Sébastien Villéger’s research while affiliated with French National Centre for Scientific Research and other places

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Publications (174)


Figure 1: Covariations and dimensionality of twenty-nine fish-based contributions to Nature (green) and People (blue) on tropical reefs worldwide.
The covariations of contributions are represented in the two first PCA axes (Mg = Magnesium, N = Nitrogen, P = Phosphorus). Total fish biomass, reported by color gradient, increases with the first dimension of the PCA (A and B). (A) and (B) represent the same PCA, yet contributions are highlighted in color according to their classification: either Nature-for-Nature (A), or Nature-for-People (B). (A) Only well-represented contributions are displayed (cos² > 0.25): phylogenetic entropy, evolutionary distinctiveness and elasmobranch diversity are not represented. The inset displays eigenvalues of PCA axis in percent, and the cumulative curve of variance explained. The black dot represents the dimensionality required to parsimoniously describe covariations of contributions according to the elbow method (9 dimensions, 84% of variance explained; see Fig. S3). (B) All contributions are represented. (C) Dot sizes are proportional to the importance of a contribution in the total variance for a given PCA axis. Gray background indicates negative correlation with the dimension, white background indicates positive correlation. The importance of PCA dimensions in the total variance is reported as a percentage below. To see the PCA-biplot with all contributions and color-blind friendly colors, refer to Fig. S4.
Figure 2. The four corners of the NN vs. NP spectrum and management strategies (A) At the global scale, NN and NP scores are weakly correlated (r = 0.24, p < 0.001). The dashed lines indicate for each color the 50% quantile of the NN 3 NS gradient. Therefore, the dashed curved lines encompass 50% of the reefs. Symbols for reefs that are 5% outliers of each quarter are highlighted with black borders (see Figure S7 for details of outliers). (B) Protection status (no-take reserves, restricted areas, fished areas) does not strongly influence reef categories in the NN-NP space (chi-squared = 28.2, df = 6, p < 0.01, Cramer's V = 0.11). (C) Geographic distribution of the 5% of reef outliers in each NN-NP category and their management status.
Figure 3: Human well-being in Nature: which future for tropical reefs?
The four parts defined by the gradient of Nature protection and exploitation illustrate different possible futures, exposed by the NFF.6 “Optimizing nature for humans / Innovative commons” proposes a bio-cultural and social future where societies exploit whatever is necessary for human well-being as long as it is sustainable. “Arcology” calls for a future where people are concentrated in dense, futuristic, self-sufficient cities, surrounded by totally pristine nature. Between both, “Sharing through sparing” depicts a future where people exploit as little of nature as possible for their well-being and safeguards the remainder. Possible dynamics are highlighted in orange and red.
Table 1: Nature contributions used in this study. We divided the 29 fish-based contributions into two categories: Nature contribution for Nature (NN) and for People (NP). All metrics were calculated at the reef fish community level using data from standardized reef fish surveys. We assumed that the values of each contribution scale positively with its benefit to people or nature. Contributions identified by (*) have been log-transformed to limit the effect of asymmetric and high-magnitude distributions (see table S1 for calculation details and data sources).
Fish communities can simultaneously contribute to nature and people across the world’s tropical reefs
  • Article
  • Full-text available

October 2024

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466 Reads

One Earth

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Anthropogenic activities are eroding biodiversity and its contributions to nature and people worldwide. Yet, the dual imperative to protect nature and sustain human well-being raises potential trade-offs that remain to be quantified. Using standardized fish surveys across 1,237 tropical reefs worldwide, we converted the presence and abundance data of 1,024 species into 29 fish community contributions that primarily benefit either nature or people. We show that “Nature-for-Nature” contributions are mostly positively correlated to total fish biomass, while “Nature-for-People” contributions are more independent. Trade-offs among contributions are not the rule, with some tropical fish communities simultaneously providing high levels of different contributions. High mean contributions have been found in all tropical oceans, so sustaining healthy tropical reefs while promoting human well-being seems achievable within most countries, rather than mutually exclusive. Our framework offers an opportunity to explore different management strategies and pathways on tropical reefs between the use and sparing of nature, towards more favorable and sustainable ecological and social futures.

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Inferring the extinction risk of marine fish to inform global conservation priorities

August 2024

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297 Reads

While extinction risk categorization is fundamental for building robust conservation planning for marine fishes, empirical data on occurrence and vulnerability to disturbances are still lacking for most marine teleost fish species, preventing the assessment of their International Union for the Conservation of Nature (IUCN) status. In this article, we predicted the IUCN status of marine fishes based on two machine learning algorithms, trained with available species occurrences, biological traits, taxonomy, and human uses. We found that extinction risk for marine fish species is higher than initially estimated by the IUCN, increasing from 2.5% to 12.7%. Species predicted as Threatened were mainly characterized by a small geographic range, a relatively large body size, and a low growth rate. Hotspots of predicted Threatened species peaked mainly in the South China Sea, the Philippine Sea, the Celebes Sea, the west coast Australia and North America. We also explored the consequences of including these predicted species’ IUCN status in the prioritization of marine protected areas through conservation planning. We found a marked increase in prioritization ranks for subpolar and polar regions despite their low species richness. We suggest to integrate multifactorial ensemble learning to assess species extinction risk and offer a more complete view of endangered taxonomic groups to ultimately reach global conservation targets like the extending coverage of protected areas where species are the most vulnerable.


Refocusing the microbial rare biosphere concept through a functional lens

July 2024

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275 Reads

Trends in Ecology & Evolution

The influential concept of the rare biosphere in microbial ecology has underscored the importance of taxa occurring at low abundances yet potentially playing key roles in communities and ecosystems. Here, we refocus the concept of rare biosphere through a functional trait-based lens and provide a framework to characterize microbial functional rarity, a combination of numerical scarcity across space or time and trait distinctiveness. We demonstrate how this novel interpretation of the rare biosphere, rooted in microbial functions, can enhance our mechanistic understanding of microbial community structure. It also sheds light on functionally distinct microbes, directing conservation efforts towards taxa harboring rare yet ecologically crucial functions.


A new framework for estimating abundance of animals using a network of cameras

March 2024

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62 Reads

While many ecology studies require estimations of species abundance, doing so for mobile animals in an accurate, non‐invasive manner remains a challenge. One popular stopgap method involves the use of remote video‐based surveys using several cameras, but abundance estimates derived from this method are computed with conservative metrics (e.g., maxN computed as the maximum number of individuals seen simultaneously on a single video). We propose a novel methodological framework based on a remote‐camera network characterized by known positions and non‐overlapping field‐of‐views. This approach involves a temporal synchronization of videos and a maximal speed estimate for studied species. Such a design allows computing a new abundance metric called Synchronized maxN ( SmaxN ). We provide a proof‐of‐concept of this approach with a network of nine remote underwater cameras that recorded fish for three periods of 1 h on a fringing reef in Mayotte (Western Indian Ocean). We found that abundance estimation with SmaxN yielded up to four times higher values than maxN among the six fish species studied. SmaxN performed better with an increasing number of cameras or longer recordings. We also found that using a network of synchronized cameras for a short time period performed better than using a few cameras for a long duration. The SmaxN algorithm can be applied to many video‐based approaches. We built an open‐sourced R package to encourage its use by ecologists and managers using video‐based censuses, as well as to allow for replicability with SmaxN metric.


Automated identification of invasive rabbitfishes in underwater images from the Mediterranean Sea

January 2024

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55 Reads

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1 Citation

Aquatic Conservation Marine and Freshwater Ecosystems

Coastal ecosystems of the Mediterranean Sea are among the richest in non‐indigenous species, mostly due to the establishment of species coming from the Red Sea through the Suez Canal. Two herbivorous rabbitfishes, Siganus rivulatus and Siganus luridus , are already invasive in the south‐eastern part of the Mediterranean Sea where they cause ecological damage by overgrazing algae. The early detection and the counting of these non‐indigenous species in the rest of the Mediterranean Sea is thus a major challenge for scientists and ecosystem managers. However, analysing images from divers or remote cameras is a demanding task. Here, a dataset of 31,285 images of Siganus spp. and of six common native fishes to the Mediterranean Sea was built from 40 underwater videos recorded at three reef habitats. A deep learning algorithm was then trained to identify Siganus spp. on images containing the eight Mediterranean species. Finally, the algorithm and a post‐processing filtering were tested with an independent dataset of 2024 images. The model had a recall of 0.92 for the Siganus genus (i.e., two Siganus species combined). After a confidence‐based post‐processing, the recall increased to 0.98 with only 4 out of 272 images of Siganus spp. being misclassified. Accuracy reached a score of 0.61 meaning that experts would have to discard false positives. Images of five native species not present in the training dataset yielded similar false positive rates than species present in the training dataset. Overall, the automatic processing of images by the model and then the checking of putative Siganus images by experts required up to five times less effort than a full processing by experts. The algorithm can help to efficiently detect these two invasive fishes in underwater images to evaluate progress towards conservation objectives and accelerate citizen‐based monitoring of coastal ecosystems.



Functional changes across marine habitats due to ocean acidification

January 2024

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439 Reads

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7 Citations

Global Change Biology

Global environmental change drives diversity loss and shifts in community structure. A key challenge is to better understand the impacts on ecosystem function and to connect species and trait diversity of assemblages with ecosystem properties that are in turn linked to ecosystem functioning. Here we quantify shifts in species composition and trait diversity associated with ocean acidification (OA) by using field measurements at marine CO 2 vent systems spanning four reef habitats across different depths in a temperate coastal ecosystem. We find that both species and trait diversity decreased, and that ecosystem properties (understood as the interplay between species , traits, and ecosystem function) shifted with acidification. Furthermore, shifts in trait categories such as autotrophs, filter feeders, herbivores, and habitat-forming species were habitat-specific, indicating that OA may produce divergent responses across habitats and depths. Combined, these findings reveal the importance of connecting species and trait diversity of marine benthic habitats with key ecosystem properties to anticipate the impacts of global environmental change. Our results also generate new insights on the predicted general and habitat-specific ecological consequences of OA.


Detecting benefits of protection level on diversity facets in a sea of temporal scarcity

January 2024

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51 Reads

Aquatic Conservation Marine and Freshwater Ecosystems

The establishment of protected areas to face global diversity declines has mainly prioritized taxonomic diversity, leaving aside phylogenetic and functional diversities, which determine ecosystem functioning and resilience. Furthermore, the assessment of protected areas' effectiveness is mainly done using short‐duration surveys (<2 h), which may undermine the detection of rare species. Through a long‐duration video approach, reef fish taxonomic, phylogenetic and functional facets of diversity were assessed for 3 days within a fully protected area and a nearby poorly protected area in Mayotte Island (Western Indian Ocean). We found that temporally rare species contributed to more than 60% of the taxonomic facet and 85% of the functional facet of biodiversity found on each site. Those rare species, which harbour the most distinct trait values, also make reef fish diversity particularly vulnerable to their loss. Taxonomic, phylogenetic and functional richness were similar between the fully protected area and the poorly protected area, while the species, lineage and trait compositions were markedly different. These results pinpoint the importance of considering taxonomic, functional and phylogenetic dissimilarities while assessing protected areas' effectiveness, instead of using only richness. In addition, benefits of the fully protected area were detected only using more than 15 h of video survey, which emphasizes the importance of long‐duration remote approaches to capture the within‐ and between‐day temporal variations.


Variation in the number of bites across trophic groups and sites. The number of bites by all fish from a trophic group was counted for 5-min sequences over 10 m² (5 quadrats of 2 m² surveyed each by a camera)
Heatmaps of corallivores (a), herbivores (b) and invertivores (c) feeding activities. Colors reflect the number of bites recorded on 10 m² for five minutes. Classes were defined to represent one eighth of the span of the feeding activity recorded across the two sites. The top row of each feeding activity is the heatmap of N’Gouja, while the bottom row reflects the heatmap of Bouéni. Dark vertical bars represent the delimitations of the time slots (07:30–08:30, 11:45–12:45, 16:00–17:00)
Total bite number per species for each feeding activity and site. Corallivory (a), herbivory (b), and invertivory (c) are expressed per species (y axis) as the overall number of bites across all 24 sequences of 5 min over 10 m² (x axis). For each of the three feeding activities, the left plot represents data for N’Gouja and the right plot represents data for Bouéni. Bars are colored if the species is only seen in the N’Gouja (green) or in Bouéni (brown) and are gray if present on both sites
Species contribution to the five sequences showing the highest feeding activities. Corallivory (a), herbivory (b), and invertivory (c) are expressed as the number of bites per five minutes per 10 m² (y axis). Colors represent species contributions in decreasing numbers of bites per unit of time. Species gathered as “Others” are species whose activity represented less than 10% of the total activity of the feeding event. For each of the three feeding activities, the left graph represents data for N’Gouja reef and the right one represents data for Bouéni reef
Remote video surveys unveil the diurnal variability of trophic-based processes by fishes on coral reefs

October 2023

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73 Reads

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2 Citations

Coral Reefs

Feeding activities by fishes are among the key ecological processes that sustain coral reef functioning. Those trophic-based processes are known to vary across space and across seasons or years. However, there is still little knowledge about their variability within and between days as well as whether these processes are dominated by the same species across time. Using remote underwater cameras, we quantified rates of three feeding activities (corallivory, herbivory and invertivory) for three one-hour time slots (morning, midday, afternoon) over two days on two coral reefs around Mayotte Island (Western Indian Ocean). Feeding activities were highly variable at within and between-day scales and concentrated in a few pulses. Herbivory was the highest in the afternoon which aligns with previous findings regarding activity of herbivorous fishes. Corallivory was the highest in the morning, which highlights the advantage of long-duration benthic remote underwater videos to accurately assess all trophic activities. Trophic-related processes were dominated by the same few species in both sites and across time of the day. This study pinpoints the importance of including within-day and between-day variations when studying ecological processes, as neglecting these variations may introduce biases into our understanding of these processes.


Citations (72)


... 0 E). S. smaris males build their nest on soft bottoms seabed. Spawning ground covers large areas (2.2-28 ha) from the lower limit of Posidonia oceanica (Delile 1813) seagrass meadows to near −50 m depth (Andromède océanologie, 2023, 2024; Deter et al., 2024). This video was therefore captured in this zone, over a substrate made of coarse sand. ...

Reference:

Sound production in wild Mediterranean blonde ray Raja brachyura
Gigantic breeding colonies of a marine fish in the Mediterranean

Current Biology

... Biodiversity in diverse ecosystems is increasingly under threat due to rapid global changes. Notably, global warming and the introduction of invasive alien species (IAS) and non-indigenous species (NIS) often act in tandem, aggravating their impact on ecosystems [1]. The Mediterranean coastal regions are a prime example of these biodiversity changes. ...

Automated identification of invasive rabbitfishes in underwater images from the Mediterranean Sea
  • Citing Article
  • January 2024

Aquatic Conservation Marine and Freshwater Ecosystems

... Natural marine volcanic vent systems release CO 2 into the water column, locally acidifying the seawater to pH levels expected later this century [16]. At CO 2 vents in Papua New Guinea and Ischia, Italy, species richness, habitat complexity, and functional diversity decrease with decreasing pH along natural gradients [17][18][19], with calcifying species being most affected [16][17][18][19][20]. In Ischia, two species of coral, the symbiotic Cladocora caespitosa and the asymbiotic Astroides calycularis, have recently been found growing near CO 2 vents [18,21]. ...

Functional changes across marine habitats due to ocean acidification

Global Change Biology

... The current special issue explores the growing diversity of methods for quantifying reef functions, including videobased methods (Collins et al. 2023;Magneville et al. 2023), or the integration of remote-sensing ; two areas in which information on reef functions has benefited greatly from technological advances (e.g. DiFiore et al. 2019; Madin et al. 2019;Schiettekatte et al. 2022b). ...

Remote video surveys unveil the diurnal variability of trophic-based processes by fishes on coral reefs

Coral Reefs

... Reef planktivores typically account for a large proportion of daily fish production in reef systems , harvesting allochthonous nutrient subsidies that allow to bypass local energetic constraints imposed by nutrient-poor and/or degraded reef environments (Campbell et al., 2020;Gove et al., 2016;Morais et al., 2021). Although the specific mechanisms require further investigation, reef planktivores might be facilitating the recovery of fish populations on the volcanic delta through (i) fertilizing benthic habitats with highly nutritious detritus via fish faeces (Rempel et al., 2022;Schiettekatte et al., 2023) and (ii) serving as prey for large piscivorous fishes (Skinner et al., 2019). ...

The role of fish feces for nutrient cycling on coral reefs

Oikos

... In England, over six million non-native common carp Cyprinus carpio were consented by the fishery regulator to be released into inland waters for angling between 1998 and 2008 (Britton et al., 2010), despite recognition that this species is an ecological engineer that has strong bottom-up and top-down effects (Britton, 2022;Carvalho & Moss, 1995;Skeate et al., 2022). These stocked fishes can alter the tangled-web by modifying the patterns of size distribution in communities, trophic-structuring (inverting the trophic pyramid by releasing individuals of relatively high trophic position ;Eby et al., 2006) and functional, genotype and phenotype diversity (Gimenez et al., 2023; Figure 1). The release of hatchery-reared and domesticated fishes can lead to the presence of individuals that can behave differently to the resident conspecifics (Cucherousset & Olden, 2020), and these stocked conspecifics can have stronger ecological impacts than alien fishes through their higher abundances (Buoro et al., 2016). ...

Stocking practices shape the taxonomic and functional diversity of fish communities in gravel pit lakes

Fisheries Management and Ecology

... For instance, null models and hierarchical modeling of species communities (HMSC) can be used to determine the dominant processes in fish communities based on functional traits to guide conservation strategies (Mori et al. 2015;Montanyès, Weigel, and Lindegren 2023). With accurate species trait databases, eDNA metabarcoding can effectively detect the functional diversity and trait composition of fish communities (Marques et al. 2021;Condachou et al. 2023). Recently, some studies have shown great potential for incorporating eDNA into the inference of ecological processes in fish communities, such as determining the main driving processes of river fish community assembly at the watershed level (Gu et al. 2023;Shi et al. 2023;Li et al. 2024). ...

Inferring functional diversity from environmental DNA metabarcoding

... These findings highlight that fish abundance alone does not accurately reflect herbivory activity (Bejarano et al., 2017;Fox and Bellwood, 2008;Magneville et al., 2023). ...

Long‐duration remote underwater videos reveal that grazing by fishes is highly variable through time and dominated by non‐indigenous species

... The physical structure of a coral reef often comprises contiguous and distinct habitat zones, such as the fringing reef, shallow back reef lagoon, reef crest, and different depths on fore reef slope (Goreau, 1959;Huston, 1985). These habitat zones are well known to differ in multiple environmental factors such as light, turbidity, wave energy, current speed, temperature, and nutrients, and to comprise distinct coral reef communities as a result (Burgess et al., 2010;Connolly et al., 2005;Guadayol et al., 2014;Johnston, Wyatt, et al., 2022;Karlson & Cornell, 1998;Pérez-Rosales et al., 2022;Reid et al., 2019;Wyatt et al., 2020Wyatt et al., , 2023. Habitat zones are also differentially affected by disturbances, such as heatwaves, cyclones, coralivorous Crown-of-Thorns seastar outbreaks, land-based pollution, and over-fishing (Baird et al., 2018;Crosbie et al., 2019;Donovan et al., 2020;Penin et al., 2007;Sully & van Woesik, 2020). ...

Mesophotic coral ecosystems of French Polynesia are hotspots of alpha and beta generic diversity for scleractinian assemblages

... In addition to coral reefs, fish-associated fauna are one of the most studied groups in deep habitats (Ajemian et al. 2015;. Recently, Loiseau et al. (2022) proposed five different categories to describe the refuge potential of deep reefs based on fish assemblages: (1) not refugia (the taxonomic and functional diversity of fish in shallow and deep reefs are completely different), (2) partial refugia (deep reefs are equally or less diverse than shallow reefs, but both contain exclusive species and traits), (3) functional refugia (only functional diversity is similar between shallow and deep reefs), (4) full refugia (shallow and deep reefs exhibit the same taxonomic and functional diversity), and (5) enriched refugia (deep reefs have the same diversity as shallow reefs and also contain exclusive species and traits). When analyzing a particular case in the Indian Ocean, the authors found that functional richness was similar between shallow and deep reefs, despite the significant decrease in fish species richness and biomass as depth increased. ...

Mesophotic reefs are not refugia for neither taxonomic nor functional diversity of reef fishes

Coral Reefs