2014
DOI: 10.14411/fp.2014.028
|View full text |Cite
|
Sign up to set email alerts
|

Neotropical Monogenoidea. 58. Three new species of Gyrodactylus (Gyrodactylidae) from Scleromystax spp. (Callichthyidae) and the proposal of COII gene as an additional fragment for barcoding gyrodactylids

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

1
17
0

Year Published

2014
2014
2021
2021

Publication Types

Select...
9
1

Relationship

1
9

Authors

Journals

citations
Cited by 26 publications
(18 citation statements)
references
References 51 publications
1
17
0
Order By: Relevance
“…Regarding the guppy parasites, the three Gyrodactylus species examined each possess two to three genetic lineages, diverging by 5.7 to 17.2%. This is in the range of the divergence observed between published sequences for described species in this genus (4% divergence between G. salaris vs G. thymalli , and 39% between G. thymalli vs G. corydori [ 61 63 ]), which confirms that cryptic speciation is common within this genus [ 17 ]. In the case of G. bullatarudis , the two cryptic lineages had overlapping geographical ranges in both the Caroni and Oropouche drainages.…”
Section: Discussionsupporting
confidence: 71%
“…Regarding the guppy parasites, the three Gyrodactylus species examined each possess two to three genetic lineages, diverging by 5.7 to 17.2%. This is in the range of the divergence observed between published sequences for described species in this genus (4% divergence between G. salaris vs G. thymalli , and 39% between G. thymalli vs G. corydori [ 61 63 ]), which confirms that cryptic speciation is common within this genus [ 17 ]. In the case of G. bullatarudis , the two cryptic lineages had overlapping geographical ranges in both the Caroni and Oropouche drainages.…”
Section: Discussionsupporting
confidence: 71%
“…For most gyrodactylid and dactylogyrid monogeneans, a small set of established mitochondrial gene fragments (coding for cox 1, cox 2, nad 2 and 16S rRNA) are the most variable markers available. These were applied in population genetics and demography [ 41 , 42 ], in barcoding [ 43 , 44 ], in phylogeography [ 45 48 ], to detect hybridisation [ 18 ] and to elucidate the phylogeny of closely related species [ 49 ] or genera [ 21 , 50 ] or of higher-order taxa in monogeneans [ 51 ] and other flatworms (e.g. tapeworms [ 52 ]).…”
Section: Discussionmentioning
confidence: 99%
“…The polymerase chain reaction (PCR) for the 18S rDNA fragment was optimized with an initial denaturation at 95°C for 5 min, succeeded by 40 cycles as follows: denaturation at 95°C for 30 s, annealing for 45 s at 50–55ºC, extension at 72°C for 45 s, and final extension 72°C for 5 min. The PCR program for the MT‐CO2 gene followed that of Bueno‐Silva and Boeger (2014): 5 min at 95ºC, followed by 40 cycles of 30 s at 94ºC, 45 s at 42–50ºC (gradient), 45 s at 72ºC and finally 4 min at 72ºC. Each amplification reaction contained 20–40 ng of template DNA, 3 mM MgCl 2 , 1X PCR‐Buffer (Invitrogen), 0.4 mM dNTP, 0.5 pmoles of each primer and 1U Platinum Taq polymerase (Invitrogen) in a total volume of 25 µl.…”
Section: Methodsmentioning
confidence: 99%