2008
DOI: 10.14411/eje.2008.019
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Sycophila pistacina (Hymenoptera: Eurytomidae): A valid species

Abstract: Abstract. Sycophila pistacina (Rondani), which was previously synonymized with Sycophila biguttata (Swederus), is revalidated. Morphological, morphometric and molecular data confirm its status as a separate species. Diagnostic characters are provided for distinguishing it from S. biguttata. The nomenclature of the S. biguttata complex is updated.

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Cited by 10 publications
(7 citation statements)
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“…The ITS2 fragment also usually possesses nucleotide differences between close species pairs (Coleman 2003) and is often an effective tool for species diagnosis (Hackett et al 2000;Hung et al 2004;Ben-David et al 2007). Both COI and ITS2 have been shown to be effective in tracing species boundaries in varied hymenopteran groups (Dowton & Austin 2001;Alvarez & Hoy 2002;Pinto et al 2002;Scheffer & Grissell 2003;Jousselin et al 2004;Jiang et al 2006a,b;Lotfalizadeh et al 2008).…”
Section: Introductionmentioning
confidence: 99%
“…The ITS2 fragment also usually possesses nucleotide differences between close species pairs (Coleman 2003) and is often an effective tool for species diagnosis (Hackett et al 2000;Hung et al 2004;Ben-David et al 2007). Both COI and ITS2 have been shown to be effective in tracing species boundaries in varied hymenopteran groups (Dowton & Austin 2001;Alvarez & Hoy 2002;Pinto et al 2002;Scheffer & Grissell 2003;Jousselin et al 2004;Jiang et al 2006a,b;Lotfalizadeh et al 2008).…”
Section: Introductionmentioning
confidence: 99%
“…For most of the parasitoids we examined, we amplified a fragment of the 3′ region of COI using the forward primer Jerry (5′-CAACATTTATTTTGATTTTTTGG-3′) and reverse primer Pat (5′-TCCAATGCACTAATCTGCCATATTA-3′) (Ghararieh, Bruford, Dawah, Fernandes, & Dodd, 2006;Simon et al, 1994) with the PCR protocol described in Lotfalizadeh, Delvare, and Rasplus (2008). For most of the parasitoids we examined, we amplified a fragment of the 3′ region of COI using the forward primer Jerry (5′-CAACATTTATTTTGATTTTTTGG-3′) and reverse primer Pat (5′-TCCAATGCACTAATCTGCCATATTA-3′) (Ghararieh, Bruford, Dawah, Fernandes, & Dodd, 2006;Simon et al, 1994) with the PCR protocol described in Lotfalizadeh, Delvare, and Rasplus (2008).…”
Section: Dna Extraction and Amplificationmentioning
confidence: 99%
“…For the mitochondrial gene cytochrome oxidase I (COI) gene, we amplified two nonoverlapping fragments. For most of the parasitoids we examined, we amplified a fragment of the 3′ region of COI using the forward primer Jerry (5′-CAACATTTATTTTGATTTTTTGG-3′) and reverse primer Pat (5′-TCCAATGCACTAATCTGCCATATTA-3′) (Ghararieh, Bruford, Dawah, Fernandes, & Dodd, 2006;Simon et al, 1994) with the PCR protocol described in Lotfalizadeh, Delvare, and Rasplus (2008). In addition, we amplified a fragment that corresponds with the "Barcode" region of COI using a novel forward primer "EurytomidF" (5′-CCWGGKTCWTTAATTGGRAATGATC-3′) and the commonly used barcode reverse primer HCO (Simon et al, 1994) using the PCR protocol described in Hebert, Penton, Burns, Janzen, and Hallwachs (2004).…”
Section: Dna Extraction and Amplificationmentioning
confidence: 99%
“…Mitochondrial cytochrome c oxidase I (COI) and nuclear ribosomal DNA internal transcribed spacer 2 (ITS2) were sequenced to clarify species boundaries and to match genders. Both COI and ITS2 have been shown to effectively identify species of hymenopteran insects (Dowton et al 2001;Alvarez & Hoy 2002;Pinto et al 2002;Scheffer & Grissell 2003;Jousselin et al 2004;Jiang et al 2006a,b;Lotfalizadeh et al 2008;Li et al 2010). One to 11 individuals (depending on availability) of each species as determined by females and each of the distinguishable male morph were sequenced.…”
Section: Dna Extraction Pcr and Sequencingmentioning
confidence: 99%