mg/g DM) are higher than those of Oregon canberries    (4.95&#150;9.80 mg/g DM) berries (Wada and Ou 2002) and bayberries (3.60&#45;4.46    mg/g DM) (Zhongxiang <i>et al</i>. 2007).</font><font face="verdana" size="2">&nbsp;</font></p>  	    <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>  	 <table width="75%" border="0" align="center">   <tr>      <td>    <p align="center"><font face="verdana" size="2"><b><a name="T1"></a>Table          1.</b> Polyphenol contents of various olive stones. </font></p></td>   </tr>   <tr>      <td>    <p align="center"><img src="/fbpe/img/maderas/2012nahead/tabla1_aop0812.jpg" width="592" height="243"></p></td>   </tr>   <tr>      <td>    
<p align="center"><font face="verdana" size="2">Three replicates of          each sample. S.D: standard deviation.</font></p></td>   </tr> </table>     ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2">FT&#45;MIR spectroscopy can be    used to address qualitative and quantitative analyses. In this view, comparison    with literature data provides preliminary information for the compositional    characterization of FT&#45;MIR bands of olives stones samples. Spectra of different    olives stones are presented in <a href="#F2">figure 2</a>. For the three varieties    the spectra seem very similar. By means of FT&#45;MIR spectroscopy, the original    structure of different polyphenols can be clearly distinguished. The peak around    1285 cm<sup>&#45;1</sup> indicates a characteristic feature for the flavonoid&#45;based    tannins. This peak was assigned to the ethereal C&#45;O stretching vibration    (Socrates, 2001, Edelmann and Lendl 2002) arising from the pyran&#45;derived    ring structure of this class of tannins. Two broader peaks at around 1350 cm<sup>&#45;1</sup>    and between 1290 and 1150 cm<sup>&#45;1</sup> can be observed in the spectra    of gallic acid, tannic acid (gallotannin) and in the ellagitannin preparation    with shifts in exact peak position and deviations in peak shape. Both peaks    can be assigned to the combination of C&#45;O stretching and O&#45;H deformation    vibrations (Socrates 2001, Edelmann and Lendl 2002).</font></p>  	 <table width="75%" border="0" align="center">   <tr>      <td>    <p align="center"><a name="F2"></a><img src="/fbpe/img/maderas/2012nahead/fig2_aop0812.jpg" width="453" height="283"></p></td>   </tr>   <tr>      <td>    
<p align="center"><font face="verdana" size="2"><b>Figure 2.</b> IR          spectra of Haouzia, Menara and Moroccan Picholine olive stones.</font></p></td>   </tr> </table>     <p align="center">&nbsp;</p>  	     <p align="justify"><font face="verdana" size="2"><b>Thermal study of different    olive stones</b></font></p>  	     <p align="justify"><font face="verdana" size="2">Thermogravimetric analysis can    check the thermal decomposition and thermal stability of the olive stones. <a href="#F3">Figure    3</a> shows the TGA curve of the Moroccan Picholine, Menara and Haouzia varieties    in air atmosphere at a heating rate of 5&deg;C/min, result that matches to typical    findings for the decomposition of other lignocellulosic materials. Two steps    can be differentiated in the TGA curves: I&#45; Up to 200 &deg;C, the weight    loss corresponds to moisture release; II&#45; The main weight loss takes place    between 200 and 400&deg;C. In this temperature range, two decomposition processes    are well defined, with maximum weight loss rates appearing at 245 and 330&deg;C.    The first step can be attributed to the group of reactions involved in hemicellulose    degradation (&Oacute;rf&atilde;o <i>et al.</i> 1999, Williams and Besler 1993),    and the second one to those related to the thermal decomposition of cellulose    (&Oacute;rf&atilde;o <i>et al.</i> 1999, Williams and Besler 1993).</font></p>  	     <p align="justify"><font face="verdana" size="2">The curve also shows that thermal    degradation began to occur only after the materials have absorbed certain amounts    of heat energy. Heat initiated the degradation processes and the breakdown of    the structure by causing molecular chain ruptures. The results obtained with    thermogravimetric analysis confirm that at 195 &deg;C they risk no degradation    of the olive stones.</font></p>  	 <table width="75%" border="0" align="center">   <tr>      <td>    <p align="center"><font face="verdana" size="2"><a name="F3"></a><img src="/fbpe/img/maderas/2012nahead/fig3_aop0812.jpg" width="550" height="324"></font></p></td>   </tr>   <tr>      <td>    
<p align="center"><font face="verdana" size="2"><b>Figure 3</b>. TGA          graphical analysis for Menara, Haouzia and Moroccan Picholine olive stone          varieties</font></p></td>   </tr> </table>     <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>  	    ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2"><b>Decay resistance of the particleboard composites</b></font></p>  	     <p align="justify"><font face="verdana" size="2">Weight losses of the particleboard    composites caused by fungal decay after 16 weeks are shown in <a href="#T2">table    2</a>. We can see that the control particleboard was attacked by both decay    fungi (<i>Coriolus versicolor</i> and <i>Coniophora puteana</i>) with weight    losses near 40%. This proves that the fungus was virulent and the test of durability    was valid according to the relevant European Norm 113 (EN 113, 1996). The values    of weight losses for all other particleboard panels decreased. Laboratory tests    have shown that the addition of olive stones (5, 10 and 15%) is very effective    in preventing attack by both decay fungi. We also observed that particleboard    with Moroccan Picholine (5, 10 or 15%) showed considerable resistance to both    the decay fungi compared with particleboard with Haouzia (5, 10 or 15%) and    Menara (5, 10 or 15%).</font></p>  	     <p align="justify"><font face="verdana" size="2">Results in <a href="#T2">table    2</a> seem to indicate that <i>Coniophora puteana</i> could be more efficient    in wood degradation than <i>Coriolus versicolor</i>. This may be due to the    differences between their decay mechanisms. This tendency has been previously    observed by Nemli <i>et al.</i> (2006) and Moubarik <i>et al.</i> (2009).</font><font face="verdana" size="2">&nbsp;</font></p>  	    <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>  	 <table width="75%" border="0" align="center">   <tr>      <td>    <p align="center"><font face="verdana" size="2"><b><a name="T2"></a>Table          2</b>. Weight loss of composite in presence of olive stones after exposure          to both decay fungi    <br>         </font><font face="verdana" size="2"> (<i>Coriolus versicolor</i> and          <i>Coniophora puteana</i>). </font></p>       </td>   </tr>   <tr>      <td>    <div align="center"><img src="/fbpe/img/maderas/2012nahead/tabla2_aop0812.jpg" width="600" height="380"></div></td>   </tr>   <tr>      <td>    
<p align="center"><font face="verdana" size="2">Ten replicates of each          decay fungus. S.D: standard deviation.</font></p></td>   </tr> </table>     <p align="center">&nbsp;</p>  	    <p align="justify"><font face="verdana" size="2"><strong>Fungicide effect of olive    stones</strong></font></p>     ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2"><a href="#T3">Table 3</a> shows    the effect of olive stones (Picholine, Haouzia and Menara) concentration on    fungal development. A decrease in fungal development for both decay fungi <i>Coriolus    versicolor</i> and <i>Coniophora puteana</i> is observed on incorporation of    olive stones into the culture medium. The results in <a href="#T3">table 3</a>    confirm the fungicide effect of olive stones that contributes to improve the    total resistance of the particleboard composites.</font></p>  	    <p align="justify"><font face="verdana" size="2">Hart and Hillis (1972) have demonstrated that the presence of phenolic compounds improves the durability of wood. Further studies evaluating the fungicide effect of phenolic compounds (tannins) also confirmed this activity (Pizzi and Conradie 1986, Charrier <i>et al.</i> 1995, Aloui <i>et al.</i> 2004, Cornelius <i>et al.</i> 2004, Moubarik <i>et al</i>. 2009).</font></p>  	    <p align="justify"><font face="verdana" size="2"></font></p>  	 <table width="75%" border="0" align="center">   <tr>      <td>    <p align="center"><font face="verdana" size="2"><b><a name="T3"></a>Table          3.</b> Effect of olive stone concentrations on fungus development. </font></p></td>   </tr>   <tr>      <td>    <div align="center"><img src="/fbpe/img/maderas/2012nahead/tabla3_aop0812.jpg" width="580" height="356"></div></td>   </tr>   <tr>      <td>    
<p align="center"><font face="verdana" size="2">Ten replicates of each          fungal development. S.D: standard deviation.</font></p></td>   </tr> </table>     <p align="center">&nbsp;</p>  	    <p align="justify"><font face="verdana" size="2"><b>&nbsp;</b></font></p>  	     <p align="justify"><font face="verdana" size="3"><b>CONCLUSION</b></font></p>  	    <p align="justify"><font face="verdana" size="2">The present work proposes an innovative valorization of olive stones for particleboard production. The result of polyphenols extraction from Moroccan Picholine variety growing in the province of Beni Mellal had the higher contents of total phenolic compounds (11.32 mg/g DM), followed by Haouzia (4.55 mg/g DM) and Menara (3.56 mg/g DM) variety. The thermogravimetric analysis shows no significant degradation of the three olive stones varieties at temperature less than 195 &deg;C. A good correlation was observed between the resistance to fungi and the concentration of olive stones. A decrease in fungal development for both decay fungi <i>Coriolus versicolor</i> and <i>Coniophora puteana</i> is observed after olive stones incorporation into the culture medium. The results of the present work contribute to the valorization of olive stones in the Mediterranean countries and especially in Morocco that has an ambitious agricultural strategy called "Green Morocco".</font></p>  	    ]]></body>
<body><![CDATA[<p align="justify"><font face="verdana" size="2"></font></p>  	     <p align="justify"><font face="verdana" size="3"><b>ACKNOWLEDGMENT</b></font></p>     <p align="justify"><font face="verdana" size="2">The authors would like to thank    the INRA (Beni Mellal and Marrakech) for their olives collection.</font></p>  	    <p align="justify"><font face="verdana" size="2">&nbsp;</font></p>  	     <p align="justify"><font face="verdana" size="3"><b>REFERENCES</b></font></p>     <!-- ref --><p align="justify"><font face="verdana" size="2"><b>Aloui, F.; Ayadi, N.; Charrier,    F.; Charrier, B. 2004.</b> Durability of European oak (<em>Quercus petraea</em>    and <em>Quercus robur</em>) against white rot fungi (<i>Coriolus versicolor</i>):    relations with phenol extractives. <i>Holz als Roh&#45; und Werkstoff</i> 62(4):286&#45;290.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=3068941&pid=S0718-221X201200030000800001&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></font></p>  	     <!-- ref --><p align="justify"><font face="verdana" size="2"><b>Besnard, G.; Hern&aacute;ndez,    P.; Khadari, B.; Dorado, G.; Savolainen, V. 2011.</b> Genomic profiling of plastid    DNA variation in the Mediterranean olive tree. <i>BMC Plant Biology</i> 11:80p.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=3068943&pid=S0718-221X201200030000800002&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></font></p>  	     <!-- ref --><p align="justify"><font face="verdana" size="2"><b>Charrier, B.; Haluk, J. 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<p><font size="2">Received: 07.02.2012 Accepted: 16.05.2012</font></p> </font>       ]]></body><back>
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