2018
DOI: 10.1017/s0022149x1800072x
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The first record of Ligophorus Euzet & Suriano, 1977 (Monogenea: Dactylogyridae) on Crenimugil buchanani (Teleostei: Muglidae) from Thailand based on morphological and molecular analyses

Abstract: Ligophorus satunensis n. sp. was collected from the bluetail mullet, Crenimugil buchanani (Bleeker, 1853), caught off Satun, Thailand, representing the first report of the Ligophorus species in Thailand. The new species is most similar to Ligophorus fenestrum Soo & Lim, 2012 in its fenestrated dorsal hamuli, a ventral bar with a long, bifurcated anteromedian protuberance (AMP) without lateral pieces, and a non-sclerotized vagina. However, it differs from the latter in its dorsal hamuli (up to two layers of fen… Show more

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Cited by 4 publications
(4 citation statements)
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“…Monogeneans of Ligophorus Euzet et Suriano, 1977 are specific gill parasites of fish from the family Mugilidae Jarocki, 1822. The genus currently includes 66 nominal species (Euzet & Suriano, 1977; Dmitrieva et al , 2007, 2012, 2013a; Abdallah et al , 2009; Soo & Lim, 2012, 2013; El Hafidi et al , 2013a, b; Kritsky et al , 2013; Sarabeev et al , 2013; Marchiori et al , 2015; Rodríguez-González et al , 2015a, 2015b; Khang et al , 2016; Pakdee et al , 2018). Identification of Ligophorus species is based mainly on the morphology of hard structures of the haptor and the distal parts of the female and male reproductive systems (Euzet & Suriano, 1977; Sarabeev et al , 2013).…”
Section: Introductionmentioning
confidence: 99%
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“…Monogeneans of Ligophorus Euzet et Suriano, 1977 are specific gill parasites of fish from the family Mugilidae Jarocki, 1822. The genus currently includes 66 nominal species (Euzet & Suriano, 1977; Dmitrieva et al , 2007, 2012, 2013a; Abdallah et al , 2009; Soo & Lim, 2012, 2013; El Hafidi et al , 2013a, b; Kritsky et al , 2013; Sarabeev et al , 2013; Marchiori et al , 2015; Rodríguez-González et al , 2015a, 2015b; Khang et al , 2016; Pakdee et al , 2018). Identification of Ligophorus species is based mainly on the morphology of hard structures of the haptor and the distal parts of the female and male reproductive systems (Euzet & Suriano, 1977; Sarabeev et al , 2013).…”
Section: Introductionmentioning
confidence: 99%
“…Many species are very morphologically similar to each other, creating difficulties for delimitation of species (Euzet & Suriano, 1977; Dmitrieva et al , 2007, 2013a). Some of them were distinguished on the basis of DNA sequence data (Marchiori et al , 2015; Pakdee et al , 2018). However, these data are discrete or insufficient, representing 127 sequences of the different parts of the nuclear DNA ribosomal cluster for only 32 species (), including 12 species from the Mediterranean Sea and two species from the Azov Sea (Mollaret et al , 2000; Plaisance et al , 2005; Blasco-Costa et al , 2012; Rodríguez-González et al , 2015a), two species from the West Atlantic Ocean off Brasilia (Marchiori et al , 2015), 14 species from the East Indian Ocean off Malaysia (Soo et al , 2015; Khang et al , 2016) and for three species from the South China Sea (Wu et al , 2006, 2007; Pakdee et al , 2018).…”
Section: Introductionmentioning
confidence: 99%
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“…The 18S, ITS1, 5.8S and 28S fragments were obtained for 12 species from the Mediterranean Sea and 2 species from the Black Sea (Blasco-Costa et al, 2012;Rodríguez-González et al, 2015). For two species off the coast of Brazil, 18S, ITS1, 5.8S and 28S were sequenced (Marchiori et al, 2015), and 18S, 28S and ITS1 fragments were obtained for 14 species from the Indian Ocean (Soo et al, 2015;Khang et al, 2016;Pakdee et al, 2019). Several studies (Blasco-Costa et al, 2012;Rodríguez-González et al, 2015;Khang et al, 2016) have compared morphological and genetic variability, showing a greater degree of congruence between phylogenetic reconstructions based on these data, suggesting that the use of ribosomal cluster sequences for genotyping species of this genus is promising.…”
Section: Introductionmentioning
confidence: 99%