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Medicinal plants are quite popular in the medicine development process because they contain bioactive chemicals. Traditional medicine has made extensive use of Crataegus orientalis L., which also has significant biological effects. In this study, essential oils (EOs) of C. orientalis var. orientalis collected from Tokat-Türkiye were isolated by hydrodistillation. Chemical constituents were detected by GC-MS and benzaldehyde (%52.75), α-terpineol (%16.86), germacrene D (%7.03) and caryophyllene (%6.77) were determined as major components. Moreover, antioxidant analyses including DPPH•, ABTS+• and FRAP tests were carried out. EOs displayed good the DPPH activity (IC50, 12.21, µg/mL) in comparison to the standard BHT (IC50, 10.23 µg/mL). The same trend was observed for ABTS and FRAP assays.

Heracleum platytaenium Boiss. has been used in traditional medicine. Antioxidant effect of essential oil as well as extracts of H. platytaenium was investigated. The essential oil was acquired by hydro distillation using a Clevenger type apparatus and GC-MS was used to analyze the essential oil compounds. Antioxidant capacity including ABTS+•, DPPH• scavenging and reducing power activity tests were carried out for essential oil and extracts. Moreover, total phenolic and total flavonoid contents were investigated. n-Octyl acetate (36.5%), apiole (24.9%), and elemicin (20.8%) were the chief products of essential oil. The essential oil and extracts exhibited from weak to moderate activity. The total phenol varied from 19.01 to 130.99 mg GAE/g extract and total flavonoid was fluctuated from 2.0 to 118.4 mg QE/g extract. The most DPPH• scavenging effect was observed in EtOAc extract (IC50 = 24.09 mg ml –1). The ABTS•+ scavenging effect of EtOAc extract was better than synthetic antioxidants BHA, BHT and Trolox.

Collected blue-green algae (cyanobacteria) from freshwater sites throughout Tokat province and its outlying areas were isolated in laboratory environment and their morphological systematics were determined and also their species identifications were studied by molecular methods. Seven different species of blue-green algae collected from seven different sites were isolated by purifying in cultures in laboratory environment. DNA extractions were made from isolated cells and extracted DNAs were amplified by using PCR. Cyanobacteria specific primers were used to amplify 16S rRNA and phycocyanine gene regions using PCR. Phylogenetic identification of species were conducted by evaluation of obtained sequence analysis data by using computer software. According to species identification by sequence analysis, it was seen that molecular data supports morphological systematics.