Redescriptions of Ligophorus cephali Rubtsova, Balbuena, Sarabeev, Blasco-Costa &amp; Euzet, 2006 and L. chabaudi Euzet &amp; Suriano, 1977 (Monogenea: Ancyrocephalidae), with notes on the functional morphology of the copulatory organ

Дмитриева, Е. В.; Gerasev, P. I.; Merella, Paolo; Pugachev, O.

doi:10.1007/s11230-009-9192-8

Cited by 15 publications

(4 citation statements)

References 7 publications

(27 reference statements)

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“…But at a large scale, due to coastal nature of mullets, vicariance may explain the occurrence of a large portion of parasite species as, for example, in such widely distributed M. cephalus [43]. Current literature data of Dmitrieva et al [50], Sarabeev et al [17] and the present observations indicate that among the helminth fauna parasitizing this fish only one dactylogyrid monogeneans, Ligophorus chabaudi, was reported in both regions, while all other species of monogeneans, digeneans, acanthocephalans and nematodes occur only in the Mediterranean or in the Sea of Japan ( [8][9][10][11][12][13][14][15]17,18,33], the present study).…”

Section: Discussionmentioning

confidence: 99%

Helminth species richness of introduced and native grey mullets (Teleostei: Mugilidae)

Sarabeev

2015

Parasitology International

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Section: Discussionmentioning

confidence: 99%

Helminth species richness of introduced and native grey mullets (Teleostei: Mugilidae)

Sarabeev

2015

Parasitology International

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“…For Scanning Electron Microscopy (SEM), some samples of several monogenean species were hydrated, placed in 1% osmium tetroxide overnight, dehydrated in ethanol, air dried and mounted on stubs with double-sided adhesive tape and sputter coated with gold-palladium and examined in Jeol JSM-6510LV at an accelerating voltage of 10 kV. The taxonomic classification and identification of the parasites observed were done on the basis of Bychovskaya-Pavlovskaya et al (1962), Gusev (1985), Sarabeev et al (2005), Dmitrieva et al (2009aDmitrieva et al ( , 2009b, Dzika et al (2009). Infection prevalence and mean intensity were calculated in accordance with Bush et al (1997).…”

Section: Methodsmentioning

confidence: 99%

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Öztürk¹,

Özer²

2014

Turk. J. Fish. Aquat. Sci.

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This comprehensive research study was conducted to determine the monogenean fauna of 16 fish species belonging to Cyprinidae, Mugilidae, Gobiidae, Percidae, Cyprinodontidae, Gasterosteidae, Cobitidae, Atherinidae, Poecilidae and Sygnidae in Lower Kızılırmak Delta located by the coasts of the Black Sea in the northern part of Turkey. A total of 1049 fish specimens were collected during the period between December 2010 and November 2011. Gyrodactylus proterorhini, G. cyprini, G. arcuatus, Dactylogyrus extensus, D. chalcalburni, D. difformis, Ancyrocephalus paradoxus, Ligophorus mediterraneus, L. cephali, Solostamenides mugilis and Paradiplozoan homoion were identified to the specific level while oneGyrodactylus and one Salsuginus species were identified only to the generic level. Some monogeneans were found to be specific to some host families, especially Ligophorus for Mugilidae and Dactylogyrus for Cyprinidae. Prevalence (%) and intensity indices were determined and discussed for each monogenean species and/or genus on respective hosts. All the monogenean species were recorded for the first time in the Lower Kızılırmak Delta. Gyrodactylus cyprini and Ancyrocephalus paradoxus represented new parasite records for Turkey.

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“…Parasite descriptions that allow the complete retrocalculation of landmarks are scarce and involve the additional use of angles (e.g. Ernst et al, 2000;Dmitrieva et al, 2007Dmitrieva et al, , 2009. As a consequence, a significant proportion of diagnoses published over the last decades do not properly characterise the shape of the haptoral hard parts.…”

Section: Bibliographic Reviewmentioning

confidence: 99%

Putting in shape – towards a unified approach for the taxonomic description of monogenean haptoral hard parts

Vignon

2011

Syst Parasitol

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Among monogeneans, haptoral hard parts provide prominent morphological characters upon which identifications are largely based. Traditionally, morphometric approaches are based on the use of arbitrary collections of linear distance measurements between landmarks. An exhaustive review of the specific diagnoses published in the journal Systematic Parasitology highlights the fact that an intricately important number of measurements are used to describe the same morphological features. Hence, this does not allow relevant comparison between studies and may have caused confusion in the literature. More importantly, a significant proportion of diagnoses commonly used do not maximize the amount of information available from morphological features, and sets of linear measurements between landmarks do not properly allow the complete reconstruction of the shape of haptoral hard parts. Given this prominent bias and the disparate use of traditional methodologies, I suggest the use of alternative methods in systematic parasitology that fully take into consideration the shape of morphological features. In addition to these considerations, a move toward placing shape at the centre of automated species recognition would be mutually beneficial for both taxonomists and non-taxonomists.

show abstract

Redescriptions of Ligophorus cephali Rubtsova, Balbuena, Sarabeev, Blasco-Costa & Euzet, 2006 and L. chabaudi Euzet & Suriano, 1977 (Monogenea: Ancyrocephalidae), with notes on the functional morphology of the copulatory organ

Cited by 15 publications

References 7 publications

Helminth species richness of introduced and native grey mullets (Teleostei: Mugilidae)

Helminth species richness of introduced and native grey mullets (Teleostei: Mugilidae)

Untitled

Putting in shape – towards a unified approach for the taxonomic description of monogenean haptoral hard parts

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