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The laboratory unfired stabilized clay specimens were identified using X-ray diffraction technique.
The specimens were identified using the test and spines of the sea urchin.
The specimens were identified using the ossicle of the sea cucumber.
The specimens were identified using ossicles obtained from the epidermal tissues of dorsal and ventral surfaces of the body wall (Kiani et al. 2014).
The plant specimens that were preserved as herbarium specimens were identified using the standard reference for this purpose [42], compared with specimens from the Department of Plant Resources, and identified with the help of taxonomists from the Department of Plant Phytotechny at the USAMVB Timisoara.
Specimens were identified using the "A_B_C" format where: "A" denotes the concrete strength (L for low and H for high); "B" denotes the number of fabric plies (0, 1 or 4); and "C" denotes the replicate number (1 3 or average).
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During periods of suspected outbreaks, where a high volume of specimens is expected, we recommended that specimens be identified using visual identification, as the fastest processing method, to select "G.
specimens was identified using the SINE PCR protocol (Santolamazza et al., 2008).
The genome composition for each specimen was identified using isozyme analysis, karyotyping, microsatellite DNA loci and/or flow cytometry.
In all previous cases of human L. hongkongensis infection and in reports of the detection of this species in animal specimens, the strains were identified using a combination of phenotypic tests and 16S rRNA gene sequencing.
The haplotypes present in the L. delicata and L. guichenoti specimens intercepted by MPI were identified using D naSP v5.10 (Librado and Rozas 2009) and were submitted to GenBank under the accession numbers JQ413190-JQ413223 (Table S1).
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