# Consumer resilience suppresses the recovery of overgrazed ecosystems

**Authors:** Nathan B. Spindel, Aaron W. E. Galloway, Julie B. Schram, Gwiisihlgaa Daniel McNeill, SG̱iids Ḵung Vanessa Bellis, Niisii Guujaaw, Jaasaljuus Yakgujanaas, Ondine Pontier, Markus Thompson, Lynn C. Lee, Daniel K. Okamoto

PMC · DOI: 10.1002/eap.70196 · 2026-03-11

## TL;DR

Sea urchins can survive in barren, overgrazed ecosystems and quickly recover when food returns, affecting ecosystem recovery.

## Contribution

The study reveals how metabolic resilience in sea urchins influences ecosystem dynamics through compensatory feeding and metabolic flexibility.

## Key findings

- Resting metabolic rates in kelp forest urchins were nearly twice those in barren urchins, but feeding rates were similar.
- Diet quality strongly affects energy conversion efficiency, with diverse, PUFA-rich diets improving nutrient assimilation.
- Starvation increases bacterial biomarkers in urchins, while algal diets enrich essential fatty acids.

## Abstract

Many heterotroph species perish when faced with severe food limitation; others can persist, adapt, and thrive. Sea urchins are emblematic of this paradox: they can overgraze kelp forests to form barren habitats, but can then survive for decades in these nutritionally depauperate seascapes. Understanding the mechanisms enabling persistence under starvation and rapid recovery when food returns provides insights into how consumer resilience shapes ecosystem dynamics. We quantified how food abundance, quality, deprivation, and reintroduction influence bioenergetic performance in the red sea urchin (Mesocentrotus franciscanus), integrating field observations of kelp forest and barren populations with a controlled feeding experiment. We measured respiration, feeding rates, gonadal growth, and fatty acid biomarkers to test how habitat history and diet jointly govern metabolic plasticity and nutrient assimilation. Resting metabolic rates (RMRs) were nearly twofold higher in kelp forest urchins than in barren conspecifics; yet, feeding rates were equivalent across habitats, indicating that metabolic depression does not constrain food intake. Reciprocal shifts emerged in the experiment: starvation reduced RMR and lipid reserves in kelp forest urchins, while feeding elevated both traits in barren urchins to levels comparable with kelp forest conspecifics. These results demonstrate rapid physiological compensation in response to both food deprivation and reintroduction. Diet quality strongly modulated performance. Urchins fed nutritionally poor monospecific diets consumed more biomass and calories than those on diverse, polyunsaturated fatty acid (PUFA)‐rich diets, but did so with markedly lower efficiency of conversion to gonadal tissue. Fatty acid assimilation revealed that starvation elevated bacterial and biofilm biomarkers in tissues, whereas algal diets enriched essential PUFA profiles, particularly when diets were diverse. These results highlight that both quantity and quality of food influence consumer recovery trajectories, with nutritional geometry shaping efficiency of energy and nutrient use. Together, our findings show that M. franciscanus exhibits pronounced metabolic resilience, allowing persistence in barren habitats and rapid reactivation of grazing and reproduction when food becomes available. This work links nutritional ecology to ecosystem feedbacks by showing how compensatory feeding and metabolic flexibility enable consumers to maintain pressure on primary producers, thereby influencing the stability, hysteresis, and recovery of degraded ecosystems.

## Linked entities

- **Species:** Mesocentrotus franciscanus (taxon 1328066)

## Full-text entities

- **Diseases:** malnutrition (MESH:D044342), nutritional deficits (MESH:D009748), Metabolic depression (MESH:D008659), FA (MESH:D008067), starvation (MESH:D013217)
- **Chemicals:** lipid (MESH:D008055), DHA (MESH:D004281), chloroform (MESH:D002725), sulfuric acid (MESH:C033158), PUFA (MESH:D005231), hexane (MESH:D006586), fatty acid methyl esters (-), helium (MESH:D006371), 16:1n-7 (MESH:C008757), FA (MESH:D005227), carbohydrates (MESH:D002241), toluene (MESH:D014050), amino acid (MESH:D000596), water (MESH:D014867), essential amino acids (MESH:D000601), oxygen (MESH:D010100), gold (MESH:D006046), NaCl (MESH:D012965), methanol (MESH:D000432), C (MESH:D002244), N (MESH:D009584)
- **Species:** PX clade (clade) [taxon 569578], Campylobacteraceae (family) [taxon 72294], Chondracanthus corymbiferus (species) [taxon 35177], Achromobacter (genus) [taxon 222], Nereocystis luetkeana (species) [taxon 117523], Mesocentrotus franciscanus (species) [taxon 1328066], Homo sapiens (human, species) [taxon 9606], Echinoidea (sea urchin, class) [taxon 7625], Paracentrotus lividus (common sea urchin, species) [taxon 7656], Ulva sp. (species) [taxon 2812607], Vibrio (genus) [taxon 662], Danthonia californica (California oat grass, species) [taxon 65975], Dilsea californica (species) [taxon 31417]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12976660/full.md

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Source: https://tomesphere.com/paper/PMC12976660