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Robert B. Allen

Bio: Robert B. Allen is an academic researcher from Landcare Research. The author has contributed to research in topics: Beech & Population. The author has an hindex of 47, co-authored 113 publications receiving 7172 citations. Previous affiliations of Robert B. Allen include Forest Research Institute & University of Cambridge.
Topics: Beech, Population, Ecosystem, Nothofagus, Canopy


Papers
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Journal ArticleDOI
TL;DR: Using wood-decaying fungi as a model system, direct manipulation of early immigration history resulted in three-fold differences in fungal species richness and composition and differences of the same magnitude in the rate of decomposition and carbon release from wood.
Abstract: Community assembly history is increasingly recognized as a fundamental determinant of community structure. However, little is known as to how assembly history may affect ecosystem functioning via its effect on community structure. Using wood-decaying fungi as a model system, we provide experimental evidence that large differences in ecosystem functioning can be caused by small differences in species immigration history during community assembly. Direct manipulation of early immigration history resulted in three-fold differences in fungal species richness and composition and, as a consequence, differences of the same magnitude in the rate of decomposition and carbon release from wood. These effects - which were attributable to the history-dependent outcome of competitive and facilitative interactions - were significant across a range of nitrogen availabilities observed in natural forests. Our results highlight the importance of considering assembly history in explaining ecosystem functioning.

528 citations

Journal ArticleDOI
TL;DR: This study is the first to build the effects of competition and environment into Enquist's model of tree growth, and shows that competitive interactions alter the scaling of mean growth rate with size, whereas altitude does not influence the scaled of potential growth rates with size.
Abstract: Summary 1 Understanding the factors influencing tree growth is central to forest ecology because of the significance of growth to forest structure and biomass. One of the simplest, yet most controversial growth models, proposed by Enquist and colleagues, predicts that stem-diameter growth scales as the one-third power of stem diameter. Recent analyses of large-scale data sets have challenged the generality of this theory and highlighted the influence of resource competition on the scaling of growth with size. 2Here we explore the factors regulating the diameter growth of 3334 trees of mountain beech (Nothofagus solandri var. cliffortioides) growing in natural single-species forests in New Zealand. Maximum-likelihood modelling was used to quantify the influences of tree size, altitude, the basal area of taller neighbours (BL) and the basal area of all neighbours (BT) on growth. Our interpretation of the models assumed that taller neighbours compete for light whereas all neighbours compete for nutrients. 3The regression analyses indicate that competition for light has a strong influence on the growth of small trees, whereas competition for nutrients affects trees of all sizes. These findings are consistent with experimental manipulation studies showing that competition for light and nutrients inhibits the growth of small mountain beech trees, and fertilizer application studies showing that nitrogen limits the growth of large trees. 4Tree growth declined with altitude. The regression analyses suggest that the intensity of light competition also declines with altitude, when trees with similar BT and BL values were compared along the gradient. These results are consistent with observations that trees become stunted and have more open canopies at high altitudes. 5Our study is the first to build the effects of competition and environment into Enquist's model of tree growth. We show that competitive interactions alter the scaling of mean growth rate with size, whereas altitude does not influence the scaling of potential growth rate with size.

378 citations

Journal ArticleDOI
TL;DR: There was evidence that P limitation and retrogressive forests developed on old soils, but N limitation on very young soils was not apparent because of inputs from an abundant N-fixing shrub.
Abstract: The aim of this study was to examine how shifts in soil nutrient availability along a soil chronosequence affected temperate rainforest vegetation. Soil nutrient availability, woody plant diversity, composition and structure, and woody species leaf and litter nutrient concentrations were quantified along the sequence through ecosystem progression and retrogression. In this super-wet, high leaching environment, the chronosequence exhibited rapid soil development and decline within 120000 years. There were strong gradients of soil pH, N, P and C, and these had a profound effect on vegetation. N:P(leaf) increased along the chronosequence as vegetation shifted from being N- to P- limited. However, high N:P(leaf) ratios, which indicate P-limitation, were obtained on soils with both high and low soil P availability. This was because the high N-inputs from an N-fixing shrub caused vegetation to be P-limited in spite of high soil P availability. Woody species nutrient resorption increased with site age, as availability of N and P declined. Soil P declined 8-fold along the sequence and P resorption proficiency decreased from 0.07 to 0.01%, correspondingly. N resorption proficiency decreased from 1.54 to 0.26%, corresponding to shifts in mineralisable N. Woody plant species richness, vegetation cover and tree height increased through ecosystem progression and then declined. During retrogression, the forest became shorter, more open and less diverse, and there were compositional shifts towards stress-tolerant species. Conifers (of the Podocarpaceae) were the only group to increase in richness along the sequence. Conifers maintained a lower N:P(leaf) than other groups, suggesting superior acquisition of P on poor soils. In conclusion, there was evidence that P limitation and retrogressive forests developed on old soils, but N limitation on very young soils was not apparent because of inputs from an abundant N-fixing shrub.

340 citations

Journal ArticleDOI
01 May 2002-Ecology
TL;DR: High intra- and intergeneric synchrony is demonstrated in mast seeding by 17 species of New Zealand plants from four families across >150 000 km2, and synchronous fruiting by these species was associated with anomalously high temperatures the summer before seedfall, a cue linked with the La Nina phase of ...
Abstract: Masting, the intermittent production of large flower or seed crops by a population of perennial plants, can enhance the reproductive success of participating plants and drive fluctuations in seed-consumer populations and other ecosystem components over large geographic areas. The spatial and taxonomic extent over which masting is synchronized can determine its success in enhancing individual plant fitness as well as its ecosystem-level effects, and it can indicate the types of proximal cues that enable reproductive synchrony. Here, we demonstrate high intra- and intergeneric synchrony in mast seeding by 17 species of New Zealand plants from four families across >150 000 km2. The synchronous species vary ecologically (pollination and dispersal modes) and are geographically widely separated, so intergeneric synchrony seems unlikely to be adaptive per se. Synchronous fruiting by these species was associated with anomalously high temperatures the summer before seedfall, a cue linked with the La Nina phase of ...

295 citations

Journal ArticleDOI
TL;DR: In this paper, the authors used the shifting mosaic of patches model to explore the ways in which competitive thinning and disturbance influence tree-size distributions, and to consider the effects of temporal variability in disturbance frequency on the size structure of forests.
Abstract: Summary 1Tree-size distributions are changing in many natural forests around the world, and it is important to understand the underlying processes that are causing these changes. Here we use a classic conceptual framework – the shifting mosaic of patches model – to explore the ways in which competitive thinning and disturbance influence tree-size distributions, and to consider the effects of temporal variability in disturbance frequency on the size structure of forests. 2We monitored 250 stands of Nothofagus solandri var. cliffortiodes (mountain beech), randomly distributed over 9000 hectares, for 19 years. Mountain beech is a light-demanding species that forms monospecific forests in New Zealand mountains. For the purposes of our model, we assumed that each stand functions as an even-aged population: it is initiated by a pulse of recruitment, undergoes competitive thinning as it matures, and is eventually destroyed by a disturbance event. The tree-size distribution of the whole forest is driven partly by the frequency and temporal patchiness of disturbance events and partly by competitive processes within the constituent stands. 3Temporal changes in stem density and mean tree size were observed to be remarkably similar in all young stands, indicating that a consistent packing rule operates during this phase of stand development. A popular idea in the self-thinning literature is that the maintenance of constant leaf area index (LAI) provides the mechanism for this packing rule, but our analyses suggest that LAI increased by about 30% during the thinning phase. We use leaf economic theory to develop a new packing rule based on light interception, and argue that LAI increases with stand age because of changes in canopy organisation. 4Smaller trees were significantly more likely to die than larger trees within the young stands. Tree-diameter distributions within young stands were left skewed but those of older populations were normally distributed. These observations are consistent with asymmetric competition winnowing out small, suppressed trees from young stands but having less effect in older stands. 5Large-scale disturbances created gaps of sufficient size to allow mass recruitment of seedlings in about 0.8% of stands each year. Older stands were most susceptible to such large-scale disturbance, but the trend was weak. 6The diameter-distribution of the whole Nothofagus forest was found to be approximately exponential in form. Simulation models only produced realistic diameter distributions when competitive packing rules and disturbance were included. Therefore, the shifting mosaic model provides a general framework for understand the ways in which these mortality processes determine forest size structure. 7The diameter distribution of the forest was not in equilibrium over the 19-year study. Using simulation models, we show that temporal variability in disturbance frequency can generate enormous deviations in tree-diameter distributions away from the long-term mean, leading us to conclude that modern-day disequilibrium in natural forests may be the legacy of past disturbance events.

266 citations


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Book
21 Mar 2002
TL;DR: An essential textbook for any student or researcher in biology needing to design experiments, sample programs or analyse the resulting data is as discussed by the authors, covering both classical and Bayesian philosophies, before advancing to the analysis of linear and generalized linear models Topics covered include linear and logistic regression, simple and complex ANOVA models (for factorial, nested, block, split-plot and repeated measures and covariance designs), and log-linear models Multivariate techniques, including classification and ordination, are then introduced.
Abstract: An essential textbook for any student or researcher in biology needing to design experiments, sample programs or analyse the resulting data The text begins with a revision of estimation and hypothesis testing methods, covering both classical and Bayesian philosophies, before advancing to the analysis of linear and generalized linear models Topics covered include linear and logistic regression, simple and complex ANOVA models (for factorial, nested, block, split-plot and repeated measures and covariance designs), and log-linear models Multivariate techniques, including classification and ordination, are then introduced Special emphasis is placed on checking assumptions, exploratory data analysis and presentation of results The main analyses are illustrated with many examples from published papers and there is an extensive reference list to both the statistical and biological literature The book is supported by a website that provides all data sets, questions for each chapter and links to software

9,509 citations

Journal ArticleDOI
TL;DR: A new and simple method to find indicator species and species assemblages characterizing groups of sites, and a new way to present species-site tables, accounting for the hierarchical relationships among species, is proposed.
Abstract: This paper presents a new and simple method to find indicator species and species assemblages characterizing groups of sites The novelty of our approach lies in the way we combine a species relative abundance with its relative frequency of occurrence in the various groups of sites This index is maximum when all individuals of a species are found in a single group of sites and when the species occurs in all sites of that group; it is a symmetric indicator The statistical significance of the species indicator values is evaluated using a randomization procedure Contrary to TWINSPAN, our indicator index for a given species is independent of the other species relative abundances, and there is no need to use pseudospecies The new method identifies indicator species for typologies of species releves obtained by any hierarchical or nonhierarchical classification procedure; its use is independent of the classification method Because indicator species give ecological meaning to groups of sites, this method provides criteria to compare typologies, to identify where to stop dividing clusters into subsets, and to point out the main levels in a hierarchical classification of sites Species can be grouped on the basis of their indicator values for each clustering level, the heterogeneous nature of species assemblages observed in any one site being well preserved Such assemblages are usually a mixture of eurytopic (higher level) and stenotopic species (characteristic of lower level clusters) The species assemblage approach demonstrates the importance of the ''sampled patch size,'' ie, the diversity of sampled ecological combinations, when we compare the frequencies of core and satellite species A new way to present species-site tables, accounting for the hierarchical relationships among species, is proposed A large data set of carabid beetle distributions in open habitats of Belgium is used as a case study to illustrate the new method

7,449 citations

01 Jan 2016
TL;DR: The modern applied statistics with s is universally compatible with any devices to read, and is available in the digital library an online access to it is set as public so you can download it instantly.
Abstract: Thank you very much for downloading modern applied statistics with s. As you may know, people have search hundreds times for their favorite readings like this modern applied statistics with s, but end up in harmful downloads. Rather than reading a good book with a cup of coffee in the afternoon, instead they cope with some harmful virus inside their laptop. modern applied statistics with s is available in our digital library an online access to it is set as public so you can download it instantly. Our digital library saves in multiple countries, allowing you to get the most less latency time to download any of our books like this one. Kindly say, the modern applied statistics with s is universally compatible with any devices to read.

5,249 citations

Journal ArticleDOI
TL;DR: A review of the literature reveals a significant number of early studies on biochar-type materials as soil amendments either for managing pathogens, as inoculant carriers or for manipulative experiments to sorb signaling compounds or toxins as mentioned in this paper.
Abstract: Soil amendment with biochar is evaluated globally as a means to improve soil fertility and to mitigate climate change. However, the effects of biochar on soil biota have received much less attention than its effects on soil chemical properties. A review of the literature reveals a significant number of early studies on biochar-type materials as soil amendments either for managing pathogens, as inoculant carriers or for manipulative experiments to sorb signaling compounds or toxins. However, no studies exist in the soil biologyliterature that recognize the observed largevariations ofbiochar physico-chemical properties. This shortcoming has hampered insight into mechanisms by which biochar influences soil microorganisms, fauna and plant roots. Additional factors limiting meaningful interpretation of many datasets are the clearly demonstrated sorption properties that interfere with standard extraction procedures for soil microbial biomass or enzyme assays, and the confounding effects of varying amounts of minerals. In most studies, microbial biomass has been found to increase as a result of biochar additions, with significant changes in microbial community composition and enzyme activities that may explain biogeochemical effects of biochar on element cycles, plant pathogens, and crop growth. Yet, very little is known about the mechanisms through which biochar affects microbial abundance and community composition. The effects of biochar on soil fauna are even less understood than its effects on microorganisms, apart from several notable studies on earthworms. It is clear, however, that sorption phenomena, pH and physical properties of biochars such as pore structure, surface area and mineral matter play important roles in determining how different biochars affect soil biota. Observations on microbial dynamics lead to the conclusion of a possible improved resource use due to co-location of various resources in and around biochars. Sorption and therebyinactivation of growth-inhibiting substances likelyplaysa rolefor increased abundance of soil biota. No evidence exists so far for direct negative effects of biochars on plant roots. Occasionally observed decreases in abundance of mycorrhizal fungi are likely caused by concomitant increases in nutrient availability,reducing theneedfor symbionts.Inthe shortterm,therelease ofavarietyoforganic molecules from fresh biochar may in some cases be responsible for increases or decreases in abundance and activity of soil biota. A road map for future biochar research must include a systematic appreciation of different biochar-types and basic manipulative experiments that unambiguously identify the interactions between biochar and soil biota.

3,612 citations