Browsing by Author "Senler, Naciye Gulkiz"
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Article Frontonia Anatolica N. Sp., a New Peniculid Ciliate (Protista, Ciliophora) From Lake Van, Turkey(Tubitak Scientific & Technological Research Council Turkey, 2013) Yildiz, Ismail; Senler, Naciye GulkizThe morphology, ciliature, and silverline system of a new ciliate, Frontonia anatolica n. sp., isolated from the bottom sediment of the eastern shore of Lake Van, a large alkaline lake in Eastern Anatolia Turkey, were investigated using live and silver impregnation methods. Frontonia anatolica n. sp. is characterised by an elliptical body shape; by an in-vivo body size of 101-134 x 47-67 mu m; by dorsoventral flattening of about 2:3 to 1:2; by 2 contractile vacuoles located in the anterior and posterior body parts, each with 6-7 collecting canals and 1 excretory pore; by about 93 somatic kineties; by 3 vestibular and 3-5 postoral kinetics; and by peniculi 1 and 2 each having 4 ciliary rows, and peniculus 3 having 2 ciliary rows.Article A New Approach To Dna Isolation From Dileptid Ciliates (Ciliophora: Litostomatea: Rhynchostomatia)(inst Zoology, Bas, 2020) Ural, Hilal; Bircan, Rifat; Aral, Cenk; Yildiz, Ismail; Senler, Naciye GulkizMolecular diagnostic methods have been used to supplement morphological methods in taxonomy. In this study, we used molecular methods to diagnose populations of dileptid ciliates, which commonly occur in terrestrial and semi-terrestrial habitats. Molecular investigations based on the comparison of DNA sequences have been carried out with a limited number of ciliate species due to insufficient genomic DNA for PCR because of their small population size and difficulties to maintain monocultures. The present study shows that there is a loss of DNA with conventional methods and proposes a novel approach: cells (stored at -20 degrees C or fresh) are directly subjected to PCR, without being processed by any chemical treatment. The small subunit ribosomal DNA (SSU rDNA) (18S rRNA gene) of dileptid ciliates was successfully amplified by direct PCR, without DNA extraction, for single-cell and multi-cell samples. This method has been found to be simpler and especially useful for species that are rare and have small population sizes.
