Effect of crop residue biochar on soil acidity amelioration in strongly acidic tea garden soils

Strongly acidic soil (e.g. pH < 5.0) is detrimental to tea productivity and quality. Wheat, rice and peanut biochar produced at low temperature (max 300 °C) and differing in alkalinity content were incorporated into Xuan‐cheng (Ultisol; initial pH_{soil/water = 1/2.5} 4.12) and Ying‐tan soil (Ultisol; initial pH _{soil/water = 1/2.5} 4.75) at 10 and 20 g/kg (w/w) to quantify their liming effect and evaluate their effectiveness for acidity amelioration of tea garden soils. After a 65‐day incubation at 25 °C, biochar application significantly (P < 0.05) increased soil pH and exchangeable cations and reduced Al saturation of both tea soils. Association of H⁺ ions with biochar and decarboxylation processes was likely to be the main factor neutralizing soil acidity. Further, biochar application reduced acidity production from the N cycle. Significant (P < 0.05) increases in exchangeable cations and reductions in exchangeable acidity and Al saturation were observed as the rate of biochar increased, but there were no further effects on soil pH. The lack of change in soil pH at the higher biochar rate may be due to the displacement of exchangeable acidity and the high buffering capacity of biochar, thereby retarding a further liming effect. Hence, a significant linear correlation between reduced exchangeable acidity and alkalinity balance was found in biochar‐amended soils (P < 0.05). Low‐temperature biochar of crop residues is suggested as a potential amendment to ameliorate acidic tea garden soils.     

Chaos theory and assessment of forest stakeholder attitudes towards Australian forest policy

The Regional Forest Agreement process has dominated Australian forest policy for the past decade. The RFA process set in place a mechanism by which benchmark conservation values were established for forest ecosystems, whilst addressing the needs of the timber industry. The outcomes of a number of RFA's have been fraught with controversy. Key stakeholder groups have shown disagreement with processes and outcomes of methods employed by government both in establishing conservation reserves and areas allocated to timber harvesting. This research uses non-linear techniques to examine the dynamical behavior in stakeholder responses and to identify patterns of behavior that may lead to prediction of stakeholder responses. The method developed in this research provides a bridge between social sciences and Chaos theory.¹     

New constituents from Gliricidia sepium

The heart wood of Gliricidia sepium stem yielded stigmastanol glucoside (1) and 3',4'-dihydroxy-trans-cinnamic acid octacosylester 2, along with three other known constituents.     

Nodule formation and distribution during the establishment stage of six selections of winged bean

Six selections of winged bean (syn. Indies Goa bean, Psophocarpus tetragonolobus, namely LBNC₃, LBNC_1,3 TPT₂, UPS₁₂₂, SLS₁ and SLS₆) were grown under plant-house conditions to study their nodulation patterns during the establishment stages of growth. Plants were grown in Sri Lankan sandy loam soil in which indigenous Rhizobium Bacteria specific to winged bean were present in natural form. Two weeks after emergence of seedlings the nodulation commenced, after 3 weeks the nodules began to reach their bacteroid stage and after the fourth week considerable numbers of bacteroid-stage nodules were found. The distribution of nodules followed a uniform pattern up to the third week in all the selections. They appeared mainly in the 30- and 60-mm (from the base of the seedling) root zones, later on they did not follow any special pattern in any of the selections. The nodules were not confined to either axillary or any particular root member. The selections varied in their nodulating-capacity. There were differences in nodular number and nodular mass. Selection LBNC₃ had the highest capacity for nodulation, while SLS₆ had the lowest. LBNC₃ and SLS₁ were very good nodulating selections, while UPS₁₂₂ and SLS₆ were poor ones with the indigenous winged bean Rhizobium. There was a very high positive correlation between nodule mass and shoot mass.     

A fungistatic chromene from<Emphasis Type="Italic">Ageratum conyzoides</Emphasis>

Ageratum conyzoides L. is an annual herb in the tropics and subtropics whose extracts are known to possess pharmacological and biocidal activity. We report on the bioactivity of a secondary metabolite (a chromene) isolated from the shoots ofA. conyzoides against some plant pathogenic fungi. Organic solvent extracts from the shoots were tested for antifungal activity against the plant pathogenic fungiRhizoctonia solani, Sclerotium rolfsii, Botryodiplodia theobromae, Phomopsis theae andFusarium species growingin vitro on potato dextrose agar medium. The cruden-hexane extract completely inhibited the growth ofR. solani andS. rolfsii. Then-hexane extract was chromatographed over a column of silica gel followed by activity-guided fractionation to give an antifungal principle. Structure elucidation by detailed analysis of¹H,¹³C NMR and mass spectroscopy identified the active compound as precocene II. The growth ofR. solani andS. rolfsii was completely inhibited by precocene II at a concentration of 80–100 ppm. The sclerotia ofR. solani andS. rolfsii were also completely suppressed by 150 ppm of precocene II. Sub-culture of these inhibited fungi onto precocene II-free medium restored growth of the fungus, indicating that precocene II is fungistatic. Crude or refined extracts fromA. conyzoides offer the possibility of biocontrol of plant pathogenic fungi. http://www.phytoparasitica.org posting Feb. 11, 2004.     

Ultrastructural analysis of sequential cyprinid herpesvirus 3 morphogenesis in vitro

Cyprinid herpesvirus 3 (CyHV‐3) is an alloherpesvirus, and it is the aetiological agent of koi herpesvirus disease. Although the complex morphogenic stages of the replication cycle of CyHV‐3 were shown to resemble that of other members of the Herpesvirales, detailed analysis of the sequence and timing of these events was not definitively determined. This study describes these features through a time course using cyprinid cell cultures (KF‐1 and CCB) infected with CyHV‐3 (KHV isolate, H361) and analysed by transmission electron microscopy. Rapid viral entry was noted, with high levels of intracellular virus within 1–4 h post‐infection (hpi). Intranuclear capsid assembly, paracrystalline array formation and primary envelopment of capsids occurred within 4 hpi. Between 1 and 3 days post‐infection (dpi), intracytoplasmic secondary envelopment occurred, as well as budding of infectious virions at the plasma membrane. At 5–7 dpi, the cytoplasm contained cytopathic vacuoles, enveloped virions within vesicles, and abundant non‐enveloped capsids; also there was frequent nuclear deformation. Several morphological features are suggestive of inefficient viral assembly, with production of non‐infectious particles, particularly in KF‐1 cells. The timing of this alloherpesvirus morphogenesis is similar to other members of the Herpesvirales, but there may be possible implications of using different cell lines for CyHV‐3 propagation.     

Ultrastructural morphogenesis of salmonid alphavirus 1

Studies on the ultrastructural morphogenesis of viruses give an insight into how the host cell mechanisms are utilized for new virion synthesis. A time course examining salmonid alphavirus 1 (SAV 1) assembly was performed by culturing the virus on Chinook salmon embryo cells (CHSE‐214). Different stages of viral replication were observed under electron microscopy. Virus‐like particles were observed inside membrane‐bound vesicles as early as 1 h following contact of the virus with the cells. Membrane‐dependent replication complexes were observed in the cytoplasm of the cells, with spherules found at the periphery of late endosome‐like vacuoles. The use of intracellular membranes for RNA replication is similar to other positive‐sense single‐stranded RNA (+ssRNA) viruses. The number of Golgi apparatus and associated vacuoles characterized by ‘fuzzy’‐coated membranes was greater in virus‐infected cells. The mature enveloped virions started to bud out from the cells at approximately 24 h post‐infection. These observations suggest that the pathway used by SAV 1 for the generation of new virus particles in vitro is comparable to viral replication observed with mammalian alphaviruses but with some interesting differences.     

Dimensional stability of single jersey fabrics of LincLITE® and conventional yarns. I

Dimensional constants (k values) of single jersey fabrics made from LincLITE® and conventional yarns are calculated under dry, steam, full relaxation treatments. Fabrics were made under different tightness factors such as high, medium and low with different twist factors, twist directions and feeder blending. LincLITE® yarns made to get soft and bulkier effects with yarn count of 39 tex and conventional yarns made into 39 tex and 48 tex yarn counts. Various effects on K values are analysed using correlation coefficients. K-values are increased with relaxation progression and have shown some differences between in LincLITE® and conventional fabrics, and feeder blended fabrics. Loop shape factor is highly affected by tightness factor, relaxation and feeder blending in LincLITE® fabrics, whereas twist factor not significantly effects on loop shape factor in conventional fabrics. Stitch density significantly increases with relaxation in conventional fabrics and no significant effect shows with LincLITE® fabrics.     

Improved detection and identification of the sudden oak death pathogen Phytophthora ramorum and the Port Orford cedar root pathogen Phytophthora lateralis

Early detection provides the best way to prevent introduction and establishment of alien plant pathogens. Amplification of DNA by PCR has revolutionized the detection and monitoring of plant pathogens. Most of those assays rely on the amplification of a fraction of the genome of the targeted species. With the availability of whole genomes for a growing number of fungi and oomycetes it is becoming possible to compare genomes and discover regions that are unique to a target organism. This study has applied this pipeline to develop a set of hierarchical TaqMan real-time PCR detection assays targeting DNA of all four Phytophthora ramorum lineages, and a closely related species, P. lateralis. Nine assays were generated: three targeting DNA of all P. ramorum lineages, one for each lineage of P. ramorum, one for P. lateralis and one targeting DNA of P. ramorum and P. lateralis. These assays were very accurate and sensitive, ranging from 98.7% to 100% detection accuracy of 2–10 gene copies of the targeted taxa from pure cultures or inoculated tissues. This level of sensitivity is within the lowest theoretical limit of detection of DNA. It is expected that these assays will be useful because of their high level of specificity and the ease with which they can be multiplexed because of the inherent flexibility in primer and probe design afforded by their lack of conservation in non-target species.     

Evaluating faba beans for rust resistance using detached leaves

A method was developed for testing detached leavesof faba beans for their response to rust disease.Leaves 5 to 8, counting from the shoot tip, wereexcised and maintained on a water-retaining medium,with 5 ppm gibberellic acid, in an enclosed box in atemperature-controlled glasshouse. Leaves treated inthis way remained in good health for up to 30 days.Rust spores were dispersed in a slurry of talc andwater and applied to the abaxial leaf surface. Diseasedevelopment of seven rust populations, collected fromseveral locations in eastern Australia, was monitoredfor 15 days on eight faba bean accessions. Fouraccessions were BPL lines which ICARDA claimed to havesome resistance, two were ILB lines from ICARDA whichhad been found to have stronger field resistance innorthern New South Wales, Australia, and the remainingtwo were known susceptibles. The detached-leaf testshowed that the two cultivars were susceptible, thefour BPL lines were intermediate and ILB 3107 and ILB3025 were slow-rusting. One rust population, which hadbeen stored under liquid nitrogen for several years,was less effective at inducing disease symptoms thanthe other six, which were all freshly collected. Theinteractions between host accessions and rustpopulations were statistically significant but minor,as the cultivars remained in their categories ofresistance or susceptibility. The detached-leaftechnique is thus suitable for use in screeningindividual plants for reaction to several differentpathogen species or genotypes without danger ofcross-contamination or induced resistance.