A comparison of gibberellin and cytokinin levels in normal and ‘little potato’ tubers

Summary Extracts of both normal and ‘little potato’ tubers of three varieties were bioassayed for gibberellin and cytokinin activity. The levels of activity of both gibberellins and cytokinins were greater in extracts from ‘little potato’ tubers than in extracts from normal tubers.     

Stand-replacing wildfires?: The incidence of multi-cohort and single-cohort Eucalyptus regnans and E. obliqua forests in southern Tasmania

The natural age structure of wet eucalypt forest has important implications for biodiversity conservation and the mode of wood production. Southern Tasmanian wet eucalypt forests were sampled to describe age class variation and to test the following hypotheses that relate to it: (1) Eucalyptus regnans stands are more likely to be single-cohort than Eucalyptus obliqua and mixed stands; (2) old-growth trees are associated with multi-cohort wet eucalypt forests; (3) the E. regnans stands are more multi-cohort than Victorian E. regnans stands. Data from 762 stands, all with either E. obliqua or E. regnans were analysed to determine how stand characteristics related to forest type and to the presence of old-growth trees. Over half the stands studied were multi-cohort. Stands with E. regnans had a lesser tendency towards multi-cohortness than stands lacking this species, although most old-growth stands, including those dominated by E. regnans, were multi-cohort. In contrast, most regrowth stands of all species combinations were single-cohort. The proportions of E. regnans stands that were multi-cohort were similar to some estimates from the same type of forest in Victoria. Modifications of forestry regimes in wet eucalypt forests could help to maintain the existence of these biodiverse multi-cohort forests in the landscape.     

A simulation of the development and restoration of old-growth structural features in northern hardwoods

Thinning treatments in second-growth forest may be a practical means of accelerating the development of certain old-growth structural features in regions where old stands are presently uncommon. We used CANOPY, an individual-tree model calibrated with data from thinned and unthinned stands, to simulate effects of thinning on growth rates and development of old-growth structural features in second-growth northern hardwoods. Three simulated, moderately heavy thinnings over a period of 45 years nearly doubled the predicted mean radial increment of canopy trees, percent of stand basal area in large trees, and area of canopy gaps. Compared to untreated stands, thinned stands had fewer dead trees per ha, but the dead trees were larger in size and the overall volume of snags and logs was little affected. In a 77-year old even-aged stand, moderately heavy thinning was predicted to reduce the time needed to attain the minimum structural features of an old-growth forest from 79 to 36 years. Simulated treatments in an older, uneven-aged stand gave mixed results; the moderately heavy treatment stimulated individual tree growth, but the removal of some medium-sized canopy trees in conjunction with natural mortality delayed the development of old-growth structure. Total volume of dead wood may still be deficient under the thinning regimes investigated in this study, but predicted live-tree structure 45 years after moderately heavy thinning was typical of stands in the advanced transition and steady-state stages of old-growth development. Results suggest that thinning can substantially accelerate the development of old-growth structure in pole and mature northern hardwoods, but response in older, uneven-aged stands is more modest, and treatments in these stands may need to be more conservative to achieve restoration goals.