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. 2013 Dec 30;(365):279–305. doi: 10.3897/zookeys.365.5819

Table 3.

The species for which alternative primers have been used for DNA amplification.

Taxon (no specimens) Probable reason for failure Used primer(s) Additional sequences with Folmer et al. (1994)
Acanthiophilus walkeri (1) DNA degraded, specimen stored in ethanol 70% for 7 years All 0
Bactrocera oleae (1) DNA degraded, specimen stored in ethanol 70% All 1
Plaumannimyia sp. (1) ? TEPCOI 0
Rhagoletis cerasi (1) ? TEPCOI 4
Rhagoletis cingulata (3) Taxon-specific mutation at primer site? TEPCOI 0
Rhagoletis samojlovitshae (1) DNA degraded, specimen stored in ethanol 70% for 10 years All 0
Sphenella marginata (7) Taxon-specific mutation at primer site? TEPCOI, TEP_F2, TEP_R2 & Folmer et al. (1994) 0
Tephritis nebulosa (1) DNA degraded, specimen stored in ethanol 70% for 10 years All 0
Terellia colon (1) ? TEPCOI 11
Terellia luteola (1) DNA degraded, specimen stored in ethanol 70% for 10 years TEPCOI, TEP_F2, TEP_R2 & Folmer et al. (1994) 1
Trupanea cf. metoeca (1) DNA degraded, specimen stored in ethanol 70% for 2 years TEPCOI 0
Trypeta artemisiae (2) ? TEPCOI 1
Ulidia nigripennis (1) ? TEPCOI 0
Urophora ivannikovi (1) DNA degraded, specimen stored in ethanol 70% for 10 years All 0