2014
DOI: 10.1016/j.mgene.2013.12.004
|View full text |Cite
|
Sign up to set email alerts
|

Biodiversity of the Betta smaragdina (Teleostei: Perciformes) in the northeast region of Thailand as determined by mitochondrial COI and nuclear ITS1 gene sequences

Abstract: In Thailand, there are currently five recognized species members of the bubble-nesting Betta genus, namely Betta splendens, B. smaragdina, B. imbellis, B. mahachaiensis and B. siamorientalis. In 2010, we indicated the possibility, based on COI barcoding evidence, that there might be two additional species, albeit cryptic, related to the type-locality B. smaragdina in some provinces in the northeast of Thailand. In the present study, after a more extensive survey of the northeast, and phylogenetic analyses base… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

1
21
0

Year Published

2014
2014
2022
2022

Publication Types

Select...
8

Relationship

3
5

Authors

Journals

citations
Cited by 15 publications
(22 citation statements)
references
References 30 publications
1
21
0
Order By: Relevance
“…Crude DNA extracts from fish samples were prepared according to a previous report (Kowasupat et al, 2014). Briefly, approximately 5 mg of fish muscle tissue was incubated with 180 μL of 50 mM NaOH at 95°C for 10 min.…”
Section: Pcr Amplification Of Fish Dna Sequencesmentioning
confidence: 99%
See 1 more Smart Citation
“…Crude DNA extracts from fish samples were prepared according to a previous report (Kowasupat et al, 2014). Briefly, approximately 5 mg of fish muscle tissue was incubated with 180 μL of 50 mM NaOH at 95°C for 10 min.…”
Section: Pcr Amplification Of Fish Dna Sequencesmentioning
confidence: 99%
“…Primers used for PCR amplification of fish DNA sequences listed in Table 1 included universal primers targeting eukaryotic 18S rDNA (Medlin et al, 1988), specific primers for fish COI (cytochrome c oxidase I), ITS (internal transcribed spacer), and RAG1 (recombinase activating gene 1). PCR reactions and thermocycling conditions were carried out using previously described protocols (Kowasupat et al, 2014).…”
Section: Pcr Amplification Of Fish Dna Sequencesmentioning
confidence: 99%
“…). Extracted nucleic acids were quantified using nanodrop (Thermo Scientific, Waltham, MA, USA) and was diluted to a final concentration of 100 ng μL −1 , and 2 μL of the resulting solution was determined for cytochrome oxidase I gene (COI) (Kowasupat, Panijpan, Laosinchai, Ruenwongsa, Phongdara, Wanna, Senapin & Phiwsaiya ) amplification before used as the template for the LAMP assay. Isolation and confirmation of S. putrefaciens isolates by biochemical tests and sequencing was followed according to the previous protocol (Suebsing, Kampeera, Sirithammajak, Pradeep et al .…”
Section: Methodsmentioning
confidence: 99%
“…These 5 species can be distinguished from one another morphologically, especially when the fully-grown males are in full aggressive display. Among these Thailand Betta fishes, cryptic species within B. smaragdina (Kowasupat et al 2014) are the only ones with tens of bluish-green iridescent plates on the head region covering the opercles down to the lower part of the mouth region. These plates are usually well separated and can be very small.…”
Section: Introductionmentioning
confidence: 99%