Solar Photocatalysis Using Fixed-Film TiO<Subscript>2</Subscript> for Microcystins from Colonial <Emphasis Type="Italic">Microcystis aeruginosa</Emphasis>

Microcystins (MCs) are endotoxins produced by cyanobacteria in freshwaters globally. With known potential for human health risks, rapid and effective treatment methods are needed for MCs. Previous studies have shown photocatalysis can achieve rapid half-lives with UV lamps and slurries of TiO₂. In this experiment, rates and extents of solar photocatalysis of MCs were measured using bench-scale reactors with fixed films of TiO₂ for solutions with a range of cellular:aqueous MC ratios. Since cellular MCs can be removed physically, photocatalysis rates were measured following sand filtration to discern the extent of MC removal post-filtration. Since UV energy drives photocatalysis using TiO₂, rates of removal were calculated as a function of cumulative UV insolation and time. For water containing < 10% aqueous MC, filtration removed 90% of total MC, and the subsequent photocatalysis half-life was 0.37 MJ/m² (or 111 min). For water with ~?50% aqueous MCs, filtration removed 52% of the total MCs, and the average half-life for photocatalysis was 0.38 MJ/m² (or 138 min). For the >?90% aqueous MC treatment, filtration removed 0% MCs, and the photocatalysis half-life for MCs was 0.37 MJ/m² (or 135 min). Previous studies have used clarified waters; however, results from this study are likely representative of scenarios with waters containing confounding water characteristics and use of solar light for UV, as anticipated in developing countries with less advanced water treatment methods. Photocatalysis is a rapid and effective process for decreasing concentrations of MCs and could be useful for mitigating risks from MC exposures in drinking water.     

Regeneration of mixed conifer forests under group tree selection harvest management in western Bhutan Himalayas

Group selection tree harvest has been proposed as an ecologically sustainable silvicultural technique in mixed conifer forests of the western Bhutan Himalayas. To evaluate this silvicultural technique, we studied the ecological consequences of a group selection tree harvest in mixed conifer forests by assessing 127 circular plots (71 in logged and 56 in unlogged stands) in two forest management units (FMUs). Tree species composition and diversity were similar between logged and unlogged stands. Seedling density and height growth vary by species and were influenced by logging and microsites, with generally taller seedlings found in the logged versus unlogged stands. Early successional shade-intolerant species colonized logged stands. Seedlings growing on bare soil scarified by harvesting had medium vigour while seedlings growing on bryophyte mats showed good vigour in both logged and unlogged stands. Moist sites with a northerly aspect supported profuse conifer seedling regeneration, compared to sites with a dry southerly aspect. Damage to conifer seedlings from herbivore browsing was minimal. Conifer seedling density and height growth was negatively affected by competition from herbaceous vegetation, most notably Salvia officinalis. Group selection tree harvest in southern dry exposures in spruce-dominated stands is silviculturally unsuitable because it alters tree succession.     

Ficus auriculata — its relative importance in Bhutan, farmers' preference and fodder quality

Tree leaves are important traditional fodder sources in many parts of the Himalaya, particularly during the dry winter season. Households interviewed in different regions of Bhutan used 1–13 different tree species for fodder, with Ficus auriculata standing out as the preferred and most widely used species across a range of conditions. It is preferred because of the wide range of adaptation, good nutritional qualities and palatability, and its good productivity. Ficus auriculata is also an important tree fodder in the Himalayan region of Nepal and India. Its fodder quality is far superior to paddy straw, the main winter fodder in the rice growing regions of the Himalayas. Parameters recorded in the literature for crude protein, neutral detergent fibre and acid detergent fiber are 9.5–17.3, 46.2–58.4 and 36.1–45.8%, respectively. Farmers consider it to be better than rice straw and the fodder from the tree fodder species Celtis tetrandra, Brassaiopsis hainla, Stereospermum suaveolens, Bauhinia purpurea and Litsea polyantha. Average annual fresh yield per tree was reported as 200, 120, 112, 108, 108 and 96 kg for F. auriculata, Artocarpus lakoocha, Gmelina arborea, F. cunia, Litsea monopetala and Stereospermum suaveolens, respectively. Considering the current importance of F. auriculata it is imperative to carry out research exploring its potential in evolving production systems and to quantify the opportunities of improving its nutritional quality and productivity through selection.This revised version was published online in November 2005 with corrections to the Cover Date.     

The influence of time,soil moisture and exogenous factors on the survival potential of oospores and chlamydospores of Phytophthora cinnamomi

The mode of persistence of Phytophthora cinnamomi, a highly aggressive soil‐ and water‐borne pathogen, remains unclear. This study investigated the survival of viable oospores and chlamydospores of P. cinnamomi when present as free propagules in untreated soil, or in soil subject to four exogenous treatments: smoke water, fish emulsion and two fungicides (ridomil and furalaxyl). The exogenous treatments were applied under moist and dry soil conditions. Spore viability was determined by the thiazolyl blue tetrazolium bromide (MTT) staining technique, with a qPCR assay used to compare general patterns of decline. Over 96% of oospores lost viability over a period of 48 weeks irrespective of soil moisture conditions. The mean percentage viability for oospores decreased from 91% at time zero to 72, 35, 20 and 1% after 6, 12, 24 and 48 weeks, respectively. Reduction in viability of chlamydospores was more rapid than oospores, with viability declining from 92% to zero after 12 weeks. There was no significant difference between untreated soil and the exogenous treatments. The RNA‐based qPCR assay indicated a strong presence of viable oospores of P. cinnamomi up to week 12 for moist soil and week 3 for dry soil, but thereafter failed to detect RNA even though viable oospores could be detected by MTT staining. Based on the MTT staining, this study indicated that viability of P. cinnamomi oospores may be entirely lost within 1 year and that of chlamydospores within 3 months for the soil type tested. Therefore, oospores and chlamydospores when existing as free propagules in soil appear unlikely to be involved in the long‐term survival of P. cinnamomi.