This study was designed to evaluate changes in plant biomass, species richness, and diversity after application of glyphosate herbicide in several successional stages of sub-boreal spruce forest near Prince George, British Columbia, Canada. Vegetation was sampled in replicate control (reference) and treatment blocks of “herb,” “shrub,” and “shrub-tree” stages of cutover forest habitats. Volume of herb layers declined temporarily in the first post-treatment year. Shrub layers were reduced in herb and shrub stages, and shrubs and trees were reduced temporarily in the shrub-tree stage. Species richness of herbs and shrubs was similar in control and treatment blocks in the herb successional stage, but shrub richness declined on the treatment in the shrub stage. There were no consistent differences in numbers of herb, shrub, or tree species between control and treatment blocks in the shrub-tree stage. Species diversity (Simpson's index and Shannon-Wiener function) of herbaceous plants was not affected by herbicide application in any of the successional stages, but diversity of shrubs was lower in treatment than control blocks in the herb and shrub stages. Diversity of trees was reduced on treatment blocks in the shrub-tree stage. Species abundance curves of overall plant communities showed little change in the herb stage, a decline in the first post-treatment year in the shrub and shrub-tree stages, with similar patterns between control and treatment blocks in subsequent post-treatment years. The general lack of community-wide reductions in plant biomass and diversity, and the short-term duration of specific changes, suggest that conifer release treatments of plantations have no substantial, incremental effects on wildlife habitat.

Three approaches to data analysis were compared to describe competitive interactions between wheat and Italian ryegrass. Replacement series were performed using the two species at total densities of 100, 200, and 400 plants/ m2, and separate monoculture experiments for each species at densities from 33 to 800 plants/m2. Approaches to data analysis included: 1) conventional analysis of replacement series experiments, 2) development of synthetic no-interaction responses from monoculture experiments for comparison with results from mixtures, and 3) responses of the reciprocal yield of individual plants to variation in densities of the two species. Wheat was the superior competitor to ryegrass; however, the three approaches varied in ability to quantify this competitive relationship. The conventional replacement series analysis was least sensitive in describing the influences of either density or proportion on the plant association. The synthetic no-interaction approach provided the most detailed analysis of the influence of proportion on the species interaction. The reciprocal yield approach provided the simplest and most sensitive analysis of the joint influences of density and proportion. The latter approach also provided the most quantitative analysis of the influence of density on the species interaction. Plant density and species proportion are important variables for interpreting the process of plant competition.

Commercially available cabinet sprayers are not well suited for making low volume applications (<30 L/ha) of herbicides to woody forest species that can be up to 1.5 m tall. A simple, inexpensive laboratory sprayer that overcomes some limitations of commercial cabinet sprays can be built from materials readily available at local building and electronic suppliers. The only specialized equipment required is a positive displacement pump and a rotary disk atomizer. The atomizer is attached to the end of a variable height arm mounted on a laboratory cart. A positive displacement pump ensures controlled flow. The operator pushes the cart along a metal rub rail which keeps the cart tracking in a straight line. Travel speed is regulated by the operator following a marker on a clothesline-like loop of fishing line and is driven by a variable-speed drill attached to a variable voltage power supply.

When herbicide concentration was constant, absorption of 14C-glyphosate increased with increasing droplet size (326 to 977 μm). Amount of 14C-glyphosate translocated away from the treated area, expressed as percent of absorbed, increased as droplet size decreased. Herbicide concentration of the droplet was more important than droplet number or droplet size in determining glyphosate absorption and translocation. Absorption and translocation increased with increasing herbicide concentration regardless of whether droplet size or number was altered in conjunction with herbicide concentration. This relationship explained why low spray volume (increased herbicide concentration) increased herbicide efficacy. The concentration gradient between droplet and leaf, rather than droplet coverage, was the primary mechanism responsible for the observed effect. Large droplets caused localized tissue injury, which may have caused decreased translocation.

A new closed cell is presented for in situ X-ray ptychography which allows studies under gas flow and at elevated temperature. In order to gain complementary information by transmission and scanning electron microscopy, the cell makes use of a Protochips E-chipTM which contains a small, thin electron transparent window and allows heating. Two gold-based systems, 50 nm gold particles and nanoporous gold as a relevant catalyst sample, were used for studying the feasibility of the cell. Measurements showing a resolution around 40 nm have been achieved under a flow of synthetic air and during heating up to temperatures of 933 K. An elevated temperature exhibited little influence on image quality and resolution. With this study, the potential of in situ hard X-ray ptychography for investigating annealing processes of real catalyst samples is demonstrated. Furthermore, the possibility to use the same sample holder for ex situ electron microscopy before and after the in situ study underlines the unique possibilities available with this combination of electron microscopy and X-ray microscopy on the same sample.