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	<front>
		<journal-meta>
			<journal-id journal-id-type="publisher-id">GRAELL</journal-id>
			<journal-title-group>
				<journal-title>Graellsia</journal-title>
				<abbrev-journal-title abbrev-type="publisher">Graellsia</abbrev-journal-title>
			</journal-title-group>
			<issn publication-format="print">0367-5041</issn>
			<issn publication-format="electronic">1989-953X</issn>
			<issn-l>0367-5041</issn-l>
			<publisher>
				<publisher-name>Consejo Superior de Investigaciones Cient&#x00ED;ficas</publisher-name>
				<publisher-name>SAM</publisher-name>
			</publisher>
		</journal-meta>
		<article-meta>
			<article-id pub-id-type="doi">10.3989/graellsia.2021.v77.297</article-id>
			<article-id pub-id-type="publisher-id">graellsia.2021.v77.297</article-id>
			<article-categories>
				<subj-group subj-group-type="heading">
					<subject>Art&#x00ED;culo</subject>
				</subj-group>
			</article-categories>
			<title-group>
				<article-title>Notes on the diet of the Mediterranean black widow  <italic>Latrodectus tredecimguttatus</italic> (Rossi, 1790) (Araneae: Theridiidae) in South Western Iberian Peninsula</article-title>
				<trans-title-group xml:lang="es">
					<trans-title>Notas sobre la dieta de la viuda negra mediterr&#x00E1;nea <italic>Latrodectus tredecimguttatus</italic> (Rossi, 1790) (Araneae: Theridiidae) en el suroeste de la pen&#x00ED;nsula ib&#x00E9;rica</trans-title>
				</trans-title-group>
				<alt-title alt-title-type="running-head">Diet of <italic>Latrodectus tredecimguttatus</italic> in SW Iberian Peninsula</alt-title>
			</title-group>
			<contrib-group>
				<contrib contrib-type="author" corresp="yes">
					<contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-1847-3215</contrib-id>
					<name name-style="western">
						<surname>Mora-Rubio</surname>
						<given-names>Carlos</given-names>
					</name>
					<xref ref-type="aff" rid="aff-1-e138">1</xref>
					<aff id="aff-1-e138">
						<label>1</label>
						<institution>Departamento de Anatom&#x00ED;a, Biolog&#x00ED;a Celular y Zoolog&#x00ED;a, Facultad de Ciencias, Universidad de Extremadura</institution>, <addr-line>06006, Badajoz</addr-line>, <country>Espa&#x00F1;a</country>
					</aff>
					<email xlink:href="morarubioresearch@gmail.com">morarubioresearch@gmail.com</email>
				</contrib>
				<contrib contrib-type="author">
					<contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-7392-2423</contrib-id>
					<name name-style="western">
						<surname>Parejo-Pulido</surname>
						<given-names>Daniel</given-names>
					</name>
					<xref ref-type="aff" rid="aff-2-e138">2</xref>
					<aff id="aff-2-e138">
						<label>2</label>
						<institution>Instituto de Investigaci&#x00F3;n en Recursos Cineg&#x00E9;ticos, IREC (CSIC, UCLM, JCCM)</institution>, <addr-line>Ronda de Toledo, s/n, 13005, Ciudad Real</addr-line>, <country>Espa&#x00F1;a</country>
					</aff>
					<email xlink:href="dapapu96@gmail.com">dapapu96@gmail.com</email>
				</contrib>
			</contrib-group>
			<pub-date pub-type="epub">
				<day>30</day>
				<month>06</month>
				<year>2021</year>
			</pub-date>
			<pub-date pub-type="collection">
				<month>06</month>
				<year>2021</year>
			</pub-date>
			<volume>77</volume>
			<issue>1</issue>
			<elocation-id>e138</elocation-id>
			<history>
				<date date-type="received">
					<day>18</day>
					<month>09</month>
					<year>2020</year>
				</date>
				<date date-type="accepted">
					<day>11</day>
					<month>02</month>
					<year>2021</year>
				</date>
				<date date-type="available-online">
					<day>27</day>
					<month>05</month>
					<year>2021</year>
				</date>
			</history>
			<permissions>
				<license license-type="open-access" xlink:href="https://creativecommons.org/licenses/by/4.0/">
					<license-p>This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International (CC BY 4.0) License.</license-p>
				</license>
			</permissions>
			<self-uri xlink:href="GRAELL-77-1-e138.pdf"/>
			<abstract>
				<p>Predators play important roles in ecosystems due to their effects on the diversity and abundance of prey communities and, ultimately, on ecosystem functions. To understand the ecology of the predatory behavior of different groups of animals and their impact on prey communities, knowledge of prey composition is essential. The aim of this study was to determine the diet composition of a predatory arthropod, the Mediterranean black widow <italic>Latrodectus tredecimguttatus</italic> (Rossi, 1790), in the Iberian Peninsula. We found that <italic>L. tredecimguttatus</italic> may be considered a stenophagous generalist predator, feeding on nine different arthropod orders (Araneae, Coleoptera, Hemiptera, Hymenoptera, Julida, Mantodea, Orthoptera, Scorpiones and Solifugae). Hymenoptera (mostly ants) were the most common prey (58.9% of prey items) and Coleoptera (mostly Tenebrionidae) was the second most frequent (33.5% of prey items). Besides, we also found evidence of intraguild predation in this species. With this study, we contribute to the knowledge of <italic>L. tredecimguttatus</italic> ecology in the Iberian Peninsula, highlighting its role as a predator of diverse arthropods, including spiders and other predators.</p>
			</abstract>
			<trans-abstract xml:lang="es">
				<p>Los depredadores juegan un importante papel en la din&#x00E1;mica ecosist&#x00E9;mica a ra&#x00ED;z de los efectos que producen en la abundancia y diversidad de presas y, en &#x00FA;ltima instancia, en las funciones del ecosistema. Para comprender la ecolog&#x00ED;a del comportamiento depredador de los distintos grupos animales, as&#x00ED; como su impacto en las comunidades de presas, es imprescindible conocer la composici&#x00F3;n de especies presa. El prop&#x00F3;sito de este estudio ha sido determinar la composici&#x00F3;n de la dieta de un artr&#x00F3;podo depredador, la viuda negra mediterr&#x00E1;nea <italic>Latrodectus tredecimguttatus</italic> (Rossi, 1790) en la pen&#x00ED;nsula ib&#x00E9;rica. Encontramos que <italic>L. tredecimguttatus</italic> puede considerarse un depredador generalista esten&#x00F3;fago, que se alimenta de nueve &#x00F3;rdenes distintos de artr&#x00F3;podos (Araneae, Coleoptera, Hemiptera, Hymenoptera, Julida, Mantodea, Orthoptera, Scorpiones y Solifugae). Los himen&#x00F3;pteros (en su mayor&#x00ED;a hormigas) fueron las presas m&#x00E1;s comunes (58.9% del total) y los cole&#x00F3;pteros (en su mayor&#x00ED;a Tenebrionidae) fueron los segundos m&#x00E1;s comunes (33.5% del total). Adem&#x00E1;s, hemos encontrado evidencias de depredaci&#x00F3;n intra-gremio en esta especie. Con este trabajo, se contribuye al conocimiento de la ecolog&#x00ED;a de <italic>L. tredecimguttatus</italic> en la pen&#x00ED;nsula ib&#x00E9;rica, destacando su papel como depredador de diversos artr&#x00F3;podos, donde se incluyen ara&#x00F1;as y otros depredadores.</p>
			</trans-abstract>
			<kwd-group>
				<kwd>ecology</kwd>
				<kwd>intraguild predation</kwd>
				<kwd>niche breadth</kwd>
				<kwd>predation</kwd>
				<kwd>prey composition</kwd>
			</kwd-group>
			<kwd-group xml:lang="es">
				<kwd>ecolog&#x00ED;a</kwd>
				<kwd>depredaci&#x00F3;n intra-gremio</kwd>
				<kwd>amplitud de nicho</kwd>
				<kwd>depredaci&#x00F3;n</kwd>
				<kwd>composici&#x00F3;n de presas</kwd>
			</kwd-group>
			<counts>
				<page-count count="6"/>
			</counts>
		</article-meta>
	</front>
	<body>
		<sec sec-type="intro" id="sec-1-e138">
			<title>Introduction</title>
			<p>Spiders (Araneae) constitute a large group of predatory arthropods, as they are located on the top trophic levels of many invertebrate food webs. This group has adapted to many habitats and ecological niches, developing different feeding behaviors depending on the species life-history (<xref ref-type="bibr" rid="ref-27-e138">Wise, 1993</xref>). They are predominantly generalist polyphagous predators capable of feeding on a wide variety of insects and other arthropods (<xref ref-type="bibr" rid="ref-5-e138">Hayes &#x0026; Lockley, 1990</xref>), thus providing access to different nutrients that are not commonly found in a single prey species (<xref ref-type="bibr" rid="ref-23-e138">Toft &#x0026; Wise, 1999</xref>). However, a minority of spider species are specialists, such as ant-eating spiders (<xref ref-type="bibr" rid="ref-1-e138">Cushing, 2012</xref>). Furthermore, species from this order use different prey-capture methods, classified broadly in two groups: web-building and non-web-building (hunting) spiders (<xref ref-type="bibr" rid="ref-25-e138">Uetz, 1991</xref>). As for web building spiders, they construct complex webs using thread which is produced from their silk glands, and its web structure ranges from simple to complex two- and three-dimensional designs. The main function of this silken structure is to trap prey (mostly insects) and to transmit vibrations to the resident spider (<xref ref-type="bibr" rid="ref-26-e138">Vollrath, 2005</xref>).</p>
			<p>The black widow spider genus <italic>Latrodectus</italic> Walckneaer, 1805 is included among the groups of generalists and web-building spiders. It constitutes one of the best-studied spider genera as it entails medical importance due to the potential danger of its venom for large mammals, including humans (<xref ref-type="bibr" rid="ref-3-e138">Garb <italic>et al.,</italic> 2004</xref>). This genus is represented by about 32 recognized species that are distributed worldwide (<xref ref-type="bibr" rid="ref-28-e138">World Spider Catalog, 2020</xref>). Of these 32 species, only <italic>Latrodectus tredecimguttatus</italic> (Rossi, 1790) and <italic>L. lilianae</italic> (<xref ref-type="bibr" rid="ref-10-e138">Melic, 2000</xref>) co-exist in the Iberian Peninsula, and these can be easily differentiated based on opisthosomal coloration. <italic>L. tredecimguttatus</italic> is widely distributed in this territory, with a seasonal activity period from May to November. This species builds simple nests very close to the ground under stones or branches, with bell-shaped three-dimensional webs, where it waits for prey to be trapped (<xref ref-type="bibr" rid="ref-10-e138">Melic, 2000</xref>).</p>
			<p>Regarding the diet composition of <italic>Latrodectus</italic> species, a number of studies have been carried out in different countries: <xref ref-type="bibr" rid="ref-20-e138">Shulov (1940)</xref> on <italic>L. tredecimguttatus</italic> in Palestine; <xref ref-type="bibr" rid="ref-21-e138">Shulov &#x0026; Weissmann (1959)</xref> on <italic>L. pallidus</italic> O. Pickard-Cambridge, 1872, <italic>L. revivensis</italic> Shulov, 1948 and <italic>L. tredecimguttatus</italic> in Israel; <xref ref-type="bibr" rid="ref-18-e138">Ross (1981)</xref>, <xref ref-type="bibr" rid="ref-8-e138">Mackay (1982)</xref> and <xref ref-type="bibr" rid="ref-19-e138">Salomon (2011)</xref> on <italic>L. hesperus</italic> Chamberlin et Ivie, 1935 in North America; <xref ref-type="bibr" rid="ref-12-e138">Nyffeler <italic>et al.</italic> (1988)</xref> and <xref ref-type="bibr" rid="ref-16-e138">Rocha-Dias &#x0026; Kobler (1999)</xref> on <italic>L. mactans</italic> (F.) in USA and Brazil, respectively; <xref ref-type="bibr" rid="ref-15-e138">Pompozzi <italic>et al.</italic> (2013)</xref> on <italic>L. mirabilis</italic> (Holmberg, 1876) in Argentina and <xref ref-type="bibr" rid="ref-22-e138">Taucare-R&#x00ED;os &#x0026; Canals (2015)</xref> on <italic>L. geometricus</italic> C. L. Koch, 1841 in Chile. In the Iberian Peninsula, only <xref ref-type="bibr" rid="ref-7-e138">H&#x00F3;dar &#x0026; S&#x00E1;nchez-Pi&#x00F1;ero (2002)</xref> investigated <italic>L. lilianae</italic>. All of these studies have shown that <italic>Latrodectus</italic> diet consists mainly in Coleoptera and Formicidae, with other prey groups being much less common.</p>
			<p>In order to understand the ecology and the predatory behavior of the different groups of spiders, knowledge of prey composition is essential. Following the work of researchers cited above about <italic>Latrodectus</italic> diet, the aim of this study was to determine the diet composition of the Mediterranean black widow <italic>L. tredecimguttatus</italic> in South Western Iberian Peninsula during the summer and early autumn period.</p>
		</sec>
		<sec sec-type="materialsmethods" id="sec-2-e138">
			<title>Material and methods</title>
			<p>The fieldwork was carried out in the Llanos de Olivenza area, near the locality of Olivenza (southwestern Spain) from July to October 2019, where a population of <italic>L. tredecimguttatus</italic> was previously recorded (<xref ref-type="bibr" rid="ref-11-e138">Mora-Rubio &#x0026; P&#x00E9;rez-Bote, 2018</xref>). During this period, most of adult black widows were active, with well-developed webs and they had produced their egg sacs. The climate is typically Continental-Mediterranean, with relatively cold wet winters and dry hot summers. Specifically, the <italic>L. tredecimguttatus</italic> population was located in a holm-oak dehesa of <italic>Quercus ilex</italic> subesp. <italic>ballota</italic> L. (38&#x00B0;41'0.7'' N, 7&#x00B0;06'0.1&#x0201D; W, 267 m alt.) with low bovine cattle, and with abundant <italic>Ulex eriocladus</italic> (C. Vicioso) shrubs. All individuals were found in an arid hollow with low herbaceous plants and shrubs, used as a cattle pond (dry during the study period), or surrounding this area.</p>
			<p>The study area was sampled weekly in search of black widow webs throughout the study period. During these months, new occupied webs were discovered and recorded. From each web, all prey items that remained in the nest silk were collected, trying to disturb the spiders as little as possible, and they were analyzed and identified in the laboratory using a stereoscopic binocular microscope IBD45B.</p>
			<p>The dietary niche breadth of <italic>L. trecedimgutattus</italic> at the study area was calculated using the standardized Levins' index (B<sub>A</sub>) as B<sub>A</sub> = [(1/&#x003A3;&#x003C1;i<sup>2</sup>)-1] / (n-1). This index indicates how uniformly resources are used for the studied group, where p<sub>i</sub> is the proportion of consumed prey of the prey category i and n is the total number of prey categories available. The range of B<sub>A</sub> varies from 0, when the population uses one prey category exclusively, to 1, when the population uses all prey categories in equal proportions (<xref ref-type="bibr" rid="ref-2-e138">Feinsinger <italic>et al.,</italic> 1981</xref>).</p>
		</sec>
		<sec sec-type="results" id="sec-3-e138">
			<title>Results</title>
			<p>A total of 15 webs of adult females <italic>L. tredecimguttatus</italic> were found throughout the study period. Some of the individuals died of natural causes, and only 3 specimens survived until the end of the fieldwork (late October). 7 out of 15 webs were found in natural cavities (lagomorph excavations, small slopes or little holes as a result of cattle trampling) (<xref ref-type="fig" rid="fig-1-e138">Fig. 1</xref>) or artificial ones (holes in the ground as a result of a local soil plow); 7 out of 15 were found beneath small <italic>Ulex eriocladus</italic> shrubs; and only 1 out of 15 was found beneath a rock.</p>
			<fig id="fig-1-e138">
				<label>Fig. 1</label>
				<caption>
					<title>Female of <italic>L. tredecimguttatus</italic> in the study area. Arrows point to prey (ants) captured in the web.</title>
					<p xml:lang="es">Fig. 1.&#x02014; Hembra de <italic>L. tredecimguttatus</italic> en la zona de estudio. Las flechas se&#x00F1;alan las presas (hormigas) capturadas en la tela.</p>
				</caption>
				<graphic id="gra-1-e138" xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="GRAELL-77-1-e138-f1-G.png"/>
			</fig>
			<p>We collected a total of 355 prey items from nine different arthropod orders (Araneae, Coleoptera, Hemiptera, Hymenoptera, Julida, Mantodea, Orthoptera, Scorpiones and Solifugae) during the three months of fieldworks, whose abundance data are represented in detail in <xref ref-type="table" rid="taw-1-e138">Table 1</xref> and <xref ref-type="fig" rid="fig-2-e138">Figure 2</xref>. The dietary niche breadth of <italic>L. tredecimguttatus</italic> (B<sub>A</sub>) was 0.146, indicating that a large proportion of its diet is comprised of a few prey orders while others are less represented in the diet.</p>
			<table-wrap id="taw-1-e138" orientation="portrait" position="float">
				<label>Table 1</label>
				<caption>
					<title>Composition of captured prey by 15 female <italic>L. tredecimguttatus</italic> individuals at a site near Olivenza, southwestern Spain, between July and October 2019.</title>
					<p xml:lang="es">Tabla 1.&#x02014; Composici&#x00F3;n de la presas capturadas por 15 hembras de <italic>L. tredecimguttatus</italic> en una zona cercana a Olivenza, suroeste de Espa&#x00F1;a, entre julio y octubre de 2019.</p>
				</caption>
				<table id="tab-1-e138" frame="hsides" border="1" rules="all">
					<thead>
						<tr>
							<th align="center" valign="middle">Prey Order</th>
							<th align="center" valign="middle">Prey Family</th>
							<th align="center" valign="middle">Prey Species</th>
							<th align="center" valign="middle">Prey number</th>
							<th align="center" valign="middle">%</th>
						</tr>
					</thead>
					<tbody>
						<tr>
							<td rowspan="18" align="left" valign="middle">
								<bold>Coleoptera</bold>
							</td>
							<td align="left" valign="middle">Buprestidae</td>
							<td align="left" valign="middle">
								<italic>Acmaeoderella</italic> sp. Cobos, 1955</td>
							<td align="center" valign="middle">1</td>
							<td align="center" valign="middle">0.282</td>
						</tr>
						<tr>
							<td align="left" valign="middle">Carabidae</td>
							<td align="left" valign="middle">
								<italic>Steropus ebenus</italic> (Quensel, 1806)</td>
							<td align="center" valign="middle">2</td>
							<td align="center" valign="middle">0.563</td>
						</tr>
						<tr>
							<td rowspan="3" align="left" valign="middle">Curculionidae</td>
							<td align="left" valign="middle">
								<italic>Coniocleonus nigrosuturatus</italic> (Goeze, 1777)</td>
							<td align="center" valign="middle">1</td>
							<td rowspan="3" align="left" valign="middle">5.352</td>
						</tr>
						<tr>
							<td align="left" valign="middle">
								<italic>Cycloderes</italic> sp. Sahlberg, 1823</td>
							<td align="center" valign="middle">13</td>
						</tr>
						<tr>
							<td align="left" valign="middle">Indet.</td>
							<td align="center" valign="middle">5</td>
						</tr>
						<tr>
							<td align="left" valign="middle">Meloidae</td>
							<td align="left" valign="middle">
								<italic>Berberomeloe castuo</italic> S&#x00E1;nchez-Vialas, 2019</td>
							<td align="center" valign="middle">1</td>
							<td align="center" valign="middle">0.282</td>
						</tr>
						<tr>
							<td align="left" valign="middle">Scarabaeidae</td>
							<td align="left" valign="middle">Indet.</td>
							<td align="center" valign="middle">3</td>
							<td align="center" valign="middle">0.845</td>
						</tr>
						<tr>
							<td rowspan="10" align="left" valign="middle">Tenebrionidae</td>
							<td align="left" valign="middle">
								<italic>Alphasida</italic> sp. Escalera, 1905</td>
							<td align="center" valign="middle">4</td>
							<td rowspan="10" align="left" valign="middle">25.35</td>
						</tr>
						<tr>
							<td align="left" valign="middle">
								<italic>Blaps hispanica</italic> Laporte, 1840</td>
							<td align="center" valign="middle">1</td>
						</tr>
						<tr>
							<td align="left" valign="middle">
								<italic>Crypticus</italic> sp. Latreille, 1817</td>
							<td align="center" valign="middle">20</td>
						</tr>
						<tr>
							<td align="left" valign="middle">
								<italic>Micrositus</italic> sp. Mulsant &#x0026; Rey, 1854</td>
							<td align="center" valign="middle">3</td>
						</tr>
						<tr>
							<td align="left" valign="middle">
								<italic>Misolampus</italic> sp. Latreille, 1807</td>
							<td align="center" valign="middle">1</td>
						</tr>
						<tr>
							<td align="left" valign="middle">
								<italic>Pimelia evorensis</italic> Reitter, 1916</td>
							<td align="center" valign="middle">1</td>
						</tr>
						<tr>
							<td align="left" valign="middle">
								<italic>Scaurus uncinus</italic> (Forster, 1771)</td>
							<td align="center" valign="middle">36</td>
						</tr>
						<tr>
							<td align="left" valign="middle">
								<italic>Sepidium bidentatum</italic> Solier, 1843</td>
							<td align="center" valign="middle">11</td>
						</tr>
						<tr>
							<td align="left" valign="middle">
								<italic>Tentyria</italic> sp. Latreille, 1802</td>
							<td align="center" valign="middle">12</td>
						</tr>
						<tr>
							<td align="left" valign="middle">Indet.</td>
							<td align="center" valign="middle">1</td>
						</tr>
						<tr>
							<td align="left" valign="middle">Indet.</td>
							<td align="left" valign="middle">-</td>
							<td align="center" valign="middle">3</td>
							<td align="center" valign="middle">0.845</td>
						</tr>
						<tr>
							<td align="left" valign="middle">
								<bold>Hemiptera</bold>
							</td>
							<td align="left" valign="middle">Lygaeidae</td>
							<td align="left" valign="middle">
								<italic>Xanthochilus saturnius</italic> (Rossi, 1790)</td>
							<td align="center" valign="middle">1</td>
							<td align="center" valign="middle">0.282</td>
						</tr>
						<tr>
							<td rowspan="6" align="left" valign="middle">
								<bold>Hymenoptera</bold>
							</td>
							<td rowspan="2" align="left" valign="middle">Formicidae</td>
							<td align="left" valign="middle">
								<italic>Messor barbarus</italic> Linnaeus, 1767</td>
							<td align="center" valign="middle">96</td>
							<td rowspan="2" align="left" valign="middle">57.46</td>
						</tr>
						<tr>
							<td align="left" valign="middle">Indet.</td>
							<td align="center" valign="middle">108</td>
						</tr>
						<tr>
							<td rowspan="3" align="left" valign="middle">Mutillidae</td>
							<td align="left" valign="middle">
								<italic>Ronisia</italic> sp. Costa, 1858</td>
							<td align="center" valign="middle">1</td>
							<td rowspan="3" align="left" valign="middle">1.127</td>
						</tr>
						<tr>
							<td align="left" valign="middle">
								<italic>Tropidotilla litoralis</italic> (Petagna, 1787)</td>
							<td align="center" valign="middle">1</td>
						</tr>
						<tr>
							<td align="left" valign="middle">Indet.</td>
							<td align="center" valign="middle">2</td>
						</tr>
						<tr>
							<td align="left" valign="middle">Tiphiidae</td>
							<td align="left" valign="middle">
								<italic>Meria</italic> sp. Illiger, 1807</td>
							<td align="center" valign="middle">1</td>
							<td align="center" valign="middle">0.282</td>
						</tr>
						<tr>
							<td align="left" valign="middle">
								<bold>Mantodea</bold>
							</td>
							<td align="left" valign="middle">Indet.</td>
							<td align="left" valign="middle">-</td>
							<td align="center" valign="middle">1</td>
							<td align="center" valign="middle">0.282</td>
						</tr>
						<tr>
							<td rowspan="3" align="left" valign="middle">
								<bold>Orthoptera</bold>
							</td>
							<td rowspan="3" align="left" valign="middle">Acrididae</td>
							<td align="left" valign="middle">
								<italic>Calliptamus</italic> sp. Serville, 1831</td>
							<td align="center" valign="middle">5</td>
							<td rowspan="3" align="left" valign="middle">5.07</td>
						</tr>
						<tr>
							<td align="left" valign="middle">
								<italic>Dociostaurus genei</italic> (Ocskay, 1832)</td>
							<td align="center" valign="middle">12</td>
						</tr>
						<tr>
							<td align="left" valign="middle">Indet.</td>
							<td align="center" valign="middle">1</td>
						</tr>
						<tr>
							<td align="left" valign="middle">
								<bold>Julida</bold>
							</td>
							<td align="left" valign="middle">Indet.</td>
							<td align="left" valign="middle">-</td>
							<td align="center" valign="middle">1</td>
							<td align="center" valign="middle">0.282</td>
						</tr>
						<tr>
							<td align="left" valign="middle">
								<bold>Solifugae</bold>
							</td>
							<td align="left" valign="middle">Daesiidae</td>
							<td align="left" valign="middle">
								<italic>Gluvia dorsalis</italic> (Latreille 1817)</td>
							<td align="center" valign="middle">1</td>
							<td align="center" valign="middle">0.282</td>
						</tr>
						<tr>
							<td align="left" valign="middle">
								<bold>Scorpiones</bold>
							</td>
							<td align="left" valign="middle">Buthidae</td>
							<td align="left" valign="middle">
								<italic>Buthus</italic> sp. Leach, 1815</td>
							<td align="center" valign="middle">1</td>
							<td align="center" valign="middle">0.282</td>
						</tr>
						<tr>
							<td rowspan="3" align="left" valign="middle">
								<bold>Araneae</bold>
							</td>
							<td align="left" valign="middle">Sparassidae</td>
							<td align="left" valign="middle">
								<italic>Eusparassus dufouri</italic> Simon, 1932</td>
							<td align="center" valign="middle">1</td>
							<td align="center" valign="middle">0.282</td>
						</tr>
						<tr>
							<td align="left" valign="middle">Salticidae</td>
							<td align="left" valign="middle">Indet.</td>
							<td align="center" valign="middle">1</td>
							<td align="center" valign="middle">0.282</td>
						</tr>
						<tr>
							<td align="left" valign="middle">Indet.</td>
							<td align="left" valign="middle">-</td>
							<td align="center" valign="middle">2</td>
							<td align="center" valign="middle">0.563</td>
						</tr>
					</tbody>
				</table>
			</table-wrap>
			<fig id="fig-2-e138">
				<label>Fig. 2</label>
				<caption>
					<title>Abundance of different prey orders (%) found in <italic>L. tredecimguttatus</italic> webs.</title>
					<p xml:lang="es">Fig. 2.&#x02014; Abundancia de los distintos &#x00F3;rdenes de presas (%) encontradas en redes de <italic>L. tredecimguttatus</italic>.</p>
				</caption>
				<graphic id="gra-2-e138" xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="GRAELL-77-1-e138-f2-G.png"/>
			</fig>
			<p>Of the two major prey orders [Hymenoptera (58.9%) and Coleoptera (33.5%)], most hymenopteran prey items were ants (Formicidae) (97.6%) and the family Tenebrionidae (75.6%) predominated in coleopteran prey items.</p>
		</sec>
		<sec sec-type="discussion" id="sec-4-e138">
			<title>Discussion</title>
			<p>Our results showed that <italic>L. tredecimguttatus</italic> can be classified as a stenophagous generalist predator (B<sub>A</sub> = 0.146), a trophic category which includes species with generalized adaptations and with a narrow diet breadth in which predominates a certain taxon (<xref ref-type="bibr" rid="ref-13-e138">Pek&#x00E1;r &#x0026; Toft, 2015</xref>). Nonetheless, their diet is polyphagous, given that the spiders preyed upon nine different arthropod orders during the study period (Araneae, Coleoptera, Hemiptera, Hymenoptera, Julida, Mantodea, Orthoptera, Scorpiones and Solifugae). The most abundant order was Hymenoptera (58.9%) followed by Coleoptera (33.5%). These results are consistent with previous works on <italic>Latrodectus</italic> species whose diet was composed mainly of ants, like <italic>L. pallidus</italic> (<xref ref-type="bibr" rid="ref-21-e138">Shulov &#x0026; Weissmann, 1959</xref>), <italic>L. mactans</italic> (75% of the total prey items) (<xref ref-type="bibr" rid="ref-12-e138">Nyffeler <italic>et al.</italic>, 1988</xref>) and <italic>L. mirabilis</italic> (&#x003E;86%) (<xref ref-type="bibr" rid="ref-15-e138">Pompozzi <italic>et al.,</italic> 2013</xref>). Nevertheless, Coleoptera and Isopoda were the most frequent prey orders in the diets of <italic>L. lilianae</italic> and <italic>L. geometricus</italic>, representing 65-82% and 47.64% of the prey total for these two species respectively (<xref ref-type="bibr" rid="ref-7-e138">H&#x00F3;dar &#x0026; S&#x00E1;nchez-Pi&#x00F1;ero, 2002</xref>; <xref ref-type="bibr" rid="ref-22-e138">Taucare-R&#x00ED;os &#x0026; Canals, 2015</xref>). Moreover, Coleoptera was the most common in the diet of <italic>L. hesperus</italic> (61%), followed by Hymenoptera (26%) (<xref ref-type="bibr" rid="ref-19-e138">Salomon, 2011</xref>). In other studies of this species, <xref ref-type="bibr" rid="ref-20-e138">Shulov (1940)</xref> and <xref ref-type="bibr" rid="ref-21-e138">Shulov &#x0026; Weissmann (1959)</xref> also discovered that Tenebrionidae and Formicidae were the most-abundant prey families consumed, so we conclude that <italic>L. tredecimguttatus</italic> feeds primarily on these two insect groups. Notwithstanding, we would not know if these prey families are selected among others since no prey abundance or availability were sampled in this study.</p>
			<p>In addition, the diet composition of black widows may depend on a variety of factors. First, widow spiders do not actively select prey but rather sit and wait for individuals that, when walking through the area, are trapped in the capture web (<xref ref-type="bibr" rid="ref-7-e138">H&#x00F3;dar &#x0026; S&#x00E1;nchez-Pi&#x00F1;ero, 2002</xref>). In addition, web location (very close to the ground) makes epigeic prey more likely to be captured. Thus, their diet will depend on the arthropod fauna available surrounding the web. Moreover, the faunal composition varies between regions and habitats (e. g. <xref ref-type="bibr" rid="ref-17-e138">Rosenzweig, 1995</xref>; <xref ref-type="bibr" rid="ref-6-e138">Hillebrand, 2004</xref>), so it is not rare to find differences in prey order composition and abundance between <italic>Latrodectus</italic> species and across habitats. Nevertheless, there is a consistent pattern of ants and Coleoptera as the dominant prey groups in <italic>Latrodectus</italic> diets.</p>
			<p>Moreover, other factors such as habitat characteristics and prey ecology must be considered, since seasonal patterns of prey affect their availability in an area (<xref ref-type="bibr" rid="ref-9-e138">McReynolds &#x0026; Polis, 1987</xref>; <xref ref-type="bibr" rid="ref-24-e138">Uetz, 1990</xref>; <xref ref-type="bibr" rid="ref-7-e138">H&#x00F3;dar &#x0026; S&#x00E1;nchez-Pi&#x00F1;ero, 2002</xref>). Most of the previous works of <italic>Latrodectus</italic> diets took place over a longer period or in different months than the current study when focused on species that differ in the activity period from <italic>L. tredecimguttatus</italic>. In contrast to these works, the prey composition of our study was made up of species whose activity period overlaps with late summer, like different families of Arachnida, most Hymenoptera, Orthoptera, or Tenebrionidae beetles. For example, the order Isopoda, whose activity is limited by the humidity of the environment (<xref ref-type="bibr" rid="ref-4-e138">Garcia, 2015</xref>), was detected in great abundance in the <italic>L. lilianae</italic> diet (<xref ref-type="bibr" rid="ref-7-e138">H&#x00F3;dar &#x0026; S&#x00E1;nchez-Pi&#x00F1;ero, 2002</xref>) during a year of sampling, while no individuals of that order were found in this study. Extreme and dry weather conditions of Extremadura in 2019 during the four summer-autumn months of sampling or the presence of different Isopoda species with different ecology could explain this absence. In contrast, ants were very abundant in the area throughout the study period, as were Tenebrionidae (Mora-Rubio &#x0026; Parejo-Pulido, pers. obs.), so they were the most available prey for the spiders in the environment (although not necessarily a preferred prey), and this could explain the low value of B .</p>
			<p>Additionally, we found that other predators such as mantids, scorpions, solpugids and other spiders are included in the black widow diet. These results support other works that found intraguild predation, often of immature prey stages, in generalist predators (<xref ref-type="bibr" rid="ref-14-e138">Polis, 1988</xref>) and even in <italic>Latrodectus</italic> species (<xref ref-type="bibr" rid="ref-20-e138">Shulov, 1940</xref>; <xref ref-type="bibr" rid="ref-21-e138">Shulov &#x0026; Weissmann, 1959</xref>; <xref ref-type="bibr" rid="ref-12-e138">Nyffeler <italic>et al.,</italic> 1988</xref>; <xref ref-type="bibr" rid="ref-7-e138">H&#x00F3;dar &#x0026; S&#x00E1;nchez-Pi&#x00F1;ero, 2002</xref>; <xref ref-type="bibr" rid="ref-19-e138">Salomon, 2011</xref>; <xref ref-type="bibr" rid="ref-15-e138">Pompozzi <italic>et al.,</italic> 2013</xref>). In this way, potential competitors are eliminated, although there are risks of being killed by the prey.</p>
			<p>In conclusion, we found that <italic>L. tredecimguttatus</italic> can be considered a stenophagous generalist predator, whose diet consists mainly of Hymenoptera (mostly ants) and Coleoptera (mostly Tenebrionidae). This study contributes to the knowledge of the ecology of this Mediterranean species in the Iberian Peninsula, highlighting its role as a predator of diverse arthropods, including spiders and other predators.</p>
		</sec>
	</body>
	<back>
		<ack id="ack-1-e138">
			<title>Acknowledgements</title>
			<p>We are grateful to Antonio J. Vel&#x00E1;zquez, Gin&#x00E9;s Rodr&#x00ED;guez, Luis Rozas and Rafael Obreg&#x00F3;n for helping with the identification of some of the Curculionidae, Orthoptera, Scarabaeidae and Tenebrionidae individuals, respectively. We also thank Catherine Scott and Laura P&#x00E9;rez Zarcos for reviewing and providing suggestions to improve this manuscript.</p>
		</ack>
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