BeckerFraserPhotos December 2011 photograph 2327
Images, UC QuakeStudies
A photograph captioned by BeckerFraserPhotos, "This used to be someone's garden on Kirsten Place in New Brighton. Liquefaction creates interesting patterns".
A photograph captioned by BeckerFraserPhotos, "This used to be someone's garden on Kirsten Place in New Brighton. Liquefaction creates interesting patterns".
Photograph captioned by BeckerFraserPhotos, "Looking east along Hereford Street through the CBD with the Botanic Gardens at the bottom. The grid pattern shows very clearly".
A photograph captioned by BeckerFraserPhotos, "A concrete-block wall from a building on the corner of Colombo and Gloucester Streets which has fallen in an interesting pattern during demolition".
Photograph captioned by BeckerFraserPhotos, "Damaged pavement in the alley between the Salvation Army Citadel and the Crowne Plaza on Durham Street. The paving tiles have separated in a pattern reminiscent of a zip".
Tree mortality is a fundamental process governing forest dynamics, but understanding tree mortality patterns is challenging because large, long-term datasets are required. Describing size-specific mortality patterns can be especially difficult, due to few trees in larger size classes. We used permanent plot data from Nothofagus solandri var. cliffortioides (mountain beech) forest on the eastern slopes of the Southern Alps, New Zealand, where the fates of trees on 250 plots of 0.04 ha were followed, to examine: (1) patterns of size-specific mortality over three consecutive periods spanning 30 years, each characterised by different disturbance, and (2) the strength and direction of neighbourhood crowding effects on sizespecific mortality rates. We found that the size-specific mortality function was U-shaped over the 30-year period as well as within two shorter periods characterised by small-scale pinhole beetle and windthrow disturbance. During a third period, characterised by earthquake disturbance, tree mortality was less size dependent. Small trees (,20 cm in diameter) were more likely to die, in all three periods, if surrounded by a high basal area of larger neighbours, suggesting that sizeasymmetric competition for light was a major cause of mortality. In contrast, large trees ($20 cm in diameter) were more likely to die in the first period if they had few neighbours, indicating that positive crowding effects were sometimes important for survival of large trees. Overall our results suggest that temporal variability in size-specific mortality patterns, and positive interactions between large trees, may sometimes need to be incorporated into models of forest dynamics.