ArticleGlobal change biology2025
Location-Scale Meta-Analysis and Meta-Regression as a Tool to Capture Large-Scale Changes in Biological and Methodological Heterogeneity: A Spotlight on Heteroscedasticity.
Article in Global change biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
2 citing papers in PubMed.
- A New Effect Size for Meta-Analysis of Magnitude: lnM.Ecology letters · 2026Article
- Location-scale models and cross validation to advance quantitative evidence synthesis.Ecology · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors.
Funding
Abstract
Heterogeneity is a defining feature of ecological and evolutionary meta-analyses. While conventional meta-analysis and meta-regression methods acknowledge heterogeneity in effect sizes, they typically assume this heterogeneity is constant across studies and levels of moderators (i.e., homoscedasticity). This assumption could mask potentially informative patterns in the data. Here, we introduce and develop a location-scale meta-analysis and meta-regression framework that models both the mean (location) and variance (scale) of effect sizes. Such a framework explicitly accommodates heteroscedasticity (differences in variance), thereby revealing when and why heterogeneity itself changes. This capability, we argue, is crucial for understanding responses to global environmental change, where complex, context-dependent processes may shape both the average magnitude and the variability of biological responses. For example, differences in study design, measurement protocols, environmental factors, or even evolutionary history can lead to systematic shifts in variance. By incorporating hierarchical (multilevel) structures and phylogenetic relationships, location-scale models can disentangle the contributions from different levels to both location and scale parts. We further attempt to extend the concepts of relative heterogeneity and publication bias into the scale part of meta-regression. With these methodological advances, we can identify patterns and processes that remain obscured under the constant variance assumption, thereby enhancing the biological interpretability and practical relevance of meta-analytic results. Notably, almost all published ecological and evolutionary meta-analytic data can be re-analysed using our proposed analytic framework to gain new insights. Altogether, location-scale meta-analysis and meta-regression provide a rich and holistic lens through which to view and interpret the intricate tapestry woven with ecological and evolutionary data. The proposed approach, thus, ultimately leads to more informed and context-specific conclusions about environmental changes and their impacts.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.