ArticleEcology2025
Ecological meta-analyses often produce unwarranted results.
Article in Ecology, 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.
- Knowledge gaps and areas for synthesis in experimental studies of context-dependent predation risk.Ecology · 2026Review
- Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
Abstract
Meta-analysis (MA), a powerful tool for synthesizing reported results, is influential in ecology. While ecologists have long been well-informed on the potential problems associated with nonindependence in experimental work (e.g., pseudoreplication), they have, until recently, largely neglected this issue in MA. However, results used in MAs are likely much more similar when they come from the same locality, system, or laboratory. A simple and common form of nonindependence in MA arises when multiple data points, that is, observed effect sizes, come from the same paper. We obtained original data from 20 published MAs, reconstructed the published analyses, and then, for 14 that had not accounted for a paper effect, used three approaches to evaluate whether within-paper nonindependence was a problem. First, we found that "nonsense" explanatory variables added to the original analyses were statistically significant (p < 0.05) far more often than the expected 5% (25%-50% for four nonsense variables). For example, the number of vowels in the first author's name had a significant effect 50% of the time. Second, we found that an added dummy variable, which was randomly assigned at one of two levels, was statistically significant an average of 38% of the time, far exceeding the expected 5%. Even after including a random paper effect in the analyses, there was still an excess of significant results, suggesting that the within-paper nonindependence was more complex than modeled with the random paper effect. Third, we repeated the original MAs that did not include random paper effects (n = 14 MAs) but added a random paper effect to each revised analysis. In 12 out of the 14 MAs, an added random effect was statistically significant (indicating group nonindependence that was not accounted for in the original analyses), and often the original inferences were substantially altered. Further, incorporating random paper effects was not a sufficient solution to nonindependence. Thus, problems resulting from nonindependence are often substantial, and accounting for the problem will likely require careful consideration of the details of the potential dependence among observed effect sizes. MAs that do not properly account for this problem may reach unwarranted conclusions.
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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.