Effects of Hydrophilic Polymer on the Survival of Buttonwood Seedlings Grown Under Drought Stress

The effect of 0.0 (control), 0.1, 0.2, 0.4, and 0.6% of the hydrophilic polymer “Stockosorb K-400” hydrogel (HG) on survival and growth of buttonwood (Conocarpus erectus L.) seedlings grown in sandy soil under drought stress was investigated. The ability of the soil to retain water increased with increasing hydrogel concentrations. The highest level of the HG was capable of changing the typical sandy soil to a loam or even silty clay in terms of water potential and water content. The highest HG concentration prolonged the time of water loss from the soil by about 66% more than the control soil. During drought stress, the seedlings grown in 0.6% HG-mixed soil survived three times as long as those grown in the control soil. Shoot and root growth increased significantly in HG-amended soil as compared with non-amended soil. Plant water potential increased significantly with HG application, thus it aided in the establishment and growth of C. erectus seedlings under water stress conditions. There were no significant differences between 0.4% and 0.6%. The study indicated that an amendment of soil with 0.4% to 0.6% of the hydrophilic polymer “Stockosorb K-400” can be used in arid and semi-arid areas to enhance the drought tolerance of C. erectus seedlings.     

An optimised protocol for molecular identification of Eimeria from chickens

Molecular approaches supporting identification of Eimeria parasites infecting chickens have been available for more than 20 years, although they have largely failed to replace traditional measures such as microscopy and pathology. Limitations of microscopy-led diagnostics, including a requirement for specialist parasitological expertise and low sample throughput, are yet to be outweighed by the difficulties associated with accessing genomic DNA from environmental Eimeria samples. A key step towards the use of Eimeria species-specific PCR as a sensitive and reproducible discriminatory tool for use in the field is the production of a standardised protocol that includes sample collection and DNA template preparation, as well as primer selection from the numerous PCR assays now published. Such a protocol will facilitate development of valuable epidemiological datasets which may be easily compared between studies and laboratories. The outcome of an optimisation process undertaken in laboratories in India and the UK is described here, identifying four steps. First, samples were collected into a 2% (w/v) potassium dichromate solution. Second, oocysts were enriched by flotation in saturated saline. Third, genomic DNA was extracted using a QIAamp DNA Stool mini kit protocol including a mechanical homogenisation step. Finally, nested PCR was carried out using previously published primers targeting the internal transcribed spacer region 1 (ITS-1). Alternative methods tested included sample processing in the presence of faecal material, DNA extraction using a traditional phenol/chloroform protocol, the use of SCAR multiplex PCR (one tube and two tube versions) and speciation using the morphometric tool COCCIMORPH for the first time with field samples.