The potential of kauri (Agathis australis) for paleoclimate research is well established. Multiple treering chronologies have been derived from living and sub-fossil material and growth-climate relationships have been identified. Work has progressed to the stage where raw ring-width data and chronologies covering the last half of the second millennium can confidently be placed in the public domain, to facilitate multiproxy paleoclimate studies. This paper outlines progress in deriving kauri tree-ring chronologies, summarises data availability and quality, and explores the scope for developing composite chronologies. Statistical quality control of the available data was undertaken, following application of an "optimum" standardisation technique. Variations in sample depth with time and between sites result in a complex evolving pattern of chronology quality across sites. Analysis of inter-site statistical relationships identified a pervasive regionalscale signal in kauri with some minor secondary patterns. In light of the strong common signal, a kauri master chronology was built by pooling tree-ring series. Analysis of the quality of this chronology indicates that high-quality master chronologies can be derived for A.D. 1597-1996 from as few as 25 trees from seven sites.

Considerable research has occurred in recent years to build Agathis australis (D. Don) Lindley (kauri) tree-ring chronologies for paleoclimate applications and to identify statistical relationships between kauri tree rings and climate. This paper reports on a multi-year study of the seasonal growth of kauri, designed to assist in the interpretation of identified statistical relationships, and to determine if kauri’s seasonal growth characteristics are dependent on tree size. To achieve this, 43 kauri (0.09-2.00 m diameter) at Huapai Scientific Reserve were fitted with vernier bands to measure circumference change over 3-4 growing seasons. Absolute (mm) and relative (proportion of total ring) monthly growth rates were calculated for each tree and statistics characterizing the timing of growth were calculated (e.g. date corresponding to 50% of growth). Tree size-related differences were assessed by splitting the data into three subsets based on size, then comparing the monthly growth rates and growth timing statistics for the subsets. The growth timing statistics were also correlated with tree diameter. A key finding is the strong dominance of spring growth, with October and November alone accounting for 38-50% of the total ring width. This result is consistent across age cohorts, although the largest trees tended to peak in November, rather than October. This indicates that kauri tree rings are likely to have value in terms of reconstructing spring conditions; consistent with reported statistical relationships between kauri tree rings and the El Niño-Southern Oscillation phenomenon. High inter-tree variance in growth rates characterized the results, but little of this variance was accounted for by tree size. Although relationships between tree size and growth characteristics were generally weak and inconsistent, they are considered sufficient to warrant a precautionary approach in the development of tree-ring chronologies for climate reconstruction purposes.

The traditional approach to standardizing tree-ring time series is to divide raw ring widths by a fitted curve. Although the derived ratios are conceptually elegant and have a more homogenous variance through time than simple differences, residual heteroscedasticity associated with variance dependence on local mean ring width may remain. Incorrect inferences about climate forcing may result if this heteroscedasticity is not corrected for, or at least recognized (with appropriate caveats). A new variance stabilization method is proposed that specifically targets this source of heteroscedasticity. It is based on stabilizing the magnitude of differences from standardization curves to a common reference local mean ring width and uses data pooled from multiple radii. Application of the method to a multi-site kauri (Agathis australis (D. Don) Lindley) data set shows that (a) the heteroscedasticity issue addressed may be generic rather than radius-specific, at least for some species, (b) variance stabilization using pooled data works well for standardization curves of variable flexibility, (c) in the case of kauri, simple ratios do not appear to be significantly affected by this cause of heteroscedasticity, and (d) centennial-scale variance trends are highly sensitive to the analytical methods used to build tree-ring chronologies.

The growth and productivity of kauri (Agathis australis (D. Don) Lindl.) in even-aged single-species planted stands and mixed-aged second-growth natural stands has been studied. Stand-level models of height, basal area and whole-tree volume were developed. Kauri growth and productivity in planted stands up to 83 years old were compared to that of natural stands that were up to 196 years of age. Within natural stands, the effect of thinning treatments on growth and productivity was also assessed. Models of growth and productivity were initially developed for each of the three different kauri stand types independently (planted, second-growth unthinned and thinned). Combined data sets allowed for the development of single models that were able to fit all stands. A Schumacher equation with local slope parameter and asymptote bounded at 45 m gave the best fit for height growth, while a von Bertalanffy-Richards equation in difference form with local slope parameter gave the best fit for basal area growth. Kauri in all stand types were found to be slow to establish with little height growth in planted stands for the first five years after planting, and for the first 25 years in natural stands. Similar trends were observed for basal area and whole-tree volume development. Models developed in this study are relevant only to kauri in the “ricker” or monopodial form irrespective of age, and for stands from 320-2000 stems/ha. Kauri growth and productivity in planted stands was substantively better than that in second-growth stands. Planted kauri had height increment of 0.4 m/yr for periods of up to 30 years. At age 50, planted kauri was predicted to be 20 m in height, over twice the height of kauri in natural stands, and to be 28.1 m by 100 years. Basal area at age 50 averaged 64.9 m2/ha for all planted stands, and was predicted to be 98.2 m2/ha at age 100. Whole-tree volume was predicted to increase by 11.7 m3/ha/annum for all stands, but was as high as 20.6 m3/ha/yr in one 70 year old stand. The maximum productivity of kauri was observed in one high-performing young kauri planted stand where whole-tree volume increment in excess of 30 m3/ha/yr were predicted for a period from age 15-30. Carbon sequestration was calculated from the volume model and predicted to be 316 t C/ha and 1168 t CO2/ha at age 100. Mortality of kauri in planted stands was as high as 3.9%/yr for individual stands, over their entire rotation to date. For all stands, mortality averaged 0.56%/yr. The highest mortality occurred in the years before the first assessment and averaged 0.64%/yr for all stands. From the first to the last assessment mortality averaged 0.30%/yr. Where mortality in individual stands was above the average rate the dominant cause was drought. The growth and productivity of kauri in second-growth stands was only marginally improved by thinning to reduce competition. The volume removed in thinning operations had not been replaced in the (up to) 50 years since thinning treatments were applied. At age 150, the predicted height of kauri in unthinned control and thinned stands were identical at 25.9 m. Basal area at age 150 was 64.5 m2/ha in unthinned stands and 52.6 m2/ha in thinned stands. Whole-tree volume was predicted to be 681 m3/ha in unthinned and 549 m3/ha in thinned stands. Volume increment peaked at 5.2 m3/ha/yr in unthinned stands and 4.7 m3/ha/yr in thinned stands. This study has shown that the worst growth and productivity of kauri in planted stands was better than that of the best natural stands. The difference in performance between plantation and second-growth kauri was most likely a result of a combination of lower site quality characteristics (soil type and fertility), stand structure and within-stand competition of natural stands. The data for planted kauri came from 31 permanent sample plots located in 25 planted stands. These stands ranged in age from 14-83 years at the last assessment, and ranged in stand density from 218-1800 stems/ha. The overall number of planted stands and plots from which data was available to develop models was small in comparison to many exotic forest species datasets. The majority of the planted stands were not silviculturally treated after planting, and considerable variation in establishment methods was recorded. The results of productivity from the models developed for planted kauri should therefore be considered to be conservative. The results of this study indicate an opportunity to grow kauri in plantations on good quality sites for the production of high quality sapwood timber over rotations of 60 years or less. They also indicate that second-growth stands will produce usable volumes of timber, but only over extended periods of time. To ensure that kauri in planted stands can meet the potential observed during the development of these models, a series of well-managed stands on a range of sites is urgently required where the effects of timely silviculture, including initial stand density, can be assessed, quantified and reported on. Further research on selection and breeding for the species would improve the early establishment and growth of planted kauri resulting in a reduced rotation length. Research on long-term management strategies that include continuous cover forestry may make the species an attractive proposition for carbon forestry and/or for the production of high quality, naturally durable heartwood. The dataset compiled for this study was the best data available. While it cannot as yet be used to develop prescriptions for the establishment and maintenance of planted kauri stands, it does provide clues and directions that should be pursued in further research, however.

Replication is a key principle in tree-ring research. Dendrochronologists strive to maximise sample size to enhance the "signal" in tree-ring chronologies, often relying on crossdating to provide an effective quality control filter. However, is crossdating alone a sufficient quality test for incorporating a series into a site chronology? We address this question using an objective and automated "chronology stripping" method designed to maximise the chronology's "Expressed Population Signal" (EPS), by iteratively removing series which lower chronology EPS. A 15-site data set of Agathis australis (D. Don) Lindley is used to demonstrate the method. Results suggest that modest benefits may be gained by chronology stripping, but the quality control implicit in crossdating is indeed effective, at least for Agathis australis.

Content removed due to copyright restriction: Knapp M., Stockler K., Havell D., Delsuc F., Sebastiani F. & Lockhart P.J. (2005) Relaxed molecular clock provides evidence for long-distance dispersal of Nothofagus (southern beech). Plos biology 3(1), 38-43 / New Zealand has long been regarded as a key to understanding discontinuous distributions in the Southern Hemisphere. The archipelago is a fragment of the ancient super continent Gondwana. It has been isolated for 80 million years, has an excellent fossil record, and some of its most ancient biota such as the Southern Beeches (Nothofagus) and the Araucariaceae show disjunct distribution patterns with relatives on other fragments of Gondwana. Some of the most controversial problems of Southern Hemisphere biogeography with wide ranging implications involve New Zealand taxa. Three of them have been addressed in this thesis. The transoceanic relationships of the genus Nothofagus have long been regarded as an iconic example of a distribution pattern resulting from the break up of Gondwana. Phylogenetic analyses presented here show that, though most of the extant distribution of the genus is indeed shaped by tectonic events, Southern Beeches have crossed the Tasman Sea between Australia and New Zealand at least twice during the Tertiary period These results, together with findings of studies on other plant and animal taxa, emphasise the importance of dispersal but at the same time raise the question of whether any New Zealand taxa can be considered Gondwanan relicts. There is no geological evidence for the continuous existence of land throughout the Tertiary in the New Zealand area. However, molecular clock analyses presented in this thesis indicate that Agathis australis (New Zealand Kauri) diverged from its closest Australian relative prior to the Oligocene, or period of greatest submergence during the Tertiary. Thus these findings reject the hypothesis of the complete drowning of the New Zealand landmass during the Tertiary. They cannot reject the hypothesis of Stöckler et al. (2002) that the New Zealand Kauri lineage has persisted on the archipelago since its separation from Gondwana. Explanations for forest distribution patterns within the New Zealand islands themselves are diverse. New Zealand Nothofagus species show distribution gaps that are not explained by recent environmental factors alone. Early Miocene tectonic events and alternatively Pleistocene climates have been proposed as causes for this disjunct distribution pattern. Phylogeographic analyses reported in this thesis suggest that severe Pliocene and Pleistocene climates as well as Pliocene and Pleistocene tectonic events have shaped present day distribution and diversification of Nothofagus species in New Zealand.

The objective of this thesis is to develop an ecological economic framework for the assessment and establishment of protected areas (PAs) that are aimed at conserving forests and biodiversity. The framework is intended to be both rigorous and relevant to the decision-making process. Constructivism is adopted as the paradigm guiding the research process of the thesis, after firstly examining also positivist philosophy and ???post-normal??? scientific methodology. The tenets of both ecological and environmental economics are then discussed. An expanded model of human behaviour, which includes facets derived from institutional economics and socioeconomics as well as aspects of neoclassical economics, is outlined. The framework is further developed by considering, from a contractarian view point, the implications of intergenerational equity for biodiversity conservation policies. The issues of intragenerational distribution and allocation are then considered. In this regard, cost-benefit analysis (CBA), as applied to the valuation of forests, PAs, and biodiversity, is critically reviewed. A participatory approach to decision-making, which may also include CBA, is then proposed. The resulting ecological economic framework may be thus summarised: (a) ecosystem use patterns should be chosen on the basis of their sustainability, distributional, and efficiency aspects; (b) systems of PAs should be established in order to achieve minimal intergenerational equity; (c) intragenerational equity requires the correction of the asymmetrical distribution of the costs and benefits arising from the establishment of PAs; (d) the institutional features relevant to the environmental-economic issues being analysed should be considered; and (e) the decision-making process should be participatory and action oriented. The framework is applied to two case studies in Vanuatu. These applications detail (a) stakeholders??? views and trade-offs faced in relation to forest management (b) modes of participatory research and decision-making, (c) forms of compensation that may be adopted in correcting asymmetrical distributions of the costs and benefits of PAs, and (d) institutional influences on ecosystems use and implications for conservation projects. The institutional arrangements developed for the establishment of the PAs are presented. The application of this ecological economic framework has resulted in the formal establishment of one PA and the identification and assessment of five other PAs.

The objective of this thesis is to develop an ecological economic framework for the assessment and establishment of protected areas (PAs) that are aimed at conserving forests and biodiversity. The framework is intended to be both rigorous and relevant to the decision-making process. Constructivism is adopted as the paradigm guiding the research process of the thesis, after firstly examining also positivist philosophy and ???post-normal??? scientific methodology. The tenets of both ecological and environmental economics are then discussed. An expanded model of human behaviour, which includes facets derived from institutional economics and socioeconomics as well as aspects of neoclassical economics, is outlined. The framework is further developed by considering, from a contractarian view point, the implications of intergenerational equity for biodiversity conservation policies. The issues of intragenerational distribution and allocation are then considered. In this regard, cost-benefit analysis (CBA), as applied to the valuation of forests, PAs, and biodiversity, is critically reviewed. A participatory approach to decision-making, which may also include CBA, is then proposed. The resulting ecological economic framework may be thus summarised: (a) ecosystem use patterns should be chosen on the basis of their sustainability, distributional, and efficiency aspects; (b) systems of PAs should be established in order to achieve minimal intergenerational equity; (c) intragenerational equity requires the correction of the asymmetrical distribution of the costs and benefits arising from the establishment of PAs; (d) the institutional features relevant to the environmental-economic issues being analysed should be considered; and (e) the decision-making process should be participatory and action oriented. The framework is applied to two case studies in Vanuatu. These applications detail (a) stakeholders??? views and trade-offs faced in relation to forest management (b) modes of participatory research and decision-making, (c) forms of compensation that may be adopted in correcting asymmetrical distributions of the costs and benefits of PAs, and (d) institutional influences on ecosystems use and implications for conservation projects. The institutional arrangements developed for the establishment of the PAs are presented. The application of this ecological economic framework has resulted in the formal establishment of one PA and the identification and assessment of five other PAs.

The long-tailed bat (Chalinolobus tuberculatus) is a threatened species endemic to New Zealand. Historical anecdotes indicate that long-tailed bat populations have declined. However, it is unknown if all populations have declined and if declines are historical or ongoing. Thus, the development and implementation of a national network of long-tailed bat monitoring sites is a priority of the Department of Conservation's Bat Recovery Plan. Potentially, information gained from a national monitoring programme would assist conservation managers to target resources towards those areas where bat populations are declining and provide baseline information to assist managers to gauge the impact of management techniques on bat populations. Of critical importance is that unless it can be demonstrated that long-tailed bat populations have declined and that, that decline is real, management will not be initiated. The aim of this research was to investigate aspects of the ecology of long-tailed bats that would influence the development of a monitoring programme. The distribution, roost selection, habitat use, and activity patterns of a long-tailed bat population that persisted in the Waitakere Ranges, Auckland, were investigated. A study of the Waitakere Ranges long-tailed bat population was significant because (1) the Waitakere Ranges is the northern most location at which long-tailed bats have been researched; (2) the study was the first to be conducted on a long-tailed bat population that persisted in kauri Agathis australis dominated forest remnants; (3) the long-tailed bat population in the Waitakere Ranges is the only known extant population in close proximity to a major urban area; and (4) the factors that are attributed to long-tailed bat population declines (i.e., forest clearance, predation and urbanisation; O'Donnell, 2000) are likely to be ongoing and intensified in the Waitakere Ranges. Twenty roosts were located. Most roosts (85%) were in kauri, 2 were in mature rimu (Dacrydium cupressinum) and 1 was in a kahikatea (Dacrycarpus dacrydioides). All roosts were in large, live, emergent trees. Mean height of roost trees was 38.4 ± 1.3 m and average DBH was 186 ± 12 cm. The entrances of six roost cavities were identified all were located in minor lateral branches in the crown of the tree and were primarily near the tip of branches. Roosts were a mean height of 24.6 ± 3.7 m above ground level. It was argued that roosts in the crowns of kauri were inaccessible to terrestrial mammalian predators. Twenty-eight roost watches were conducted. The average number of bats counted leaving roosts was 10.0 ± 1.5 (maximum = 24). Roosts were occupied by radio-tagged bats for an average of 2.0 ± 0.4 days, and 11 (55 %) were occupied for only one day. Roost size was the lowest reported for long-tailed bats. Roost switching also appeared higher than in other populations that have been studied. It was argued that morepork predation may have a significant impact on the population viability of the population. As in other studies long-tailed bats were found to forage over modified habitats including over farmland, dwellings, orchards and along streams and roads with little vehicular traffic. Long-tailed bats foraged throughout the Waitakere Ranges and their foothills. Bat activity was highly variable. Of the environmental variables analysed, temperature was found to have the greatest influence on bat activity. There were seasonal and habitat influences on bat activity. The relationship between sample sizes, variation in bat detection rates and desired statistical power using automatic bat detectors to monitor populations of bats was explored. A power analysis on activity data collected with automatic bat detectors indicated that declines in bat populations would need to be reflected in declines of greater than fifty percent in bat activity before monitoring programmes would have sufficient power to detect declines in activity. It was recommended that monitoring programmes should concentrate on intensive presence – absence surveys rather than long-term studies at a few sites.