2016
DOI: 10.1038/srep34372
|View full text |Cite
|
Sign up to set email alerts
|

Formal nomenclature and description of cryptic species of the Encyrtus sasakii complex (Hymenoptera: Encyrtidae)

Abstract: With the recent development of molecular approaches to species delimitation, a growing number of cryptic species have been discovered in what had previously been thought to be single morpho-species. Molecular methods, such as DNA barcoding, have greatly enhanced our knowledge of taxonomy, but taxonomy remains incomplete and needs a formal species nomenclature and description to facilitate its use in other scientific fields. A previous study using DNA barcoding, geometric morphometrics and mating tests revealed… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

1
36
0

Year Published

2018
2018
2022
2022

Publication Types

Select...
7
1

Relationship

1
7

Authors

Journals

citations
Cited by 21 publications
(37 citation statements)
references
References 71 publications
(84 reference statements)
1
36
0
Order By: Relevance
“…1), finding congruent support for three species-level genetic clusters (hereafter cluster A, B and C), which comprised one or more of the six previously identified lineages as described in Daniel F. Marchán et al, (2017). The well-supported putative species identified in Carpetania demanded a full, detailed taxonomic description: several authors have stressed the necessity of going a step further from cryptic species identification (Jörger & Schrödl, 2013;Wang et al, 2016). To this end, this work will build upon the framework provided by Marchán et al (submitted), with the following objectives: i) identify genomewide nucleotidic positions to be used as diagnostic characters in species description (molecular taxonomy); ii) explore further morphometric and internal anatomic characters to reinforce species description; iii) formally describe the species within Carpetania; iv) compare genomic and barcode genetic distances to validate the widespread use of the latter.…”
Section: Introductionmentioning
confidence: 81%
“…1), finding congruent support for three species-level genetic clusters (hereafter cluster A, B and C), which comprised one or more of the six previously identified lineages as described in Daniel F. Marchán et al, (2017). The well-supported putative species identified in Carpetania demanded a full, detailed taxonomic description: several authors have stressed the necessity of going a step further from cryptic species identification (Jörger & Schrödl, 2013;Wang et al, 2016). To this end, this work will build upon the framework provided by Marchán et al (submitted), with the following objectives: i) identify genomewide nucleotidic positions to be used as diagnostic characters in species description (molecular taxonomy); ii) explore further morphometric and internal anatomic characters to reinforce species description; iii) formally describe the species within Carpetania; iv) compare genomic and barcode genetic distances to validate the widespread use of the latter.…”
Section: Introductionmentioning
confidence: 81%
“…Consider the noisy candidate characters at positions 8,19,20, and 23 in Fig. 1 and a k-window of size k = 5.…”
Section: Examplementioning
confidence: 99%
“…In the character-based approach, each position of an alignment represents a molecular character which may adopt different states in gene sequence data (e.g., nucleotides and deletions). Diagnostic molecular characters are included in taxon diagnoses (e.g., of protists [5] or animals [1,[6][7][8]). However, data from (potentially) related taxa for comparison with the type species are often lacking or difficult to obtain [9].…”
mentioning
confidence: 99%
“…For Diaspididae, COI sequences were obtained using the primer pairs reported in Morse and Normark (2006) and the 28S sequences (D2 and D3 regions) were obtained using primer 28S-F3633 and 28S-b (Rugman-Jones, Hoddle, & Stouthamer, 2010;Whiting, Carpenter, Wheeler, & Wheeler, 1997). The protocols for PCR followed Wang et al (2016). PCR products were sequenced using ABI technology.…”
Section: Dna Extraction Amplification and Sequencingmentioning
confidence: 99%