2004
DOI: 10.1073/pnas.0406166101
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Ten species in one: DNA barcoding reveals cryptic species in the neotropical skipper butterflyAstraptes fulgerator

Abstract: Astraptes fulgerator, first described in 1775, is a common and widely distributed neotropical skipper butterfly (Lepidoptera: Hesperiidae). We combine 25 years of natural history observations in northwestern Costa Rica with morphological study and DNA barcoding of museum specimens to show that A. fulgerator is a complex of at least 10 species in this region. Largely sympatric, these taxa have mostly different caterpillar food plants, mostly distinctive caterpillars, and somewhat different ecosystem preferences… Show more

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Cited by 3,079 publications
(2,585 citation statements)
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References 31 publications
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“…Finally, the accuracy of the DNA-based identifications is tightly dependent on the coverage of the DNA barcode reference libraries used to assign the sequences generated through NGS to known taxa [e.g. 17,21,28,189,[205][206][207][208][209].…”
Section: Resultsmentioning
confidence: 99%
See 2 more Smart Citations
“…Finally, the accuracy of the DNA-based identifications is tightly dependent on the coverage of the DNA barcode reference libraries used to assign the sequences generated through NGS to known taxa [e.g. 17,21,28,189,[205][206][207][208][209].…”
Section: Resultsmentioning
confidence: 99%
“…Compared to morphological characters, DNA barcodes presents several advantages: (1) intraspecific phenotypic variation often These detailed specimens and barcode records ensure the reproducibility of the PCR and sequencing protocols by providing contact of the peoples involved in generating DNA barcodes. In addition, it enables the continuous updating of the identification of specimens by the community of users and facilitates the use of DNA barcodes for further taxonomic studies [21,[27][28][29][30][31]183]. To further improve the quality of DNA barcode data, the BARCODE data standard as been implemented in GenBank for the records that are compliant with the following requirements: 1.…”
Section: Dna Barcoding: a Solution To The Taxonomic Impediment?mentioning
confidence: 99%
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“…Afterwards they were centrifuged for 10 s at 3,000 r.p.m. The primers used were: for COI (676 bp) LCO 1490 (5′-GGTCAACAAATCATAA AGATATTGG-3′) 34 and Nancy (5′-CCCGGTAAAATTAAAATATAAACTTC-3′) 35 , or (658 bp) LepF1 (5′-ATTCAACCAATCATAAAGATATTGG-3) and LepR1 (5′-TAAACTTCTGGATGTCCAAAAAATCA-3′) 36 ; for ND1 (790-794 bp) 5′-CTGTTCGATCATTAAAATCTTAC-3′ (forward) 37 and 5′-ATCAAAAG GAGCTCGATTAGTTTC-3′ (reverse) 38 ; for ITS2 (684 bp) ITS3 (5′-GCATCGAT GAAGAACGCAGC-3′) and ITS4 (5′-TCCTCCGCTTATTGATATGC-3′) 39 ; for Wg (403 bp) Wg1 (5′-GARTGYAARTGYCAYGGYATGTCTGG-3′) and Wg2 (5′-ACTICGCRCACCARTGGAATGTRCA-3′) 40 ; for CAD (571 bp) CADFa (5′-GDATGGTYGATGAAAATGTTAA-3′) and CADRa (5′-CTCATRTCGTAAT CYGTRCT-3′). Double-stranded DNA was amplified in 25 µl volume reactions: 13.22 µl ultra pure (HPLC quality) water, 2.5 µl 10× buffer, 4.5 µl 25 mM MgCl 2 , 0.25 µl 100 mM dNTP, 1.2 µl of each primer (10 mM), 0.13 µl Taq DNA Gold Polymerase (Qiagen) and 2 µl of extracted DNA.…”
Section: Methodsmentioning
confidence: 99%
“…2011) or barcode gaps lead to the recognition of new species upon further study (Hebert et al. 2004; Bickford et al. 2007).…”
Section: Introductionmentioning
confidence: 99%