MétaCan
Menu
Retour à la cohorte
Enregistrement W4414750653 · doi:10.3389/fmars.2025.1702410

Editorial: Impacts of climate change on seaweeds

2025· article· en· W4414750653 sur OpenAlexaboutno aff
Christopher E. Cornwall, Denisa M. Berbece, Caitlin O. Blain, Maggie D. Johnson, Samuel Starko

Notice bibliographique

RevueFrontiers in Marine Science · 2025
Typearticle
Langueen
DomaineEarth and Planetary Sciences
ThématiqueMarine and coastal plant biology
Établissements canadiensnon disponible
Organismes subventionnairesTertiary Education CommissionOcean FoundationForest Foundation
Mots-clésClimate changeEcosystemEffects of global warming on oceansOcean acidificationMarine ecosystemGlobal warmingEffects of global warmingSedimentation

Résumé

récupéré en direct d'OpenAlex

Climate change is drastically altering the composition and abundance of seaweed-dominated ecosystems throughout our oceans. Ocean warming and associated intensifying marine heatwaves (Wernberg et al., 2016; Bunting et al., 2024; Trautmann et al., 2024; Gendall et al., 2025; Khen et al., 2025), ocean acidification (Koch et al., 2013; Comeau and Cornwall, 2016), and deoxygenation (Altieri et al., 2021) can all impact the physiology of seaweeds and the ecological roles that they play. Ocean warming can cause long-term shifts in the ranges of seaweed species, usually in the form of range retractions at warm edges and expansions at cool edges (Straub et al., 2016). Marine heatwaves can elicit acute heat stress in seaweeds, drive subsequent mortality, and result in phase shifts from one ecosystem type to another (Wernberg et al., 2016; Wernberg et al., 2024). Ocean acidification causes the slow transformation of ecosystems from those dominated by coralline algal substrate to those characterised by a variety of turfing seaweeds or microalgae (Cornwall et al., 2024). Increasing intensity of ocean deoxygenation and frequency of acute localized events will likely exacerbate the effects of localized threats, but the effects of deoxygenation on seaweed communities remain poorly understood compared to other climate change-linked stressors (Altieri et al., 2021). Additionally, increased sedimentation caused by land use changes and increased storm frequencies brought on by climate change (termed 'coastal darkening'), is also an important stressor of seaweed communities (Blain et al., 2021). Increased sedimentation can interact with other stressors (e.g., temperature) or act on its own to alter the composition and function of seaweed-dominated ecosystems (Wernberg et al., 2024). To better predict and project how seaweed-dominated ecosystems will fare in the future, we require extensive further evidence regarding how the effects of climate change will manifest on seaweeds of all types across temperate, tropical, and polar regions. Ocean warming is likely to have extensive impacts on the physiology and ecology of seaweeds. Trautmann et al. (2024) examine the impacts of ocean warming on the kelp Laminaria digitata in the Arctic during the winter months. They test the hypothesis that ocean warming during the Polar Night would reduce survivability due to increased metabolism and resource consumption under a period of complete darkness. They found a reduction in energy stores, an increase in metabolic rates, and a decline in various biochemical compounds under winter warming. Despite a reduction in physiological health, specimens that underwent warming remained in relatively healthy condition, indicating that winter warming may not necessarily cause a significant decline in L. digitata populations in the High Arctic, at least in the near future. Wu et al. (2024) investigated the combined effects of ocean warming and eutrophication on the competition dynamics between two bloom-forming seaweed species, Ulva prolifera (green tide) and Sargassum horneri (golden tide). The results show that while both seaweeds thrive with increasing temperatures and nutrients up to 25°C, both had rapid declines in growth, pigment concentration, and photosynthetic activity at 30°C. Furthermore, under eutrophic conditions, Ulva prolifera outcompeted Sargassum horneri, particularly at higher temperatures. Collectively, these results suggest that ocean warming and eutrophication, associated with climate change, will facilitate the dominance of green tide blooms. Zhang et al. (2024) assessed the photosynthetic, growth response of the rhodophyte Gracilariopsis lemaneiformis when exposed to four different nutrient conditions (full factorial high and low N and P) and two temperatures (20 and 23°C). They found photosynthetic and growth rates of this species generally only increased by higher levels of both nutrients (N+P), but that there were minimal effects of temperature. Bunting et al. (2024) assessed how marine heatwaves of differing intensities and durations impacted sporophytes of the giant kelp Macrocystis pyrifera in a laboratory experiment in Aotearoa New Zealand. They find that increasing both the duration (from 3 to 6 weeks) and intensity (from 18°C to 20 or 22°C) of marine heatwaves act to reduce the growth of M. pyrifera. Moreover, temperatures over 22°C were found to have particularly strong negative impacts on growth, as this was the only temperature treatment to cause mortality, especially in the 6-week duration treatment. This indicates marine heatwaves above 20°C will be especially problematic for this species in situ. Understanding the drivers of kelp forest stability under ocean warming requires long-term, spatially explicit datasets. Multiple papers in this Research Topic develop such datasets using satellite-based remote sensing and uncover patterns of change in kelp forests across Western Canada. Despite its extensive ~26,000 km coastline, the trajectories of Western Canada's kelp forests have remained largely unexplored until recently, even with clear evidence of localised climate impacts (Schroeder et al., 2020; Watson et al., 2021; Mora-Soto et al., 2024; Starko et al., 2024; Wernberg et al., 2024). Gendall et al. (2025) combined archival charts with satellite imagery to reveal century-scale changes in Macrocystis forests of Haida Gwaii, including a persistent loss in the early 1970s likely driven by ocean warming. This is one of the earliest examples of climate-driven kelp loss globally (Wernberg et al., 2024). These declines were isolated to the warmest parts of the region, with nearby areas remaining stable. Mora-Soto et al. (2024) extend this perspective to bull kelp (Nereocystis luetkeana) in the Salish Sea, demonstrating that recent warming caused major kelp losses in the warmer, inner parts of the region. Notably, these declines occurred during the 2014–2016 marine heatwave, which had extensive impacts on kelp along the west coast of North America (Starko et al., 2025). However, cooler areas were much more stable and did not experience these same declines, similar to the findings of Gendall et al. (2025). Finally, Man et al. (2025) focus on kelp forest dynamics in the Broughton Archipelago and report high persistence of canopy kelps from 1984–2023, suggesting this cool region may serve as a climate refuge. Khen et al. (2025) assessed 11 years of benthic seaweed cover on the coral reefs of Palmyra Atoll in the tropical central Pacific. In addition to identifying that seaweed communities were dominated by calcareous taxa on the fore reef and by fleshy taxa on the reef terrace, they also found that marine heatwaves associated with El Niño years (2009, 2015) dramatically altered seaweed abundances. Fleshy seaweed tended to dominate reef communities after these periods of warming, while calcifying green seaweeds in the genus Halimeda declined. Palmyra Atoll's relatively pristine reefs, provide an opportunity to understand long-term patterns in seaweed community dynamics in the absence of direct local human impacts. Climate change will not only impact seaweed ecology, but also impact their utility in aquaculture. Veenhof et al. (2024) provide a summary of climate change related challenges to this industry, contrasted by the various opportunities that seaweed aquaculture presents to enhance ecosystem resilience. The primary challenges experienced are those caused by changes to physical factors (such as ocean warming and acidification), an increase in extreme weather events, and a heightened prevalence of disease and herbivory (particularly by invasive species). To overcome these challenges, Veenhof et al. present the following recommendations: a) selection of restoration and aquaculture sites that balance climate change impacts and species responses; b) utilising genetic advancements to inform selective breeding and hybridization, microbiome manipulation, and priming strategies; and c) progressing aquaculture towards approaches that maximize both restoration and cultivation. Lui et al. 2025 examines challenges in Neopyropia yezoensis (laver) cultivation in Jiangsu Province, China, focusing on the challenges it faces due to climate change. Warming sea temperatures, extreme weather, and high-density cultivation lead to crop failures, diseases, intra-specific competition and economic losses. The paper proposes strategies for sustainable, climate-resilient development, such as cultivating heat-resistant alternatives like N. haitanensis, relocating cultivation to cooler regions, integrating multi-trophic aquaculture systems (IMTA), and aligning the industry with carbon credit markets to improve future ecological and economic outcomes. These measures aim to ensure long-term productivity while mitigating environmental impacts. Collectively, these studies emphasise the importance of local environmental conditions in mediating seaweed responses to ocean warming (Figure 1). This underscores the need for locally tailored conservation and management strategies to protect these vital ecosystems. Local variability in temperature extremes, ocean acidification, nutrient concentrations, and seasonality will all influence the response of seaweeds to ocean warming and marine heatwaves. This editorial highlights an urgent need for more experimental and observational work that tests the role of multiple environmental drivers on seaweed ecology and physiology. Figure 1: Impacts of climate change on seaweed ecosystems reviewed in this Research Topic. Importantly, ocean warming and marine heatwaves will have large consequences for kelp forest and coral/seaweed ecosystems, as well as seaweed aquaculture. The effects of temperature will also be highly modified by local contexts and drivers, such as nutrient and sediment levels. Marine heat waves and warming Eutrophication Extreme weather Impacts of Climate Change on Seaweed communities Kelp Forests Coral/seaweed communities Seaweed aquaculture Disease and herbivory Coastal darkening +CO2 Ocean acidification Baseline/healthy seaweed systems Kelp Forests Coral/seaweed communities Seaweed aquaculture Climate impacted seaweed systems Growth Distribution Seaweed dominance Quality and growth

Récupéré en direct depuis OpenAlex et désinversé. Les résumés ne sont pas conservés dans cette base de données : les index inversés représentent 8,6 Go des 9,3 Go de texte de la base, et le serveur dispose de 13 Go libres.

Comment cette classification a été obtenuedéplier

Prédiction machine sur la base complète

Imitation des enseignants

Ni prévalence calibrée, ni vérité terrain. Validation humaine à venir. Le volet Gemma est une étiquette directe du modèle pour chaque travail de la base, lue sur la notice réduite au titre. Le volet Codex est un classifieur appris des 10 348 étiquettes directes de Codex et calibré sur les taux pondérés de l'échantillon; les champs sans appui suffisant ne portent aucun appel Codex. Le mode candidate est l'union des deux volets; le consensus est leur intersection. Ces sorties portent le statut machine_predicted_unvalidated et ne sont pas des étiquettes humaines.

score de la tête « metaresearch » (Codex)0,003
score de la tête « metaresearch » (Gemma)0,014
Version: metacan-v3-hybrid-931329e0061cStatut de validation: machine_predicted_unvalidated
Catégories candidatesaucune
Catégories consensuellesaucune
DomaineSignal candidat: aucune · Signal consensuel: aucune
Devis d'étudeSignal candidat: Sans objet · Signal consensuel: Sans objet
GenreSignal candidat: Éditorial · Signal consensuel: Éditorial
Score de désaccord entre enseignants0,041
Score d'incertitude au seuil0,137

Scores du classifieur distillé par catégorie (deux têtes)

CatégorieCodexGemma
Métarecherche0,0030,014
Méta-épidémiologie (sens strict)0,0030,001
Méta-épidémiologie (sens large)0,0030,003
Bibliométrie0,0030,001
Études des sciences et des technologies0,0020,002
Communication savante0,0060,004
Science ouverte0,0030,001
Intégrité de la recherche0,0110,011
Charge utile insuffisante (le modèle a refusé de juger)0,0410,028

Scores machine (provisoires)

Les deux têtes enseignantes du modèle étudiant, lues sur ce travail. Un score ordonne la base pour la relecture; il n'affirme jamais une catégorie, et le statut de validation accompagne chaque rangée tel quel.

Scores de référence d'un modèle non mature (critères de maturité non atteints, 7 itérations). Un score ordonne; il n'affirme jamais une catégorie.

Tête enseignante Opus0,008
Tête enseignante GPT0,224
Écart entre enseignants0,216 · la distance entre les deux têtes enseignantes sur ce seul travail
Statut de validationscore_only:v0-immature-baseline · tel quel depuis la passe de notation : score_only signifie que le nombre peut ordonner les travaux, et qu'aucune étiquette de catégorie n'en découle

Classification

machine, non validée

Prédiction automatique; un appel candidat d’une seule source (Gemma direct ou Codex distillé), pas un consensus.

Les modèles n’ont appliqué aucune catégorie : rien dans la taxonomie ne correspondait à ce travail.
Devis d'étudeSans objet
Domainenon disponible
GenreÉditorial

Le détail, modèle par modèle et score par score, se trouve en fin de page sous « Comment cette classification a été obtenue ».

En bref

Citations1
Publié2025
Routes d'admission1
Résumé présentoui

Explorer davantage

Même revueFrontiers in Marine ScienceMême sujetMarine and coastal plant biologyTravaux en français237 207