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<article article-type="research-article" dtd-version="1.0" specific-use="sps-1.6" xml:lang="es" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">
	<front>
		<journal-meta>
			<journal-id journal-id-type="publisher-id">rfnam</journal-id>
			<journal-title-group>
				<journal-title>Revista Facultad Nacional de Agronomía, Medellín</journal-title>
				<abbrev-journal-title abbrev-type="publisher">Rev.Fac.Nal.Agr.Medellín</abbrev-journal-title>
			</journal-title-group>
			<issn pub-type="ppub">0304-2847</issn>
			<publisher>
				<publisher-name>Facultad de Ciencias Agrarias - Universidad Nacional de Colombia</publisher-name>
			</publisher>
		</journal-meta>
		<article-meta>
			<article-id pub-id-type="doi">10.15446/rfna.v70n2.64519</article-id>
			<article-categories>
				<subj-group subj-group-type="heading">
					<subject>Artículos</subject>
				</subj-group>
			</article-categories>
			<title-group>
				<article-title>Diaspididae en <italic>Citrus spp.</italic> (Rutaceae) de Colombia: Nuevos registros y una clave taxonómica para su identificación</article-title>
				<trans-title-group xml:lang="en">
					<trans-title>Diaspididae on <italic>Citrus spp.</italic> (Rutaceae) from Colombia: New records and a taxonomic key to their identification</trans-title>
				</trans-title-group>
			</title-group>
			<contrib-group>
				<contrib contrib-type="author">
					<name>
						<surname>Ramos-Portilla</surname>
						<given-names>Andrea Amalia</given-names>
					</name>
					<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
					<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
				</contrib>
				<contrib contrib-type="author">
					<name>
						<surname>Caballero</surname>
						<given-names>Alejandro</given-names>
					</name>
					<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
				</contrib>
			</contrib-group>
			<aff id="aff1">
				<label>1</label>
				<institution content-type="original"> Dirección técnica de Sanidad Vegetal. Instituto Colombiano Agropecuario (ICA). Carrera 41 No. 17-81. Bogotá, Colombia.</institution>
				<institution content-type="normalized">Instituto Colombiano Agropecuario</institution>
				<institution content-type="orgdiv1">Dirección técnica de Sanidad Vegetal</institution>
				<institution content-type="orgname">Instituto Colombiano Agropecuario</institution>
				<addr-line>
					<named-content content-type="city">Bogotá</named-content>
				</addr-line>
				<country country="CO">Colombia</country>
			</aff>
			<aff id="aff2">
				<label>2</label>
				<institution content-type="original"> Facultad de Ciencias Agrarias. Universidad Nacional de Colombia. A.A. 14490, Bogotá, Colombia. lacaballeror@unal.edu.co</institution>
				<institution content-type="normalized">Universidad Nacional de Colombia</institution>
				<institution content-type="orgdiv1">Facultad de Ciencias Agrarias</institution>
				<institution content-type="orgname">Universidad Nacional de Colombia</institution>
				<addr-line>
					<named-content content-type="city">Bogotá</named-content>
				</addr-line>
				<country country="CO">Colombia</country>
				<email>Colombia</email>
				<email>lacaballeror@unal.edu.co</email>
			</aff>
			<pub-date pub-type="epub-ppub">
				<season>May-Aug</season>
				<year>2017</year>
			</pub-date>
			<volume>70</volume>
			<issue>2</issue>
			<fpage>8139</fpage>
			<lpage>8154</lpage>
			<history>
				<date date-type="received">
					<day>22</day>
					<month>07</month>
					<year>2016</year>
				</date>
				<date date-type="accepted">
					<day>08</day>
					<month>03</month>
					<year>2017</year>
				</date>
			</history>
			<permissions>
				<license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by-nc-sa/4.0/" xml:lang="es">
					<license-p>Este es un artículo publicado en acceso abierto bajo una licencia Creative Commons</license-p>
				</license>
			</permissions>
			<abstract>
				<title>RESUMEN</title>
				<p>En este manuscrito se registra por primera vez para Colombia a <italic>Aonidiella comperei</italic>; los especímenes se encontraron asociados a ramas, hojas y frutos de <italic>Citrus</italic> x <italic>latifolia</italic> (Rutaceae) en el departamento del Tolima. Además, se verifica la asociación <italic>Parlatoria ziziphi</italic> y <italic>Citrus</italic> x <italic>limonia</italic> (Rutaceae), a partir de recolecciones en campo; hasta la fecha, su único registro para el país provenía de especímenes interceptados en puertos de entrada en Estados Unidos. Se provee información de características en campo y en montaje en lámina para <italic>A. comperei</italic>, al igual que una clave taxonómica de especies de Diaspididae presentes en <italic>Citrus</italic> spp. de Colombia.</p>
			</abstract>
			<trans-abstract xml:lang="en">
				<title>ABSTRACT</title>
				<p>In this manuscript <italic>Aonidiella comperei</italic> is reported for the first time in Colombia; the specimens were found associated with branches, leaves and fruits of <italic>Citrus</italic> x <italic>latifolia</italic> (Rutaceae) in the department of Tolima. Also we obtained physical evidence of the association of <italic>Parlatoria ziziphi</italic> and <italic>Citrus</italic> x <italic>limonia</italic> (Rutaceae) in Colombia from a sample collected in the field; until this paper the only record of <italic>P. ziziphi</italic> in the country came from specimens intercepted in a quarantine inspection at a port of entry in the United States. Field and slide-mounted characteristics are provided for <italic>A. comperei</italic>. Also a taxonomic key to species of Diaspididae present on <italic>Citrus</italic> spp. in Colombia is given.</p>
			</trans-abstract>
			<kwd-group xml:lang="es">
				<title>Palabras clave:</title>
				<kwd>Coccomorpha</kwd>
				<kwd>Especies invasivas</kwd>
				<kwd>Región neotropical</kwd>
				<kwd>Nuevos hospedantes</kwd>
				<kwd>Plaga</kwd>
			</kwd-group>
			<kwd-group xml:lang="en">
				<title>Keywords:</title>
				<kwd>Coccomorpha</kwd>
				<kwd>Invasive species</kwd>
				<kwd>Neotropical region</kwd>
				<kwd>New host</kwd>
				<kwd>Pest</kwd>
			</kwd-group>
			<counts>
				<fig-count count="18"/>
				<table-count count="1"/>
				<equation-count count="0"/>
				<ref-count count="54"/>
				<page-count count="16"/>
			</counts>
		</article-meta>
	</front>
	<body>
		<p>The Diaspididae (Hemiptera: Coccomorpha), commonly known as “armored scale insects”, is one of the most speciose families in that infraorder, and it is composed of 2650 species in 400 genera (<xref ref-type="bibr" rid="B20">García <italic>et al.</italic>, 2016</xref>). Armored scales occur on a wide variety of host plants encompassing more than 1,380 plant genera in 182 plant families (<xref ref-type="bibr" rid="B39">Miller and Davidson, 2005</xref>). This family is particularly important in agriculture and wild vegetation (<xref ref-type="bibr" rid="B54">Zamudio and Claps, 2005</xref>) because it includes numerous highly prolific species that can reach high populations and become serious pests of several crops (<xref ref-type="bibr" rid="B9">Claps and Teran, 2001</xref>).</p>
		<p>On <italic>Citrus</italic> spp. (Rutaceae) there are records of 112 species of Diaspididae (<xref ref-type="bibr" rid="B20">García <italic>et al.</italic>, 2016</xref>), of which 19 have been recorded in Colombia (<xref ref-type="bibr" rid="B4">Balachowsky, 1959</xref>, <xref ref-type="bibr" rid="B4">1959a</xref>; <xref ref-type="bibr" rid="B16">Figueroa, 1946</xref>, <xref ref-type="bibr" rid="B17">1952</xref>, <xref ref-type="bibr" rid="B18">1977</xref>; <xref ref-type="bibr" rid="B19">Gallego and Vélez, 1992</xref>; <xref ref-type="bibr" rid="B23">Kondo, 2001</xref>; <xref ref-type="bibr" rid="B22">Kondo <italic>et al.</italic>, 2012</xref>; <xref ref-type="bibr" rid="B40">Mosquera, 1979</xref>; <xref ref-type="bibr" rid="B43">Posada, 1989</xref>).</p>
		<p>The genus <italic>Aonidiella</italic> Berlese and Leonardi 1896 has 32 species described around the world, and includes pest species such as <italic>Aonidiella aurantii</italic> (Maskell), it is considered as the most injurious pest of citrus crops around the world (<xref ref-type="bibr" rid="B38">Miller and Davison 1990</xref>), <italic>Aonidiella citrina</italic> (Coquillett) in citrus (<xref ref-type="bibr" rid="B13">EFSA PLH Panel, 2014</xref>); <italic>
 <bold>Aonidiella eremocitri</bold>
</italic> McKenzie on oil palm and coconut (<xref ref-type="bibr" rid="B27">Mariau, 1998</xref>); <italic>
 <bold>Aonidiella gracilis</bold>
</italic> (Balachowsky) on cacao (<xref ref-type="bibr" rid="B26">Liegeois, 1944</xref>); <italic>
 <bold>Aonidiella inornata</bold>
</italic> (McKenzie) on papaya (<xref ref-type="bibr" rid="B25">Lee and Wen, 1977</xref>) and mango (<xref ref-type="bibr" rid="B8">Chua and Wood, 1990</xref>); <italic>
 <bold>Aonidiella orientalis</bold>
</italic> (Newstead) recorded as a pest of several agricultural crops such as citrus (<xref ref-type="bibr" rid="B45">Rose, 1990</xref>), tea (<xref ref-type="bibr" rid="B41">Nagarkatti and Sankaran, 1990</xref>), date palm (<xref ref-type="bibr" rid="B44">Rajagopal and Krishnamoorty, 1996</xref>), palms and ornamentals (<xref ref-type="bibr" rid="B12">Dekle, 1976</xref>), papaya (<xref ref-type="bibr" rid="B14">Elder et al., 1998</xref>) and mango (<xref ref-type="bibr" rid="B48">Swirski et al., 2002</xref>); and <italic>Aonidiella taxus</italic> Leonardi recorded causing damage to <italic>Taxus</italic> sp. and <italic>Podocarpus</italic> sp. trees (<xref ref-type="bibr" rid="B35">Miller and Davidson, 1990</xref>). In Colombia, only <italic>A. orientalis</italic> has been hitherto recorded (<xref ref-type="bibr" rid="B23">Kondo, 2001</xref>; <xref ref-type="bibr" rid="B43">Posada, 1989</xref>).</p>
		<p>Before this study, <italic>Aonidella comperei</italic> McKenzie was recorded in 22 countries in the Neotropical and Oriental regions (García <italic>et al.</italic>, 2016). In the Neotropics, <italic>A. comperei</italic> has been recorded in Brazil (<xref ref-type="bibr" rid="B11">Culik et al., 2008</xref>; <xref ref-type="bibr" rid="B28">Martins et al., 2004</xref>), Dominica (<xref ref-type="bibr" rid="B34">McKenzie, 1946</xref>), Guadeloupe (<xref ref-type="bibr" rid="B1">Balachowsky, 1957</xref>), Guatemala (<xref ref-type="bibr" rid="B34">McKenzie, 1946</xref>), Haiti (<xref ref-type="bibr" rid="B34">McKenzie, 1946</xref>) Martinique (<xref ref-type="bibr" rid="B1">Balachowsky, 1957</xref>), Puerto Rico (<xref ref-type="bibr" rid="B31">Martorell, 1976</xref> ), Saint Martin (<xref ref-type="bibr" rid="B32">Matile and Etienne, 2006</xref>) and the U.S. Virgin Islands (<xref ref-type="bibr" rid="B42">Nakahara, 1983</xref>).</p>
		<p><italic>Aonidiella comperei</italic> is considered an important pest species of papaya, <italic>Carica papaya</italic> L. (Caricaceae) in Brazil because it has a widespread distribution and frequent occurrence; it causes cosmetic damage to fruit and weakens it host plant, and is also of concern as a pest of quarantine significance (Martins <italic>et al</italic>., 2014). It is a polyphagous species, affecting 14 plant species belonging to 12 families: <italic>Annona muricata</italic> L. (Annonaceae) (<xref ref-type="bibr" rid="B31">Martorell, 1976</xref>), <italic>Cocos nucifera</italic> L. (Arecaceae) (<xref ref-type="bibr" rid="B34">McKenzie, 1946</xref>), <italic>Pluchea odorata</italic> (L.) (Asteraceae) (<xref ref-type="bibr" rid="B53">Williams and Watson, 1988</xref>), <italic>Carica papaya</italic> (<xref ref-type="bibr" rid="B29">Martins <italic>et al.</italic>, 2004</xref>), <italic>Cucurbita maxima</italic> Duchesne (Cucurbitaceae) (<xref ref-type="bibr" rid="B51">Velasquez, 1971</xref>), <italic>Diospyros</italic> sp. (Ebenaceae) (<xref ref-type="bibr" rid="B53">Williams and Watson, 1988</xref>), <italic>Annesijoa</italic> sp. (Euphorbiaceae) (<xref ref-type="bibr" rid="B53">Williams and Watson 1988</xref>), <italic>Ficus</italic> sp. (Moraceae) (<xref ref-type="bibr" rid="B53">Williams and Watson, 1988</xref>), <italic>Musa</italic> sp. (Musaceae) (<xref ref-type="bibr" rid="B53">Williams and Watson, 1988</xref>), <italic>Morinda citrifolia</italic> L. (Rubiaceae) (<xref ref-type="bibr" rid="B53">Williams and Watson, 1988</xref>), <italic>Citrus aurantifolia</italic> Swingle (<xref ref-type="bibr" rid="B34">McKenzie, 1946</xref>), <italic>Citrus maxima</italic> (Burm.) (<xref ref-type="bibr" rid="B34">McKenzie, 1946</xref>), <italic>Citrus</italic> sp. (Rutaceae) (<xref ref-type="bibr" rid="B33">McKenzie, 1937</xref>) and <italic>Vitis</italic> sp. (Vitaceae) (<xref ref-type="bibr" rid="B34">McKenzie, 1946</xref>).</p>
		<p><italic>Parlatoria ziziphi</italic> (Lucas) is a cosmopolitan species (<xref ref-type="bibr" rid="B20">Garcia <italic>et al.</italic>, 2016</xref>), known to occur in Africa, Asia, Central and South America, Europe, Oceania, and the West Indies (<xref ref-type="bibr" rid="B39">Miller and Davidson, 2005</xref>). The species is considered to have a very limited host range, probably <italic>Citrus</italic> spp., <italic>Murraya</italic> spp., <italic>Poncirus</italic> spp., and <italic>Severinia</italic> spp., with <italic>Citrus</italic> spp. being the predominant host (<xref ref-type="bibr" rid="B37">Miller and Davidson, 2005</xref>). In Colombia this species was recorded by <xref ref-type="bibr" rid="B7">Blackburn and Miller (1984)</xref> based on information from the United States Department of Agriculture, without information about its hosts.</p>
		<p><italic>Parlatoria ziziphi</italic> is known as “the black parlatoria scale” and it has long been considered one of the major pests of citrus in certain areas (<xref ref-type="bibr" rid="B39">Miller and Davidson, 2005</xref>). Heavy infestations of this scale cause chlorosis and premature leaf drop, dieback of twigs and branches, stunting and distortion of fruit, and premature fruit drop and perhaps the most characteristic damage is the virtually unremovable scale cover on the fruit (<xref ref-type="bibr" rid="B37">Miller and Davidson, 2005</xref>). <xref ref-type="bibr" rid="B5">Beardsley and González (1975)</xref> and <xref ref-type="bibr" rid="B35">Miller and Davidson (1990)</xref> considered this species as a serious world pest.</p>
		<p>The purpose of this paper is to provide new biological information of <italic>Aonidiella</italic> 
 <italic>comperei</italic> and <italic>Parlatoria ziziphi</italic>. We report for the first time <italic>A. comperei</italic> and <italic>P. ziziphi</italic> on <italic>Citrus</italic> spp. in Colombia. Brief diagnoses of the adult females are given for both species. An updated list and a taxonomic key of all species of Diaspididae recorded on <italic>Citrus</italic> spp. (Rutaceae) from Colombia is provided.</p>
		<sec sec-type="materials|methods">
			<title>MATERIALS AND METHODS</title>
			<p>Samples of scales insects were collected on fruits and leaves of Key lime, <italic>Citrus</italic> x <italic>latifolia</italic> Tanaka ex Q. Jiménez (Rutaceae) from commercial crops in the department of Tolima, by the first author as part of plant health surveillance activities conducted by the Colombian Agricultural Institute (ICA) and on leaves of <italic>Citrus</italic> x <italic>limonia</italic> (L.) Osbeck (Rutaceae) in the department of Atlántico by entomologist Oscar Dix. </p>
			<p>Slide-mounted specimens were prepared according to the protocol by <xref ref-type="bibr" rid="B47">Siresena <italic>et al</italic>. (2013)</xref>; however, the exposure time to which the specimens were subjected to the chemical reagents was modified. The specimens are deposited at the “Universidad Nacional Agronomía Bogotá” UNAB entomological museum, Facultad de Ciencias Agrarias, Universidad Nacional de Colombia, Sede Bogotá, Bogotá, Cundinamarca, Colombia. Imaging analysis was done under a phase contrast microscope Nikon Eclipse E600 and the software Image Pro Insight v 8.0. </p>
			<p>Specimens were identified by checking the morphological descriptions of <xref ref-type="bibr" rid="B33">McKenzie (1937)</xref>, <xref ref-type="bibr" rid="B6">Beardsley (1966)</xref>, <xref ref-type="bibr" rid="B39">Miller and Davidson (2005)</xref> and by using the keys by <xref ref-type="bibr" rid="B6">Beardsley (1966)</xref>, <xref ref-type="bibr" rid="B53">Williams and Watson (1988)</xref> and <xref ref-type="bibr" rid="B37">Miller and Davidson (2005)</xref>. The taxonomic key of species of Diaspididae of <italic>Citrus</italic> spp. for Colombia is based on morphological external features of the adult female. The species included in the key correspond to those recorded on <italic>Citrus</italic> spp. from Colombia by <xref ref-type="bibr" rid="B4">Balachowsky (1959)</xref>, <xref ref-type="bibr" rid="B16">Figueroa (1946</xref>, <xref ref-type="bibr" rid="B17">1952</xref>, <xref ref-type="bibr" rid="B18">1977</xref>), <xref ref-type="bibr" rid="B19">Gallego and Vélez (1992)</xref>, <xref ref-type="bibr" rid="B23">Kondo (2001)</xref> and <xref ref-type="bibr" rid="B43">Posada (1989)</xref>. </p>
		</sec>
		<sec sec-type="results|discussion">
			<title>RESULTS AND DISCUSSION</title>
			<p><italic>Aonidiella comperei</italic><xref ref-type="bibr" rid="B33">McKenzie 1937</xref>, 327. Type data: INDIA: Bombay, Calaba, on <italic>Citrus</italic> sp. </p>
			<p><italic>Chrysomphalus comperei</italic> Lindinger 1957: 545 </p>
			<p>
				<fig id="f1">
					<label>Figure 1</label>
					<caption>
						<title>Fruit (left) and branch (right) of Citrus x latifolia infested with Aonidiella comperei.</title>
					</caption>
					<graphic xlink:href="0304-2847-rfnam-70-02-08139-gf1.jpg"/>
				</fig>
			</p>
			<sec>
				<title>Field characteristics</title>
				<p>The female scale is circular, smooth, flat, light brown in the center, surrounded by a white halo (<xref ref-type="fig" rid="f2">Figure 2A</xref>). The insect is reniform, membranous and yellow when it is young (<xref ref-type="fig" rid="f2">Figure 2B</xref>) and it turns orange and sclerotized at maturity (<xref ref-type="fig" rid="f2">Figure 2C</xref>). The female has two nymphal instars, all of them slightly darker than the adult female (<xref ref-type="fig" rid="f2">Figure 2D</xref>).</p>
				<p>
					<fig id="f2">
						<label>Figure 2</label>
						<caption>
							<title>Live specimens of Aonidiella comperei. A. Two stages of development, N1: first-instar nymph, N2: second-instar nymph B. Adult female cover. C. Young adult female separated from its scale; D. Mature adult female after removal of scale.</title>
						</caption>
						<graphic xlink:href="0304-2847-rfnam-70-02-08139-gf2.jpg"/>
					</fig>
				</p>
			</sec>
			<sec>
				<title>Slide-mounted characters</title>
				<p>The adult female is reniform, highly sclerotized at maturity (<xref ref-type="fig" rid="f3">Figure 3A</xref>). The following features are given by <xref ref-type="bibr" rid="B33">McKenzie (1937)</xref>: pygidium not heavily sclerotized; three pairs of lobes present, the median pair only slightly larger than the second pair (<xref ref-type="fig" rid="f3">Figure 3B</xref>); paraphyses small, short, and slender; tubular ducts broad and conspicuous (<xref ref-type="fig" rid="f3">Figure 3C</xref>); anal opening large; venter with a few small ducts, situated close to the margin of the pygidium; perivulvar pores present, in two groups only, of apparently no more than two pores in each group (<xref ref-type="fig" rid="f3">Figure 3D</xref>). The differences between A. comperei and A. orientalis are listed in <xref ref-type="table" rid="t1">Table 1</xref>.</p>
				<p>
					<fig id="f3">
						<label>Figure 3</label>
						<caption>
							<title>Slide-mounted features of Aonidiella comperei: A. Reniform and highly sclerotized mature adult female. B. Three pairs of lobes present on the pygidium, the median pair (a) only slightly larger than the second pair (b). C. Tubular ducts. D. Perivulvar pores in two groups, each with two pores. E. Prosomatic lobes well developed. F. Fringed plates lateral to third lobe.</title>
						</caption>
						<graphic xlink:href="0304-2847-rfnam-70-02-08139-gf3.jpg"/>
					</fig>
				</p>
				<p>
					<table-wrap id="t1">
						<label>Table 1</label>
						<caption>
							<title>Morphological differences between Aonidiella orientalis and A. comperei, showed as attributes. Character states taken from <xref ref-type="bibr" rid="B6">Beardsley (1966)</xref>, <xref ref-type="bibr" rid="B33">Mckenzie (1937)</xref> and <xref ref-type="bibr" rid="B53">Williams and Watson (1988)</xref>.</title>
						</caption>
						<graphic xlink:href="0304-2847-rfnam-70-02-08139-gt1.jpg"/>
					</table-wrap>
				</p>
			</sec>
			<sec>
				<title>Material studied</title>
				<p><bold>
 <italic>Aonidiella comperei</italic>
</bold> McKenzie. Colombia, Tolima, Chicoral, vereda Las Mercedes, finca El Diamante, 318 m.a.s.l., 04°13′41.34″ N, 75°00′11.1636″ W, 18th november 2015, coll. A. Ramos ex. leaves, branches and fruits of key lime, <italic>Citrus</italic> x <italic>latifolia</italic> (Rutaceae), 32♀♀, Catalogue No. UNAB 1837; Tolima, Espinal, vereda La Morena, Citriexpinal, 331 m.a.s.l., 04°13ʹ59.62ʺ N, 74°54ʹ23.96ʺ W, 2nd march 2016, coll. A. Ramos, ex. stored fruits of key lime, <italic>Citrus</italic> x <italic>latifolia</italic> (Rutaceae). 10♀♀, Catalogue No. UNAB 1837.</p>
				<p><bold>NOTE</bold>: The scale insects were found in high populations (<xref ref-type="fig" rid="f1">Figure 1</xref>).</p>
			</sec>
			<sec>
				<title><bold>
 <italic>Parlatoria ziziphi</italic> (Lucas)</bold></title>
				<p><italic>Coccus ziziphi</italic> Lucas, 1853: xxix. Type data: FRANCE: on <italic>Ziziphus pinnachristi</italic>. Syntypes, female. Described: female.</p>
				<p><italic>Chermes aurantii</italic> Boisduval, 1867: 338-339. [Synonymized by McKenzie, 1945: 54].</p>
				<p><italic>Parlatoria lucassi</italic> Targioni Tozzetti, 1868: 735. Nomen nudum.</p>
				<p><italic>Parlatoria</italic> (<italic>Websteriella</italic>) <italic>ziziphus</italic> (Lucas); Ramakrishna Ayyar, 1919: 26. Change of combination.</p>
				<p><italic>Apteronidia ziziphi</italic> (Lucas); Lindinger, 1934: 62. Change of combination.</p>
				<p><italic>Diaspis ziziphus</italic> (Lucas); Lindinger, 1934: 62. Change of combination.</p>
				<p><italic>Parlatoreopsis ziziphi</italic> (Lucas); Kawai, 1972: 23. Change of combination.</p>
			</sec>
			<sec>
				<title>Field characters</title>
				<p>According to <xref ref-type="bibr" rid="B39">Miller and Davidson (2005)</xref> the adult female cover is flat, broadly elongate oval, black with narrow white fringe, with two or three longitudinal ridges, shed skins marginal, black, primary component of cover second shed skin; white; body of newly matured adult female yellow brown, margin of body lateral of mouthparts with a small lobe; normally on leaves, also on branches and fruit. </p>
			</sec>
			<sec>
				<title>Slide-mounted characters </title>
				<p>The description and character states that differentiates <italic>P. ziziphi</italic> from others species of <italic>Parlatoria</italic> agrees well with those proposed by <xref ref-type="bibr" rid="B39">Miller and Davidson (2005)</xref>: body oval, length usually less than two times the greatest width; presence of perivulvar pores; marginal macroducts barrel shaped, length of ducts usually less than three times width of inner end of duct; a barrel shaped macroduct present between median lobes; plates or gland spines in space between median and second lobes with at least two apical fimbriations, usually more; with conspicuous ear-like lobes on body margin laterad of mouthparts. </p>
				<p>The differences between <italic>P. ziziphi</italic> and others species of <italic>Parlatoria</italic> present on <italic>Citrus</italic> spp. in Colombia are given in the key. </p>
			</sec>
			<sec>
				<title>Material studied</title>
				<p><bold>
 <italic>Parlatoria ziziphi</italic>
</bold> (Lucas). Colombia, Atlántico, Sabanagrande, Vda Los Caracoles, 9 m of altitude, 10°47’16.3” N, 74°46’07.2” W, 8th december 2015, coll. O. Dix; E. Palacino ex. <italic>Citrus</italic> 
 <italic>x limonia</italic> (Rutaceae), 23♀♀, Catal. UNAB 1885. </p>
				<p><bold>Updated list of species of Diaspididae on</bold> Citrus <bold>spp. from Colombia.</bold> Author(s) after the colon (:) correspond to whom recorded each species.</p>
				<p><italic>Acutaspis scutiformis</italic> (Cockerell, 1893): <xref ref-type="bibr" rid="B18">Figueroa (1977)</xref>.</p>
				<p><italic>Aonidiella comperei</italic> (<xref ref-type="bibr" rid="B33">McKenzie, 1937</xref>): Present study.</p>
				<p><italic>Aspidiotus nerii</italic> (Costa, 1829): <xref ref-type="bibr" rid="B19">Gallego and Vélez (1992)</xref>, <xref ref-type="bibr" rid="B22">Kondo et al. (2012)</xref>, <xref ref-type="bibr" rid="B43">Posada (1989)</xref>.</p>
				<p><italic>Aulacaspis tubercularis</italic> (Newstead, 1906): <xref ref-type="bibr" rid="B22">Kondo et al. (2012)</xref>, <xref ref-type="bibr" rid="B43">Posada (1989)</xref>.</p>
				<p><italic>Chrysomphalus aonidum</italic> (Linnaeus, 1758): <xref ref-type="bibr" rid="B4">Balachowsky (1959)</xref>, <xref ref-type="bibr" rid="B16">Figueroa (1946</xref>, <xref ref-type="bibr" rid="B17">1952</xref>, <xref ref-type="bibr" rid="B18">1977</xref>), <xref ref-type="bibr" rid="B19">Gallego and Vélez (1992)</xref>, <xref ref-type="bibr" rid="B22">Kondo et al. (2012)</xref>, <xref ref-type="bibr" rid="B40">Mosquera (1979)</xref>, <xref ref-type="bibr" rid="B43">Posada (1989)</xref>.</p>
				<p><italic>Chrysomphalus dictyospermi</italic> (Morgan, 1889): <xref ref-type="bibr" rid="B16">Figueroa (1946</xref>, <xref ref-type="bibr" rid="B17">1952</xref>, <xref ref-type="bibr" rid="B18">1977</xref>), <xref ref-type="bibr" rid="B19">Gallego and Vélez (1992)</xref>, <xref ref-type="bibr" rid="B22">Kondo et al. (2012)</xref>, <xref ref-type="bibr" rid="B40">Mosquera (1979)</xref>, <xref ref-type="bibr" rid="B43">Posada (1989)</xref>.</p>
				<p><italic>Hemiberlesia lataniae</italic> (Signoret, 1869): <xref ref-type="bibr" rid="B22">Kondo et al. (2012)</xref>, <xref ref-type="bibr" rid="B43">Posada (1989)</xref>.</p>
				<p><italic>Hemiberlesia palmae</italic> (Cockerell, 1892): <xref ref-type="bibr" rid="B22">Kondo et al. (2012)</xref>, <xref ref-type="bibr" rid="B43">Posada (1989)</xref>.</p>
				<p><italic>Ischnaspis longirostris</italic> (Signoret, 1882): <xref ref-type="bibr" rid="B4">Balachowsky (1959)</xref>, <xref ref-type="bibr" rid="B19">Gallego and Vélez (1992)</xref>
					<xref ref-type="bibr" rid="B22">Kondo et al. (2012)</xref>, <xref ref-type="bibr" rid="B40">Mosquera (1979)</xref>, <xref ref-type="bibr" rid="B43">Posada (1989)</xref>.</p>
				<p><italic>Lepidosaphes beckii</italic> (Boisduval, 1868): <xref ref-type="bibr" rid="B4">Balachowsky (1959)</xref>, <xref ref-type="bibr" rid="B17">Figueroa (1952</xref>, <xref ref-type="bibr" rid="B18">1977</xref>), <xref ref-type="bibr" rid="B19">Gallego and Vélez (1992)</xref>, <xref ref-type="bibr" rid="B40">Mosquera (1979)</xref>, <xref ref-type="bibr" rid="B23">Kondo (2001)</xref>, <xref ref-type="bibr" rid="B22">Kondo <italic>et al.</italic> (2012)</xref>.</p>
				<p><italic>Lepidosaphes gloverii</italic> (Packard, 1869): <xref ref-type="bibr" rid="B4">Balachowsky (1959)</xref>, <xref ref-type="bibr" rid="B17">Figueroa (1952</xref>, <xref ref-type="bibr" rid="B18">1977</xref>), <xref ref-type="bibr" rid="B23">Kondo (2001)</xref>, <xref ref-type="bibr" rid="B22">Kondo <italic>et al.</italic> (2012)</xref>, <xref ref-type="bibr" rid="B40">Mosquera (1979)</xref>, <xref ref-type="bibr" rid="B43">Posada (1989)</xref>.</p>
				<p><italic>Lopholeucaspis</italic> sp.: <xref ref-type="bibr" rid="B40">Mosquera (1979)</xref>, <xref ref-type="bibr" rid="B43">Posada (1989)</xref>.</p>
				<p><italic>Parlatoria cinerea</italic> (Hadden in Doane and Hadden, 1909): <xref ref-type="bibr" rid="B23">Kondo (2001)</xref>, <xref ref-type="bibr" rid="B22">Kondo <italic>et al.</italic> (2012)</xref>, <xref ref-type="bibr" rid="B40">Mosquera (1979)</xref>, <xref ref-type="bibr" rid="B43">Posada (1989)</xref>.</p>
				<p><italic>Parlatoria pergandii</italic> (Comstock, 1881): <xref ref-type="bibr" rid="B23">Kondo (2001)</xref>, <xref ref-type="bibr" rid="B22">Kondo <italic>et al.</italic> (2012)</xref>, <xref ref-type="bibr" rid="B40">Mosquera (1979)</xref>, <xref ref-type="bibr" rid="B43">Posada (1989)</xref>.</p>
				<p><italic>Parlatoria ziziphi</italic> (Lucas, 1853): <xref ref-type="bibr" rid="B7">Blackburn and Miller (1984)</xref>
				</p>
				<p><italic>Pinnaspis aspidistrae</italic> (Signoret, 1869): <xref ref-type="bibr" rid="B17">Figueroa (1952</xref>, <xref ref-type="bibr" rid="B18">1977</xref>), <xref ref-type="bibr" rid="B22">Kondo et al. (2012)</xref>, <xref ref-type="bibr" rid="B40">Mosquera (1979)</xref>, <xref ref-type="bibr" rid="B43">Posada (1989)</xref>.</p>
				<p><italic>Pinnaspis strachani</italic> (Cooley, 1898): <xref ref-type="bibr" rid="B4">Balachowsky (1959)</xref>, <xref ref-type="bibr" rid="B22">Kondo et al. (2012)</xref>, <xref ref-type="bibr" rid="B40">Mosquera (1979)</xref>, <xref ref-type="bibr" rid="B43">Posada (1989)</xref>.</p>
				<p><italic>Pseudaonidia trilobitiformis</italic> (Green, 1896): <xref ref-type="bibr" rid="B22">Kondo et al. (2012)</xref>, <xref ref-type="bibr" rid="B40">Mosquera (1979)</xref>, <xref ref-type="bibr" rid="B43">Posada (1989)</xref>.</p>
				<p><italic>Selenaspidus articulatus</italic> (Morgan, 1889): <xref ref-type="bibr" rid="B4">Balachowsky (1959)</xref>, <xref ref-type="bibr" rid="B22">Kondo et al. (2012)</xref>, <xref ref-type="bibr" rid="B40">Mosquera (1979)</xref>, <xref ref-type="bibr" rid="B43">Posada (1989)</xref>.</p>
				<p><italic>Unaspis citri</italic> (Comstock, 1881): <xref ref-type="bibr" rid="B4">Balachowsky (1959)</xref>, <xref ref-type="bibr" rid="B17">Figueroa (1952</xref>, 1977), <xref ref-type="bibr" rid="B19">Gallego and Vélez (1992)</xref>, <xref ref-type="bibr" rid="B23">Kondo (2001)</xref>, <xref ref-type="bibr" rid="B22">Kondo <italic>et al.</italic> (2012)</xref>, <xref ref-type="bibr" rid="B40">Mosquera (1979)</xref>, <xref ref-type="bibr" rid="B43">Posada (1989)</xref>.</p>
				<p><bold>Key to subfamilies, genera and species of Diaspididae on</bold> Citrus <bold>spp. from Colombia</bold> (Compiled from <xref ref-type="bibr" rid="B6">Beardsley (1966)</xref>, <xref ref-type="bibr" rid="B10">Claps and Wolff (2003)</xref>, <xref ref-type="bibr" rid="B24">Kosztarab (1996)</xref>, <xref ref-type="bibr" rid="B34">McKenzie (1946)</xref>, <xref ref-type="bibr" rid="B39">Miller (2005)</xref>, <xref ref-type="bibr" rid="B37">Miller and Davidson (2005)</xref> and <xref ref-type="bibr" rid="B52">Watson (2016)</xref>).</p>
				<p>1. Macroducts normally of the “one-barred type”, length of each one at least six times the width; second pygidial lobes unilobulate; anterior spiracles usually without associated pores; antennae of adult female usually bearing only one seta; pygidial plates present in second instar if not in adult; gland spines absent; duct tubercles absent; body circular or pyriform (Figure. 4A) … <bold>
 <italic>Aspidiotinae</italic>
</bold> …12 </p>
				<p>1’. Macroducts of the “two barred” type, length of each one rarely longer than three times their width; second pygidial lobes uni-or bilobulate; anterior spiracles usually with associated pores; antennae of adult female often bearing more than one seta; pygidial plates or gland spines often present in second instar if not in the adult; gland spines present or absent; duct tubercles may be present; body usually elongate spindle-shaped, rarely pyriform (<xref ref-type="fig" rid="f4">Figure 4B</xref>) … <bold>
 <italic>Diaspidinae</italic>
</bold> …2 </p>
				<p>
					<fig id="f4">
						<label>Figure 4</label>
						<caption>
							<title>Habitus with magnified structures of two main subfamilies of Diaspididae. A. Aspidiotinae (Illustration from <xref ref-type="bibr" rid="B36">Miller and Davidson 1998</xref>); B. <italic>Diaspidinae</italic>. Illustration by Davidson (Miller, 2005).</title>
						</caption>
						<graphic xlink:href="0304-2847-rfnam-70-02-08139-gf4.jpg"/>
					</fig>
				</p>
				<p>2. Adult female with second lobes bilobulate (<xref ref-type="fig" rid="f5">Figure 5A</xref>); gland spines usually present, occasionally replaced by plates; pores often associated with anterior and posterior spiracles; marginal macroducts usually with the long axis of each orifice perpendicular to margin; antennae each usually with two or more setae … 6 </p>
				<p>2’.Adult female with second lobes unilobulate (<xref ref-type="fig" rid="f5">Figure 5B</xref>); gland spines absent, plates usually present; spiracular pores associated with anterior spiracles only; marginal macroducts often with the long axis of each orifice oriented parallel to margin; antenna with one or more setae … 3 </p>
				<p>
					<fig id="f5">
						<label>Figure 5</label>
						<caption>
							<title>A. Pigydium with second lobe bilobulate; B. Pigydium with second lobe unilobulate. Illustrations taken from <xref ref-type="bibr" rid="B39">Miller and Davidson (2005)</xref>.</title>
						</caption>
						<graphic xlink:href="0304-2847-rfnam-70-02-08139-gf5.jpg"/>
					</fig>
				</p>
				<p>3. Antenna with two to six setae; adult female pupillarial; body more or less elongate; plates, if present, confined to pygidium; marginal pygidial ducts not enlarged; abdominal disc pores sometimes present on some prepygidial segments … <bold>
 <italic>Lopholeucaspis sp</italic>
</bold> . </p>
				<p>3’ Antenna with one seta; adult female usually not pupillarial; body oval to circular (elongate if pupillarial); plates often present on pre pygidium and pygidium; marginal pygidial ducts often enlarged; abdominal disc pores never present on some prepygidial segments … <bold>
 <italic>Parlatoria</italic>
</bold> (Targioni Tozzetti) … 4 </p>
				<p>4. With a large, conspicuous, lateral and membranous lobe on each side of head, marginal to each anterior spiracle; female scale composed principally of a large black second exuvium … <bold>
 <italic>Parlatoria ziziphi</italic>
</bold> (Lucas) (<xref ref-type="fig" rid="f6">Figure 6</xref>). </p>
				<p>4’ Without such a membranous lobe on each side of head; female scale cover not largely black … 5 </p>
				<p>
					<fig id="f6">
						<label>Figure 6</label>
						<caption>
							<title>Habitus of Parlatoria ziziphi (Lucas) with magnified structures. Illustration taken from <xref ref-type="bibr" rid="B39">Miller and Davidson (2005)</xref>.</title>
						</caption>
						<graphic xlink:href="0304-2847-rfnam-70-02-08139-gf6.jpg"/>
					</fig>
				</p>
				<p>5. Dorsum of pygidium with two longitudinal rows of macroducts on each side of pygidium on abdominal segments six and seven, extending cephalad to well anterior of anal opening; three plates between third and fourth lobs … <bold>
 <italic>Parlatoria cinerea</italic>
</bold> (Hadden in Doane and Hadden) (<xref ref-type="fig" rid="f7">Figure 7A</xref>) </p>
				<p>5’. Dorsum of pygidium without such rows of macroducts; macroducts not found anterior to anal opening on these segments; four plates between third and fourth lobes … Parlatoria pergandii (Comstock) (<xref ref-type="fig" rid="f7">Figure 7B</xref>) </p>
				<p>
					<fig id="f7">
						<label>Figure 7</label>
						<caption>
							<title>Habitus with magnified structures of: A. <italic>Parlatoria cinerea</italic> (Hadden in Doane &amp; Hadden) (Illustration taken from <xref ref-type="bibr" rid="B21">Gerson 1977</xref>); B. <italic>
 <bold>Parlatoria pergandii</bold>
</italic> (Comstock). Illustration taken from <xref ref-type="bibr" rid="B39">Miller and Davidson (2005)</xref>.</title>
						</caption>
						<graphic xlink:href="0304-2847-rfnam-70-02-08139-gf7.jpg"/>
					</fig>
				</p>
				<p>6. Median lobes zygotic (<xref ref-type="fig" rid="f8">Figure 8A</xref>) … 7. </p>
				<p>6’. Median lobes not zygotic (although crowding or secondary sclerotization may make this difficult to see) (<xref ref-type="fig" rid="f8">Figure 8B</xref>) … 9 </p>
				<p>
					<fig id="f8">
						<label>Figure 8</label>
						<caption>
							<title>A. Median lobes zygotic; B. Median lobes not zygotic. Illustrations taken from <xref ref-type="bibr" rid="B52">Watson (2016)</xref>.</title>
						</caption>
						<graphic xlink:href="0304-2847-rfnam-70-02-08139-gf8.jpg"/>
					</fig>
				</p>
				<p>7. Gland spines and macroducts absent from area anterior to abdominal segment 1; body of characteristic shape, with head, prothorax, and mesothorax swollen and rectangular; lateral margin side of prothorax on older females with 1 swollen tubercle on each side of body; labium set in groove, with sclerotized areas on each side … <bold>
 <italic>Aulacaspis tubercularis</italic>
</bold> (Newstead) (<xref ref-type="fig" rid="f9">Figure 9</xref>). </p>
				<p>7’.Gland spines and macroducts present anterior to abdominal segment 1; head, prothorax, and mesothorax not swollen; without lateral tubercles on lateral margin side of prothorax on older females; labium set not in groove, without sclerotized areas on each side … <bold>
 <italic>Pinnaspis</italic>
</bold> (Cockerell) … 8 </p>
				<p>
					<fig id="f9">
						<label>Figure 9</label>
						<caption>
							<title>Habitus with magnified structures of <italic>
 <bold>Aulacaspis tubercularis</bold>
</italic> (Newstead). Illustration taken from <xref ref-type="bibr" rid="B39">Miller and Davidson (2005)</xref>.</title>
						</caption>
						<graphic xlink:href="0304-2847-rfnam-70-02-08139-gf9.jpg"/>
					</fig>
				</p>
				<p>8. Preanal sclerosis lacking or represented by light sclerotized patch; median lobes protrude less than or about same distance as second lobes; posterior spiracles each with one to 12 pores, four pores on average … <bold>
 <italic>Pinnaspis aspidistrae</italic>
</bold> (Signoret) (<xref ref-type="fig" rid="f10">Figure 10A</xref>) </p>
				<p>8’. Preanal sclerosis represented by sclerotized bar; median lobes protrude beyond or about same distance as second lobes; posterior spiracles each with 0 to four pores, two pores on average … <bold>
 <italic>Pinnaspis strachani</italic>
</bold> (Cooley) (<xref ref-type="fig" rid="f10">Figure 10B</xref>) </p>
				<p>
					<fig id="f10">
						<label>Figure 10</label>
						<caption>
							<title>Habitus with magnified structures of: A. <italic>
 <bold>Pinnaspis aspidistrae</bold>
</italic> (Signoret) B. <italic>Pinnaspis strachani</italic> (Cooley). Illustrations taken from <xref ref-type="bibr" rid="B39">Miller and Davidson (2005)</xref>.</title>
						</caption>
						<graphic xlink:href="0304-2847-rfnam-70-02-08139-gf10.jpg"/>
					</fig>
				</p>
				<p>9. Median lobes with only a pair of marginal setae between their bases … 11 </p>
				<p>9’. Median lobes with only a pair of gland spines between their bases … <bold>
 <italic>Lepidosaphes</italic>
</bold> (Schlectendal) … 10 </p>
				<p>10. Mature female without sclerotized pattern on thorax; without sclerotized dermal pockets on thorax; macroducts on dorsal margin of prothorax present … <bold>
 <italic>Lepidosaphes beckii</italic>
</bold> (Boisduval) (<xref ref-type="fig" rid="f11">Figure 11A</xref>) </p>
				<p>10’. Mature female with distinctive pattern of punctures on dorsum of thorax extending to ventral margin; with sclerotized dermal pockets on pro- and mesothorax; macroducts on dorsal margin of prothorax absent … <bold>
 <italic>Lepidosaphes gloverii</italic>
</bold> (Packard) (<xref ref-type="fig" rid="f11">Figure 11B</xref>) </p>
				<p>
					<fig id="f11">
						<label>Figure 11</label>
						<caption>
							<title>Habitus with magnified structures of: A. <italic>
 <bold>Lepidosaphes beck</bold>
</italic> ii (Boisduval); B. <italic>Lepidosaphes gloverii</italic> (Packard). Illustrations taken from <xref ref-type="bibr" rid="B39">Miller and Davidson (2005)</xref>.</title>
						</caption>
						<graphic xlink:href="0304-2847-rfnam-70-02-08139-gf11.jpg"/>
					</fig>
				</p>
				<p>11. Dorsum of pygidium with a coarse ‘lattice-work’ sclerotized pattern … <bold>
 <italic>Ischnaspis longirostris</italic>
</bold> (Signoret) (<xref ref-type="fig" rid="f12">Figure 12A</xref>) </p>
				<p>11’. Dorsum of pygidium without such a sclerotized pattern; with four or fewer perivulvar pores on each side of body … <bold>
 <italic>Unaspis citri</italic>
</bold> (Comstock) (<xref ref-type="fig" rid="f12">Figure 12B</xref>) </p>
				<p>
					<fig id="f12">
						<label>Figure 12</label>
						<caption>
							<title>Habitus with magnified structures of: A. <italic>
 <bold>Ischnaspis longirostris</bold>
</italic> (Signoret); B. <italic>
 <bold>Unaspis citri</bold>
</italic> (Comstock). Illustrations taken from <xref ref-type="bibr" rid="B39">Miller and Davidson (2005)</xref>.</title>
						</caption>
						<graphic xlink:href="0304-2847-rfnam-70-02-08139-gf12.jpg"/>
					</fig>
				</p>
				<p>12. Dorsal surface of pygidium with a conspicuous mosaic or areolate appearance … <bold>
 <italic>Pseudaonidia trilobitiformis</italic>
</bold> (Green) (<xref ref-type="fig" rid="f13">Figure 13A</xref>) </p>
				<p>12’. Dorsal surface of pygidium without mosaic areolate pattern … 13 </p>
				<p>
					<fig id="f13">
						<label>Figure 13</label>
						<caption>
							<title>A. Habitus with magnified structures of <italic>Pseudaonidia trilobitiformis</italic> (Green). Illustration from <xref ref-type="bibr" rid="B39">Miller and Davidson (2005)</xref>; B. Pygidial apex acute, forming an angle of 90° or less of <italic>
 <bold>Acutaspis scutiformis</bold>
</italic> (Cockerell). Illustration taken from <xref ref-type="bibr" rid="B52">Watson (2016)</xref>.</title>
						</caption>
						<graphic xlink:href="0304-2847-rfnam-70-02-08139-gf13.jpg"/>
					</fig>
				</p>
				<p>13. Pygidial margin with paraphyses present, these sometimes small (arising from bases of lobes or from the margin itself); paraphyses sometimes present lateral to the outer lobes … 14 </p>
				<p>13’. Pygidial margin without paraphyses … 19 </p>
				<p>14. Pygidial apex acute, forming an angle of 90° or less, although basal half of pygidium may be broad (<xref ref-type="fig" rid="f13">Figure 13B</xref>); pygidial margins tending to be concave and sclerotized; plates confined to interlobular spaces … <bold>
 <italic>Acutaspis scutiformis</italic>
</bold> (Cockerell) </p>
				<p>14’. Pygidial apex more or less broad, forming an angle greater than 90°; pygidial margins convex or straight, with or without sclerotization; plates often present lateral to third lobes … 15 </p>
				<p>15. Mature specimens with prosoma very enlarged and sclerotized, usually reniform so its lateral lobes more or less enclose the pygidium. If prosoma not reniform at maturity (A. orientalis), then paraphyses between second and third lobes never longer than the lobes … <bold>
 <italic>Aonidiella comperei</italic>
</bold> McKenzie (<xref ref-type="fig" rid="f14">Figure 14</xref>) </p>
				<p>15’. Mature specimens with prosoma membranous or sclerotized, not expanded sufficiently to become reniform; paraphyses between second and third lobes shorter or longer than the lobes … 16 </p>
				<p>
					<fig id="f14">
						<label>Figure 14</label>
						<caption>
							<title>Habitus with magnified structures of <italic>Aonidiella comperei</italic><xref ref-type="bibr" rid="B33">McKenzie. Illustration taken from McKenzie (1937)</xref>.</title>
						</caption>
						<graphic xlink:href="0304-2847-rfnam-70-02-08139-gf14.gif"/>
					</fig>
				</p>
				<p>16. Paraphyses obviously longer than median lobes (<xref ref-type="fig" rid="f15">Figure 15A</xref>) … <bold>
 <italic>Chrysomphalus</italic>
</bold> (Ashmead) … 17 </p>
				<p>16’ Paraphyses same length or shorter than median lobes (<xref ref-type="fig" rid="f15">Figure 15B</xref>) … <bold>
 <italic>Hemiberlesia</italic>
</bold> (Berlese and Leonardi) … 18 </p>
				<p>
					<fig id="f15">
						<label>Figure 15</label>
						<caption>
							<title>A. Paraphyses obviously longer than median lobes; B. Paraphyses same length or shorter than <ext-link ext-link-type="uri" xlink:href="http://wbd.etibioinformatics.nl/bis/diaspididae.php?menuentry=sleutel&amp;pagenum=26">median</ext-link> lobes. Illustrations taken from <xref ref-type="bibr" rid="B39">Miller and Davidson (2005)</xref>.</title>
						</caption>
						<graphic xlink:href="0304-2847-rfnam-70-02-08139-gf15.jpg"/>
					</fig>
				</p>
				<p>17. With one cluster of macroducts on submarginal areas of prepygidial segments; plates just lateral to third lobes fringed; nine to 13 prevulvar pores on each side of pygidium … <bold>
 <italic>Chrysomphalus aonidum</italic>
</bold> (Linnaeus) (<xref ref-type="fig" rid="f16">Figure 16A</xref>) </p>
				<p>17’. Without clusters of macroducts on submarginal areas of prepygidial segments; plates just lateral to third lobes clavate; five or six prevulvar pores on each side of pygidium … <bold>
 <italic>Chrysomphalus dictyospermi</italic>
</bold> (Morgan) (<xref ref-type="fig" rid="f16">Figure 16B</xref>). </p>
				<p>
					<fig id="f16">
						<label>Figure 16</label>
						<caption>
							<title>Habitus with magnified structures of: A. <italic>Chrysomphalus aonidum</italic> (Linnaeus); B. <italic>Chrysomphalus dictyospermi</italic> (Morgan). Illustrations taken from <xref ref-type="bibr" rid="B39">Miller and Davidson (2005)</xref>.</title>
						</caption>
						<graphic xlink:href="0304-2847-rfnam-70-02-08139-gf16.jpg"/>
					</fig>
				</p>
				<p>18 Medial notch, first and second space of pygidium with band of fringe plates less strongly developed; plates in third space, if present, reduced in size, not forming such a dense uniform fringe; median lobes very close together, almost in touch; … <bold>
 <italic>Hemiberlesia lataniae</italic>
</bold> (Signoret) (<xref ref-type="fig" rid="f17">Figure 17A</xref>) </p>
				<p>18’. Medial notch, first, second and third space of pygidium with a band of broad apically fringed plates of nearly uniform; plates in third space always present in a dense, nearly uniform fringe; median lobes separated, at least in the half of the width of each median lobe … <bold>
 <italic>Hemiberlesia palmae</italic>
</bold> (Cockerell) (<xref ref-type="fig" rid="f17">Figure 17B</xref>) </p>
				<p>
					<fig id="f17">
						<label>Figure 17</label>
						<caption>
							<title>Habitus with magnified structures of A. <italic>
 <bold>Hemiberlesia lataniae</bold>
</italic> (Signoret). Illustrations taken from <xref ref-type="bibr" rid="B39">Miller and Davidson (2005)</xref>; B. <italic>
 <bold>Hemiberlesia palmae</bold>
</italic> (Cockerell). Illustrations taken from <xref ref-type="bibr" rid="B15">Ferris (1938)</xref>.</title>
						</caption>
						<graphic xlink:href="0304-2847-rfnam-70-02-08139-gf17.jpg"/>
					</fig>
				</p>
				<p>19. Prosoma strongly constricted between meso- and metathorax, and sclerotized; third lobe represented by an elongate, acute, sclerotized spine … <bold>
 <italic>Selenaspidus articulatus</italic>
</bold> (Morgan) (<xref ref-type="fig" rid="f18">Figure 18a</xref>)</p>
				<p>19’. Prosoma without strong constriction between meso- and metathorax, and usually membranous; third lobe short, either rounded or pointed, or absent … <bold>
 <italic>Aspidiotus neri</italic>
</bold> i (Costa) (<xref ref-type="fig" rid="f18">Figure 18b</xref>)</p>
				<p>
					<fig id="f18">
						<label>Figure 18</label>
						<caption>
							<title>Habitus with magnified structures of: A. <italic>
 <bold>Selenaspidus articulatus</bold>
</italic> (Morgan); B. <italic>
 <bold>Aspidiotus nerii</bold>
</italic> (Costa). Illustrations taken from <xref ref-type="bibr" rid="B39">Miller and Davidson (2005)</xref>.</title>
						</caption>
						<graphic xlink:href="0304-2847-rfnam-70-02-08139-gf18.jpg"/>
					</fig>
				</p>
			</sec>
		</sec>
		<sec sec-type="conclusions">
			<title>CONCLUSIONS</title>
			<p>The identity of <italic>Aonidella comperei</italic>, the species that is causing damage on fruits, branches and leaves of <italic>Citrus aurantifolia</italic> in Tolima, Colombia, was determined. This basic information will be useful to start studies about its biology and ecology in order to define management strategies. The knowledge about species of Diaspididae on <italic>Citrus</italic> spp. in Colombia is improved and the number of species recorded on this host and their geographical distribution is updated. </p>
		</sec>
		<sec>
			<title>ACKNOWLEDGEMENTS</title>
			<p>We thank to William King by the information and the logistic to the collect the samples of <italic>Aonidiella comperei</italic> and Oscar Dix for providing samples of <italic>Parlatoria ziziphi</italic>. Thanks to Lucia Claps and Barbara Denno for providing scientific literature. Thanks to Museo Entomológico UNAB and Instituto Colombiano Agropecuario Ica-Ceisa by the facilities to develop this research. Thanks to Takumasa Kondo and anonymous reviewers for theirs comments and suggestions. Thanks to Douglas Miller, John Davidson and Stephanie Munson (Cornell University) by the permission to use pictures and images.</p>
		</sec>
	</body>
	<back>
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