<?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>0123-4226</journal-id>
<journal-title><![CDATA[Revista U.D.C.A Actualidad & Divulgación Científica]]></journal-title>
<abbrev-journal-title><![CDATA[rev.udcaactual.divulg.cient.]]></abbrev-journal-title>
<issn>0123-4226</issn>
<publisher>
<publisher-name><![CDATA[Universidad de Ciencias Aplicadas y Ambientales]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0123-42262016000100005</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[PRELIMINARY EVALUATION OF PATHOGENS AFFECTING Eleodes longicollis punctigerus BLAISDELL (COLEOPTERA: TENEBRIONIDAE)]]></article-title>
<article-title xml:lang="es"><![CDATA[EVALUACIÓN PRELIMINAR DE PATÓGENOS QUE AFECTAN A Eleodes longicollis punctigerus BLAISDELL (COLEOPTERA: TENEBRIONIDAE)]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Quiroga-Murcia]]></surname>
<given-names><![CDATA[Daniel Estiven]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Zenner de Polanía]]></surname>
<given-names><![CDATA[Ingeborg]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Posada-Flórez]]></surname>
<given-names><![CDATA[Francisco Javier]]></given-names>
</name>
<xref ref-type="aff" rid="A03"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Universidad de Ciencias Aplicadas y Ambientales U.D.C.A Facultad de Ingeniería Agronómica Grupo de Investigación Fitosanidad]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
</aff>
<aff id="A02">
<institution><![CDATA[,Universidad de Ciencias Aplicadas y Ambientales U.D.C.A Facultad de Ingeniería Agronómica Grupo de Investigación Fitosanidad]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
</aff>
<aff id="A03">
<institution><![CDATA[,Independiente  ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
</aff>
<pub-date pub-type="pub">
<day>30</day>
<month>06</month>
<year>2016</year>
</pub-date>
<pub-date pub-type="epub">
<day>30</day>
<month>06</month>
<year>2016</year>
</pub-date>
<volume>19</volume>
<numero>1</numero>
<fpage>37</fpage>
<lpage>43</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_arttext&amp;pid=S0123-42262016000100005&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_abstract&amp;pid=S0123-42262016000100005&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_pdf&amp;pid=S0123-42262016000100005&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[The false wire-worm Eleodes longicollis punctigerus, despite of been registered more than 30 years ago, is until now considered as an emerging pest in some areas of the Sabana de Bogotá, in Colombia. Therefore, within an integrated management program, the use of biological control agents have to be considered.Under field conditions, larvae and adult wireworms were found to be affected by pathogenic microorganisms, such as Paecilomyces sp., Beauveria bassiana and Metarhizium anisopliae and nematodes. Preliminary studies to determine their pathogenicity in the laboratory were undertaken, showinging that none of them were highly pathogenic. An alternative explanation may be that E. longicollis may be tolerant to the infection or the spore concentration used was to low, because the highest larval mortality observed was only 20% with the treatment pos. Paecilomyces sp., at 1x10(7)spore concentrations. Adult mortality of 22.5% with M. anisopliae at 1x10(7)was obtained. It was also found that the insect is susceptible to nematodes. Both nematodes and fungi should be studied under other conditions, with higher concentrations, in order to be incorporated as a complement into a strategy of preventive control.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[El falso gusano alambre Eleodes longicollis punctigerus, a pesar de haberse detectado hace más de 30 años, apenas últimamente, se perfila como una plaga emergente en algunas áreas de la Sabana de Bogotá, Colombia. Por ello, dentro de un plan de manejo integrado, se plantea el uso del control biológico y, luego de encontrar en campo larvas y adultos afectados por microorganismos entomopatógenos, tales como Paecilomyces sp., Beauveria bassiana y Metarhizium anisopliae y por nematodos, se decidió determinar la patogenicidad de éstos en el laboratorio. Los resultados mostraron que ninguno de ellos es altamente patogénico, existiendo la posibilidad que el insecto es tolerante a la infección o que la concentración de esporas empleada fue muy baja, ya que la mortalidad larval máxima observada fue del 20%, con el tratamiento de pos. Paecylomices sp., concentración de esporas 1x10(7). Sobre el adulto, se observó una mortalidad del 22,5%, con el hongo M. anisopliae, a una concentración del 1x10(7); también, se detectó que el insecto es susceptible a nematodos. Se concluye que, tanto estos últimos como los hongos mencionados, deben ser estudiados bajo otras condiciones y en concentraciones más altas, para poderlos incorporar como complemento de una estrategia de control preventivo, a su debido tiempo antes de la siembra, y con condiciones de adecuada humedad del suelo.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[False wire-worm]]></kwd>
<kwd lng="en"><![CDATA[micro-biologic control]]></kwd>
<kwd lng="en"><![CDATA[fungi]]></kwd>
<kwd lng="en"><![CDATA[nematode]]></kwd>
<kwd lng="es"><![CDATA[Falso gusano alambre]]></kwd>
<kwd lng="es"><![CDATA[control microbiológico]]></kwd>
<kwd lng="es"><![CDATA[hongos]]></kwd>
<kwd lng="es"><![CDATA[nematodo]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[  <font size="2" face="verdana">     <p align="right"> <b> CIENCIAS AGROPECUARIAS-Art&iacute;culo Cient&iacute;fico</b></p>     <p align="center"><b>PRELIMINARY EVALUATION OF PATHOGENS AFFECTING <i>Eleodes longicollis punctigerus </i>BLAISDELL (COLEOPTERA: TENEBRIONIDAE)</b></p>     <p align="center"><b>EVALUACI&Oacute;N PRELIMINAR DE PAT&Oacute;GENOS QUE AFECTAN A <i>Eleodes longicollis punctigerus </i>BLAISDELL (COLEOPTERA: TENEBRIONIDAE)</b></p>     <p><b>Daniel Estiven Quiroga-Murcia<sup>1</sup>, Ingeborg Zenner de Polan&iacute;a<sup>2</sup>, Francisco  Javier Posada-Fl&oacute;rez<sup>3</sup></b></p>     <p><sup>1</sup>Joven  Investigador Grupo  de  Investigaci&oacute;n  Fitosanidad, Estudiante  Facultad  de  Ingenier&iacute;a  Agron&oacute;mica.  Universidad de Ciencias  Aplicadas  y  Ambientales  U.D.C.A, e-mail:  <a href="mailto:quirogaedaniel@hotmail.com">quirogaedaniel@hotmail.com</a></p>     <p><sup>2</sup>I.A., Ph.D.,  Docente-Investigador. U.D.C.A, e-mail: <a href="mailto:izenner@udca.edu.co">izenner@udca.edu.co</a></p>     <p><sup>3</sup> Ing. Agr&oacute;nomo,  Entom&oacute;logo Ph.D., Investigador Cient&iacute;fico Independiente, e-mail: <a href="mailto:fjavierposada@hotmail.com">fjavierposada@hotmail.com</a></p>     <p>Rev. U.D.C.A Act. &amp; Dic. Cient. 19(1): 37-43, Enero-Junio, 2016</p> <hr>     <p><b>SUMMARY</b></p>     ]]></body>
<body><![CDATA[<p>The false wire-worm <i>Eleodes longicollis  punctigerus</i>, despite of been  registered  more  than  30  years  ago,  is until now considered as an emerging pest in some areas of the Sabana de  Bogot&aacute;,   in  Colombia.  Therefore,  within an  integrated management program,  the use of biological control agents  have  to  be  considered.Under field conditions,   larvae  and adult  wireworms were found  to  be  affected  by pathogenic microorganisms,  such   as <i>Paecilomyces </i>sp., <i>Beauveria bassiana </i>and <i>Metarhizium  anisopliae </i>and   nematodes. Preliminary studies  to  determine  their pathogenicity  in the laboratory  were undertaken, showinging  that  none  of them were highly pathogenic. An alternative explanation  may be that <i>E. longicollis </i>may  be  tolerant  to  the  infection  or the spore  concentration used  was to low, because the  highest larval  mortality observed  was only 20% with the  treatment pos. <i>Paecilomyces </i>sp., at 1x10<sup>7</sup>spore concentrations. Adult mortality of 22.5% with <i>M. anisopliae </i>at 1x10<sup>7</sup>was obtained.  It was also found that the insect is susceptible  to nematodes. Both  nematodes and  fungi should  be  studied  under  other conditions,   with  higher   concentrations,  in  order   to   be incorporated as a complement into a strategy  of preventive control.</p>     <p><b>   Key words:</b> False  wire-worm, micro-biologic  control,  fungi, nematode.</p>   <hr>     <p><b>RESUMEN</b></p>     <p>   El falso gusano  alambre <i>Eleodes  longicollis  punctigerus, </i>a pesar  de haberse detectado hace  m&aacute;s  de 30 a&ntilde;os,  apenas &uacute;ltimamente, se perfila como una plaga emergente en algunas  &aacute;reas de la Sabana de Bogot&aacute;,  Colombia. Por ello, dentro de un plan de manejo  integrado,  se plantea  el uso del control biol&oacute;gico  y, luego  de encontrar en campo  larvas y adultos afectados  por  microorganismos  entomopat&oacute;genos,   tales como <i>Paecilomyces </i>sp<i>., Beauveria  bassiana </i>y <i>Metarhizium anisopliae </i>y  por   nematodos,  se   decidi&oacute;   determinar  la patogenicidad de  &eacute;stos   en  el  laboratorio.   Los  resultados  mostraron que  ninguno  de  ellos es  altamente patog&eacute;nico, existiendo  la  posibilidad  que  el  insecto  es  tolerante  a  la infecci&oacute;n o que  la concentraci&oacute;n de esporas  empleada fue muy  baja,  ya que  la mortalidad  larval m&aacute;xima  observada  fue del 20%, con  el tratamiento de pos. <i>Paecylomices </i>sp., concentraci&oacute;n de esporas  1x10<sup>7</sup>. Sobre el adulto, se observ&oacute; una  mortalidad  del 22,5%,  con  el hongo <i>M. anisopliae</i>, a una  concentraci&oacute;n del  1x10<sup>7</sup>;  tambi&eacute;n,   se  detect&oacute;   que  el insecto es susceptible  a nematodos. Se concluye que, tanto estos  &uacute;ltimos  como  los  hongos   mencionados, deben  ser estudiados bajo otras condiciones y en concentraciones m&aacute;s altas, para poderlos  incorporar  como  complemento de una estrategia  de control  preventivo, a su debido  tiempo  antes  de la siembra,  y con condiciones de adecuada humedad del suelo.</p>     <p><b>   Palabras clave:</b> Falso gusano alambre, control microbiol&oacute;gico,  hongos, nematodo.</p> <hr>     <p><b>INTRODUCTION</b></p>     <p>Biological control  has  been  for years a tool for population  management of insect crop pests,  being defined by Nicholls (2008) as the use of beneficial organisms against  pests  that cause  damage. This concept of biological  control  can  be based  on the principle that in nature  all organisms possess  antagonists,  which  either  compete  or  eliminate  them,   a process  being essential for life equilibrium (Hanson,  1993).</p>     <p>   Microorganisms  are  components of biological  control,  the so   called   entomopathogens,  including   viruses,   bacteria, protozoa,   rickettsia,  fungi  and  nematodes, which  can  be found affecting insects,  establishing  symbiotic relationships such  as  parasitism   and  also  causing   disease   and  death,  contributing   therefore  to  the  natural  regulation   of  insect populations  (Lacey &amp; Kaya, 2007).</p>     <p>   Currently,   many   organisms   are   studied    and    used    in microbiological  control  programs. Successful   alternatives, using  entomopathogenic fungi to control  arthropod pests, inhabiting water and soil environments have been developed, using   primarily   the   genera <i>Metharhizium</i>, <i>Beauveria</i>, <i>Sporothrix</i>,  Nomuraea, <i>Paecilomyces </i>among  others  (Alves  &amp; Lopes, 2008). According to Posada  &amp; Pava-Ripoll (2010), <i>Bacillus </i>spp., <i>Beauveria  bassiana </i>(Moniliales: Moniliaceae) and <i>Metharizum anisopliae </i>(Hypocreales:  Clavicipitaceae) are the most studied fungi being mentioned in the literature, to  control  several  insect  pests.  Vieira  Tiago <i>et  al. </i>(2014) also highlighted <i>M. anisopliae </i>as the fungus  species  most studied  and  used  for control  purposes, due,  among  other characteristics, to its persistence in the soil.</p>     <p>   Nematodes have  multiple  relationships   with insects;  they can  be  parasites,  affecting  their  reproductive  ability (Kaya &amp; Stock,  1997),  but they can also enter insects  and release bacteria  that  are  responsible   for the  individual's death  by septicemia  (Rosales <i>et al</i>. 2009).</p>     ]]></body>
<body><![CDATA[<p>   Both  fungi and  nematodes are  recommended as  biological control agents of insect pests in crops of economic importance; such is the case  of <i>B. bassiana </i>for the management of the coffee berry borer (<i>Hypothenemus hampei</i>).This fungus is the most commonly  used and widely distributed natural enemy of this pest (Posada &amp; Pava-Ripoll, 2010).</p>     <p><i>Beauveria bassiana</i> is also efficient against tenebrionids such as <i>Alphitobius  diaperinus</i> in chicken  houses  (Steinkraus <i>et al.</i> 1991)  and  against <i>Tribolium  castaneum </i>pest  of stored grains (Pedrini <i>et al. </i>2010). <i>Metharizium anisopliae </i>is used to control insects of several families of the Order Coleoptera,  such  as  Curculionidae  and  Scarabidae, common pests  of rice,  citrus and  sugarcane (Nicholls Estrada,  2008).  It also affects wireworms of the genus <i>Agriotes </i>(Elateridae) (Kabaluk &amp; Ericsson, 2007; Ericsson <i>et al. </i>2007). Another species, <i>M. brunneum </i>has been inclusive, evaluated  against  ticks of the genus  Ixodes (Acari: Ixodidae).</p>     <p>  The  nematode  genera <i>Steinernema </i>and <i>Heterorhabditis </i>form   part   of  the   integrated    management  program    of <i>Premnotrypes  vorax </i>and <i>Tecia  solanivora </i>in potato  crops  (Maggiorani &amp; Gudi&ntilde;o,  1996). <i>Steinernema feltiae </i>and <i>S</i>. <i>carcocapsae </i>(Rhabditia  Steinernematidae) are  considered as  promising  tenebrionid  control  agents  for <i>A. diaperinus </i>(Geden <i>et al. </i>1987) and <i>Cyanaeus angustus </i>(Nansen <i>et al.</i>  2013), respectively.</p>     <p>   The false wire-worm, recently identified as <i>Eleodes longicollis  punctigera </i>Blaisdell, by Dr. Charles A. Triplehorn, Ohio State University, United States,  based  on  specimens sent  by Dr. Francisco  Javier  Posada  Fl&oacute;rez,  and  previously referenced  in  Colombia  as <i>Eleodes  omissoides </i>Blaisdell (Coleoptera: Tenebrionidae),  causes  seed  losses  of various plant species, especially  grasses   and  seedlings   that  reach   germination. Larvae and adults of the pest are considered a limiting factor in the affected crops, because the attack requires replanting, and  the  use  of insecticides  that  increase  costs  (Quiroga- Murcia &amp; Posada-Fl&oacute;rez, 2013; Zenner de Polan&iacute;a <i>et al</i>. 2014; Calkins &amp; Kirk, 1973;  Rogers <i>et al. </i>1988).  It is worthwhile mentioning, that <i>E. longicollis  punctigerus </i>was recorded  for the first time in Mexico and  described  by Blaisdell in 1935,  but in this country apparently it never became a pest.</p>     <p>   Information on the genus <i>Eleodes </i>is scarce and the literature refers primarily to the taxonomy  and the description  of new species from Mexico and the United States (Triplehorn, 2010; Triplehorn &amp; Cifuentes, 2011; Triplehorn &amp; Thomas, 2011); South-American data  outside  those  from Colombia,  to our knowledge, do not exist.</p>     <p><i>Eleodes  longicollis  punctigera </i>receives the common name  of  false  wireworm  because  of  the  larval  resemblance  to the  larvae  of the  family Elateridae  (Coleoptera)  which  are considered the true wire-worms. This generic name  is given to  the  larvae  of  various  insects  of  the  genera <i>Epitragus</i>, <i>Anaedus</i>, <i>Blapstinus</i>, <i>Lobometopon </i>and <i>Ulus </i>spp. (Saunders <i>et al. </i>1998), all of the family Tenebrionidae, known pests  of rice, sorghum, corn, pineapple,  cotton  and pastures.</p>     <p>Previously   identified   as <i>E.   omissoides </i>in   Colombian publications  and in the newsletter Entomological  Notes and News (NNE), the insect was first recorded in the department of Boyac&aacute; in 1977 and then in Cundinamarca in 1980 attacking pea  (<i>Pisum   sativum</i>)  seeds.   From   then   on  the  bulletin sporadically  mentions   the  insect  in  several  municipalities of  Cundinamarca such  as  Madrid, Mosquera,  Bojac&aacute;  and Facatativ&aacute;   and   Tunja  (Boyac&aacute;).  In  addition,   the  authors observed that the insect is susceptible  to entomopathogenic fungi and nematodes. The susceptibility of <i>E. longicollis </i>was intended  to  be  confirmed  with this research, even  though  according   to  Pears  (2009)  false  wire-worms  do  not  have registered  biological control agents.</p>     <p>   This study, evaluated the potential of some naturally occurring entomopathogens, found  at  ''El Remanso'',   research   unit  of the  University of Applied and  Environmental  Sciences,  U.D.C.A Bogot&aacute;,  Colombia. These biocontrol agents  can be part of a sustainable control that could be integrated  into a management program  of <i>E. longicollis.</i></p>     <p><b>MATERIALS AND METHODS</b></p>     <p>Most studies,  if not stated  otherwise, were carried out under laboratory conditions,  18 &plusmn; 3&deg;C, 80% R.H. at the University.</p>     ]]></body>
<body><![CDATA[<p><b>Collection,  breeding  and survey:</b> The collection  of adults, larvae, pupae and eggs of the pest was done at ''El Remanso'', during  three   sampling   periods.   Two-hundred   adults   and some  larvae were hand  captured. Adults were separated by sex, resulting in 100 males and 100 females,  then placed in sterile soil and  fed corn and  wheat seeds,  and  cooked  rice. Their unaccounted F1 larval progeny was separated and fed with wheat.  Eggs  obtained  from  31  adults  of one  sample date were counted, obtaining 70 eggs, from which 58 larvae emerged. Larvae were placed in sterilized moistened soil and fed with cooked rice.</p>     <p>Adults were in rectangular plastic containers  (22 x 14 x 8cm high),  fed  with corn  and  wheat  seeds.   Most adults  died, observing  a survival of 15  after 10  months. Many of them were  found  dead   with  signs  of  cannibalism;   while other showed signs of fungal infection, such as a rigid appearance, absence of odor  and  apparent absence of fungal infection signs.  Dead  adults  were placed  in vials with moist  soil to observe sporulation.</p>     <p>   During  the  first  month   larvae  affected   by <i>Metharhizum anisopliae </i>and <i>Beauveria   bassiana </i>and   adults   affected by <i>M. anisopliae </i>were detected; two months   later  spores  of the fungus  identified as possibly belonging  to the genus <i>Paecilomyces </i>were observed  expanding  on the soil surface, proceeding  from  one   larva.  No  signs   or  symptoms  of nematode infection were detected.</p>     <p>   <b>Isolation  and  culture  of  entomopathogenic organisms: </b>After sporulation,  the fungi obtained  from the insects  were placed  in moist  plastic  growing chambers, and  introduced  to a PDA (potato,  dextrose  agar) medium  inside polystyrene incubators, to obtain the fungal growth and development. A culture of the fungus  pos. <i>Paecilomyces </i>was conducted in PDA obtaining a very good growth.</p>     <p>   Once pure fungal cultures were obtained the effective SDLYM medium   (Kaya &amp; Stock,  1997),  was  prepared.   SDLYM  is composed of Agar-Sabouraud, milk, egg yolk, agar, dextrose and yeast extract.</p>     <p>  Because   no   nematodes  were  found   in  false  wireworm larvae, they were collected  from the white grub <i>Clavipalpus</i> <i>ursinus </i>at El Remanso. These  larvae were placed  in plastic containers  with sterilized soil and  moisture  at field capacity. Approximately  one  month   later,  two  larvae  with  possible symptoms  of  nematode  infection  (showing  brown  color) were observed. <i>Clavipalpus ursinus </i>larvae were introduced  in modified White traps,  which consist  of plastic vials with a foam disc to prevent mites, from entering, that fed on the filter paper and the insect's cadavers.  After obtaining nematodes, a solution of 20 JI / cm<sup>3</sup>was prepared  and within the same  White traps,  false wire-worm larvae of diverse instars  were inoculated.</p>     <p>   <b>Inoculation and evaluation of pathogenicity: </b>To determine  the   fungal   pathogenicity    on <i>E   longicollis </i>larvae,   280 plastic  vials, filled with 6g  of previously sterilized soil were prepared,  placing one larva per vial for each fungus species.  As  control  40 untreated larvae were used.  Fungi  produced in the above mentioned medium  were applied to the larvae at two concentrations. Mortality was assessed every second day during 60 days for a total of 21 evaluations; during each observation distilled water, depending on the soil moisture,  and two wheat grains as larval food were added  to the vial.</p>     <p>   Treatments  corresponded  to  the   inoculation   with  native strains of <i>Metarhizum</i>, <i>Beauveria </i>and pos. <i>Paecylomices </i>at concentrations of 1x10<sup>5</sup> and  1x10<sup>7</sup>,  and  the control  which consisted   of distilled water.  For  this  purpose, spore  count was performed  by dilution of a concentrated solution, using a hemocytometer (Kaya &amp; Stock, 1997; V&eacute;lez <i>et al. </i>1997).</p>     <p>   Since  only adults  infected  by <i>M. anisopliae </i>were detected, the experiment was performed  with this fungus, extracted two months  before  inoculation  and  propagated in the  medium  SDLYM and  with a control.  A solution  of 1x10<sup>7</sup>  spores  was applied.  Twenty females  and  20 males  per treatment, same  number   for  the  control  were  evaluated;  for  a  total  of  80 experimental units. During 20 days a total of eight observations were made, each every second day; and during this observation time food and water was provided as necessary.</p>     <p>   To test the pathogenic nematode effect, those  recovered  in the  white grubs,  belonging  to the  family Sterneinematidae (indentified using) (Kaya &amp; Stock, 1997). Seventy two plastic vials, 36 for each  treatment for each  treatment, (nematode inoculation  and  control), with 6g of previously dried soil for 48 h received 3mL of distilled water. After 24 hours  one <i>E. longicollis </i>larva and  a corn  grain  was introduced  in each vial.  Larval instars  were not  determined at the  start  of the experiment and they varied from two-five instars. A nematode solution,  containing  20Jl/cm<sup>3</sup>was prepared  (Saenz,  2003), which has been the most  effective treatment invading larvae of <i>Clavipalpus ursinus </i>(Coleoptera). To each vial 1cm<sup>3</sup>of the solution was applied;  evaluations  were performed  every 72 hours for 15 days.</p>     ]]></body>
<body><![CDATA[<p> The  soil was kept  moist  applying  if  necessary,   every third day 1cm<sup>3</sup>of water.  When  noting  dead  larvae, the  cadaver was  extracted,  washed  with a  solution  of water  and  0.5% hypochlorite, and placed in a modified White trap to confirm the presence of nematodes.</p>     <p>   Data were analyzed with a qualitative approach and a descriptive- comprehensive scope,  calculating and interpreting the larval and adult percent  mortality.</p>     <p><b>RESULTS AND DISCUSSION</b></p>     <p>Symptoms  with  the   treatments  with <i>Metharizium </i>were dots  and  brown spots  on the cuticle of the larva; the spots were observed  8-10 days before the insect's death.  Later a slight change in the color of the larva was noted  and a rigid consistency   was  detected. After death,  a  white  mycelium initiated  at  the  ventral  side  between   the  junction  of  the externits  and  pleurits.  Confirmation  of the  fungal  infection was made when an olive green sporulation was detected and under  the microscope spores  in columns  appearance were observed.</p>     <p>   When  infected  with <i>Beauveria</i>, the  larva revealed  a  dark coloration   at  its  anal  area;  dead   individuals  had  a  rigid consistency   and  the  translucent  larvae  showed  a  whitish color. The initial appearance of mycelium showed where the dark  spot  was originally perceived,  then  covered  the  entire body. <i>Beauveria </i>infection was confirmed  by the observation of the spores  which provided a powdery appearance to the larva and by small spherical sacks covering the body (Posada &amp; Pava-Ripoll, 2010).  Under  the  microscope the  globular spores,  characteristics of this fungus, were detected.</p>     <p>   Finally, in the  case  of pos. <i>Paecilomyces </i>the  fungus  did not  produce  spots,  but  a  total  color  change of the  whole dead body; the color ranged  from intense  yellow to salmon  red. The larva was quite rigid and  a few days after death,  a rough texture of the cuticle was detected. The occurrence of white mycelium  started  between  the  abdominal  segments; although  no fungal sporulation was observed, the symptoms and  signs  were identical  to  those  observed  in the  original specimens, from which the inoculum  was taken.</p>     <p>   <a href="#f1">Figure  1</a> shows  the  percentage of larval mortality after 15 days of inoculation.  Before this all larvae were alive, except for   those   exposed   to   1x10<sup>5</sup>of  pos. <i>Paecilomyces, </i>all treatments produced the death  of 5% of the 20 inoculated  larvae. A maximum of 20% mortality throughout the trial was observed  only with the high dose  of this fungus  at day 60. The  concentration 1x10<sup>5</sup> achieved  15% mortality after two months. The  higher  dose,  1x10<sup>7</sup>of <i>M. anisopliae </i>caused  12.5% mortality, while the same  high dose of <i>B. bassiana </i>at day 60 showed only 7.5% mortality.</p>         <p><a name="f1"></a></p>    <p align="center"><img src="img/revistas/rudca/v19n1/v19n1a05f1.jpg"></p>     <p>   Only <i>Paecilomyces </i>revealed a tendency to increase mortality over  time.   The  other   pathogens  did  not   improve   their mortality rate, <i>Metarhizium </i>from day 42 and <i>Beauveria </i>from day 36 on after inoculation.</p>     ]]></body>
<body><![CDATA[<p>   Although, in general terms, all pathogens initiated their action and  killed <i>E. longicollis </i>larvae, it was required  a relatively  long time for an increase  in larval mortality. It is known that the three fungi are not fast acting. The low efficiency may be due to a natural larval tolerance  to the infection process, i.e. the penetration of spores through the cuticle. For this action, entomopathogenic  fungi  produce    extracellular   enzymes, whose  function  in  the  pathogenicity   corresponds  to  the suppression of the  immune  system  and  dissolution  of the insect cuticle, among  others (Gomes Fernandes <i>et al. </i>2012; Tiemi Ito <i>et al. </i>2007).  It is possible,  that  the production of these  enzymes  from the  strains  used  in this work was not appropriate  to  achieve  a  proper  penetration  through   the chitin constituting  the cuticle of <i>E. longicollis  punctigerus.</i></p>     <p>   The same  consideration may be true for the low pathogenic action of <i>M. anisopliae </i>against males and females at 1x10<sup>7</sup>. Mortality of the first insects  was detected after six days, with three  dead  males  and  one  dead  female.  Three  days  later increased to 12% mortality with one more insect of each sex, for a total of five males (25%) and three females (15%) dead.</p>     <p>   In <a href="#f2">figure 2</a> results using the nematode, <i>Steinernema </i>sp., at a concentration of 20 infective juveniles / cm<sup>3</sup>is shown.  At day  three  one  dead  individual was initially detected; at day ten 22.2% of dead larvae and at the end of the experiment 12 individuals representing 33.3%. The figure 2 shows  a clear trend  of increased larval mortality over time.  Nansen <i>et al. </i>(2013)  mention  that  the most  important  conditions  for the development and  the  infection  of  another   Tenebrionidae, <i>Cynaeus angustus, </i>by nematodes is soil moisture,  which in this experiment  was apparently  adequate for the movement and   action   of  the   nematode.  Maybe  the   relatively  low efficiency has to do with the origin of the nematode, which was obtained from a beetle of another family, having a certain influence. Although nematodes are not considered specific, Geden <i>et al</i>. (1985) obtained  satisfactory results controlling larvae  of  another   tenebrionid, <i>A.  diaperinus, </i>dispersing infective  juveniles  of <i>Steinernema  feltiae </i>to  the  floor  of poultry houses.</p>         <p><a name="f2"></a></p>    <p align="center"><img src="img/revistas/rudca/v19n1/v19n1a05f2.jpg"></p>     <p>   Comparing  the maximum  larval mortality produced by fungi and  nematodes, it appears that  the  latter  causes   a  faster and  increased mortality  of  larvae  of  the  false  wire-worm, thus  showing  an  advantage for the  possible  use  within a management program  of the insect.</p>     <p>   The  results   of  these   preliminary  experiments   revealed  a lower mortality  rate  as  expected,   based   on  previous  field observations. Apparently, the insect is tolerant to infection by these  fungi, at least under  the conditions  of the trial. In the case <i>M. anisopliae</i>, the low mortality rate can be attributed to   adverse   environmental   conditions,   since   infection   is influenced by temperature, moisture and particular conditions  such as pH, organic matter content  and texture, among  other physical properties  (Posada  &amp; Pava-Ripoll, 2010;  Bidochka <i>et al. </i>1998;  Quesada-Moraga <i>et al. </i>2007)  not evaluated  in this  study.  These  and  other  experimental  conditions   also influence  the  efficiency of <i>B.  bassiana. </i>Steinkraus <i>et  al</i>. (1991)  showed  that  the  susceptibility to  the  fungus  in the tenebrionid <i>Alphitobius diaperinus</i>, is influenced by the hosts instar, the substrate and the formulation of the inoculum.</p>     <p>   In  addition,   it  should   be   noted   that   the   experiments  were   conducted  with  soil   and   although    the   presence of  micro,   meso   and   macro   organisms  were  controlled, conditions   such   as  the  vials  moisture,   temperature  and soil  characteristics were difficult to control.  They influence infection by microorganisms and the insects contact  with the microorganism or its infective structures.</p>     <p>   The  contact   of  microorganisms  with  the  host   is  a  very important  factor  that  should  be  taken  into  account  when assessing its pathogenicity.   In this  context,  low larval and adult susceptibility may be due to the low affinity of fungi with the  rigid exoskeleton.  In the  case  of nematodes, a certain soil humidity is required,  sufficient to allow their movement through the soil and recognize the host to infect.</p>     <p>   Another factor to consider,  as mentioned above,  is that the soil used was completely free of any organism,  differing from natural  conditions  were  mites,  springtails  and  insects  not susceptible to the infection of the microorganisms evaluated, could  serve  as  means   of  transport   so  that  larvae  of  the target  species  could  come  into contact  with the  pathogen employed.</p>     ]]></body>
<body><![CDATA[<p>   From this preliminary and basic research, it can be concluded that  both,  the  entomopathogenic fungi and  the  nematode could be part of an integrated  management program  of the false  wire-worm,  once  a  suitable  dose  of inoculation  and the conditions  of optimal field condition  for adult and larval infection are established. Also it is considered important  to study the molecular  affinity of spores  of entomopathogenic and the insects instar.</p>     <p>   <b>Acknowledgment: </b>The authors thank the U.D.C.A for funding the  research  under  the  context  of ''young researcher'', first author  of this article. <u>Conflicts of interest</u>:  This manuscript was prepared  and revised with the participation of all authors,  who declare that there is no conflict of interest that could put in danger  the validity of the results.</p>     <p><b>BIBLIOGRAPHY</b></p>     <!-- ref --><p>1.   ALVES, S.B.;  LOPES, R.B. 2008.  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