Stochastic flowering phenology in Dactylis glomerata populations described by Markov chain modelling

Genetic diversity and structure of natural Dactylis glomerata L. populations revealed by morphological and microsatellite-based (SSR/ISSR) markers.

Dactylis glomerata L. is an important forage species in the Mediterranean region, and in other regions with a similar climate. Genetic material from 3 locations in north, central, and south Greece was studied, using morphological traits, SSR, and ISSR molecular markers. Morphological analysis revealed differences among the geographic locations studied for all morphological traits, except the nu...

Increased Meiotic Irregularity Accompanying Inbreeding in Dactylis Glomerata L.

Fungal Diversity The endophytic mycobiota of the grass Dactylis glomerata

Fungal endophytes were isolated from asymptomatic and symptomatic plants of Dactylis glomerata sampled in different ecosystems in Spain. Fungi were identified using morphological, as well as molecular methods based on internal transcribed spacer (ITS) and ribosomal DNA sequencing. Molecular data provided a framework for identification and assessing the phylogenetic position of isolates. One hun...

Identification of orchardgrass (Dactylis glomerata L.) cultivars by using simple sequence repeat markers.

The accurate identification of orchardgrass (Dactylis glomerata L.) cultivars is necessary to ensure purity for consumers, the effective utilization of cultivars, and to protect the intellectual property for breeders. Therefore, this study aimed to use SSR to construct DNA fingerprinting of orchardgrass cultivars. The genetic diversity of 32 orchardgrass cultivars originated from 21 countries, ...

Optimization of SCoT-PCR reaction system in Dactylis glomerata by orthogonal design.

The effects of 5 factors (template DNA, Mg(2+), dNTPs, Taq DNA polymerase, and primer) on the polymerase chain reaction (PCR) were investigated to optimize the start codon targeted polymor-phism (SCoT)-PCR system of Dactylis glomerata L., using an orthogo-nal design L16 (4(5)). A suitable SCoT-PCR system for D. glomerata was established; the 20 μL reaction volume contained 3.0 mM Mg(2+), 0.2 mM...