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Repeatability for Gaussian and non-Gaussian data: a practical guide for biologists
- BIOL REV CAMB PHILOS SOC 85:935–956
, 2010
"... Repeatability (more precisely the common measure of repeatability, the intra-class correlation coefficient, ICC) is an important index for quantifying the accuracy of measurements and the constancy of phenotypes. It is the proportion of phenotypic variation that can be attributed to between-subject ..."
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Repeatability (more precisely the common measure of repeatability, the intra-class correlation coefficient, ICC) is an important index for quantifying the accuracy of measurements and the constancy of phenotypes. It is the proportion of phenotypic variation that can be attributed to between-subject (or between-group) variation. As a consequence, the non-repeatable fraction of phenotypic variation is the sum of measurement error and phenotypic flexibility. There are several ways to estimate repeatability for Gaussian data, but there are no formal agreements on how repeatability should be calculated for non-Gaussian data (e.g. binary, proportion and count data). In addition to point estimates, appropriate uncertainty estimates (standard errors and confidence intervals) and statistical significance for repeatability estimates are required regardless of the types of data. We review the methods for calculating repeatability and the associated statistics for Gaussian and non-Gaussian data. For Gaussian data, we present three common approaches for estimating repeatability: correlation-based, analysis of variance (ANOVA)-based and linear mixed-effects model (LMM)-based methods, while for non-Gaussian data, we focus on generalised linear mixed-effects models (GLMM) that allow the estimation of repeatability on the original and on the underlying latent scale. We also address a number of methods for calculating standard errors, confidence intervals and statistical significance; the most accurate and recommended methods are parametric bootstrapping, randomisation tests and Bayesian approaches. We advocate the use of LMM-
Egg size and food abundance interactively affect juvenile growth and behaviour. Funct Ecol
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The shape of things to come: woodland herb niche contraction begins during recruitment in mesic forest microhabitat.
- Proceedings of the Royal Society B,
, 2010
"... Natural abundance is shaped by the abiotic requirements and biotic interactions that shape a species' niche, yet these influences are rarely decoupled. Moreover, most plant mortality occurs during early life stages, making seed recruitment critical in structuring plant populations. We find tha ..."
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Natural abundance is shaped by the abiotic requirements and biotic interactions that shape a species' niche, yet these influences are rarely decoupled. Moreover, most plant mortality occurs during early life stages, making seed recruitment critical in structuring plant populations. We find that natural abundance of two woodland herbs, Hexastylis arifolia and Hepatica nobilis, peaks at intermediate resource levels, a pattern probably formed by concurrent abiotic and biotic interactions. To determine how this abundance patterning reflects intrinsic physiological optima and extrinsic biotic interactions, we translocate adults and seeds to novel locations across experimentally extended abiotic gradients. These experiments indicate that the plant distributions probably reflect biotic interactions as much as physiological requirements, and that adult abundance provides a poor indication of the underlying niche requirements. The positive response exhibited by adult transplants in the wettest conditions is offset by increased fungal attack on buried seeds consistent with peak natural abundance where soil moisture is intermediate. This contraction of niche space is best described by Connell's model-species are limited by physiological tolerances where resources are low and biotic interactions where resources are high.
Global quantification of contrasting leaf life span strategies for deciduous and evergreen species in response to environmental conditions.
- Global Ecology and Biogeography
, 2012
"... ABSTRACT Aim Species with deciduous and evergreen leaf habits typically differ in leaf life span (LLS). Yet quantification of the response of LLS, within each habit, to key environmental conditions is surprisingly lacking. The aim of this study is to quantify LLS strategies of the two leaf habits u ..."
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ABSTRACT Aim Species with deciduous and evergreen leaf habits typically differ in leaf life span (LLS). Yet quantification of the response of LLS, within each habit, to key environmental conditions is surprisingly lacking. The aim of this study is to quantify LLS strategies of the two leaf habits under varying temperature, moisture and nutrient conditions, using a global database. We hypothesize that deciduous LLS reflects the length of the growing season, avoiding unfavourable conditions regardless of the cause. Evergreen species adjust to unfavourable periods and amortize lower net carbon gains over several growing seasons, with increasing LLS associated with increasingly short favourable versus unfavourable season lengths. Location Global. Methods Data on LLS and environmental variables were compiled from global datasets for 189 deciduous and 506 evergreen species across 83 study locations. Individual and combined effects of measures of seasonality of temperature, water and nutrient availability on length of the growing season and on LLS were quantified using linear mixed models. The best models for predicting LLS were obtained using Akaike's information criterion (AIC) and DAIC. Results The LLS of deciduous and evergreen species showed opposite responses to changes in environmental conditions. Under unfavourable conditions, deciduous LLS decreases while evergreen LLS increases. A measure of temperature alone was the best predictor of the growing season. The LLS of deciduous species was independent of environmental conditions after expressing LLS in relation to the number of growing seasons. Evergreen species, on the other hand, adjusted to unfavourable conditions by increasing LLS up to four growing seasons. Contrary to expectations, variation in LLS was best explained solely by temperature, instead of by combined measures of temperature, moisture and nutrient availability. Shifts in the photosynthesis to respiration balance might provide a physiological explanation. Main conclusions Temperature, and not drought or nutrient availability, is the primary driver of contrasting responses of LLS for different leaf habit types.
Can catch share fisheries better track management targets? Fish Fish doi: 10.1111/j.1467–2979.2011.00429.x
, 2012
"... Methods 269 Data sources 270 Response variables and covariates 271 Types of response variables 271 ..."
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Methods 269 Data sources 270 Response variables and covariates 271 Types of response variables 271
The relationship between body mass and field metabolic rate among individual birds and mammals
- J. Anim. Ecol
, 2013
"... 1. The power-law dependence of metabolic rate on body mass has major implications at every level of ecological organization. However, the overwhelming majority of studies examin-ing this relationship have used basal or resting metabolic rates, and/or have used data consist-ing of species-averaged ma ..."
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1. The power-law dependence of metabolic rate on body mass has major implications at every level of ecological organization. However, the overwhelming majority of studies examin-ing this relationship have used basal or resting metabolic rates, and/or have used data consist-ing of species-averaged masses and metabolic rates. Field metabolic rates are more ecologically relevant and are probably more directly subject to natural selection than basal rates. Individual rates might be more important than species-average rates in determining the outcome of ecological interactions, and hence selection. 2. We here provide the first comprehensive database of published field metabolic rates and body masses of individual birds and mammals, containing measurements of 1498 animals of 133 spe-cies in 28 orders. We used linear mixed-effects models to answer questions about the body mass scaling of metabolic rate and its taxonomic universality/heterogeneity that have become classic areas of controversy. Our statistical approach allows mean scaling exponents and taxonomic heterogeneity in scaling to be analysed in a unified way while simultaneously accounting for nonindependence in the data due to shared evolutionary history of related species. 3. The mean power-law scaling exponents of metabolic rate vs. body mass relationships were
Pastoral Herding Strategies and Governmental Management Objectives: Predation Compensation as a Risk Buffering Strategy in the Saami Reindeer Husbandry
, 2011
"... # The Author(s) 2011. This article is published with open access at Springerlink.com Abstract Previously it has been found that an important risk buffering strategy in the Saami reindeer husbandry in Norway is the accumulation of large herds of reindeer as this increases long-term household viabilit ..."
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# The Author(s) 2011. This article is published with open access at Springerlink.com Abstract Previously it has been found that an important risk buffering strategy in the Saami reindeer husbandry in Norway is the accumulation of large herds of reindeer as this increases long-term household viability. Nevertheless, few studies have investigated how official policies, such as economic compensation for livestock losses, can influence pastoral strategies. This study investigated the effect of received predation compensation on individual husbandry units ’ future herd size. The main finding in this study is that predation compensation had a positive effect on husbandry units ’ future herd size. The effect of predation compensation, however, was nonlinear in some years, indicating that predation compensation had a positive effect on future herd size only up to a certain threshold whereby adding additional predation compensation had little effect on future herd size. More importantly, the effect of predation compensation was positive after controlling for reindeer density, indicating that for a given reindeer density husbandry units receiving more predation compensation performed better (measured as the size of future herds) compared to husbandry units receiving less compensation.
2010 Host–parasite coevolution: genetic variation in a virus population and the interaction with a host
- TAG Theor. Appl. Genet
, 1993
"... Hosts and their parasites are bound up in an intimate and perpetual arms race. Hosts are under selection to develop resistance towards costly parasite infections. A parasite’s fitness in turn rests entirely on it being able to overcome ..."
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Hosts and their parasites are bound up in an intimate and perpetual arms race. Hosts are under selection to develop resistance towards costly parasite infections. A parasite’s fitness in turn rests entirely on it being able to overcome
Plant functional group identity and diversity determine biotic resistance to invasion by an exotic grass
- J Ecol
, 2013
"... 1. Biotic resistance, the ability of species in a community to limit invasion, is central to our under-standing of how communities at risk of invasion assemble after disturbances, but it has yet to trans-late into guiding principles for the restoration of invasion-resistant plant communities. We com ..."
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1. Biotic resistance, the ability of species in a community to limit invasion, is central to our under-standing of how communities at risk of invasion assemble after disturbances, but it has yet to trans-late into guiding principles for the restoration of invasion-resistant plant communities. We combined experimental, functional, and modelling approaches to investigate processes of community assembly contributing to biotic resistance to an introduced lineage of Phragmites australis, a model invasive species in North America. We hypothesized that (i) functional group identity would be a good pre-dictor of biotic resistance to P. australis, while species identity effect would be redundant within functional group (ii) mixtures of species would be more invasion resistant than monocultures. 2. We classified 36 resident wetland plants into four functional groups based on eight functional traits. We conducted two competition experiments based on the additive competition design with P. australis and monocultures or mixtures of wetland plants. As an indicator of biotic resistance, we calculated a relative competition index (RCIavg) based on the average performance of P. australis in competition treatment compared with control. To explain diversity effect further, we partitioned it into selection effect and complementarity effect and tested several diversity–interaction models. 3. In monoculture treatments, RCIavg of wetland plants was significantly different among functional
Paths to statistical fluency for ecologists
- Frontiers in Ecology and the Environment 8
, 2010
"... (Article begins on next page) The Harvard community has made this article openly available. Please share how this access benefits you. Your story matters. Citation Ellison, Aaron M. and Brian Dennis. Forthcoming. Paths to statistical fluency for ecologists. Frontiers in Ecology and the ..."
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(Article begins on next page) The Harvard community has made this article openly available. Please share how this access benefits you. Your story matters. Citation Ellison, Aaron M. and Brian Dennis. Forthcoming. Paths to statistical fluency for ecologists. Frontiers in Ecology and the