14 research outputs found
In vitro mycorrhization of micropropagated plants: studies on Castanea sativa Mill.
In vitro mycorrhization can be made by several axenic and nonaxenic
techniques but criticism exists about their artificiality and inability to
reproduce under natural conditions. However, artificial mycorrhization under
controlled conditions can provide important information about the physiology
of symbiosis. Micropropagated Castanea sativa plants were inoculated with
the mycorrhizal fungus Pisolithus tinctorius after in vitro rooting. The
mycorrhizal process was monitored at regular intervals in order to evaluate the
mantle and hartig net formation, and the growth rates of mycorrhizal and
nonmycorrhizal plants. Plant roots show fungal hyphae adhesion at the surface
after 24 hours of mycorrhizal induction. After 20 days a mantle can be
observed and a hartig net is forming although the morphology of the epidermal
cells remains unaltered. At 30 days of root–fungus contact the hartig net is
well developed and the epidermal cells are already enlarged. After 50 days of
mycorrhizal induction, growth was higher for mycorrhizal plants than for
nonmycorrhizal ones. The length of the major roots was lower in mycorrhizal
plants after 40 days. Fresh and dry weights were higher in mycorrhizal plants
after 30 days. The growth rates of chestnut mycorrhizal plants are in agreement
with the morphological development of the mycorrhizal structures observed at
each mycorrhizal time. The assessment of symbiotic establishment takes into
account the formation of a mantle and a hartig net that were already developed
at 30 days, when differences between fresh and dry weights of mycorrhizal and
nonmycorrhizal plants can be quantified. In vitro conditions, mycorrhization
influences plant physiology after 20 days of root–fungus contact, namely in
terms of growth rates. Fresh and dry weights, heights, stem diameter and
growth rates increased while major root growth rate decreased in mycorrhizal
plants.Springe
Additional file 8: Table S8. of Regulatory networks underlying mycorrhizal development delineated by genome-wide expression profiling and functional analysis of the transcription factor repertoire of the plant symbiotic fungus Laccaria bicolor
List and sequences of primers used for qPCR. (XLSX 9Ă‚Â kb
Examining the Effects of the Destroying Ammunition, Mines and Explosive Devices on the Presence of Heavy Metals in Soil of Open Detonation Pit; Part 2: Determination of Heavy Metal Fractions
As a result of the destruction of ammunition, mines, and explosive devices by the method of open detonation, the increased concentration of heavy metals is often recorded in the soil of military polygons, which is a serious ecological problem. However, in order to determine the potential risk of such locations to the environment, it is necessary to determine, in addition to the total content, the forms in which the metals are present. In this paper, a sequential extraction method was used to analyze the six fractions of five heavy metals (cadmium, lead, nickel, copper, and zinc) in the soil of the polygon for destruction of ammunition, mines, and explosive devices. Samples were collected from the place of direct detonation (so-called pits) and from the edge of the pit. The aim of this research is determination of metal speciation in order to obtain a better insight in their mobility and risk arising from this. The results showed that heavy metals are predominantly present in the residual, oxide, and organic fractions. Cd and Cu were also significantly present in the mobile fractions due to conducted activities on the polygon. To assess the potential environmental risk of soil, the risk assessment code (RAC) and individual (ICF) and global (GCF) contamination factors were used. According to the RAC, the mobility and bioavailability of the analyzed heavy metals decreases in the following order: Cd gt Cu gt Zn gt Pb gt Ni. ICF results show low to moderate risk, while GCF results show low risk in terms of heavy metal contamination in the examined area