<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">OALibJ</journal-id><journal-title-group><journal-title>Open Access Library Journal</journal-title></journal-title-group><issn pub-type="epub">2333-9705</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/oalib.1103805</article-id><article-id pub-id-type="publisher-id">OALibJ-80474</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Biomedical&amp;Life Sciences</subject><subject> Business&amp;Economics</subject><subject> Chemistry&amp;Materials Science</subject><subject> Computer Science&amp;Communications</subject><subject> Earth&amp;Environmental Sciences</subject><subject> Engineering</subject><subject> Medicine&amp;Healthcare</subject><subject> Physics&amp;Mathematics</subject><subject> Social Sciences&amp;Humanities</subject></subj-group></article-categories><title-group><article-title>
 
 
  Population Dynamics of &lt;i&gt;Saissetia oleae&lt;/i&gt; (Olivier) (Hemiptera: Coccidae) on Olives
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Faiza</surname><given-names>Ilias</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Fatiha</surname><given-names>Hammadi</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib></contrib-group><aff id="aff2"><addr-line>National Institute of Plant Protection, Tlemcen, Algeria</addr-line></aff><aff id="aff1"><addr-line>Center University of Belhadj Bouchaib, Ain Temouchent, Algeria</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>faizahope@yahoo.fr(FI)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>01</day><month>11</month><year>2017</year></pub-date><volume>04</volume><issue>11</issue><fpage>1</fpage><lpage>8</lpage><history><date date-type="received"><day>4,</day>	<month>July</month>	<year>2017</year></date><date date-type="rev-recd"><day>19,</day>	<month>November</month>	<year>2017</year>	</date><date date-type="accepted"><day>22,</day>	<month>November</month>	<year>2017</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  A preliminary study on fluctuation of black scale, 
  Saissetia
   
  oleae
   
  (Olivier) (Hemiptera: Coccidae), was carried out in Algeria in order to assess population dynamics and infestation incidence on olive groves. Monitoring was conducted in two years (2014-2015) in three localities in North Algeria. The density of populations has varied from year to year and from region to region. Populations peaked in June, when crawlers eme
  rged after the egg-laying period, and decreased during several months. Additionally, 
  S.
   
  oleae
   
  can be considered a risky pest of olive groves in Algeria. Therefore, further studies on population dynamics are necessary for a better understanding of its biology in this Algeria.
 
</p></abstract><kwd-group><kwd>&lt;i&gt;Saissetia oleae&lt;/i&gt;</kwd><kwd> Dynamics</kwd><kwd> Olive</kwd><kwd> Region</kwd><kwd> Generation</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Saissetia oleae (Olivier) (Hemiptera: Coccidae), the black scale, is one of the most important pests of olive in the Mediterranean region and of citrus trees. As discussed by Tena [<xref ref-type="bibr" rid="scirp.80474-ref1">1</xref>] , Mediterranean black scale generally continues to be a problem in most coastal citrus growing areas of the world. According to Haniotakis [<xref ref-type="bibr" rid="scirp.80474-ref2">2</xref>] , black scale is considered a major secondary pest, meaning that it occurs throughout the Mediterranean region, causing damages of major economic importance locally or occasionally. As discussed by Tena [<xref ref-type="bibr" rid="scirp.80474-ref1">1</xref>] , the damages are produced when large populations are present; their feeding can cause physiological damage to the host plant through an increase in the transpiration rate and by depletion of nutrients.</p><p>In Algeria, as discussed elsewhere [<xref ref-type="bibr" rid="scirp.80474-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.80474-ref4">4</xref>] , Saissetia oleae (Olivier) (Hemiptera: Coccidae), Polliniapollini (Costa) (Hemiptera: Coccidae) and Parlatoriaoleae (Colve’e) (Hemiptera: Diaspididae) represent the most important scale of olive. S. oleae infests leaves and twigs of citrus and olives. Black scale is known by its high reproductive capacity, the number of eggs laid by the scale range from a few hundreds to 4000 as discussed elsewhere [<xref ref-type="bibr" rid="scirp.80474-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.80474-ref6">6</xref>] . After hatching, the crawlers move out of the egg chamber beneath the mother’s body and they wander over the host plant searching for a suitable place to settle, Tena [<xref ref-type="bibr" rid="scirp.80474-ref1">1</xref>] . In Mediterranean countries, this species may have one generation per year, one and a partial second generation, or two complete generations, depending on crop species, nutrition of the tree, agricultural practices, possibly different strains of S. oleae, and most importantly, climate as discussed elsewhere [<xref ref-type="bibr" rid="scirp.80474-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.80474-ref7">7</xref>] .</p><p>In Algeria, the life cycle of S. oleae remains unclear, with the reported number of generations. Moreover, no long-term and area-wide studies have been conducted to determine and compare its life cycle in olive orchards at many regions.</p></sec><sec id="s2"><title>2. Material and Methods</title><sec id="s2_1"><title>2.1. Experimental Site</title><p>The study was evaluated in the field with data gathered from 2014 and 2015 in three traditional olive groves: 1) Ain Temouchent: 35˚19'60&quot;N, 1˚4'60&quot;W, 296 m, 2) Mascara: 35˚25'0&quot;N, 0˚10'0&quot;E, 676 m, (3) SidiBel Abbes: 35˚11'38&quot;N, 0˚38'29&quot;W, 483 m, in Algeria. Neither of these olive groves received any chemical treatment during the study. The first orchard of 2 ha was 15 years old, the second of 3 ha was 9 years old and the third of 7 ha was 22 years.</p></sec><sec id="s2_2"><title>2.2. Data Collection</title><p>During the years 2014 and 2015, a sample of 40 branches, each 20 cm in length, was taken monthly and examined to determine the population density of the developmental instars (eggs, crawlers, nymphs and female adults) of five randomly selected olive trees and the relative abundance and the flight dynamics of adult on different olive organs.</p><p>The densities of first-instar and second-instar nymphs were calculated on old and young parts. The density was reported on 400 old leaves (10 leaves &#215; 40 branches) and on 200 young leaves (5 young leaves &#215; 40 branches) and the results were given per leaf. For the young branches (10 cm length), the averages were calculated per linear meter. For the old branches (25 cm length), average numbers were obtained by dividing the crawlers and nymphs found on 40 branches by 1000 cm (40 &#215; 25 cm) to have density by linear meter, as discussed by Ouguas [<xref ref-type="bibr" rid="scirp.80474-ref8">8</xref>] .</p><p>The spatial distribution of crawlers and nymphs was compared with cardinal directions all the groves. The volume of mature females was compared with the three groves and year (2014 and 2015) as main factors.</p></sec><sec id="s2_3"><title>2.3. Data Analysis</title><p>One-way analysis of variance (Anona) and Tukey’s honestly significant difference (HSD) test (p &lt; 0.05) were used to compare the means amond different generations and/or years. Although data were transformed for statistical analysis, means and standard errors based on the original data are presented in figures. Calculations were one with MINITAB 15.</p></sec></sec><sec id="s3"><title>3. Results</title><p>Figures 1-3 shows the seasonal abundance of the olive scale, S. oleae was studied for two successive years from 2014-2015 on three olive groves. The obtained results showed considerable fluctuations in abundance during the year. Populations peaked in summer (June), when crawlers emerged after the egg-laying period in April and May, and decreased during the next several months.</p><p>Crawler emergence was relatively synchronized across all groves during the first generation in July. The cumulative percentage of first instars emerged in spring-summer in each grove and year is compared in fig. The second emergence period was observed in the grove of Ain Temouchent was less synchronized and more extended. This period started in September-November and lasted until March as shows <xref ref-type="fig" rid="fig2">Figure 2</xref>. In Mascara and SidiBel Abbes groves, <xref ref-type="fig" rid="fig1">Figure 1</xref> and <xref ref-type="fig" rid="fig3">Figure 3</xref> shows one generation that peaked in June. These results due to probably to the climate change with the high temperature during the two years of study.</p><p>In the old grove of SidiBel Abbes, the eggs started to be laid in May 2014 and they reached their maximum in July (2245 eggs per linear meter) and did not reappear until May 2015 of next year with a maximum in August (4989 eggs per linear meter). Adult females, they appeared from early January to October in 2014 and appear April until October in 2015.</p><p>The crawlers densities are 0.1 to 2.52 in 2014 and 0.3 to 3.1 in 2014. We can note that the duration of different instars was longer in the two years because the rainfall was abundant and so the humidity was suitable for them.</p><p>In Ain Temouchent and Mascara groves (the young orchard), eggs appeared from Marsh to October in the two years and for the both groves. The maximum number of eggs was about 1896 eggs per linear meter in Mascara and 2341 eggs per linear meter in Ain Temouchent. The crawlers followed the same trend as in the previous orchard. Indeed, the crawlers appeared from Marsh and persisted until November in Mascara and to April until October in Ain Temouchent.</p><p>The third-instar nymphs were present in from January to December in the years 2005. As in the old orchard, the adult females were found in surveys conducted between January and November with different peaks; 39 adult females per linear meter in 2014 in Ain Temouchent and 30 adult females perlinear meter in Mascara.</p><p>Crawler density present a peak of 4.02 per old leaf as maximum and 3.01 per young leaf and a maximum of 3.3 on old branches and 1.6 on young branches. <xref ref-type="fig" rid="fig4">Figure 4</xref> shows the presence of these instars was concentrated between April and September with a high peak in 2015. Statistically, these densities varied significantly from one organ to another (P = 0.003). These immature instars showed a preference for the young leaves and branches.</p><p>Adult females that were collected during the spring and old grove laid a maximum of 3.157 eggs in olives, whereas females that were collected in autumn in young grove laid a maximum of 953.120 eggs. There was a significant relationship between ovipositing female volumes and number of eggs found beneath females as shows <xref ref-type="fig" rid="fig5">Figure 5</xref>. Female volume was variable depending on season, region, age and location on the tree.</p><p>The spatial distribution of crawlers and nymphs of S. oleae according to the cardinal directions of the tree demonstrate that the Center is the preferable</p><p>direction for the both followed by North, South directions respectively as shows <xref ref-type="fig" rid="fig6">Figure 6</xref>. The Center represents 30 crawlers per linear meter 10<sup>3</sup> and 28 nymphs per linear meter 10<sup>3</sup>. The East represents the last direction preferred by Crawlers and nymphs with 10 and 11 per linear meter 10<sup>3</sup> respectively.</p></sec><sec id="s4"><title>4. Discussion</title><p>This study presents the dynamics and densities population structure of S. oleae, including number of generations and crawler emergence periods between 2014 and 2015 in three regions of olive groves in North Algeria.</p><p>In this study, S. oleae adults appear from April to September or October, because of synchronized and concentrated crawler emergence after the egg laying period in Marsh-May. We suggest that the climate change with the high temperature in summer change or influence the development of S. oleae. Our observations are not similar to those of other western Mediterranean authors, most of</p><p>whom reported crawler emergence in June-July, as discussed elsewhere [<xref ref-type="bibr" rid="scirp.80474-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.80474-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.80474-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.80474-ref10">10</xref>] .</p><p>In our study, it’s a partial second crawler emergence in Ain Temouchent. Tena [<xref ref-type="bibr" rid="scirp.80474-ref1">1</xref>] , reported that the second generation is heterogeneous and variable depending on year, crop, and grove.</p><p>Saissetia oleae populations exhibited considerable abundance fluctuations during the year. Population density decreased for several months, especially during the summer, because of high mortality of first-instar scales, Tena [<xref ref-type="bibr" rid="scirp.80474-ref1">1</xref>] . Most eggs and crawlers that hatched during the winter perished, as discussed elsewhere [<xref ref-type="bibr" rid="scirp.80474-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.80474-ref12">12</xref>] . In Spain, Tena [<xref ref-type="bibr" rid="scirp.80474-ref1">1</xref>] , demonstrates that low temperatures synchronized the developmental stages present, and consequently, populations were strongly synchronous after the winter.</p><p>In our study, crawlers showed a preference for the young leaves and branches. These results are similar to those of Morroco. Ouguas [<xref ref-type="bibr" rid="scirp.80474-ref8">8</xref>] , who suggest that young tissues are rich in sap and tender, young crawlers can easily suck the sap. Also, these crawlers remain on the same organ and do not move far away from it as discussed by Paparatti [<xref ref-type="bibr" rid="scirp.80474-ref13">13</xref>] . Crawlers will moult after one month and then migrate to the young stems and branches of the tree, as discussed by Sekkat [<xref ref-type="bibr" rid="scirp.80474-ref14">14</xref>] .</p><p>A significant relationship between female volume and number of eggs that they contained are beneath their bodies. This relation was also observed by Pereira [<xref ref-type="bibr" rid="scirp.80474-ref10">10</xref>] in olive groves and Tena [<xref ref-type="bibr" rid="scirp.80474-ref1">1</xref>] in olive and citrus groves. The volume of the female represents its potential fecundity more accurately than the number of eggs found in a particular moment as discussed by Tena [<xref ref-type="bibr" rid="scirp.80474-ref1">1</xref>] .</p><p>S. oleae showed a preference to the Center direction. The North, Center and the East are the favorite spot for Parlatoriaziziph scale in Algeria as discussed by Belguendouz [<xref ref-type="bibr" rid="scirp.80474-ref15">15</xref>] . They reported that, larvas, nymphs and femellesadultesprefered the Center and North directions. It’s due to the conditions climatiques, microclimatiques of the region and the nutriments elements necessary for the development and reproduction.</p><p>Our result showed that climate has a big influence upon scale spread and infestation, it’s showed an important level’s infestation especially on autumn and spring season, also, young organs are more infested than the old organs. Also, this study showed also, that Saissetia oleae population was very important in the center direction where the humidity is high with low mild temperature and light.</p></sec><sec id="s5"><title>Cite this paper</title><p>Ilias, F. and Hammadi, F. (2017) Population Dynamics of Saissetia oleae (Olivier) (Hemiptera: Coccidae) on Olives. Open Access Library Journal, 4: e3805. https://doi.org/10.4236/oalib.1103805</p></sec></body><back><ref-list><title>References</title><ref id="scirp.80474-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Tena, A., Soto, A., Vercher, R. and Garcia-Mari, F. (2007) Density and Structure of Saissetiaoleae (Hemiptera: Coccidae) Populations on Citrus and Olives: Relative Importance of the Two Annual Generations. Environmental Entomology, 36, 700-706. https://doi.org/10.1093/ee/36.4.700</mixed-citation></ref><ref id="scirp.80474-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Haniotakis, G.E. (2005) Olive Pest Control: Present Status and Prospects. Proceedings of the IOBC/WPRS Conference on Integrated Protection of Olive Crops, Chania, 29-31 May 2003.</mixed-citation></ref><ref id="scirp.80474-ref3"><label>3</label><mixed-citation publication-type="other" xlink:type="simple">Moghaddam, M. and Tavaloli, M. 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