ReviewEcology letters2025
Harnessing Nutritional Niches to Explore Fungus-Animal Symbioses.
Review in Ecology letters, 2025. 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.
- Harnessing Nutritional Niches to Explore Fungus-Animal Symbioses.Ecology letters · 2025Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
Abstract
Fungus-animal symbioses have evolved countless times across the tree of life. While the stability of these mutualistic or parasitic interkingdom interactions often depends on optimised nutrient exchange, we lack a framework to explore whether animal-derived nutrients are optimal for fungal symbionts. This conceptual gap has constrained studies about the ecological success and evolutionary stability of fungus-animal symbioses. We use Nutritional Geometry (NG) to harness nutritional niche theory and identify the crucial nutritional niche dimensions of fungi that mediate symbiotic stability. We hypothesise that these fungal nutritional niche dimensions are governed by symbiotic role (mutualist vs. pathogen), degree of animal host control over nutritional competition (monoculture vs. polyculture), and breadth of host associations (specialist vs. generalist). We explore the promise of integrating NG with advanced imaging and -omics approaches to test coevolutionary hypotheses at precise microscales where fungus and animal cells trade nutrients. We conclude that niche-based theory can advance studies of coevolutionary dynamics from arms races to the emergence of economically important pathogens.
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Registered trials
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