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I-IV ventral view; 3, chaetotaxy of the head; 4, thorax and abdomen chaetotaxy.</p>" ] ] ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "José G. Palacios-Vargas, Maira Montejo-Cruz" "autores" => array:2 [ 0 => array:2 [ "nombre" => "José G." "apellidos" => "Palacios-Vargas" ] 1 => array:2 [ "nombre" => "Maira" "apellidos" => "Montejo-Cruz" ] ] ] ] ] "idiomaDefecto" => "en" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S1870345314729872?idApp=UINPBA00004N" "url" => "/18703453/0000008500000004/v1_201504220301/S1870345314729872/v1_201504220301/en/main.assets" ] "itemAnterior" => array:18 [ "pii" => "S1870345314729859" "issn" => "18703453" "doi" => "10.7550/rmb.43875" "estado" => "S300" "fechaPublicacion" => "2014-12-01" "aid" => "72985" "copyright" => "Universidad Nacional Autónoma de México" "documento" => "article" "licencia" => "http://creativecommons.org/licenses/by-nc-nd/4.0/" "subdocumento" => "fla" "cita" => "Revista Mexicana de Biodiversidad. 2014;85:1024-31" "abierto" => array:3 [ "ES" => true "ES2" => true "LATM" => true ] "gratuito" => true "lecturas" => array:2 [ "total" => 1080 "formatos" => array:3 [ "EPUB" => 22 "HTML" => 760 "PDF" => 298 ] ] "en" => array:12 [ "idiomaDefecto" => true "titulo" => "Echinostome cercariae from <span class="elsevierStyleItalic">Biomphalaria straminea</span> (Mollusca: Planorbidae) in a ricefield from northeastern Argentina" "tienePdf" => "en" "tieneTextoCompleto" => "en" "tieneResumen" => array:2 [ 0 => "en" 1 => "es" ] "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "1024" "paginaFinal" => "1031" ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Echinocercarias de <span class="elsevierStyleItalic">Biomphalaria straminea</span> (Mollusca: Planorbidae) en un campo de arroz del noreste de Argentina" ] ] "contieneResumen" => array:2 [ "en" => true "es" => true ] "contieneTextoCompleto" => array:1 [ "en" => true ] "contienePdf" => array:1 [ "en" => true ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:7 [ "identificador" => "fig0005" "etiqueta" => "Figure 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 614 "Ancho" => 973 "Tamanyo" => 52330 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Prevalence of larval trematode infections in <span class="elsevierStyleItalic">B. straminea</span> from a rice field in Corrientes province during 2 rice cultivation cycles, black bar: December 2010 - May 2011 (n= number of collected snails: 3 494); gray bar: December 2011 - May 2012 (n<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>2 016).</p>" ] ] ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "María Virginia Fernández, Monika Inés Hamann, Margarita Ostrowski-de Núñez" "autores" => array:3 [ 0 => array:2 [ "nombre" => "María Virginia" "apellidos" => "Fernández" ] 1 => array:2 [ "nombre" => "Monika Inés" "apellidos" => "Hamann" ] 2 => array:2 [ "nombre" => "Margarita Ostrowski-de" "apellidos" => "Núñez" ] ] ] ] ] "idiomaDefecto" => "en" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S1870345314729859?idApp=UINPBA00004N" "url" => "/18703453/0000008500000004/v1_201504220301/S1870345314729859/v1_201504220301/en/main.assets" ] "en" => array:19 [ "idiomaDefecto" => true "titulo" => "First record of <span class="elsevierStyleItalic">Litomosoides pardinasi</span> (Nematoda: Onchocercidae) in native and exotic rodents from Chile" "tieneTextoCompleto" => true "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "1032" "paginaFinal" => "1037" ] ] "autores" => array:1 [ 0 => array:3 [ "autoresLista" => "Carlos Landaeta-Aqueveque, Juliana Notarnicola, Juana P. Correa, Andrea Yáñez-Meza, AnaLía Henríquez, Pedro E. Cattan, Carezza Botto-Mahan, Fernando Torres-Pérez" "autores" => array:8 [ 0 => array:3 [ "nombre" => "Carlos" "apellidos" => "Landaeta-Aqueveque" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">1</span>" "identificador" => "aff0005" ] ] ] 1 => array:4 [ "nombre" => "Juliana" "apellidos" => "Notarnicola" "email" => array:1 [ 0 => "julinota@cepave.edu.ar" ] "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">2</span>" "identificador" => "aff0010" ] ] ] 2 => array:3 [ "nombre" => "Juana P." "apellidos" => "Correa" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">3</span>" "identificador" => "aff0015" ] ] ] 3 => array:3 [ "nombre" => "Andrea" "apellidos" => "Yáñez-Meza" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">4</span>" "identificador" => "aff0020" ] ] ] 4 => array:3 [ "nombre" => "AnaLía" "apellidos" => "Henríquez" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">5</span>" "identificador" => "aff0025" ] ] ] 5 => array:3 [ "nombre" => "Pedro E." "apellidos" => "Cattan" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">3</span>" "identificador" => "aff0015" ] ] ] 6 => array:3 [ "nombre" => "Carezza" "apellidos" => "Botto-Mahan" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">4</span>" "identificador" => "aff0020" ] ] ] 7 => array:3 [ "nombre" => "Fernando" "apellidos" => "Torres-Pérez" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">6</span>" "identificador" => "aff0030" ] ] ] ] "afiliaciones" => array:6 [ 0 => array:3 [ "entidad" => "Departamento de Patología y Medicina Preventiva, Facultad de Ciencias Veterinarias, Universidad de Concepción. Vicente Méndez 595, Chillán. Chile." "etiqueta" => "1" "identificador" => "aff0005" ] 1 => array:3 [ "entidad" => "Centro de Estudios Parasitológicos y de Vectores, CCT La Plata, Consejo Nacional de Investigaciones Científicas y Técnicas. Calle 2, Núm. 584, La Plata (1900), Buenos Aires, Argentina." "etiqueta" => "2" "identificador" => "aff0010" ] 2 => array:3 [ "entidad" => "Departamento de Ciencias Biológicas Animales, Facultad de Ciencias Veterinarias y Pecuarias, Universidad de Chile. Santa Rosa 11735, Santiago Chile." "etiqueta" => "3" "identificador" => "aff0015" ] 3 => array:3 [ "entidad" => "Depatamento de Ciencias Ecológicas, Facultad de Ciencias, Universidad de Chile. Las Palmeras 3425, Ñuñoa, Santiago Chile." "etiqueta" => "4" "identificador" => "aff0020" ] 4 => array:3 [ "entidad" => "Facultad de Recursos Naturales y Medicina Veterinaria, Universidad Santo Tomás. Manuel Rodríguez 060, Temuco, Chile." "etiqueta" => "5" "identificador" => "aff0025" ] 5 => array:3 [ "entidad" => "Instituto de Biología, Pontificia Universidad Católica de Valparaíso. Valparaíso 2373223, Chile." "etiqueta" => "6" "identificador" => "aff0030" ] ] ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Primer registro de <span class="elsevierStyleItalic">Litomosoides pardinasi</span> (Nematoda: Onchocercidae) en roedores nativos y exóticos de Chile" ] ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:7 [ "identificador" => "fig0005" "etiqueta" => "Figure 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 1836 "Ancho" => 973 "Tamanyo" => 164133 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall"><span class="elsevierStyleItalic">Litomosoides pardinasi</span> from <span class="elsevierStyleItalic">Rattus rattus</span>. A, buccal capsule lateral view; B, posterior extremity of male showing the spicules and cloacal papillae.</p>" ] ] ] "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Introduction</span><p id="par0005" class="elsevierStylePara elsevierViewall">Worms of the genus <span class="elsevierStyleItalic">Litomosoides</span> Chandler, 1931 are filarioid parasites of the thoracic and abdominal cavities of bats, marsupials, and rodents of the families Ctenomyidae, Echimyidae, Sciuridae, and Cricetidae (<a class="elsevierStyleCrossRef" href="#bib0050">Esslinger, 1973</a>; <a class="elsevierStyleCrossRef" href="#bib0030">Bain et al., 1989</a>; <a class="elsevierStyleCrossRefs" href="#bib0125">Notarnicola et al., 2002, 2010</a>). They occur in Neotropical and southern Nearctic regions. Most of the <span class="elsevierStyleItalic">Litomosoides</span> species occur in South America, including Venezuela (6 species), Colombia (10 species), Peru (3 species), Bolivia (5 species), Argentina (8 species), Brazil (11 species), and Uruguay (1 species) (<a class="elsevierStyleCrossRef" href="#bib0155">Travassos, 1919</a>; <a class="elsevierStyleCrossRef" href="#bib0050">Esslinger, 1973</a>; <a class="elsevierStyleCrossRefs" href="#bib0025">Bain et al., 1980, 1989</a>; <a class="elsevierStyleCrossRef" href="#bib0035">Brant and Gardner, 1997</a>; <a class="elsevierStyleCrossRef" href="#bib0110">Moraes Neto et al., 1997</a>; <a class="elsevierStyleCrossRefs" href="#bib0120">Notarnicola et al., 2000, 2002</a>; <a class="elsevierStyleCrossRefs" href="#bib0135">Notarnicola and Navone, 2002, 2011</a>; <a class="elsevierStyleCrossRefs" href="#bib0080">Guerrero et al., 2002, 2003, 2011</a>).</p><p id="par0010" class="elsevierStylePara elsevierViewall">All the records of <span class="elsevierStyleItalic">Litomosoides</span> species have been reported in native host species, with the exception of some specimens of <span class="elsevierStyleItalic">Litomosoides sigmodontis</span> Chandler, 1931 found in one individual of the exotic <span class="elsevierStyleItalic">Rattus norvegicus</span> Berkenhout, 1769 —originally mentioned as <span class="elsevierStyleItalic">Mus decumanus</span>— from 131 specimens trapped in Caracas, Venezuela (<a class="elsevierStyleCrossRef" href="#bib0160">Vogel and Gabaldon, 1932</a>).</p><p id="par0015" class="elsevierStylePara elsevierViewall">Among the species of this genus, <span class="elsevierStyleItalic">Litomosoides pardinasi</span><a class="elsevierStyleCrossRef" href="#bib0140">Notarnicola and Navone, 2011</a> is the southernmost worldwide record described in cricetid rodents from Neuquén, Argentina (<a class="elsevierStyleCrossRef" href="#bib0140">Notarnicola and Navone, 2011</a>). These authors found <span class="elsevierStyleItalic">L. pardinasi</span> in <span class="elsevierStyleItalic">Phyllotis xanthopygus</span> Waterhouse, 1837 with a prevalence of 25% and a mean intensity of 7.2, and in <span class="elsevierStyleItalic">Oligoryzomys longicaudatus</span> Bennett, 1832 with 33% and 6, respectively.</p><p id="par0020" class="elsevierStylePara elsevierViewall">In Chile, several studies have reported helminths in rodents (e.g., <a class="elsevierStyleCrossRef" href="#bib0015">Babero and Cattan, 1975</a>; <a class="elsevierStyleCrossRef" href="#bib0045">Durette-Desset et al., 1976</a>; <a class="elsevierStyleCrossRefs" href="#bib0090">Landaeta-Aqueveque et al., 2007a, 2007b</a>), but none have reported filarioid species. Filarioids in Chile include <span class="elsevierStyleItalic">Dipetalonema reconditum</span> Grassi, 1980, <span class="elsevierStyleItalic">D. dracunculoides</span> Cobbold, 1870, and <span class="elsevierStyleItalic">Dirofilaria repens</span> Railliet and Henry, 1911 in dogs (<a class="elsevierStyleCrossRef" href="#bib0010">Alcaíno et al., 1984</a>; <a class="elsevierStyleCrossRef" href="#bib0105">López et al., 2012</a>), and <span class="elsevierStyleItalic">Setaria equina</span> Abildgaard, 1789 in horses (<a class="elsevierStyleCrossRef" href="#bib0005">Alcaíno and Gorman, 1999</a>). Argentina and Chile share several rodent species and some are known to be hosts for this group of nematodes in Argentina.</p><p id="par0025" class="elsevierStylePara elsevierViewall">This study reports the first record of <span class="elsevierStyleItalic">L. pardinasi</span> in rodents of Chile. We also report new hosts and the first record of <span class="elsevierStyleItalic">L. pardinasi</span> in the exotic rodent <span class="elsevierStyleItalic">Rattus rattus</span> Linnaeus, 1758. Finally we discuss the evolution of the host-parasite associations of this nematode.</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Materials and methods</span><p id="par0030" class="elsevierStylePara elsevierViewall">We sampled 1 150 native and exotic rodents between the latitudes 31°30'32” S, 35°08'13” S, and between 0 and 1 100<span class="elsevierStyleHsp" style=""></span>m asl in central Chile, for a total of 19 sampling sites. Localities covered heterogeneous landscapes encompassing several eco-regions, ranging from arid- Mediterranean, to humid-Mediterranean. Rodents were analyzed for the presence of intestinal, peritoneal, and pleural helminths. Trapped native species consisted of 344 <span class="elsevierStyleItalic">Abrothrix olivaceus</span> Waterhouse, 1837, 10 <span class="elsevierStyleItalic">Abrothrix longipilis</span> Waterhouse, 1837, 58 <span class="elsevierStyleItalic">O. longicaudatus</span>, 119 <span class="elsevierStyleItalic">Phyllotis darwini</span> Waterhouse, 1837 (Cricetidae), 183 <span class="elsevierStyleItalic">Octodon degus</span> Molina, 1782 (Octodontidae), and 7 <span class="elsevierStyleItalic">Abrocoma bennetti</span> Waterhouse, 1837 (Abrocomidae), and the exotic rodents were 161 <span class="elsevierStyleItalic">R. rattus</span>, 87 <span class="elsevierStyleItalic">R. norvegicus</span>, and 181 <span class="elsevierStyleItalic">Mus musculus</span> Linnaeus, 1758 (Muridae). Rodents were trapped with Sherman traps baited with rolled oats, and killed using isoflurane anesthesia. Captures followed all ethical guidelines of the Bioethical Committee of the Facultad de Ciencias Veterinarias y Pecuarias, Universidad de Chile, and were performed with the permission of the Chilean Agriculture and Livestock Bureau (Servicio Agrícola y Ganadero of Chile) and the Chilean National Forest Corporation (Corporación Nacional Forestal).</p><p id="par0035" class="elsevierStylePara elsevierViewall">Worms were recovered directly from the peritoneal and pleural cavities and preserved in 70% ethanol. For examination, samples were cleared with ethanol-glycerin solution and observed under light microscope (Olympus BX51); drawings were made with the aid of a drawing tube. Some worms were studied under Scanning Electron Microscope (SEM Hitachi TM 3000, Pontificia Universidad Católica de Chile, Facultad de Ciencias Biológicas). Measurements are given in micrometers unless otherwise stated; mean values follow the range in parentheses; when two specimens are given, measurements are separated by semicolons.</p><p id="par0040" class="elsevierStylePara elsevierViewall">Prevalence (P) and mean intensity (MI) were calculated following <a class="elsevierStyleCrossRef" href="#bib0040">Bush et al. (1997)</a>. Fisher's exact test was used to compare prevalences and the negative binomial regression methodology (NBR) was used to analyze intensities. Comparisons with Argentinean P and MI correspond to these reported by <a class="elsevierStyleCrossRef" href="#bib0140">Notarnicola and Navone (2011)</a>. Statistical analyses were performed in R environment (R Core Team, Vienna, Austria, <a href="http://www.R-project.org/">http://www.R-project.org/</a>).</p><p id="par0045" class="elsevierStylePara elsevierViewall">Voucher specimens of worms were deposited at the Museo Nacional de Historia Natural de Chile, Invertebrate Collection (MNHNCL/NEM), and voucher specimen of rodents were deposited at the Museo Nacional de Historia Natural de Chile - Vertebrate Collection (MNHN), and the Patricio Sánchez Reyes Flora and Fauna Collection (UCK) -Pontificia Universidad Católica de Chile.<a name="p1034"></a></p></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Results</span><p id="par0050" class="elsevierStylePara elsevierViewall">The filarioids were identified as <span class="elsevierStyleItalic">L. pardinasi</span> according to the morphological and morphometric characters stated by <a class="elsevierStyleCrossRef" href="#bib0140">Notarnicola and Navone (2011)</a>. Specimens show the following characters: the shape of the buccal capsule displays an anterior enlargement in the cuticularized segment (<a class="elsevierStyleCrossRef" href="#fig0005">Fig. 1A</a>); the left spicule is constituted with a handle longer than the blade; blade consisting of a filament; the right spicule is well cuticularized, with a prominent dorsal heel and a terminal cap; the tail is attenuated with one pair of ad-cloacal papillae and three to four pairs of slightly asymmetric postcloacal papillae (<a class="elsevierStyleCrossRef" href="#fig0005">Fig. 1B</a>); the arrangement of the head papillae consists of two dorsal cephalic papillae near the amphids and four labial papillae (<a class="elsevierStyleCrossRef" href="#fig0010">Fig. 2A</a>); the area rugosa constituted by transverse ridges made of small longitudinal crests (<a class="elsevierStyleCrossRef" href="#fig0010">Fig. 2B</a>); and the position of the vulva, posterior to the esophago-intestinal junction. Measurements of the specimens are included in <a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>.</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="tbl0005"></elsevierMultimedia><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0040">Taxonomic summary</span><p id="par0055" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">Hosts and localities: Oligoryzomys longicaudatus</span> Bennett, 1832 from Los Queñes (35°08'13” S, 70°45'19” W), UCK 423; from Polpaico (33°09' S, 70°53' W), MNHN 1598; from Rinconada de Maipú (33°29' S, 70°49' W), PM84,<a name="p1035"></a></p><p id="par0060" class="elsevierStylePara elsevierViewall">PM183, PM184, PM204, PM207, PM233, PM264, PM266; from Calera de Tango (33°38' S, 70°47' W), PL186. <span class="elsevierStyleItalic">Phyllotis darwini</span> Waterhouse, 1837 from Las Chinchillas National Reserve (31°30' S, 71°06' W), MNHN 1599, Dn56, T66, L56, K56. <span class="elsevierStyleItalic">Rattus rattus</span> from Fundo El Bosque (33°32' S, 70°48' W), M180; from La Pintana (33°34' S, 70°37' W), M145, Chile.</p><p id="par0065" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">Site of infection:</span> abdominal and peritoneal cavities.</p><p id="par0070" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">Specimens deposited:</span> voucher specimens at the Museo Nacional de Historia Natural de Chile, Invertebrates Collection numbers MNHNCL/NEM 11853; 11854; 11855.</p><p id="par0075" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">Remarks. Litomosoides pardinasi</span> was found in the peritoneal and thoracic cavities of 11 <span class="elsevierStyleItalic">O. longicaudatus</span> (P<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>18.9%; MI<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>57.3) and 5 <span class="elsevierStyleItalic">P. darwini</span> (P<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>4.2%; MI<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>10), and in the peritoneal cavity of 2 <span class="elsevierStyleItalic">R. rattus</span> (P<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>1.24%; MI<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>22.5) captured in 7 areas located in Chile. Total prevalence and total mean intensity in native host species were 9% and 42.5, respectively. <span class="elsevierStyleItalic">Phyllotis darwini</span> showed significantly lower prevalence than <span class="elsevierStyleItalic">O. longicaudatus</span> (<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>0.003), and non-significantly higher prevalence than <span class="elsevierStyleItalic">R. rattus</span>.</p><p id="par0080" class="elsevierStylePara elsevierViewall">When comparing our data with that from Argentina, total prevalence in Chile, excluding <span class="elsevierStyleItalic">R. rattus</span> (9%, n<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>177), was significantly lower than in Argentina (25.5%, n<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>47) (<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>0.005). When comparing prevalence from the same host genus, in Chilean <span class="elsevierStyleItalic">P. darwini</span> it was significantly lower (4.2%, n<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>119) than in the Argentinean <span class="elsevierStyleItalic">P. xanthopygus</span> (25%, n<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>44) (<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.001), while prevalence in Chilean <span class="elsevierStyleItalic">O. longicaudatus</span> (19%, n<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>58) was not significantly different from that of the Argentinean <span class="elsevierStyleItalic">O. longicaudatus</span> (33.3%, n<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>3) (<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>0.490). The total mean intensity in Chile excluding <span class="elsevierStyleItalic">R. rattus</span> (42.5) was significantly higher than in Argentina (7.08) (Likelihood ratio test (LRt): <span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>0.001). Analyzing by host species or genus, there were no significant differences between the mean intensities of <span class="elsevierStyleItalic">O. longicaudatus</span> from Chile (57.3) and Argentina (6) (LRt: <span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>0.150); the same was observed between the <span class="elsevierStyleItalic">Phyllotis</span> spp. (<span class="elsevierStyleItalic">P. darwini</span>: 10 vs. <span class="elsevierStyleItalic">P. xanthopygus:</span> 7.2; LRt: <span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>0.560).</p></span></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0045">Discussion</span><p id="par0085" class="elsevierStylePara elsevierViewall">Here we report the first record of <span class="elsevierStyleItalic">L. pardinasi</span> in Chile and expand the host record to <span class="elsevierStyleItalic">P. darwini</span> and <span class="elsevierStyleItalic">R. rattus.</span> Identification was based on morphological attributes and supported by morphometric characters. Most of the measurements of Chilean <span class="elsevierStyleItalic">L. pardinasi</span> averaged between the minimum and maximum measurements of Argentinean samples (<a class="elsevierStyleCrossRef" href="#bib0140">Notarnicola and Navone, 2011</a>). However some differences were observed: female tails of <span class="elsevierStyleItalic">L. pardinasi</span> found in <span class="elsevierStyleItalic">O. longicaudatus</span> from Chile are shorter than those obtained from Argentina, while the female tail from the specimen found in <span class="elsevierStyleItalic">R. rattus</span> is similar to the specimen of <span class="elsevierStyleItalic">O. longicaudatus</span> from Argentina (855 versus 800<span class="elsevierStyleHsp" style=""></span>μm; <a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>). Male worms from the three host species found in Chile presented shorter tails than those found in Argentina. The<a name="p1036"></a> Chilean specimens also had shorter left spicules (153–241<span class="elsevierStyleHsp" style=""></span>μm versus 210–270<span class="elsevierStyleHsp" style=""></span>μm). However, the spicular ratio from Chilean specimens fit within the range of the specimens from Argentina (i. e., 1:1.96 in <span class="elsevierStyleItalic">P. darwini;</span> 1:2.12 in <span class="elsevierStyleItalic">O. longicaudatus</span>, and 1:1.91 in <span class="elsevierStyleItalic">R. rattus</span> from Chile versus a range of 1:1.8 to 1:2.4 in <span class="elsevierStyleItalic">P. xanthopygus</span> and 1:2.09 in <span class="elsevierStyleItalic">O. longicaudatus</span> from Argentina). Morphometric variability was reported within other <span class="elsevierStyleItalic">Litomosoides</span> species and these observations were attributed to differences in the host species and/or geographic distribution (<a class="elsevierStyleCrossRef" href="#bib0050">Esslinger, 1973</a>; <a class="elsevierStyleCrossRef" href="#bib0030">Bain et al., 1989</a>; <a class="elsevierStyleCrossRef" href="#bib0080">Guerrero et al., 2002</a>; <a class="elsevierStyleCrossRef" href="#bib0115">Notarnicola 2005</a>; <a class="elsevierStyleCrossRef" href="#bib0130">Notarnicola et al., 2010</a>).</p><p id="par0090" class="elsevierStylePara elsevierViewall">Prevalences and mean intensities of <span class="elsevierStyleItalic">L. pardinasi</span> in <span class="elsevierStyleItalic">O. longicaudatus</span> from Chile and Argentina showed non-significant differences, while in <span class="elsevierStyleItalic">Phyllotis</span> spp. the prevalence from the Chilean specimens was significantly lower than in Argentina. Thus, it appears that <span class="elsevierStyleItalic">L. pardinasi</span> is well established in <span class="elsevierStyleItalic">O. longicaudatus</span> based on the similarities in their prevalences and mean intensities in Chile and Argentina. In contrast, this filarioid species seems to be recently acquired by <span class="elsevierStyleItalic">P. darwini</span> and the exotic <span class="elsevierStyleItalic">R. rattus</span> in Chile, based on the significantly lower prevalence, suggesting that this parasitism is a result of a recent host-switching phenomenon. Moreover, of the 16 <span class="elsevierStyleItalic">Litomosoides</span> species registered in Sigmodontinae rodents, 6 are present in Akodontini, 9 in Oryzomyini —including <span class="elsevierStyleItalic">L. pardinasi</span>—, and 1 in both Akodontini and Oryzomyini. <span class="elsevierStyleItalic">Litomosoides pardinasi</span> is the unique species registered in Phyllotini. This result supports the hypothesis that <span class="elsevierStyleItalic">L. pardinasi</span> primarily colonized the Oryzomyini tribe and later, by different phenomena of host-switching, colonized the Phyllotini (<span class="elsevierStyleItalic">P. xanthopygus</span> in Argentina and <span class="elsevierStyleItalic">P. darwini</span> in Chile) and the exotic host <span class="elsevierStyleItalic">R. rattus</span>. The host-switching phenomenon was frequently reported between native rodents living in sympatry (<a class="elsevierStyleCrossRef" href="#bib0080">Guerrero et al., 2002</a>; <a class="elsevierStyleCrossRef" href="#bib0115">Notarnicola, 2005</a>; <a class="elsevierStyleCrossRef" href="#bib0140">Notarnicola and Navone, 2011</a>).</p><p id="par0095" class="elsevierStylePara elsevierViewall"><a class="elsevierStyleCrossRef" href="#bib0160">Vogel and Gabaldon (1932)</a> reported the presence of adults and microfilariae of <span class="elsevierStyleItalic">L. sigmodontis</span> in <span class="elsevierStyleItalic">R. norvegicus</span> from Caracas, Venezuela. This filarioid species was also found to parasitize the cotton rat <span class="elsevierStyleItalic">Sigmodon hispidus</span> Say and Ord, 1825 from Mexico and USA (<a class="elsevierStyleCrossRef" href="#bib0145">Ochoterena and Caballero, 1932</a>; <a class="elsevierStyleCrossRef" href="#bib0055">Forrester and Kinsella, 1973</a>). Female specimens of <span class="elsevierStyleItalic">L. pardinasi</span> found in <span class="elsevierStyleItalic">R. rattus</span> presented microfilariae in the uterus, indicating that its life cycle can be completed in the host and can be transmitted to other hosts. All these results confirm that filarioid species are able to colonize allochthonous rodents when they share microhabitats with parasitized native rodents.</p><p id="par0100" class="elsevierStylePara elsevierViewall">The mite <span class="elsevierStyleItalic">Ornithonyssus bacoti</span> Hirst, 1913 (Acari, Macronyssidae) has been reported as a vector for several species of <span class="elsevierStyleItalic">Litomosoides</span> in rodents as well as in bats (<a class="elsevierStyleCrossRefs" href="#bib0025">Bain et al., 1980, 2002</a>). Another study showed that <span class="elsevierStyleItalic">Hoplopleura travassosi</span> Werneck, 1932 (Anoplura, Hoplopleuridae) presented positive association with <span class="elsevierStyleItalic">Litomosoides bonaerensis</span> Notarnicola, Bain and Navone 2000 (<a class="elsevierStyleCrossRef" href="#bib0100">Lareschi et al., 2003</a>). In Chile, <span class="elsevierStyleItalic">O. bacoti</span> has been recorded in several native and allochthonous rodents (<a class="elsevierStyleCrossRef" href="#bib0085">Jofré et al., 2009</a>; <a class="elsevierStyleCrossRef" href="#bib0150">Peña Oyarce, 2009</a>); whereas <span class="elsevierStyleItalic">H. travassosi</span> and <span class="elsevierStyleItalic">Hoplopleura aitkeni</span> Johnson, 1972 have been found in <span class="elsevierStyleItalic">O. longicaudatus</span> and <span class="elsevierStyleItalic">P. darwini</span>, respectively, in a geographic range that encompasses this work (<a class="elsevierStyleCrossRefs" href="#bib0060">González-Acuña et al., 2003; 2005</a>). The presence of these arthropods in native and allochthonous rodents provide more information to the hypothesis that filarioids are transmitted by these vectors in rodents living in sympatry.</p></span></span>" "textoCompletoSecciones" => array:1 [ "secciones" => array:10 [ 0 => array:3 [ "identificador" => "xres479579" "titulo" => "Abstract" "secciones" => array:1 [ 0 => array:1 [ "identificador" => "abst0005" ] ] ] 1 => array:2 [ "identificador" => "xpalclavsec501899" "titulo" => "Key words" ] 2 => array:3 [ "identificador" => "xres479580" "titulo" => "Resumen" "secciones" => array:1 [ 0 => array:1 [ "identificador" => "abst0010" ] ] ] 3 => array:2 [ "identificador" => "xpalclavsec501900" "titulo" => "Palabras clave" ] 4 => array:2 [ "identificador" => "sec0005" "titulo" => "Introduction" ] 5 => array:2 [ "identificador" => "sec0010" "titulo" => "Materials and methods" ] 6 => array:3 [ "identificador" => "sec0015" "titulo" => "Results" "secciones" => array:1 [ 0 => array:2 [ "identificador" => "sec0020" "titulo" => "Taxonomic summary" ] ] ] 7 => array:2 [ "identificador" => "sec0025" "titulo" => "Discussion" ] 8 => array:2 [ "identificador" => "xack147154" "titulo" => "Acknowledgments" ] 9 => array:1 [ "titulo" => "Literature cited" ] ] ] "pdfFichero" => "main.pdf" "tienePdf" => true "fechaRecibido" => "2014-02-25" "fechaAceptado" => "2014-07-07" "PalabrasClave" => array:2 [ "en" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Key words" "identificador" => "xpalclavsec501899" "palabras" => array:7 [ 0 => "host-switching" 1 => "nematodes" 2 => "filarioid" 3 => "sigmodontine rodents" 4 => "<span class="elsevierStyleItalic">Oligoryzomys</span>" 5 => "<span class="elsevierStyleItalic">Phyllotis</span>" 6 => "Rattus" ] ] ] "es" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Palabras clave" "identificador" => "xpalclavsec501900" "palabras" => array:7 [ 0 => "cambio de hospedero" 1 => "nemátodos" 2 => "filarias" 3 => "roedores sigmodontinos" 4 => "<span class="elsevierStyleItalic">Oligoryzomys</span>" 5 => "<span class="elsevierStyleItalic">Phyllotis</span>" 6 => "<span class="elsevierStyleItalic">Rattus</span>" ] ] ] ] "tieneResumen" => true "resumen" => array:2 [ "en" => array:2 [ "titulo" => "Abstract" "resumen" => "<span id="abst0005" class="elsevierStyleSection elsevierViewall"><p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">We report the first record of <span class="elsevierStyleItalic">Litomosoides pardinasi</span> in native and exotic rodents from Chile. <span class="elsevierStyleItalic">Litomosoides pardinasi</span>, described in the Argentine Patagonia parasitizing <span class="elsevierStyleItalic">Phyllotis xanthopygus</span> and <span class="elsevierStyleItalic">Oligoryzomys longicaudatus</span>, was found in Chile parasitizing the peritoneal and thoracic cavities of <span class="elsevierStyleItalic">O. longicaudatus</span> (prevalence (P)= 18.9%, mean intensity (MI)= 57.3) and <span class="elsevierStyleItalic">Phyllotis darwini</span> (P<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>4.2%, MI<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>10), and in the peritoneal cavity of <span class="elsevierStyleItalic">Rattus rattus</span> (P<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>1.24%; MI<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>22.5). Total P in native rodents from Chile was significantly lower than in Argentina, while the total MI was higher. Prevalence and MI of <span class="elsevierStyleItalic">L. pardinasi</span> in <span class="elsevierStyleItalic">O. longicaudatus</span> from Chile and Argentina showed non-significant differences; prevalence in <span class="elsevierStyleItalic">P. darwini</span> from Chile was significantly lower than in <span class="elsevierStyleItalic">P. xanthopygus</span> from Argentina and than in Chilean <span class="elsevierStyleItalic">O. longicaudatus</span>. Our results, together with those from Argentina, support the hypothesis that <span class="elsevierStyleItalic">L. pardinasi</span> is well established in <span class="elsevierStyleItalic">O. longicaudatus</span>, but seems to be recently acquired by <span class="elsevierStyleItalic">P. darwini</span> and the exotic <span class="elsevierStyleItalic">R. rattus</span>. Considering the known host distribution of <span class="elsevierStyleItalic">Litomosoides</span> species among the sigmodontines, our results also support the hypothesis that <span class="elsevierStyleItalic">L. pardinasi</span> first colonized the Oryzomyini tribe and later, by different phenomena of host-switching, colonized the Phyllotini tribe and the exotic <span class="elsevierStyleItalic">R. rattus</span>.</p></span>" ] "es" => array:2 [ "titulo" => "Resumen" "resumen" => "<span id="abst0010" class="elsevierStyleSection elsevierViewall"><p id="spar0025" class="elsevierStyleSimplePara elsevierViewall"><span class="elsevierStyleItalic">Litomosoides pardinasi</span> es registrada por primera vez en roedores nativos y exóticos de Chile. La especie <span class="elsevierStyleItalic">Litomosoides pardinasi</span>, parásita de <span class="elsevierStyleItalic">Phyllotis xanthopygus</span> y <span class="elsevierStyleItalic">Oligoryzomys longicaudatus</span> en la Patagonia Argentina, fue encontrada en Chile parasitando la cavidad torácica y abdominal de <span class="elsevierStyleItalic">O. longicaudatus</span> (prevalencia (P)= 18.9%, intensidad media (MI)= 57.3) y de <span class="elsevierStyleItalic">Phyllotis darwini</span> (P<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>4.2%, MI<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>10), y la cavidad abdominal del roedor exótico <span class="elsevierStyleItalic">Rattus rattus</span> (P<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>1.24%; MI<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>22.5). La P total en roedores nativos de Chile fue significativamente menor que la P de Argentina, en tanto la MI total fue significativamente mayor. La P y MI de <span class="elsevierStyleItalic">L. pardinasi</span> en <span class="elsevierStyleItalic">O. longicaudatus</span> de Chile y Argentina no mostraron diferencias significativas; la P en <span class="elsevierStyleItalic">P. darwini</span> de Chile fue significativamente menor que la de <span class="elsevierStyleItalic">P. xanthopygus</span> de Argentina y que la de <span class="elsevierStyleItalic">O. longicaudatus</span> de Chile. Considerando la distribución de las especies de <span class="elsevierStyleItalic">Litomosoides</span> entre los sigmodontinos, estos resultados apoyan la hipótesis que <span class="elsevierStyleItalic">L. pardinasi</span> está bien establecida en <span class="elsevierStyleItalic">O. longicaudatus</span> y que posiblemente haya sido recientemente adquirida por <span class="elsevierStyleItalic">P. darwini</span> y <span class="elsevierStyleItalic">R. rattus.</span> Así, <span class="elsevierStyleItalic">L. pardinasi</span> colonizó primero a la Tribu Oryzomyini y posteriormente por un fenómeno de cambio de hospedero a la Tribu Phyllotini y a <span class="elsevierStyleItalic">R. rattus</span>.<a name="p1033"></a></p></span>" ] ] "multimedia" => array:3 [ 0 => array:7 [ "identificador" => "fig0005" "etiqueta" => "Figure 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 1836 "Ancho" => 973 "Tamanyo" => 164133 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall"><span class="elsevierStyleItalic">Litomosoides pardinasi</span> from <span class="elsevierStyleItalic">Rattus rattus</span>. A, buccal capsule lateral view; B, posterior extremity of male showing the spicules and cloacal papillae.</p>" ] ] 1 => array:7 [ "identificador" => "fig0010" "etiqueta" => "Figure 2" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr2.jpeg" "Alto" => 1500 "Ancho" => 972 "Tamanyo" => 235636 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">Scanning electron microphotographs of <span class="elsevierStyleItalic">Litomosoides pardinasi</span>. A, anterior extremity showing the labial papillae (black arrows), cephalic papillae (black star), and amphids (white arrows); B, detail of the area rugosa at mid-length.</p>" ] ] 2 => array:7 [ "identificador" => "tbl0005" "etiqueta" => "Table 1" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "tabla" => array:2 [ "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><th class="td" title="table-head " align="left" valign="middle" scope="col" style="border-bottom: 2px solid black"> \t\t\t\t\t\t\n \t\t\t\t</th><th class="td" title="table-head " align="center" valign="middle" scope="col" style="border-bottom: 2px solid black"><span class="elsevierStyleItalic">P. darwini</span> \t\t\t\t\t\t\n \t\t\t\t</th><th class="td" title="table-head " align="center" valign="middle" scope="col" style="border-bottom: 2px solid black"><span class="elsevierStyleItalic">O. longicaudatus</span> \t\t\t\t\t\t\n \t\t\t\t</th><th class="td" title="table-head " align="center" valign="middle" scope="col" style="border-bottom: 2px solid black"><span class="elsevierStyleItalic">R. rattus</span> \t\t\t\t\t\t\n \t\t\t\t</th></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td" title="table-entry " align="left" valign="middle">Females \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">(n<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>2) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">(n<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>6) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">(n<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>2) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="table-entry " align="left" valign="middle">Body length (mm) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">55.4<a class="elsevierStyleCrossRef" href="#tblfn0005"><span class="elsevierStyleSup">*</span></a> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">56.1 (36.2–72.2) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">53.3 <a class="elsevierStyleCrossRef" href="#tblfn0010"><span class="elsevierStyleSup">†</span></a> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="table-entry " align="left" valign="middle">Maximum width \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">– \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">244 (190–325) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">310<a class="elsevierStyleCrossRef" href="#tblfn0010"><span class="elsevierStyleSup">†</span></a> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="table-entry " align="left" valign="middle">Width at vulva \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">186; 207.7 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">177.1 (160–200) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">170.5 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="table-entry " align="left" valign="middle">Buccal capsule (L<span class="elsevierStyleHsp" style=""></span>×<span class="elsevierStyleHsp" style=""></span>W) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">19<span class="elsevierStyleHsp" style=""></span>×<span class="elsevierStyleHsp" style=""></span>9; 22<span class="elsevierStyleHsp" style=""></span>×<span class="elsevierStyleHsp" style=""></span>9 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">18 (15–20)<span class="elsevierStyleHsp" style=""></span>×<span class="elsevierStyleHsp" style=""></span>8 (7–10) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">19<span class="elsevierStyleHsp" style=""></span>×<span class="elsevierStyleHsp" style=""></span>8; 25<span class="elsevierStyleHsp" style=""></span>×<span class="elsevierStyleHsp" style=""></span>12 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="table-entry " align="left" valign="middle">Esophagus length \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">415; 533 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">529 (432–645) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">496; 567 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="table-entry " align="left" valign="middle">Tail length \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">– \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">260 (225–312) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">855 † \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="table-entry " align="left" valign="middle">Vulva to apex \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">772; 961 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">1 132 (925–1 335) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">1 271; 1 559 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="table-entry " align="left" valign="middle">Males \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">(n<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>3) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">(n<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>5) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">(n<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>6) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="table-entry " align="left" valign="middle">Body length (mm) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">21.5 (20.3–22.7) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">15.5 (10.2–18.7) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">18.1 (15–22.2) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="table-entry " align="left" valign="middle">Maximum width \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">99 (83–108) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">127 (100–140) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">111 (105–120) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="table-entry " align="left" valign="middle">Buccal capsule (L<span class="elsevierStyleHsp" style=""></span>×<span class="elsevierStyleHsp" style=""></span>W) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">19 (16–22) × 8 (6–9) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">17 (16–20)<span class="elsevierStyleHsp" style=""></span>×<span class="elsevierStyleHsp" style=""></span>7 (5–8) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">18 (13–20) × 7 (6–9) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="table-entry " align="left" valign="middle">Esophagus length \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">423 (418–427) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">405 (350–462) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">452 (424–475) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="table-entry " align="left" valign="middle">Tail length \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">139 (99–186) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">132 (115–160) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">146 (125–170) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="table-entry " align="left" valign="middle">Left spicule \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">199 (180–217) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">222 (170–241) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">210 (153–232) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="table-entry " align="left" valign="middle">Handle \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">112 (93–130) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">132 (115–150) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">107 (93–124) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="table-entry " align="left" valign="middle">Right spicule \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">101 (96–108) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">105 (87–117) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">116 (85–197) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="table-entry " align="left" valign="middle">Area rugosa length \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">1 622 (1 333–2 046) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">1 514 (1 350–1 700) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="center" valign="middle">1 467 (1 162–1 725) \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab757999.png" ] ] ] "notaPie" => array:2 [ 0 => array:3 [ "identificador" => "tblfn0005" "etiqueta" => "*" "nota" => "<p class="elsevierStyleNotepara" id="npar0005">From 1 entire specimen.</p>" ] 1 => array:3 [ "identificador" => "tblfn0010" "etiqueta" => "†" "nota" => "<p class="elsevierStyleNotepara" id="npar0010">One entire female found in this host.</p>" ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">Measurements of <span class="elsevierStyleItalic">Litomosoides pardinasi</span> parasitizing 3 different hosts in Chile</p>" ] ] ] "bibliografia" => array:2 [ "titulo" => "Literature cited" "seccion" => array:1 [ 0 => array:2 [ "identificador" => "bibs0005" "bibliografiaReferencia" => array:32 [ 0 => array:3 [ "identificador" => "bib0005" "etiqueta" => "Alcaíno and Gorman, 1999" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Parásitos de los animales domésticos en Chile" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:2 [ 0 => "H. 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Gardner" ] ] ] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:6 [ "tituloSerie" => "Journal of Parasitology" "fecha" => "1997" "volumen" => "83" "paginaInicial" => "700" "paginaFinal" => "705" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/9267414" "web" => "Medline" ] ] ] ] ] ] ] ] 7 => array:3 [ "identificador" => "bib0040" "etiqueta" => "Bush et al., 1997" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Parasitology meets ecology on its own terms: Margolis et al. revisited" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:4 [ 0 => "A.O. Bush" 1 => "K.D. Lafferty" 2 => "J.M. Lotz" 3 => "A.W. 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JN is a member of Conicet.</p>" "vista" => "all" ] ] ] "idiomaDefecto" => "en" "url" => "/18703453/0000008500000004/v1_201504220301/S1870345314729860/v1_201504220301/en/main.assets" "Apartado" => null "PDF" => "https://static.elsevier.es/multimedia/18703453/0000008500000004/v1_201504220301/S1870345314729860/v1_201504220301/en/main.pdf?idApp=UINPBA00004N&text.app=https://www.elsevier.es/" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S1870345314729860?idApp=UINPBA00004N" ]
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2020 April | 7 | 5 | 12 |
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