Click
here to close Hello! We notice that
you are using Internet Explorer, which is not supported by Echinobase
and may cause the site to display incorrectly. We suggest using a
current version of Chrome,
FireFox,
or Safari.
PLoS One
2019 Feb 22;142:e0212485. doi: 10.1371/journal.pone.0212485.
Show Gene links
Show Anatomy links
The impact of fishing on a highly vulnerable ecosystem, the case of Juan Fernández Ridge ecosystem.
Porobic J
,
Fulton EA
,
Parada C
,
Frusher S
,
Ernst B
,
Manríquez P
.
???displayArticle.abstract???
The Juan Fernández Ridge (JFRE) is a vulnerable marine ecosystem (VME) located off the coast of central Chile formed by the Juan Fernández Archipelago and a group of seamounts. This ecosystem has unique biological and oceanographic features, characterized by: small geographical units, high degree of endemism with a high degree of connectivity within the system. Two fleets have historically operated in this system: a long term coastal artisanal fishery associated with the Islands, focused mainly on lobster, and a mainland based industrial demersal finfish fishery operating on the seamounts which is currently considered overexploited. The management of these fisheries has been based on a classical single-species approach to determine output controls (industrial fleet) and a mixed management system with formal and informal components (artisanal fleet). There has been growing interest in increasing the exploitation of fisheries, and modernization of the fishing fleet already operating in the JFRE. Under this scenario of increased levels of fishing exploitation and the high level of interrelation of species it might be necessary to understand the impact of these fisheries from a holistic perspective based on a ecosystem-based modeling approach. To address these challenges we developed an Atlantis end-to-end model was configured for this ecosystem. The implemented model has a high degree of skill in representing the observed trends and fluctuations of the JFRE. The model shows that the industrial fishing has a localized impact and the artisanal fisheries have a relatively low impact on the ecosystem, mainly via the lobster fishery. The model indicates that the depletion of large sized lobster has leads to an increase in the population of sea urchins. Although this increase is not sufficient, as yet, to cause substantial flow-on effects to other groups, caution is advised in case extra pressure leads the ecosystem towards a regime shift.
???displayArticle.pubmedLink???
30794609
???displayArticle.pmcLink???PMC6386342 ???displayArticle.link???PLoS One
Fig 1. Atlantis JFRE model domain.The red square represents the area of coverage of the hydrodynamic OFES model subset. The maps in the left represent the characteristics that were considered for the division of the polygons: The geographic structure of the ridge (Islands and seamounts); Management area (Marine parks and Marine protected areas with multiple uses; MPA-MU); and areas of influence of fishing activity (Industrial and artisanal fleets).
Fig 2. The left side includes the main components (biological, physical and economic) and forcings that were considered for the JFRE model.The flowchart shows that the model runs for 35 years if after this period the model is dynamically stable it creates a new initial condition at equilibrium. When the model is already dynamically stable, the calibration process is performed to represent the conditions observed in the ecosystem.
Fig 3. In the left column are presented the time series of the biomass relative to the initial biomass of an unfished (blue line) and fished (yellow line) ecosystem.The first three rows of the right column represents the time series of simulated catches in Atlantis (red line) and observed (gray dots). For the Fur seal, the dots represented the observed abundance and the red line is the estimated abundance from Atlantis.
Fig 4. Food web of the Juan Fernández Ridge ecosystem.The code representing the functional groups can be found in Table 1.
Fig 5. Relative change in biomass (A) and abundance (B) for the scenarios with only artisanal, industrial and the historical fisheries (industrial + artisanal). An unfished ecosystem is the base case for comparisons. Note that the y-axes is the ratio of change against the starting conditions—so a -0.5 result indicates a 50% decrease and a 0.5 result indicates a 50% increase -.
Fig 6. Summary of the catch distribution for the total bait caught from artisanal fisheries (A)), the total artisanal bycatch (B)) and the industrial bycatch (C)). The upper and lower limits of boxes represent the 25th and the 75th percentile and the middle line the 50th percentile of the data distribution. The whiskers represent the range of the catches.
Fig 7. Relative change in biomass (A) and abundance (B) for the business as usual (BAU), a 50% increase in fishing effort of crustaceans (ICRUS50%), 50% increase in fishing effort for crustaceans and finfish (IBoth50%) and 100% increase in fishing effort for finfish (IFish100%). An unfished ecosystem is the base case for comparisons. Note that the y-axes is the ratio of change against the starting conditions—so a -0.5 result indicates a 50% decrease and a 0.5 result indicates a 50% increase -.
Fig 8. Relative change in catch for the last 20 years of projection for 50% increase in fishing effort of crustaceans (ICRUS50%), a 50% increase in fishing effort for crustaceans and finfish (IBoth50%) and 100% increase in fishing effort for finfish (IFish100%).The catches from a business as usual scenario is the base case for comparisons. Note that the y-axes is the ratio of change against the starting conditions—so a -0.5 result indicates a 50% decrease and a 0.5 result indicates a 50% increase -.
Clark,
The ecology of seamounts: structure, function, and human impacts.
2010, Pubmed
Clark,
The ecology of seamounts: structure, function, and human impacts.
2010,
Pubmed
Dunn,
Hypotheses of spatial stock structure in orange roughy Hoplostethus atlanticus inferred from diet, feeding, condition, and reproductive activity.
2011,
Pubmed
Friedlander,
Marine Biodiversity in Juan Fernández and Desventuradas Islands, Chile: Global Endemism Hotspots.
2016,
Pubmed
,
Echinobase
Góes,
Natural diet of the spiny lobster, Panulirus echinatus Smith, 1869 (Crustacea: Decapoda: Palinuridae), from São Pedro and São Paulo Archipelago, Brazil.
2009,
Pubmed
Halpern,
Spatial and temporal changes in cumulative human impacts on the world's ocean.
2015,
Pubmed
Heath,
Cascading ecological effects of eliminating fishery discards.
2014,
Pubmed
Horn,
Feeding habits of alfonsino Beryx splendens.
2010,
Pubmed
Levin,
Integrated ecosystem assessments: developing the scientific basis for ecosystem-based management of the ocean.
2009,
Pubmed
Ling,
Overfishing reduces resilience of kelp beds to climate-driven catastrophic phase shift.
2009,
Pubmed
,
Echinobase
Loh,
Indirect effects of overfishing on Caribbean reefs: sponges overgrow reef-building corals.
2015,
Pubmed
Olsen,
Ecosystem Model Skill Assessment. Yes We Can!
2016,
Pubmed
Porobic,
Biogeography and historical demography of the Juan Fernandez Rock Lobster, Jasus frontalis (Milne Edwards, 1837).
2013,
Pubmed
Worm,
Rebuilding global fisheries.
2009,
Pubmed