Andy Hector

Bio: Andy Hector is an academic researcher from University of Oxford. The author has contributed to research in topics: Biodiversity & Species richness. The author has an hindex of 74, co-authored 183 publications receiving 36456 citations. Previous affiliations of Andy Hector include University of Zurich & Natural Environment Research Council.

Seed mass and the competition/colonization trade-off: Competitive interactions and spatial patterns in a guild of annual plants

Abstract: Summary 1 We used neighbourhood modelling to estimate individual-level competition coefficients for seven annuals growing in limestone grassland over 2 years. We calculated the relative strength of intra- and interspecific competition and related this to differences in seed size and plant size between targets and neighbours. 2 Significant differences in the impact of neighbours on each target species were observed in half the models fitted, allowing us to reject a null hypothesis of competitive equivalence. 3 In one year we found that as the seed size or plant size of neighbours increased relative to targets, so did their competitive effect. Although this is consistent with the competition/colonization trade-off model the competitive interactions were not sufficiently asymmetric to allow coexistence. In a second year we found only weak interspecific competition and no relationship with plant or seed size. 4 We found no overall relationship between competition coefficients and the degree of segregation, contradicting the spatial segregation hypothesis for coexistence. However, segregation was linked to differences in plant traits: when targets were smaller than neighbours the degree of segregation increased with relative neighbour size. 5 Most species were positively associated with each other due to a shared preference for otherwise unvegetated patches. The degree of association was negatively correlated with differences in plant and seed size, particularly when interspecific competition was weak. This might reflect (i) decreasing overlap in microhabitat use with increasing trait divergence or (ii) density-dependent mortality. 6 Seed size is a key trait within this group of species, determining both competitive and colonizing ability. The presence of such a competition/colonization trade-off undoubtedly stabilizes community dynamics although other mechanisms may also be at work.

Biodiversity effects and transgressive overyielding

Abstract: Aims The potential for mixtures of plant species to produce more biomass than every one of their constituent species in monoculture is still controversially discussed in the literature. Here we tested how this socalled transgressive overyielding is affected by variation between and within species in monoculture yields in biodiversity experiments. Methods We use basic statistical principles to calculate expected maximum monoculture yield in a species pool used for a biodiversity experiment. Using a real example we show how between- and withinspecies variance components in monoculture yields can be obtained. Combining the two components we estimate the importance of sampling bias in transgressive overyielding analysis. Important Findings The net biodiversity effect (difference between mixture and average monoculture yield) needed to achieve transgressive overyielding increases with the number of species in a mixture and with the variation between constituent species in monoculture yields. If there is no significant variation between species, transgressive overyielding should not be calculated using the best monoculture, because in this case the difference between this species and the other species could exclusively reflect a sampling bias. The sampling bias decreases with increasing variation between species. Tests for transgressive overyielding require replicated species’ monocultures. However, it can be doubted whether such an emphasis on monocultures in biodiversity experiments is justified if an analysis of transgressive overyielding is not the major goal.

Local loss and spatial homogenization of plant diversity reduce ecosystem multifunctionality

Abstract: Biodiversity is declining in many local communities while also becoming increasingly homogenized across space. Experiments show that local plant species loss reduces ecosystem functioning and services, but the role of spatial homogenization of community composition and the potential interaction between diversity at different scales in maintaining ecosystem functioning remains unclear, especially when many functions are considered (ecosystem multifunctionality). We present an analysis of eight ecosystem functions measured in 65 grasslands worldwide. We find that more diverse grasslands—those with both species-rich local communities (α-diversity) and large compositional differences among localities (β-diversity)—had higher levels of multifunctionality. Moreover, α- and β-diversity synergistically affected multifunctionality, with higher levels of diversity at one scale amplifying the contribution to ecological functions at the other scale. The identity of species influencing ecosystem functioning differed among functions and across local communities, explaining why more diverse grasslands maintained greater functionality when more functions and localities were considered. These results were robust to variation in environmental drivers. Our findings reveal that plant diversity, at both local and landscape scales, contributes to the maintenance of multiple ecosystem services provided by grasslands. Preserving ecosystem functioning therefore requires conservation of biodiversity both within and among ecological communities.

Biodiversity effects on ecosystem functioning change along environmental stress gradients

Abstract: Positive relationship between biodiversity and ecosystem functioning has been observed in many studies, but how this relationship is affected by environmental stress is largely unknown. To explore this influence, we measured the biomass of microalgae grown in microcosms along two stress gradients, heat and salinity, and compared our results with 13 published case studies that measured biodiversity-ecosystem functioning relationships under varying environmental conditions. We found that positive effects of biodiversity on ecosystem functioning decreased with increasing stress intensity in absolute terms. However, in relative terms, increasing stress had a stronger negative effect on low-diversity communities. This shows that more diverse biotic communities are functionally less susceptible to environmental stress, emphasises the need to maintain high levels of biodiversity as an insurance against impacts of changing environmental conditions and sets the stage for exploring the mechanisms underlying biodiversity effects in stressed ecosystems.

Analysis of variance with unbalanced data: an update for ecology & evolution

Abstract: 1. Factorial analysis of variance (anova) with unbalanced (non-orthogonal) data is a commonplace but controversial and poorly understood topic in applied statistics. 2. We explain that anova calculates the sum of squares for each term in the model formula sequentially (type I sums of squares) and show how anova tables of adjusted sums of squares are composite tables assembled from multiple sequential analyses. A different anova is performed for each explanatory variable or interaction so that each term is placed last in the model formula in turn and adjusted for the others. 3. The sum of squares for each term in the analysis can be calculated after adjusting only for the main effects of other explanatory variables (type II sums of squares) or, controversially, for both main effects and interactions (type III sums of squares). 4. We summarize the main recent developments and emphasize the shift away from the search for the 'right' anova table in favour of presenting one or more models that best suit the objectives of the analysis.

The Theory of Island Biogeography

Abstract: Preface to the Princeton Landmarks in Biology Edition vii Preface xi Symbols Used xiii 1. The Importance of Islands 3 2. Area and Number of Speicies 8 3. Further Explanations of the Area-Diversity Pattern 19 4. The Strategy of Colonization 68 5. Invasibility and the Variable Niche 94 6. Stepping Stones and Biotic Exchange 123 7. Evolutionary Changes Following Colonization 145 8. Prospect 181 Glossary 185 References 193 Index 201

Human biochemical genetics

Abstract: So far in this course we have dealt entirely with the evolution of characters that are controlled by simple Mendelian inheritance at a single locus. There are notes on the course website about gametic disequilibrium and how allele frequencies change at two loci simultaneously, but we didn’t discuss them. In every example we’ve considered we’ve imagined that we could understand something about evolution by examining the evolution of a single gene. That’s the domain of classical population genetics. For the next few weeks we’re going to be exploring a field that’s actually older than classical population genetics, although the approach we’ll be taking to it involves the use of population genetic machinery. If you know a little about the history of evolutionary biology, you may know that after the rediscovery of Mendel’s work in 1900 there was a heated debate between the “biometricians” (e.g., Galton and Pearson) and the “Mendelians” (e.g., de Vries, Correns, Bateson, and Morgan). Biometricians asserted that the really important variation in evolution didn’t follow Mendelian rules. Height, weight, skin color, and similar traits seemed to

A safe operating space for humanity

Abstract: Identifying and quantifying planetary boundaries that must not be transgressed could help prevent human activities from causing unacceptable environmental change, argue Johan Rockstrom and colleagues.

Planetary boundaries: Guiding human development on a changing planet

Abstract: The planetary boundaries framework defines a safe operating space for humanity based on the intrinsic biophysical processes that regulate the stability of the Earth system. Here, we revise and update the planetary boundary framework, with a focus on the underpinning biophysical science, based on targeted input from expert research communities and on more general scientific advances over the past 5 years. Several of the boundaries now have a two-tier approach, reflecting the importance of cross-scale interactions and the regional-level heterogeneity of the processes that underpin the boundaries. Two core boundaries—climate change and biosphere integrity—have been identified, each of which has the potential on its own to drive the Earth system into a new state should they be substantially and persistently transgressed.

Effects of biodiversity on ecosystem functioning: a consensus of current knowledge

Abstract: Humans are altering the composition of biological communities through a variety of activities that increase rates of species invasions and species extinctions, at all scales, from local to global. These changes in components of the Earth's biodiversity cause concern for ethical and aesthetic reasons, but they also have a strong potential to alter ecosystem properties and the goods and services they provide to humanity. Ecological experiments, observations, and theoretical developments show that ecosystem properties depend greatly on biodiversity in terms of the functional characteristics of organisms present in the ecosystem and the distribution and abundance of those organisms over space and time. Species effects act in concert with the effects of climate, resource availability, and disturbance regimes in influencing ecosystem properties. Human activities can modify all of the above factors; here we focus on modification of these biotic controls. The scientific community has come to a broad consensus on many aspects of the re- lationship between biodiversity and ecosystem functioning, including many points relevant to management of ecosystems. Further progress will require integration of knowledge about biotic and abiotic controls on ecosystem properties, how ecological communities are struc- tured, and the forces driving species extinctions and invasions. To strengthen links to policy and management, we also need to integrate our ecological knowledge with understanding of the social and economic constraints of potential management practices. Understanding this complexity, while taking strong steps to minimize current losses of species, is necessary for responsible management of Earth's ecosystems and the diverse biota they contain.