ArticleEcology2026
Location-scale models and cross validation to advance quantitative evidence synthesis.
Article in Ecology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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
1 citing paper in PubMed.
Corrections and comments
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Authors and funding
1 author.
Funding
Abstract
Quantitative evidence synthesis is a prominent path towards generality in ecology. Generality is typically discussed in terms of central tendencies, such as an average effect across a compilation of studies, and the role of heterogeneity for assessing generality is less well developed. Heterogeneity examines the transferability of ecological effects across contexts, though between-study variance is typically assumed as constant (i.e., homoscedastic). Here, I use two case studies to show how location-scale models that relax the assumption of homoscedasticity and cross validation can combine to further the goals of evidence syntheses. First, I examine scale-dependent heterogeneity for a meta-analysis of plant native-exotic species richness relationships, quantifying the relationships among unexplained effect size variation, spatial grain and extent. Second, I examine relationships among habitat fragment size, study-level covariates and unexplained variation in patch-scale species richness using a database of fragmentation studies. Heteroscedastic models quantify where effects can be transferred with more or less certainty and provide new descriptions of transferability for both case studies. Cross validation can be applied to a single or multiple models, adapted to either the goal of assessing intervention efficacy or generalization and, for the case studies examined here, showed that assuming homoscedasticity limits transferability.
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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.