Butenolide from plant-derived smoke enhances germination and seedling growth of arable weed species

We tested the applicability of the recently identified major germination cue from smoke (a butenolide 3-methyl-2Hfuro[2,3-c]pyran-2-one) on 18 weed species from non-fire prone environments. For the study species we compared the relative effectiveness of alternating temperatures, KNO₃, GA₃, smoke water and the butenolide on germination percentage, germination rate and seedling mass. We found that while smoke stimulated germination in a number of species it also had negative impacts on other species. In addition, the butenolide was effective on the widest range of species in terms of enhancing germination percentage, rate and seedling mass. However, none of the treatments, including butenolide were effective on all species. Our data demonstrate that butenolide may have wide applicability as a germination and seedling growth stimulant irrespective of whether the species come from fire-prone habitats.     

Human killer cells and natural killer cells: distinct subpopulations of Fc receptor-bearing lymphocytes

Unstimulated human peripheral blood lymphocytes were depleted of K cells, which mediate antibody-dependent cellular cytotoxicity (ADCC) without removing NK cells, which mediate natural killing (NK). K cell depletion was achieved by buoyant centrifugation removal of lymphocytes that bound to glutaraldehyde-treated P815-AB cells at high lymphocyte-to-target ratios. Likewise, NK cells were removed with glutaraldehyde-treated K562 cells without removing K cells. Furthermore, both cytotoxic cell populations were observed directly in one agarose single-cell cytotoxic assay (ASCA) using P815-AB and K562 cells simultaneously as target cells. Moreover, the percentage of total cytotoxic cells was equal to the sum of the percentage of K and NK cells observed in separate ASCA. Collectively, these results indicate that K cells and NK cells are distinct subsets of FcR-bearing lymphocytes. One subset, K cells, has more avid Fc receptors (fcR) than NK cells and are 'activated' via thier FcR to kill antibody-coated target cells. The second subset, NK cells, have less avid FcR and are not 'activated' through their FcR to kill antibody-coated target cells.     

Acceleration of high gravity yeast fermentations by acetaldehyde addition

In high gravity Saccharomyces cerevisiae fermentations containing 300 g glucose l^–1, daily addition of acetaldehyde to a total of 93 mM shortened the time required to ferment the first 250 g glucose l^–1 from 790 h to 585 h. Acetaldehyde feeding had no effect on the ethanol yield but increased by 135%, 78% and 77% the final concentrations of 2,3-butanediol, 2-methylpropanol and acetate, while decreasing that of glycerol by 14%. Controlled acetaldehyde feeding has potential as a technique for accelerating high gravity fuel or industrial ethanol fermentations and may be useful in preventing incomplete fermentations.     

Epithelial cell proliferation and migration in the developing rat gastric mucosa

To investigate cell proliferation in developing gastric antrum and fundus, proliferating gastric epithelial cells were labeled in fetal rats by intravenously injecting mothers with [³H]thymidine. In addition 14-day postnatal (dPN) rats were given [³H]thymidine intraperitoneally. Tissue was removed 1.5 hr later, and autoradiographs were prepared to identify proliferating cells. Total epithelial labeling indices (L.I.) reached a peak at 20 days gestation (dG), coincident with the appearance of pit/glands, then declined again by 22 dG (gestation end). At 18 dG, labeled cells were distributed throughout all levels of the stratified epithelia. Between 20 and 22 dG, as pit/gland development proceeded, labeled cells became concentrated in the gland bases and were only rarely seen on the surface (L.I. of surface cells <1% at 22 dG). By 14 dPN, proliferating cells were entirely absent from the epithelial surface. Approximately 15% of the endocrine cells were labeled at 22 dG, compared to only 2% at 14 dPN; zymogen cells were labeled (～6%) at 14 dPN; parietal cells did not label at any age studied. In addition, cell migration to the epithelial surface was studied in rats labeled at 22 dG, 14 dPN, or 28 dPN, and killed 1–20 days later. Migration times were slightly shorter in the 28 dPN group and were longer in fundus than antrum in all groups.     

A study of salmonid populations of the River Teify and tributaries near Tregaron

Population estimates of Salmo sular L. and Salmo trutta L. were made by electrofishing at 39 stations spaced along the main river and tributaries. Within the tributaries there was a tendency for the standing crop, the average weight of individual fish and the proportion of juvenile salmon to trout to decline in an upstream direction The survey included an ayessnient of a salmon alevin restocking project.     

Application of common predictive habitat techniques for post-border weed risk management

Weed risk assessment has become an accepted methodology for examining the likelihood and consequence of a plant species becoming invasive outside of its native range. Weed risk assessment draws upon biological and ecological information to estimate the likelihood and magnitude of the threats posed by introducing non-indigenous plants. In geographical terms, this has traditionally been understood as within a new country following importation of plant material. However, recent risk assessment development has focused more specifically on intracountry risk posed by already-present invasive plants and is referred to as post-border weed risk management. This form of assessment calls for fine-scale predictions of invasive species habitat suitability. This study applies some of the more popular and widely available habitat prediction models that represent a variety of different statistical approaches (linear regression, logistic regression, Bayesian probability, Classification and Regression Trees, Genetic Algorithm for Rule-set Production) to a single invasive plant, the vertebrate-dispersed, fleshy fruited European olive ( Olea europaea L.) in southern Australia. The relationships between the dependant ( O. europaea distribution) and independent (soil and climate) variables are used in the models to produce predictive maps for each model. Accuracy was calculated for each model output as well as a combined surface to examine whether recent calls for ensemble modelling of distributions produces improved predictions. Overall, the combined prediction demonstrated superior accuracy compared to any individual model outputs. The combined outputs can be likened to mapped gradations of predicted habitat suitability. The type of output produced in this study should form a critical component of post-border weed risk management but more importantly, the methodology will add to this important discipline.