Verbascum calycosum is an endemic plant species having considerable narrow distribution in Erzincan (Turkey) region. This species is known from only a single population and its habitats are highly threatened due to intensive human activities and soil erosion. In this study, the germination behavior of V. calycosum under different concentrations of NaCl, HCl, KNO3, GA3 (100 and 200 μM), hot-cold stratification and mechanical scarification were investigated. Seeds were exposed to a photoperiod of 8 h light/16 h dark with a 23/18 °C thermoperiod. Germination rates increased with GA3-100 µM (39%), GA3-200 µM (54.5%), mechanical scarification (34.5%) and cold stratification treatments (+4 °C, 23.25%; -20 °C, 18.25%) on the other hand, KNO3, NaCl, HCl and stratification with hot water treatments have decreased germination rates significantly when compared to the control (12.25%). Increased germination after GA3 application and mechanical scarification indicated that seeds of V. calycosum exhibited both non-deep and intermediate physiological dormancy as well as physical dormancy due to its hard seed coat. The highest speed of germination index was obtained at cold stratification of +4 °C and -20 °C (10.3). This study represents first report about seed dormancy and germination characteristics of V. calycosum. Overall, these results will provide valuable data for ex situ conservation of this rare endemic plant.
Background and Objective: Teucrium leucophyllum is endemic plant species having considerable narrow distribution in Erzincan (Turkey) Region. The aim of this study was to determine genetic diversity levels of T. leucophyllum in order to obtain data for its conservation. Method: Genomic DNA was isolated from 81 plants using CTAB method. Genetic diversity in four natural populations of T. leucophyllum was investigated by ISSR markers. A binary matrix was produced by scoring each amplified fragment as present (1) or absent (0) from each individual. The matrix was used to produce an input file and analyzed using the software programs; POPGENE 1.32 and GenAlex. Results: Twenty primers amplified a total of 434 bright and discernible bands of 220-3000 bp, of which 431 bands (PPB: 99.31%) were polymorphic in 4 populations. The genetic diversity was high at the species level; the observed number of alleles (Na) was 1.993, the effective number of alleles (Ne) was 1.404, the Nei's genetic diversity (H) was 0.263, and the Shannon's information index (I) was 0.418. A high level of gene flow (Nm: 2.208) and low-moderate genetic differentiation (Gst: 0.184) were also observed. Analysis of molecular variance showed that 11% of the total genetic diversity resided among populations, while 89% within the populations. Conclusion: Our results indicated that the conservation efforts should aim to preserve the extant populations of this endangered species in its natural habitat. Seeds could be collected from Kayacik and Bagistas populations for ex situ conservation practices.
A study of the genetic relationships among Petrorhagia taxa from Turkey was carried out using inter-simple sequence repeat (ISSR) markers. A total of 409 amplified bands were obtained by 10 ISSR primers. The polymorphism ratio was high (100%) across 45 individuals representing nine Petrorhagia taxa (P. dubia, P. prolifera, P. pamphylica, P. peroninii, P. saxifraga, P. cretica, P. alpina subsp. alpina, P. alpina subsp. olympica, P. lycica) and was sufficient to distinguish each species. Statistical analyses were performed by using POPGENE, GenAlEx6, and PAUP. An unweighted pair-group method with arithmetic mean (UPGMA) dendrogram was constructed based on Nei’s genetic distance along with outgroup species (Velezia rigida) in MEGA4. The dendrogram shows two main clusters, the first one (Cluster-I) included only P. lycica, while the cluster-II contained all other taxa. Cluster-II can be grouped in two sub-clusters, with P. prolifera and P. saxifraga constituting a first sub-cluster, the other species (P. alpina subsp. alpina, P. alpina subsp. olympica, P. cretica, P. dubia, P. peroninii and P. pamphylica) being grouped in a second sub-cluster. Both PCoA and Neighbour-Net network analysis supported the dendrogram. The study showed that ISSR technique can be successfully used in species identification and determination of the genetic relationships between Petrorhagia species distributed in Turkey.
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